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The cardiac cycle and the effects of neurohumors on myocardial contractility in the Asiatic eel Anguilla japonica, Timm. & Schle. | 52(1) | 41-5 | Comparative biochemistry and physiology. C: Comparative pharmacology | [
{
"affiliation": "",
"forename": "P H",
"identifier": "",
"initials": "PH",
"lastname": "Chow"
},
{
"affiliation": "",
"forename": "D K",
"identifier": "",
"initials": "DK",
"lastname": "Chan"
}
] | 1975-10-01 | 201 | D000109:Acetylcholine / Q000494:pharmacology*; D000818:Animals; D001794:Blood Pressure / Q000187:drug effects; D004524:Eels / Q000502:physiology*; D006321:Heart / Q000187:drug effects / Q000502:physiology*; D006339:Heart Rate / Q000187:drug effects; D006352:Heart Ventricles / Q000187:drug effects; D009200:Myocardial Contraction / Q000187:drug effects*; D009638:Norepinephrine / Q000494:pharmacology*; D016276:Ventricular Function | D016428:Journal Article | D000109:Acetylcholine; D009638:Norepinephrine | 10.1016/0306-4492(75)90010-6 | [] | false | eng | Comp Biochem Physiol C Comp Pharmacol | 7503763 | 0306-4492 | England | [] | "2024-08-13T15:33:32.631087Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Characteristics of the noradrenergic innervation of the left atrium in the chick (Gallus gallus domesticus, L.). | 52(1) | 47-9 | Comparative biochemistry and physiology. C: Comparative pharmacology | [
{
"affiliation": "",
"forename": "T",
"identifier": "",
"initials": "T",
"lastname": "Bennett"
},
{
"affiliation": "",
"forename": "T",
"identifier": "",
"initials": "T",
"lastname": "Malmfors"
}
] | 1975-10-01 | 202 | D000818:Animals; D016275:Atrial Function; D002645:Chickens / Q000502:physiology*; D003042:Cocaine / Q000494:pharmacology*; D006321:Heart / Q000294:innervation; D006325:Heart Atria / Q000187:drug effects; D006329:Heart Conduction System / Q000187:drug effects / Q000502:physiology; D009200:Myocardial Contraction / Q000187:drug effects; D010643:Phenoxybenzamine / Q000494:pharmacology*; D012601:Scopolamine / Q000494:pharmacology* | D016428:Journal Article | D010643:Phenoxybenzamine; D012601:Scopolamine; D003042:Cocaine | 10.1016/0306-4492(75)90011-8 | [] | false | eng | Comp Biochem Physiol C Comp Pharmacol | 7503763 | 0306-4492 | England | [] | "2024-08-13T15:33:32.632136Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Responsiveness of neurogenic hearts to octopamine. | 52(1) | 5-8 | Comparative biochemistry and physiology. C: Comparative pharmacology | [
{
"affiliation": "",
"forename": "D S",
"identifier": "",
"initials": "DS",
"lastname": "Grega"
},
{
"affiliation": "",
"forename": "R G",
"identifier": "",
"initials": "RG",
"lastname": "Sherman"
}
] | 1975-10-01 | 203 | D000818:Animals; D001097:Arachnida / Q000502:physiology; D004305:Dose-Response Relationship, Drug; D006321:Heart / Q000187:drug effects / Q000502:physiology*; D006339:Heart Rate / Q000187:drug effects; D008121:Nephropidae / Q000502:physiology; D009655:Octopamine / Q000494:pharmacology*; D013045:Species Specificity; D013112:Spiders / Q000502:physiology | D016428:Journal Article | D009655:Octopamine | 10.1016/0306-4492(75)90003-9 | [] | false | eng | Comp Biochem Physiol C Comp Pharmacol | 7503763 | 0306-4492 | England | [
{
"agency": "Medical Research Council",
"country": "United Kingdom",
"grant_acronym": "MRC_",
"grant_id": "G1002279"
}
] | "2024-08-13T15:33:32.633122Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Action of kainic acid on a glutamatergic synapse. | 52(1) | 51-3 | Comparative biochemistry and physiology. C: Comparative pharmacology | [
{
"affiliation": "",
"forename": "A",
"identifier": "",
"initials": "A",
"lastname": "Daoud"
},
{
"affiliation": "",
"forename": "P N",
"identifier": "",
"initials": "PN",
"lastname": "Usherwood"
}
] | 1975-10-01 | 204 | D000818:Animals; D005071:Evoked Potentials / Q000187:drug effects; D005971:Glutamates / Q000494:pharmacology*; D006110:Grasshoppers; D009119:Muscle Contraction / Q000187:drug effects; D009469:Neuromuscular Junction / Q000187:drug effects / Q000502:physiology*; D011759:Pyrrolidines / Q000494:pharmacology*; D013569:Synapses / Q000187:drug effects / Q000502:physiology* | D016428:Journal Article | D005971:Glutamates; D011759:Pyrrolidines | 10.1016/0306-4492(75)90012-x | [] | false | eng | Comp Biochem Physiol C Comp Pharmacol | 7503763 | 0306-4492 | England | [] | "2024-08-13T15:33:32.633934Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
The effects of 5-hydroxytryptamine depletors and monoamine oxidase inhibitors on color changes of the fiddler crab, Uca pugilator: further evidence in support of the hypothesis that 5-hydroxytryptamine controls the release of red pigment-dispersing hormone. | 52(1) | 55-9 | Comparative biochemistry and physiology. C: Comparative pharmacology | [
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Fingerman"
},
{
"affiliation": "",
"forename": "S W",
"identifier": "",
"initials": "SW",
"lastname": "Fingerman"
}
] | 1975-10-01 | 205 | D000064:Acclimatization; D000818:Animals; D003386:Brachyura / Q000187:drug effects / Q000502:physiology*; D002856:Chromatophores / Q000187:drug effects / Q000502:physiology*; D003116:Color; D005260:Female; D010134:Fenclonine / Q000494:pharmacology*; D006728:Hormones / Q000502:physiology; D007490:Iproniazid / Q000494:pharmacology*; D008996:Monoamine Oxidase Inhibitors / Q000494:pharmacology*; D009526:Nialamide / Q000494:pharmacology*; D012110:Reserpine / Q000494:pharmacology*; D012702:Serotonin Antagonists; D013997:Time Factors | D016428:Journal Article; D013486:Research Support, U.S. Gov't, Non-P.H.S. | D006728:Hormones; D008996:Monoamine Oxidase Inhibitors; D012702:Serotonin Antagonists; D012110:Reserpine; D007490:Iproniazid; D010134:Fenclonine; D009526:Nialamide | 10.1016/0306-4492(75)90013-1 | [] | false | eng | Comp Biochem Physiol C Comp Pharmacol | 7503763 | 0306-4492 | England | [] | "2024-08-13T15:33:32.635915Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Evidence of a gastrin-like substance in Rhinobatus productus. | 52(1) | 61-3 | Comparative biochemistry and physiology. C: Comparative pharmacology | [
{
"affiliation": "",
"forename": "D",
"identifier": "",
"initials": "D",
"lastname": "Hansen"
}
] | 1975-10-01 | 206 | D000818:Animals; D001681:Biological Assay; D004305:Dose-Response Relationship, Drug; D005260:Female; D005399:Fishes / Q000378:metabolism*; D005753:Gastric Mucosa / Q000032:analysis / Q000378:metabolism; D005755:Gastrins / Q000032:analysis* / Q000378:metabolism; D009132:Muscles / Q000032:analysis / Q000378:metabolism; D009928:Organ Specificity; D010418:Pentagastrin / Q000378:metabolism; D051381:Rats; D013045:Species Specificity; D013270:Stomach / Q000032:analysis; D013552:Swine | D016428:Journal Article | D005755:Gastrins; D010418:Pentagastrin | 10.1016/0306-4492(75)90014-3 | [] | false | eng | Comp Biochem Physiol C Comp Pharmacol | 7503763 | 0306-4492 | England | [
{
"agency": "Medical Research Council",
"country": "United Kingdom",
"grant_acronym": "MRC_",
"grant_id": "MR/K000608/1"
}
] | "2024-08-13T15:33:32.636813Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
5-hydroxytryptamine as a possible inhibitory neurotransmitter in the central nervous system of the leech, Haemopis sanguisuga. | 52(1) | 65-73 | Comparative biochemistry and physiology. C: Comparative pharmacology | [
{
"affiliation": "",
"forename": "P A",
"identifier": "",
"initials": "PA",
"lastname": "Smith"
},
{
"affiliation": "",
"forename": "J T",
"identifier": "",
"initials": "JT",
"lastname": "Fitzsimons"
},
{
"affiliation": "",
"forename": "J E",
"identifier": "",
"initials": "JE",
"lastname": "Loker"
},
{
"affiliation": "",
"forename": "R J",
"identifier": "",
"initials": "RJ",
"lastname": "Walker"
}
] | 1975-10-01 | 207 | D002490:Central Nervous System / Q000187:drug effects / Q000502:physiology*; D005724:Ganglia / Q000187:drug effects / Q000502:physiology / Q000648:ultrastructure; D007099:Imipramine / Q000494:pharmacology; D007865:Leeches / Q000502:physiology*; D008854:Microscopy, Electron; D008856:Microscopy, Fluorescence; D009020:Morphine / Q000494:pharmacology; D009474:Neurons / Q000187:drug effects / Q000502:physiology; D012701:Serotonin / Q000494:pharmacology* | D016428:Journal Article | D012701:Serotonin; D009020:Morphine; D007099:Imipramine | 10.1016/0306-4492(75)90015-5 | [] | false | eng | Comp Biochem Physiol C Comp Pharmacol | 7503763 | 0306-4492 | England | [] | "2024-08-13T15:33:32.637659Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Gastrin-like activity in an Indian python. | 52(1) | 9-10 | Comparative biochemistry and physiology. C: Comparative pharmacology | [
{
"affiliation": "",
"forename": "M O",
"identifier": "",
"initials": "MO",
"lastname": "Olowo-Okorun"
}
] | 1975-10-01 | 208 | D000818:Animals; D005260:Female; D005755:Gastrins / Q000378:metabolism*; D006632:Histamine / Q000032:analysis; D007413:Intestinal Mucosa / Q000032:analysis / Q000378:metabolism; D011708:Pylorus / Q000032:analysis / Q000378:metabolism; D012911:Snakes / Q000378:metabolism* | D016428:Journal Article | D005755:Gastrins; D006632:Histamine | 10.1016/0306-4492(75)90004-0 | [] | false | eng | Comp Biochem Physiol C Comp Pharmacol | 7503763 | 0306-4492 | England | [] | "2024-08-13T15:33:32.638595Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Kinetics of antibody--hapten reactions. | 4() | 23-54 | Contemporary topics in molecular immunology | [
{
"affiliation": "",
"forename": "A",
"identifier": "",
"initials": "A",
"lastname": "Froese"
},
{
"affiliation": "",
"forename": "A H",
"identifier": "",
"initials": "AH",
"lastname": "Sehon"
}
] | 1975 | 209 | D000937:Antigen-Antibody Reactions; D001666:Binding Sites, Antibody; D004140:Dinitrophenols / Q000276:immunology; D006241:Haptens / Q000032:analysis / Q000276:immunology*; D006863:Hydrogen-Ion Concentration; D007140:Immunoglobulin Fab Fragments / Q000032:analysis; D007158:Immunologic Techniques; D007700:Kinetics; D011487:Protein Conformation | D016428:Journal Article; D016454:Review | D004140:Dinitrophenols; D006241:Haptens; D007140:Immunoglobulin Fab Fragments | [] | false | eng | Contemp Top Mol Immunol | 0363025 | 0090-8800 | United States | [] | "2024-08-13T15:33:32.639240Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
Effects of maleate on renal reabsorption of bicarbonate. | 4() | 101-5 | Current problems in clinical biochemistry | [
{
"affiliation": "",
"forename": "P",
"identifier": "",
"initials": "P",
"lastname": "Gmaj"
},
{
"affiliation": "",
"forename": "A",
"identifier": "",
"initials": "A",
"lastname": "Hoppe"
},
{
"affiliation": "",
"forename": "S",
"identifier": "",
"initials": "S",
"lastname": "Angielski"
},
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "Rogulski"
},
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Metler"
}
] | 1975 | 211 | D000086:Acetazolamide / Q000494:pharmacology; D000255:Adenosine Triphosphate / Q000378:metabolism; D000818:Animals; D001151:Arsenic / Q000494:pharmacology; D001639:Bicarbonates / Q000378:metabolism*; D002712:Chlorides / Q000652:urine; D005919:Glomerular Filtration Rate / Q000187:drug effects; D006863:Hydrogen-Ion Concentration; D007656:Ketoglutaric Acids / Q000652:urine; D007668:Kidney / Q000187:drug effects / Q000378:metabolism*; D008298:Maleates / Q000494:pharmacology*; D011188:Potassium / Q000652:urine; D051381:Rats; D012964:Sodium / Q000652:urine | D003160:Comparative Study; D016428:Journal Article | D001639:Bicarbonates; D002712:Chlorides; D007656:Ketoglutaric Acids; D008298:Maleates; D000255:Adenosine Triphosphate; D012964:Sodium; D001151:Arsenic; D000086:Acetazolamide; D011188:Potassium | [] | false | eng | Curr Probl Clin Biochem | 0353507 | 0300-1725 | Switzerland | [] | "2024-08-13T15:33:32.641215Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
Bicarbonate inhibition of rat kidney aconitate hydratase isoenzymes. | 4() | 65-9 | Current problems in clinical biochemistry | [
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "Stepiński"
},
{
"affiliation": "",
"forename": "S",
"identifier": "",
"initials": "S",
"lastname": "Angielski"
}
] | 1975 | 212 | D000154:Aconitate Hydratase / Q000378:metabolism*; D000818:Animals; D001639:Bicarbonates / Q000494:pharmacology*; D002951:Citrates / Q000378:metabolism; D003593:Cytoplasm / Q000201:enzymology; D006836:Hydro-Lyases / Q000378:metabolism*; D006863:Hydrogen-Ion Concentration; D007527:Isoenzymes / Q000378:metabolism; D007668:Kidney / Q000201:enzymology*; D007700:Kinetics; D008928:Mitochondria / Q000201:enzymology; D051381:Rats | D016428:Journal Article | D001639:Bicarbonates; D002951:Citrates; D007527:Isoenzymes; D006836:Hydro-Lyases; D000154:Aconitate Hydratase | [] | false | eng | Curr Probl Clin Biochem | 0353507 | 0300-1725 | Switzerland | [] | "2024-08-13T15:33:32.641999Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
Influence of pH and hypoxia on the success of defibrillation. | 3(4) | 139-42 | Clinical impressions about the problem of defibrillation during states of acid-base imbalance and hypoxia have been influenced by studies involving the effect of these derangements on the ventricular fibrillation threshold. Based on body weight, energy requirements for defibrillation in normal dogs were compared to requirements in dogs subjected to commonly encountered acid-base disturbances and severe hypoxemia. No significant differences were found. Seventy-five percent of all animals in the study were electrically converted with low-to-moderate levels of energy. The incidence of spontaneous resumption of circulation following defibrillation was lowest in animals subjected to metabolic acidosis and hypoxia. The results suggest that pH and blood gas alterations, previously shown to influence the normal ventricular fibrillation threshold, do not significantly affect the normal defibrillation threshold. | Critical care medicine | [
{
"affiliation": "",
"forename": "R W",
"identifier": "",
"initials": "RW",
"lastname": "Yakaitis"
},
{
"affiliation": "",
"forename": "J D",
"identifier": "",
"initials": "JD",
"lastname": "Thomas"
},
{
"affiliation": "",
"forename": "J E",
"identifier": "",
"initials": "JE",
"lastname": "Mahaffey"
}
] | 1975 | 210 | D000137:Acid-Base Imbalance; D000138:Acidosis; D000142:Acidosis, Respiratory; D000472:Alkalosis, Respiratory; D000818:Animals; D004285:Dogs; D004554:Electric Countershock; D006863:Hydrogen-Ion Concentration; D000860:Hypoxia | D016428:Journal Article | 10.1097/00003246-197507000-00003 | [] | false | eng | Crit Care Med | 0355501 | 0090-3493 | United States | [] | "2024-08-13T15:33:32.642695Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Metabolic studies in experimental renal dysfunction resulting from maleate administration. | 4() | 86-100 | Current problems in clinical biochemistry | [
{
"affiliation": "",
"forename": "S",
"identifier": "",
"initials": "S",
"lastname": "Angielski"
},
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "Rogulski"
}
] | 1975 | 213 | D000090:Acetoacetates / Q000494:pharmacology; D000818:Animals; D001639:Bicarbonates / Q000652:urine; D002118:Calcium / Q000494:pharmacology; D003065:Coenzyme A / Q000378:metabolism; D004195:Disease Models, Animal; D005198:Fanconi Syndrome / Q000139:chemically induced*; D006863:Hydrogen-Ion Concentration; D007651:Keto Acids / Q000652:urine; D007656:Ketoglutaric Acids / Q000378:metabolism; D007785:Lactose / Q000378:metabolism; D008293:Malates / Q000097:blood; D008298:Maleates / Q000378:metabolism; D008314:Malonates / Q000494:pharmacology; D008928:Mitochondria / Q000378:metabolism; D008930:Mitochondria, Liver / Q000378:metabolism; D010085:Oxidative Phosphorylation / Q000187:drug effects; D010539:Permeability; D051381:Rats; D013466:Sulfurtransferases / Q000378:metabolism | D016428:Journal Article | D000090:Acetoacetates; D001639:Bicarbonates; D007651:Keto Acids; D007656:Ketoglutaric Acids; D008293:Malates; D008298:Maleates; D008314:Malonates; D013466:Sulfurtransferases; D007785:Lactose; D003065:Coenzyme A; D002118:Calcium | [] | false | eng | Curr Probl Clin Biochem | 0353507 | 0300-1725 | Switzerland | [] | "2024-08-13T15:33:32.643796Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
Multiple endocrine adenomatosis-I and II. | 1-51 | Current problems in surgery | [
{
"affiliation": "",
"forename": "T S",
"identifier": "",
"initials": "TS",
"lastname": "Harrison"
},
{
"affiliation": "",
"forename": "N W",
"identifier": "",
"initials": "NW",
"lastname": "Thompson"
}
] | 1975-08 | 214 | D000293:Adolescent; D000328:Adult; D002277:Carcinoma / Q000235:genetics*; D002648:Child; D002675:Child, Preschool; D005260:Female; D006801:Humans; D008297:Male; D008875:Middle Aged; D009377:Multiple Endocrine Neoplasia / Q000601:surgery; D011379:Prognosis; D013964:Thyroid Neoplasms / Q000235:genetics*; D015043:Zollinger-Ellison Syndrome | D016428:Journal Article | 10.1016/s0011-3840(75)80009-8 | [] | false | eng | Curr Probl Surg | 0372617 | 0011-3840 | United States | [] | "2024-08-13T15:33:32.644575Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||||
A randomized double-blind study of timolol in patients with essential hypertension. | 18(4) | 534-8 | Current therapeutic research, clinical and experimental | [
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "Guevara"
},
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Sukerman"
},
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Velasco"
}
] | 1975-10 | 215 | D000319:Adrenergic beta-Antagonists / Q000627:therapeutic use; D000328:Adult; D001794:Blood Pressure; D002986:Clinical Trials as Topic; D006339:Heart Rate; D006801:Humans; D006973:Hypertension / Q000188:drug therapy* / Q000503:physiopathology; D008875:Middle Aged; D010919:Placebos; D011412:Propanolamines / Q000627:therapeutic use*; D013830:Thiadiazoles / Q000627:therapeutic use | D016430:Clinical Trial; D016428:Journal Article; D016449:Randomized Controlled Trial | D000319:Adrenergic beta-Antagonists; D010919:Placebos; D011412:Propanolamines; D013830:Thiadiazoles | [] | false | eng | Curr Ther Res Clin Exp | 0372621 | 0011-393X | United States | [] | "2024-08-13T15:33:32.645536Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
[Observation of permanent teeth adjacent to teeth damaged by trauma]. | 28(11) | 1045-9 | Czasopismo stomatologiczne | [
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Szpringer"
}
] | 1975-11 | 216 | D000293:Adolescent; D002648:Child; D002675:Child, Preschool; D003790:Dental Pulp Necrosis / Q000209:etiology; D003809:Dentin, Secondary / Q000209:etiology; D003817:Dentition; D003818:Dentition, Mixed; D005500:Follow-Up Studies; D006801:Humans; D010484:Periapical Granuloma / Q000209:etiology; D018677:Tooth Injuries; D014947:Wounds and Injuries / Q000150:complications | D004740:English Abstract; D016428:Journal Article | [] | false | pol | Obserwacja zebów stałych sasiadujacych z zebami uszkodzonymi wskutek urazów | Czas Stomatol | 2984742R | 0011-4553 | Poland | [] | "2024-08-13T15:33:32.647424Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
Idiopathic hypertrophic subaortic stenosis (hypertrophic obstructive cardiomyopathy) changing concepts-1975. | 68(6) | 814-7 | Chest | [
{
"affiliation": "",
"forename": "P M",
"identifier": "",
"initials": "PM",
"lastname": "Shah"
}
] | 1975-12 | 217 | D000319:Adrenergic beta-Antagonists / Q000627:therapeutic use; D001145:Arrhythmias, Cardiac / Q000209:etiology; D006332:Cardiomegaly / Q000209:etiology; D002312:Cardiomyopathy, Hypertrophic / Q000175:diagnosis / Q000188:drug therapy / Q000209:etiology / Q000401:mortality / Q000503:physiopathology / Q000601:surgery; D004452:Echocardiography; D004562:Electrocardiography; D005500:Follow-Up Studies; D006337:Heart Murmurs; D006352:Heart Ventricles / Q000503:physiopathology; D006439:Hemodynamics; D006801:Humans; D008944:Mitral Valve Insufficiency / Q000209:etiology / Q000601:surgery | D016428:Journal Article; D016454:Review | D000319:Adrenergic beta-Antagonists | 10.1378/chest.68.6.814 | [] | false | eng | Chest | 0231335 | 0012-3692 | United States | [] | "2024-08-13T15:33:32.648233Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Pleural effusion associated with aortitis syndrome. | 68(6) | 826-8 | A patient with aortitis syndrome had a pleural effusion which subsided but reappeared with an exacerbation of aortitis symptoms while under antituberculosis treatment. The character of the fluid was that of an exudate, and the glucose concentration was normal. Clinical and laboratory features of the case suggest that the effusion was part of the aortitis syndrome per se. | Chest | [
{
"affiliation": "",
"forename": "T",
"identifier": "",
"initials": "T",
"lastname": "Kawai"
},
{
"affiliation": "",
"forename": "Y",
"identifier": "",
"initials": "Y",
"lastname": "Yamada"
},
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "Tsuneda"
},
{
"affiliation": "",
"forename": "T",
"identifier": "",
"initials": "T",
"lastname": "Aoyagi"
},
{
"affiliation": "",
"forename": "A",
"identifier": "",
"initials": "A",
"lastname": "Mikata"
}
] | 1975-12 | 218 | D000328:Adult; D001015:Aortic Arch Syndromes / Q000150:complications*; D006801:Humans; D008297:Male; D010996:Pleural Effusion / Q000032:analysis / Q000209:etiology*; D013625:Takayasu Arteritis / Q000150:complications* / Q000175:diagnosis; D014396:Tuberculosis, Pleural / Q000175:diagnosis | D002363:Case Reports; D016428:Journal Article | 10.1378/chest.68.6.826 | [] | false | eng | Chest | 0231335 | 0012-3692 | United States | [] | "2024-08-13T15:33:32.649270Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
The metabolic fate of securinine. | 1(3) | 205-15 | Chinese medical journal | [] | 1975-05 | 219 | D000470:Alkaloids / Q000378:metabolism*; D000818:Animals; D001381:Azepines; D002415:Cats; D004285:Dogs; D004912:Erythrocytes / Q000378:metabolism; D005260:Female; D000882:Haplorhini; D006572:Heterocyclic Compounds, Bridged-Ring; D006863:Hydrogen-Ion Concentration; D007668:Kidney / Q000378:metabolism; D007783:Lactones; D008099:Liver / Q000378:metabolism; D008297:Male; D051379:Mice; D009206:Myocardium / Q000378:metabolism; D009928:Organ Specificity; D010100:Oxygen / Q000494:pharmacology; D010880:Piperidines; D011817:Rabbits; D051381:Rats | D003160:Comparative Study; D016428:Journal Article | D000470:Alkaloids; D001381:Azepines; D006572:Heterocyclic Compounds, Bridged-Ring; D007783:Lactones; D010880:Piperidines; C000785:securinine; D010100:Oxygen | [] | false | eng | Chin Med J (Engl) | 7513795 | 0366-6999 | China | [] | "2024-08-13T15:33:32.650312Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
[Transplantation and preservation of tissue-typized skin in burns]. | 46(7) | 319-22 | At the Department of Plastic Surgery and Burns, Berufsgenossenschaftliche Unfalklinik Ludwigshafen-Oggersheim, a skinbank with typed skin has been established. The storage system consists of deep-freezing at -196 degrees C in liquid nitrogen. The transplantation of HL-A typed skin was evaluated from the clinical and histological point of view. Due to the effort necessary for such an undertaking this method is critically reviewed. | Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen | [
{
"affiliation": "",
"forename": "P R",
"identifier": "",
"initials": "PR",
"lastname": "Zellner"
},
{
"affiliation": "",
"forename": "I",
"identifier": "",
"initials": "I",
"lastname": "Taubert"
},
{
"affiliation": "",
"forename": "K",
"identifier": "",
"initials": "K",
"lastname": "Wegener"
}
] | 1975-07 | 220 | D002056:Burns / Q000601:surgery*; D005615:Freezing; D006087:Graft vs Host Reaction; D006680:HLA Antigens; D006650:Histocompatibility Testing; D006801:Humans; D016038:Skin Transplantation; D014021:Tissue Preservation; D014184:Transplantation, Homologous | D004740:English Abstract; D016428:Journal Article | D006680:HLA Antigens | [] | false | ger | Transplantation und Konservierung geqebetypisierter Haut bei Brandverletzten | Chirurg | 16140410R | 0009-4722 | Germany | [] | "2024-08-13T15:33:32.651097Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
[Ability of antilymphocyte sera to counteract the allogeneic inhibition of hematopoietic stem cells]. | 223(5) | 1245-7 | Doklady Akademii nauk SSSR | [
{
"affiliation": "",
"forename": "I N",
"identifier": "",
"initials": "IN",
"lastname": "Golovistikov"
}
] | 1975-08-11 | 222 | D000818:Animals; D000961:Antilymphocyte Serum / Q000494:pharmacology*; D002455:Cell Division; D002999:Clone Cells; D006084:Graft Rejection; D018380:Hematopoietic Stem Cell Transplantation; D006824:Hybridization, Genetic; D051379:Mice; D008810:Mice, Inbred C57BL; D011828:Radiation Chimera; D013154:Spleen / Q000276:immunology; D014184:Transplantation, Homologous | D016428:Journal Article | D000961:Antilymphocyte Serum | [] | false | rus | Sposobnost' antilimfotsitarnykh syvorotok syvorotok otmeniat' allogennuiu ingibitsiiu stvolovykh krovetvornykh kletok | Dokl Akad Nauk SSSR | 7505465 | 0002-3264 | Russia (Federation) | [] | "2024-08-13T15:33:32.652084Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Microenvironment of enzymes as 1 of the factors determining enzyme stability. Stabilization of soluble and immobilized horseradish peroxidase]. | 223(5) | 1256-9 | Doklady Akademii nauk SSSR | [
{
"affiliation": "",
"forename": "I V",
"identifier": "",
"initials": "IV",
"lastname": "Berezin"
},
{
"affiliation": "",
"forename": "B M",
"identifier": "",
"initials": "BM",
"lastname": "Kershengol'ts"
},
{
"affiliation": "",
"forename": "N N",
"identifier": "",
"initials": "NN",
"lastname": "Ugarova"
}
] | 1975-08-11 | 223 | D004355:Drug Stability; D005782:Gels; D006735:Horseradish Peroxidase; D006863:Hydrogen-Ion Concentration; D010544:Peroxidases; D011506:Proteins; D012709:Serum Albumin | D016428:Journal Article | D005782:Gels; D011506:Proteins; D012709:Serum Albumin; D006735:Horseradish Peroxidase; D010544:Peroxidases | [] | false | rus | Mikrookruzhenie fermentov kak odin iz faktorov, opredeliaiushchikh stabil'nost' fermentov. Stabilizatsiia restvorimoĭ i immobilizovannoĭ peroksidazy iz khrena | Dokl Akad Nauk SSSR | 7505465 | 0002-3264 | Russia (Federation) | [] | "2024-08-13T15:33:32.654076Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[3d regional meeting of the specialty field of supervisory nurses in Baden-Württemberg, Northern Group. June 25, 1975 in district hospital Heidenheim]. | 28(9) | 486-7 | Deutsche Krankenpflegezeitschrift | [
{
"affiliation": "",
"forename": "H",
"identifier": "",
"initials": "H",
"lastname": "Stängle"
}
] | 1975-09 | 224 | D003226:Congresses as Topic; D005860:Germany, West; D009745:Nursing, Supervisory | D016423:Congress | [] | false | ger | 3. Regionaltagung des Arbeitskreises Leitender Krankenschwestern und -pfleger in Baden-Württemberg, Gruppe Nord. Am 25. Juni 1975 im Kreiskrankenhaus Heidenheim | Dtsch Krankenpflegez | 0323406 | 0012-074X | Germany | [] | "2024-08-13T15:33:32.654729Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
[Polyploidization and fusion of insect cells exposed to concanavalin A]. | 223(1) | 209-12 | Doklady Akademii nauk SSSR | [
{
"affiliation": "",
"forename": "V T",
"identifier": "",
"initials": "VT",
"lastname": "Kakpakov"
},
{
"affiliation": "",
"forename": "L G",
"identifier": "",
"initials": "LG",
"lastname": "Polukarova"
}
] | 1975 | 221 | D000818:Animals; D002459:Cell Fusion / Q000187:drug effects*; D002460:Cell Line; D002478:Cells, Cultured / Q000187:drug effects; D003208:Concanavalin A / Q000494:pharmacology*; D009033:Culicidae; D004330:Drosophila; D011123:Polyploidy | D016428:Journal Article | D003208:Concanavalin A | [] | false | rus | Poliploidizatsiia i sliianie kletok nasekomykh pod vliianiem konkanavalina A | Dokl Akad Nauk SSSR | 7505465 | 0002-3264 | Russia (Federation) | [] | "2024-08-13T15:33:32.655397Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Adverse effects of anti-epileptic drugs]. | 100(38) | 1904-6 | Deutsche medizinische Wochenschrift (1946) | [
{
"affiliation": "",
"forename": "N",
"identifier": "",
"initials": "N",
"lastname": "Bohlen"
},
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Hertl"
}
] | 1975-09-19 | 225 | D000324:Adrenocorticotropic Hormone / Q000009:adverse effects; D000927:Anticonvulsants / Q000009:adverse effects*; D001463:Barbiturates / Q000009:adverse effects; D002220:Carbamazepine / Q000009:adverse effects; D003975:Diazepam / Q000009:adverse effects; D004827:Epilepsy / Q000188:drug therapy*; D005013:Ethosuximide / Q000009:adverse effects; D006801:Humans; D008617:Mephenytoin / Q000009:adverse effects; D009567:Nitrazepam / Q000009:adverse effects; D010672:Phenytoin / Q000009:adverse effects; D011324:Primidone / Q000009:adverse effects; D013388:Succinimides / Q000009:adverse effects; D013843:Thiazines / Q000009:adverse effects; D014293:Trimethadione / Q000009:adverse effects; D014635:Valproic Acid / Q000009:adverse effects | D016428:Journal Article | D000927:Anticonvulsants; D001463:Barbiturates; D013388:Succinimides; D013843:Thiazines; D011324:Primidone; D002220:Carbamazepine; D005013:Ethosuximide; D014635:Valproic Acid; D010672:Phenytoin; D000324:Adrenocorticotropic Hormone; D009567:Nitrazepam; D003975:Diazepam; D008617:Mephenytoin; D014293:Trimethadione | 10.1055/s-0028-1106478 | [] | false | ger | Nebenwirkungen antiepileptischer Medikamente | Dtsch Med Wochenschr | 0006723 | 0012-0472 | Germany | [] | "2024-08-13T15:33:32.656615Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Charge properties of human pituitary and amniotic fluid prolactins. | 2(6-7) | 379-402 | The apparent isoelectric points (pI) in isoelectric focusing (IF) of human pituitary and amniotic fluid prolactin (hPRL), both non-iodinated and iodinated, were determined. Unresolved mixtures of pituitary hPRL isohormones E and F, and of at least five isohormones found in amniotic fluid, and plasma hPRL exhibit an average pI value of 6.5 - 6.7. Transient state pH values observed or previously reported for hPRL components range from pH 5.9 to 6.8 after correction to standard conditions. At pH 8.1, the major isohormone, hPRL-F, carriers a charge of 2.2 net protons per molecule. The net charge differences among isohormones E, F and G are compatible with acquisition or loss of single charged groups per 20,000 molecular weight. This net charge is similar to that of the least prolactin-bioactive major isohormone of human growth hormone (hGH-B), while the hGH with a bioactivity comparable to that of hPRL exhibits a net charge of 3.4 valence units. The "large" isohormones J and H increased net charges, by a factor of 2-3, in direct proportion to their size increments. | Endocrine research communications | [
{
"affiliation": "",
"forename": "A D",
"identifier": "",
"initials": "AD",
"lastname": "Rogol"
},
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Ben-David"
},
{
"affiliation": "",
"forename": "R",
"identifier": "",
"initials": "R",
"lastname": "Sheats"
},
{
"affiliation": "",
"forename": "D",
"identifier": "",
"initials": "D",
"lastname": "Rodbard"
},
{
"affiliation": "",
"forename": "A",
"identifier": "",
"initials": "A",
"lastname": "Chrambach"
}
] | 1975 | 226 | D000653:Amniotic Fluid / Q000032:analysis*; D005260:Female; D006801:Humans; D006863:Hydrogen-Ion Concentration; D007525:Isoelectric Focusing; D007774:Lactation; D010902:Pituitary Gland / Q000032:analysis*; D011247:Pregnancy; D011388:Prolactin / Q000097:blood / Q000276:immunology; D011863:Radioimmunoassay | D016428:Journal Article | D011388:Prolactin | 10.1080/07435807509084162 | [] | false | eng | Endocr Res Commun | 0426337 | 0093-6391 | United States | [] | "2024-08-13T15:33:32.657366Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Human and monkey prolactin and growth hormone: separation of polymorphic forms by isoelectric focusing. | 97(4) | 855-67 | The feasibility of using isoelectric focusing for the separation of primate pituitary growth hormone from prolactin and for the characterization of polymorphic forms of these hormones was explored. In a pH 3--10 gradient, extracts of both human and cynomolgus monkey pituitaries were each resolved into 4 growth hormone components and at least 3 prolactin components, as shown by radioimmunoassay. In narrower gradients (of 2--3 pH units) greater resolution was achieved; the principal growth hormone components were well separated from the principal prolactin components but there was overlapping of some minor components. A partially purified human prolactin preparation was found to contain 4 prolactin components, one of which had a prolactin/growth hormone ratio of 760. Clinical grade human growth hormone was also resolved into at least 5 prolactin and 5 growth hormone components, many of which had higher pI values than those found in pituitary extract. Under the conditions used, both growth hormone and prolactin were found to be polymorphic with respect to isoelectric point. Some of the human prolactin components were found to contain less than 0.2% growth hormone by radioimmunoassay. Monkey growth hormone containing 0.01% prolactin was isolated. These findings demonstrate that isoelectric focusing is useful for the preparation of both growth hormone and prolactin which are essentially free of one another. Furthermore, the polymorphic forms were repeatedly found in preparations obtained by several methods and from 2 different species, suggesting that these forms are not artifacts. | Endocrinology | [
{
"affiliation": "",
"forename": "B C",
"identifier": "",
"initials": "BC",
"lastname": "Hummel"
},
{
"affiliation": "",
"forename": "G M",
"identifier": "",
"initials": "GM",
"lastname": "Brown"
},
{
"affiliation": "",
"forename": "P",
"identifier": "",
"initials": "P",
"lastname": "Hwang"
},
{
"affiliation": "",
"forename": "H G",
"identifier": "",
"initials": "HG",
"lastname": "Friesen"
}
] | 1975-10 | 227 | D000818:Animals; D013006:Growth Hormone / Q000302:isolation & purification*; D000882:Haplorhini; D006801:Humans; D006863:Hydrogen-Ion Concentration; D007525:Isoelectric Focusing; D008252:Macaca fascicularis; D010902:Pituitary Gland / Q000032:analysis*; D011388:Prolactin / Q000302:isolation & purification*; D011863:Radioimmunoassay | D016428:Journal Article; D013487:Research Support, U.S. Gov't, P.H.S. | D011388:Prolactin; D013006:Growth Hormone | 10.1210/endo-97-4-855 | [] | false | eng | Endocrinology | 0375040 | 0013-7227 | United States | [] | "2024-08-13T15:33:32.658451Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
The interaction of SO2 with proteins. | 9(3) | 265-77 | Environmental letters | [
{
"affiliation": "",
"forename": "E Y",
"identifier": "",
"initials": "EY",
"lastname": "Eickenroht"
},
{
"affiliation": "",
"forename": "E M",
"identifier": "",
"initials": "EM",
"lastname": "Gause"
},
{
"affiliation": "",
"forename": "J R",
"identifier": "",
"initials": "JR",
"lastname": "Rowlands"
}
] | 1975 | 228 | D000818:Animals; D001665:Binding Sites; D001798:Blood Proteins; D006863:Hydrogen-Ion Concentration; D009994:Osmolar Concentration; D011485:Protein Binding; D011487:Protein Conformation; D011817:Rabbits; D013050:Spectrometry, Fluorescence; D013053:Spectrophotometry; D013056:Spectrophotometry, Ultraviolet; D013447:Sulfites; D013458:Sulfur Dioxide | D003160:Comparative Study; D016428:Journal Article | D001798:Blood Proteins; D013447:Sulfites; D013458:Sulfur Dioxide | 10.1080/00139307509435855 | [] | false | eng | Environ Lett | 7610448 | 0013-9300 | United States | [] | "2024-08-13T15:33:32.660267Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Ecological observation of the 137Cs-contamination in beef of animals from the southern-Bavarian area. | 4() | 24-36 | Certain climatic and edaphic conformations in the Bavarian sub-alpine mountains and in the Alps favor above all the development of a land utilization system and farm structures similar to those in the northern part of Scandinavia. In 1963/64, the years of the highest environmental contamination up to the present, we established in 600 beef samples from the round or shoulder of male and female cattle (mainly Highland cattle) close connections between the 137Cs-contamination of green crop and the long lastnig yearly precipitation quantities, as well as certain relations between the 137Cs-contamination of meat and differences in the feeding and keeping of the animals. During summer-seasons (April-October), beef of cattle from pastures with heavy rainfall (Alps) was contaiminated by 137Cs up to 15 times more than that of confined animals. Hereby the rate of 137Cs-contamination in the meat of grazing cattle was nearly proportional to the quantities of precipitation. When confined cattle were fed on pastures in autumn after harvesting for 2 to 3 weeks, a quick increase of 137Cs-contamination of the meat was caused within this time up to values which in this district were otherwise only observed in grazing cattle. The lower 137Cs-content in meat of cattle housed during the summer season is due to the more varied fodder, which is at that time less contaminated than green crop. During the winter season (November to March), the highest contaminations in the meat of confined (Bohemian Forest) or grazing cattle (Alps) was measured when the animals in these districts were almost exclusively fed with fodder from the own farmground or with leafy silage. The highest contamination was almost regularly noticed in January, February and March, as generally during these months the highly contaminated first cut hay is fed. Here the meat was often even more contaminated than that of grazing cattle. After the quick decrease of 137Cs in fallout noticed in the years 1964 and 1965, in 1965/66 a dependance in the 137Cs-contamination of beef on the methods of keeping and feeding could still be observed in only the extreme cases (Alps, Bavarian- and Bohemian Forest); though in general, meat of animals from districts with heavy rainfall was slightly more contaminated than meat of animals from regions with less precipitation. | Environmental quality and safety | [
{
"affiliation": "",
"forename": "W",
"identifier": "",
"initials": "W",
"lastname": "Kreuzer"
}
] | 1975 | 229 | D000818:Animals; D002417:Cattle; D002588:Cesium Radioisotopes; D004463:Ecology; D005507:Food Contamination, Radioactive; D005658:Fungi; D005860:Germany, West; D006863:Hydrogen-Ion Concentration; D008460:Meat / Q000032:analysis; D010944:Plants; D011848:Radioactive Pollutants; D012987:Soil / Q000032:analysis; D012988:Soil Microbiology; D013997:Time Factors; D014197:Trees; D014887:Weather | D016428:Journal Article | D002588:Cesium Radioisotopes; D011848:Radioactive Pollutants; D012987:Soil | [] | false | eng | 76066044 | Environ Qual Saf | 0332077 | 0300-824X | United States | [] | "2024-08-13T15:33:32.660969Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Liver microsomal beta-glucuronidase and UDP-glucuronyltransferase. | 20(5) | 269-76 | Both UDP-glucuronyltransferase (GT) and beta-glucuronidase (betaG) were assayed in untreated liver microsomes. Optimum assay conditions were established with rat liver microsomes using p-nitrophenol (pNP) and its glucuronide (pNPGA) at the pH optima of GT (7.5) and betaG (4.5). The activities of the two enzymes were compared using microsomes from rats, mice, pigs, cattle and horses, with pNP, pNPGA, and phenolphthalein as substrate, in the presence of various cofactors and inhibitors at pH 7.5 and 4.5. These data disclose pronounced differences with respect to species, substrate and other experimental conditions, thereby precluding the establishment of general optimum conditions. The two enzymes were also assayed under strictly identical conditions using pNP and pNPGA and rat liver microsomes at pH 7.5 in the presence and absence of UDP-glucuronate disodium (UDPGA), activators (ATP;UDP-N-acetylglucosamine) and inhibitors. When provided with a functional level of UDPGA, both enzymes proved active under those conditions, and a conjugation-deconjugation interplay was indicated. The two processes could be selectively and totally inhibited by Zn2+ and saccharolactone. The results suggest that conjugation-deconjugation-reconjugation cycles may be operative in the metabolism of drugs in vivo, taking place already at the level of the liver endoplasmic reticulum. | Enzyme | [
{
"affiliation": "",
"forename": "I",
"identifier": "",
"initials": "I",
"lastname": "Schöllhammer"
},
{
"affiliation": "",
"forename": "D S",
"identifier": "",
"initials": "DS",
"lastname": "Poll"
},
{
"affiliation": "",
"forename": "M H",
"identifier": "",
"initials": "MH",
"lastname": "Bickel"
}
] | 1975 | 230 | D000255:Adenosine Triphosphate / Q000494:pharmacology; D000818:Animals; D002413:Cations, Divalent; D002417:Cattle; D005966:Glucuronidase / Q000378:metabolism*; D014453:Glucuronosyltransferase / Q000378:metabolism*; D006602:Hexosyltransferases / Q000378:metabolism*; D006736:Horses; D006863:Hydrogen-Ion Concentration; D007700:Kinetics; D007783:Lactones / Q000494:pharmacology; D008297:Male; D051379:Mice; D008862:Microsomes, Liver / Q000201:enzymology*; D051381:Rats; D013045:Species Specificity; D013402:Sugar Alcohols / Q000494:pharmacology; D013552:Swine; D014537:Uridine Diphosphate N-Acetylglucosamine / Q000494:pharmacology; D015032:Zinc / Q000494:pharmacology | D016428:Journal Article | D002413:Cations, Divalent; D007783:Lactones; D013402:Sugar Alcohols; D014537:Uridine Diphosphate N-Acetylglucosamine; D000255:Adenosine Triphosphate; D006602:Hexosyltransferases; D014453:Glucuronosyltransferase; D005966:Glucuronidase; D015032:Zinc | 10.1159/000458949 | [] | false | eng | Enzyme | 1262265 | 0013-9432 | Switzerland | [] | "2024-08-13T15:33:32.662161Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Biochemical aspects of renal ammonia formation in metabolic acidosis. | 20(6) | 359-80 | In omnivorous creatures, the diet is acidogenic, especially as a result of the meat content, which gives rise to phosphoric and sulphuric acids, i.e., to metabolic acidosis. In the short term, metabolic acids are buffered by tissue proteins and bicarbonate (the 'alkali reserve'). In the longer term, acid must be excreted, or neutralized with base which is also generated from the diet, by conversion of dietary amino-nitrogen to ammonia. The final steps of this process occur in the kidney, which converts circulating glutamine to ammonia, and to carbon products such as glucose and carbon dioxide, by metabolic reactions which adapt during acidosis to generate more ammonia and maintain an increased renal ammonia content. The complex mechanisms which govern the formation of ammonia, glucose and carbon dioxide from glutamine, involving the reactions of amino acids, the tricarboxylic acid cycle, and gluconeogenesis, are reviewed. | Enzyme | [
{
"affiliation": "",
"forename": "D A",
"identifier": "",
"initials": "DA",
"lastname": "Hems"
}
] | 1975 | 231 | D000138:Acidosis / Q000139:chemically induced / Q000378:metabolism* / Q000503:physiopathology; D000208:Acute Disease; D000641:Ammonia / Q000378:metabolism*; D005947:Glucose / Q000378:metabolism; D005971:Glutamates / Q000378:metabolism; D005973:Glutamine / Q000097:blood / Q000378:metabolism; D006851:Hydrochloric Acid / Q000494:pharmacology; D006863:Hydrogen-Ion Concentration; D007668:Kidney / Q000187:drug effects / Q000378:metabolism* / Q000503:physiopathology; D007672:Kidney Cortex / Q000378:metabolism; D008954:Models, Biological; D010477:Perfusion | D016428:Journal Article; D016454:Review | D005971:Glutamates; D005973:Glutamine; D000641:Ammonia; D005947:Glucose; D006851:Hydrochloric Acid | 10.1159/000458960 | [] | false | eng | Enzyme | 1262265 | 0013-9432 | Switzerland | [] | "2024-08-13T15:33:32.663134Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Studies on the mechanism of the changes in serum and liver gamma-glutamyl transpeptidase activity. I. Experimental extrahepatic cholestasis in rabbits. | 21(1) | 1-7 | Serum, liver and renal gamma-glutamyl transpeptidase (GGT) activities were studied in four groups of rabbits: controls, rabbits with obstructive extrahepatic cholestasis, rabbits with obstructive anuria, and animals with combined obstructive extrahepatic cholestasis and obstructive anuria. Serum GGT was essentially increased in rabbits with obstructive extrahepatic cholestasis, showing peak values in the combined cholestasis + obstructive anuria group, and practically normal values in animals with anuria. Liver GGT was increased in both cholestasis groups, but the increase was less prominent than the increase in serum GGT and there was no correlation between them. In both anuric groups renal GGT was reduced, probably as a result of inhibited enzyme synthesis secondary to the altered conditions for adequate renal function. The results obtained are suggestive of a probable renal involvement in the formation of the serum GGT activity level. | Enzyme | [
{
"affiliation": "",
"forename": "D",
"identifier": "",
"initials": "D",
"lastname": "Adjarov"
},
{
"affiliation": "",
"forename": "S",
"identifier": "",
"initials": "S",
"lastname": "Popov"
},
{
"affiliation": "",
"forename": "E",
"identifier": "",
"initials": "E",
"lastname": "Ivanov"
}
] | 1976 | 232 | D000818:Animals; D001652:Bile Ducts / Q000502:physiology; D002404:Catheterization; D002779:Cholestasis / Q000201:enzymology*; D007668:Kidney / Q000201:enzymology*; D008026:Ligation; D008099:Liver / Q000201:enzymology*; D008297:Male; D011817:Rabbits; D014513:Ureter / Q000502:physiology; D005723:gamma-Glutamyltransferase / Q000097:blood / Q000378:metabolism* | D016428:Journal Article | D005723:gamma-Glutamyltransferase | 10.1159/000458836 | [] | false | eng | Enzyme | 1262265 | 0013-9432 | Switzerland | [] | "2024-08-13T15:33:32.665040Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Studies on the mechanism of the changes in serum and liver gamma-glutamyl transpeptidase activity. II. Experimental hexachlorobenzene porphyria in rabbits. | 21(1) | 8-20 | The mechanism responsible for the changes in serum and liver gamma-glutamyl transpeptidase (gamma-GT) activity was studied in a model of experimental hexachlorobenzene porphyria in rabbits. Porphyria followed the administration of hexachlorobenzene in doses of 280 mumol - kg-1 body weight, which were given daily through a gastric tube over a 20-day period. Serum gamma-GT activity and the activities of the lysosomal enzymes beta-N-acetylglucosaminidase and alpha-mannosidase were increased, whereas L-aspartate: 2-oxoglutarate aminotransferase and L-alanine: 2-oxoglutarate aminotransferase and L-alanine: 2-oxoglutarate aminotransferase remained unaltered. There was a considerable increase in liver microsomal protein, gamma-GT, cytochrome P-450, anilinehydroxylase, aminopyrine-demethylase and delta-aminolevulinic acid synthase. In the liver gamma-GT was detected in the microsomes as well as in the cytoplasm where enzymatic activity was higher. The high correlation coefficient between liver gamma-GT, cytochrome P-450 and delta-aminolevulinic acid synthase witnesses a hexachlorobenzene-induced gamma-GT formation in the liver. A statistically significant correlation between serum and liver gamma-GT activity was also found. These data strongly suggest that the increase in serum gamma-GT activity may result from the induction of the enzyme in the liver. | Enzyme | [
{
"affiliation": "",
"forename": "E",
"identifier": "",
"initials": "E",
"lastname": "Ivanov"
},
{
"affiliation": "",
"forename": "L",
"identifier": "",
"initials": "L",
"lastname": "Krustev"
},
{
"affiliation": "",
"forename": "D",
"identifier": "",
"initials": "D",
"lastname": "Adjarov"
},
{
"affiliation": "",
"forename": "K",
"identifier": "",
"initials": "K",
"lastname": "Chernev"
},
{
"affiliation": "",
"forename": "I",
"identifier": "",
"initials": "I",
"lastname": "Apostolov"
},
{
"affiliation": "",
"forename": "P",
"identifier": "",
"initials": "P",
"lastname": "Dimitrov"
},
{
"affiliation": "",
"forename": "E",
"identifier": "",
"initials": "E",
"lastname": "Drenska"
},
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Stefanova"
},
{
"affiliation": "",
"forename": "V",
"identifier": "",
"initials": "V",
"lastname": "Pramatarova"
}
] | 1976 | 233 | D000118:Acetylglucosaminidase / Q000378:metabolism; D000818:Animals; D006581:Hexachlorobenzene; D008099:Liver / Q000187:drug effects / Q000201:enzymology*; D008361:Mannosidases / Q000378:metabolism; D011164:Porphyrias / Q000139:chemically induced / Q000201:enzymology* / Q000378:metabolism; D011166:Porphyrins / Q000378:metabolism; D011817:Rabbits; D005723:gamma-Glutamyltransferase / Q000097:blood / Q000378:metabolism* | D016428:Journal Article | D011166:Porphyrins; D006581:Hexachlorobenzene; D005723:gamma-Glutamyltransferase; D008361:Mannosidases; D000118:Acetylglucosaminidase | 10.1159/000458837 | [] | false | eng | Enzyme | 1262265 | 0013-9432 | Switzerland | [] | "2024-08-13T15:33:32.665991Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Changes in erythrocyte 2,3 diphosphoglycerate in women following short term maximal exercise. | 34(4) | 227-32 | 15 untrained women were subjected to a walking treadmill test to determine the influence of maximal exercise upon synthesis of erythrocyte 2,3 DPG. Although there was a 9.8% increase in the 2,3 DPG content following exercise, there was a concomitant 9.4% increase in the hemoglobin level; therefore, when 2,3 DPG is expressed as a ratio to hemoglobin (See Article), there was no significant change as a result of exercise stress. It was suggested that three additive factors produced during strenuous exercise; decreased pH; increased hemoglobin concentration; and increased CO2 production result in by-product inhibition of 2,3 DPG synthesis. It is concluded that 2,3 DPG does not provide a physiologic benefit in the adaptation of the oxygen transport system to exercise. | European journal of applied physiology and occupational physiology | [
{
"affiliation": "",
"forename": "H W",
"identifier": "",
"initials": "HW",
"lastname": "Bonner"
},
{
"affiliation": "",
"forename": "C A",
"identifier": "",
"initials": "CA",
"lastname": "Tate"
},
{
"affiliation": "",
"forename": "C K",
"identifier": "",
"initials": "CK",
"lastname": "Buffington"
}
] | 1975-12-05 | 234 | D000328:Adult; D002245:Carbon Dioxide / Q000097:blood; D004163:Diphosphoglyceric Acids / Q000096:biosynthesis / Q000097:blood*; D004912:Erythrocytes / Q000378:metabolism*; D005260:Female; D006454:Hemoglobins / Q000378:metabolism; D006801:Humans; D006863:Hydrogen-Ion Concentration; D010100:Oxygen / Q000097:blood; D010101:Oxygen Consumption; D005082:Physical Exertion | D016428:Journal Article | D004163:Diphosphoglyceric Acids; D006454:Hemoglobins; D002245:Carbon Dioxide; D010100:Oxygen | 10.1007/BF00999936 | [
{
"citation": "Annu Rev Med. 1974;25:29-38",
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] | false | eng | Eur J Appl Physiol Occup Physiol | 0410266 | 0301-5548 | Germany | [] | "2024-08-13T15:33:32.668261Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Hydroxylation of p-Coumaric acid by illuminated chloroplasts. The role of superoxide. | 55(2) | 355-60 | 1. Chloroplasts isolated from leaves of spinach-beet (Beta vulgaris L. ssp. vulgaris) do not catalyse the hydroxylation of p-coumaric acid in the dark unless a reductant (such as ascorbate, NADH or NADPH) is added. Superoxide dismutase has no effect on this reaction. 2. Illuminated chloroplasts catalyse the hydroxylation in the absence of added reductant. This reaction is completely inhibited by superoxide dismutase, but catalase has little effect. 3. Both hydroxylation in the light and hydroxylation in the dark in the presence of reductants are inhibited by diethyldithiocarbamate, EDTA, cyanide and 2-mercaptoethanol. 4. It is proposed that O-2- generated by illuminated chloroplasts is involved in the provision of a reductant to the enzyme phenolase. | European journal of biochemistry | [
{
"affiliation": "",
"forename": "B",
"identifier": "",
"initials": "B",
"lastname": "Halliwell"
}
] | 1975-07-01 | 235 | D001205:Ascorbic Acid / Q000494:pharmacology; D002109:Caffeic Acids / Q000378:metabolism; D002374:Catalase / Q000378:metabolism; D002734:Chlorophyll / Q000378:metabolism; D002736:Chloroplasts / Q000187:drug effects / Q000378:metabolism*; D002934:Cinnamates / Q000378:metabolism*; D003373:Coumaric Acids / Q000378:metabolism*; D005609:Free Radicals; D007700:Kinetics; D008027:Light; D009243:NAD / Q000494:pharmacology; D009249:NADP / Q000494:pharmacology; D010084:Oxidation-Reduction; D010100:Oxygen; D010944:Plants; D013482:Superoxide Dismutase / Q000378:metabolism | D016428:Journal Article | D002109:Caffeic Acids; D002934:Cinnamates; D003373:Coumaric Acids; D005609:Free Radicals; D009243:NAD; D002734:Chlorophyll; D009249:NADP; D002374:Catalase; D013482:Superoxide Dismutase; D001205:Ascorbic Acid; D010100:Oxygen | 10.1111/j.1432-1033.1975.tb02169.x | [] | false | eng | Eur J Biochem | 0107600 | 0014-2956 | England | [] | "2024-08-13T15:33:32.669970Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Identification of chloride-binding sites in hemoglobin by nuclear-magnetic-resonance quadrupole-relaxation studies of hemoglobin digests. | 55(2) | 385-90 | 35Cl minus-nuclear magnetic resonance (NMR) studies indicate that various digests of human hemoglobin with carboxypeptidase A and B, or a combination of the two, may be used for the identification of chloride binding sites. All the digestion products contain, like hemoglobin itself, at least two classes of binding sites, one of high, the others of low affinity. The pH dependence of the excess linewidth of the 35Cl minus NMR signal indicates that in the simple digests with either carboxypeptidase A or B, chloride is bound with high affinity at or near His-beta146-Asp-beta94 and at or near Val-alpha1-Arg-alpha141. The high-affinity sites show, in the case of the simple digests, a strong oxygen linkage which is lost in the forms digested with both carboxypeptidase A and B; this linkage may thus be correlated to the presence of conformational changes. Organic phosphates, like inositol hexaphosphate, show competition for some of the high-affinity chloride binding sites in hemoglobin and in the simple digests. This competition is likewise lost in the doubly digested hemoglobins. | European journal of biochemistry | [
{
"affiliation": "",
"forename": "E",
"identifier": "",
"initials": "E",
"lastname": "Chiancone"
},
{
"affiliation": "",
"forename": "J E",
"identifier": "",
"initials": "JE",
"lastname": "Norne"
},
{
"affiliation": "",
"forename": "S",
"identifier": "",
"initials": "S",
"lastname": "Forsén"
},
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "Bonaventura"
},
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Brunori"
},
{
"affiliation": "",
"forename": "E",
"identifier": "",
"initials": "E",
"lastname": "Antonini"
},
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "Wyman"
}
] | 1975-07-01 | 236 | D001665:Binding Sites; D002248:Carbon Monoxide / Q000097:blood; D002268:Carboxypeptidases; D002712:Chlorides / Q000097:blood*; D006454:Hemoglobins; D006801:Humans; D006863:Hydrogen-Ion Concentration; D009682:Magnetic Resonance Spectroscopy; D008433:Mathematics; D009994:Osmolar Concentration; D010446:Peptide Fragments; D010833:Phytic Acid / Q000097:blood; D011485:Protein Binding; D011487:Protein Conformation; D012965:Sodium Chloride | D016428:Journal Article | D002712:Chlorides; D006454:Hemoglobins; D010446:Peptide Fragments; D012965:Sodium Chloride; D010833:Phytic Acid; D002248:Carbon Monoxide; D002268:Carboxypeptidases | 10.1111/j.1432-1033.1975.tb02173.x | [] | false | eng | Eur J Biochem | 0107600 | 0014-2956 | England | [] | "2024-08-13T15:33:32.675376Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
The internal-alkaline pH gradient, sensitive to uncoupler and ATPase inhibitor, in growing Clostridium pasteurianum. | 55(2) | 445-53 | 1. The intracellular pH was measured in growing Clostridium pasteurianum with and acid-base equilibrium distribution method. [14C]Dimethyloxazolidinedione, [14]methylamine and [14C]acetic acid were used as "deltapH-indicators". During growth the extracellular pH decreased from 7.1 to 5.1; simultaneously the intracellular pH changed from 7.5 to 5.9. Thus, the intracellular pH was more alkaline than the extracellular pH by 0.4 to 0.8 pH-units. 2. This pH gradient (interior alkaline) was abolished by the proton conductor carbonylcyanide m-chlorophenylhydrazone and the ATPase inhibitor N,N'-dicyclohexylcarbodiimide. The pH gradient could not be demonstrated in cells depleted of an energy substrate. These results suggest that the pH gradient is formed by an ATPase-driven extrusion of protons from the cells rather than by a Donnan potential. 3. Growth of the organism was inhibited by low concentrations of both carbonylcyanide m-chlorophenylhydrazone (5 muM) and dicyclohexylcarbodiimide (5 muM). This finding suggests that the pH gradient is essential for the growing cell as it may be required for substrate accumulation and other types of transport processes. | European journal of biochemistry | [
{
"affiliation": "",
"forename": "V",
"identifier": "",
"initials": "V",
"lastname": "Riebeling"
},
{
"affiliation": "",
"forename": "R K",
"identifier": "",
"initials": "RK",
"lastname": "Thauer"
},
{
"affiliation": "",
"forename": "K",
"identifier": "",
"initials": "K",
"lastname": "Jungermann"
}
] | 1975-07-01 | 237 | D002234:Carbodiimides / Q000494:pharmacology*; D002258:Carbonyl Cyanide m-Chlorophenyl Hydrazone / Q000494:pharmacology*; D003013:Clostridium / Q000187:drug effects / Q000378:metabolism*; D004024:Dicyclohexylcarbodiimide / Q000494:pharmacology*; D004734:Energy Metabolism; D006863:Hydrogen-Ion Concentration; D009570:Nitriles / Q000494:pharmacology* | D016428:Journal Article | D002234:Carbodiimides; D009570:Nitriles; D004024:Dicyclohexylcarbodiimide; D002258:Carbonyl Cyanide m-Chlorophenyl Hydrazone | 10.1111/j.1432-1033.1975.tb02181.x | [] | false | eng | Eur J Biochem | 0107600 | 0014-2956 | England | [] | "2024-08-13T15:33:32.676334Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
D-alanyl-D-alanine carboxypeptidase in the bacterial form and L-form of Proteus mirabilis. | 55(2) | 465-73 | Membranes of the bacterial form and the stable and unstable L-forms of Proteus mirabilis contain LD and DD-carboxypeptidase. The DD-carboxypeptidase is inhibited non-competitively by penicillin G. The enzyme of the bacterial form is highly penicillin-sensitive (Ki - 4 X 10(-9) M penicillin G). Inhibition is only partly reversible by treatment with penicillinase or by dialysis against buffer. In contrast, the DD-carboxypeptidase of the unstable L-form, grown in the presence of penicillin, is 175-fold less penicillin-sensitive (Ki = 7 X 10(7) M penicillin G). Inhibition is completely reversed by penicillinase or dialysis. After inhibition by penicillin and subsequent reactivation the penicillin sensitivity of the bacterial DD-carboxtpeptidase is similar to the sensitivity of the enzyme of the unstable L-form. The hypothesis is proposed that P. mirabilis contains two DD-carboxypeptidases of different penicillin sensitivity and with different mechanisms of penicillin binding. Peptidoglycan synthesis in the cell walls of the unstable L-form is probably carried out with the help of only one DD-carboxypeptidase, viz. the completely reactivatable enzyme with the lower penicillin sensitivity. | European journal of biochemistry | [
{
"affiliation": "",
"forename": "H H",
"identifier": "",
"initials": "HH",
"lastname": "Martin"
},
{
"affiliation": "",
"forename": "C",
"identifier": "",
"initials": "C",
"lastname": "Maskos"
},
{
"affiliation": "",
"forename": "R",
"identifier": "",
"initials": "R",
"lastname": "Burger"
}
] | 1975-07-01 | 238 | D000409:Alanine; D002268:Carboxypeptidases / Q000378:metabolism*; D002462:Cell Membrane / Q000187:drug effects / Q000201:enzymology; D003605:D-Amino-Acid Oxidase; D003902:Detergents / Q000494:pharmacology; D006863:Hydrogen-Ion Concentration; D007700:Kinetics; D007740:L Forms / Q000201:enzymology*; D010400:Penicillin G / Q000494:pharmacology; D010404:Penicillin V / Q000494:pharmacology; D011513:Proteus mirabilis / Q000201:enzymology*; D011523:Protoplasts / Q000201:enzymology; D013104:Spheroplasts / Q000201:enzymology | D016428:Journal Article | D003902:Detergents; D003605:D-Amino-Acid Oxidase; D002268:Carboxypeptidases; D000409:Alanine; D010400:Penicillin G; D010404:Penicillin V | 10.1111/j.1432-1033.1975.tb02183.x | [] | false | eng | Eur J Biochem | 0107600 | 0014-2956 | England | [] | "2024-08-13T15:33:32.677547Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Pigeon-liver NAD kinase. The structural and kinetic basis of regulation of NADPH. | 55(2) | 475-83 | NAD kinase was purified from pigeon liver by an improved procedure which included chromatography on phosphocellulose. The resultant preparation was homogeneous as judged by gel electrophoresis, but electrofocusing gave indications of heterogeneity. The enzyme appeared to be of molecular weight 270000, and to consist of subunits of molecular weight 34000; it may therefore be an octomer. Kinetic studies over a wide range of substrate concentrations revealed departures from Michaelis-Menten behaviour with the substrate NAD+; these were interpreted tentatively in terms of negative homotropic interactions between identical binding sites, since thermal and chemical inactivation studies revealed no evidence for more than one type of catalytic site. The significance of the kinetics and of the type of inhibition produced by NADPH is discussed in terms of the regulation of NAD kinase activity in vivo. | European journal of biochemistry | [
{
"affiliation": "",
"forename": "D K",
"identifier": "",
"initials": "DK",
"lastname": "Apps"
}
] | 1975-07-01 | 239 | D000818:Animals; D001665:Binding Sites; D010856:Columbidae; D007525:Isoelectric Focusing; D007700:Kinetics; D008099:Liver / Q000201:enzymology*; D046911:Macromolecular Substances; D008970:Molecular Weight; D009243:NAD / Q000378:metabolism; D009249:NADP / Q000378:metabolism*; D010770:Phosphotransferases / Q000037:antagonists & inhibitors / Q000378:metabolism*; D017853:Phosphotransferases (Alcohol Group Acceptor) | D016428:Journal Article | D046911:Macromolecular Substances; D009243:NAD; D009249:NADP; D010770:Phosphotransferases; D017853:Phosphotransferases (Alcohol Group Acceptor); C021844:NAD kinase | 10.1111/j.1432-1033.1975.tb02184.x | [] | false | eng | Eur J Biochem | 0107600 | 0014-2956 | England | [] | "2024-08-13T15:33:32.679652Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Hydrogen ion changes and contractile behavior in the perfused rat heart. | 3(4) | 329-36 | The effect of acid-base alterations was analyzed using isolated rat hearts perfused at constant coronary perfusion pressure, and stimulated to contract at constant rat. The amount of shortening in the major axis and its derivative were measured to assess myocardial contractility. Both the 'respiratory' and 'metabolic' alterations affected the contractile behavior to the same extent. In the physiological range studied by us, acidosis depresses and alkalosis increases myocardial contraction. However acidosis seems to depress contractility more than the enhancement produced by the same change in pH towards the alkalotic side. When either amount of shortening or max dl/dt was plotted as a function of hydrogen ion acitvity (aH+) a linear correlation was obtained, either with pure 'metabolic' or 'respiratory' acid-base induced alterations (correlation coefficients higher than -.95; P less than .01). Our findings suggest that in the range studied by us, contraction of the perfused rat heart following acid-base alterations, is a linear function of hydrogen ion activity. | European journal of cardiology | [
{
"affiliation": "",
"forename": "H E",
"identifier": "",
"initials": "HE",
"lastname": "Cingolani"
},
{
"affiliation": "",
"forename": "A J",
"identifier": "",
"initials": "AJ",
"lastname": "Maas"
},
{
"affiliation": "",
"forename": "A N",
"identifier": "",
"initials": "AN",
"lastname": "Zimmerman"
},
{
"affiliation": "",
"forename": "F L",
"identifier": "",
"initials": "FL",
"lastname": "Meijler"
}
] | 1975-12 | 240 | D000136:Acid-Base Equilibrium; D000818:Animals; D001639:Bicarbonates / Q000097:blood; D002245:Carbon Dioxide / Q000097:blood; D006863:Hydrogen-Ion Concentration; D009200:Myocardial Contraction; D009206:Myocardium / Q000378:metabolism; D010477:Perfusion; D051381:Rats | D016428:Journal Article | D001639:Bicarbonates; D002245:Carbon Dioxide | [] | false | eng | Eur J Cardiol | 0404054 | 0301-4711 | Netherlands | [] | "2024-08-13T15:33:32.680614Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Changes of EEG and pulmonary venous admixture during a protein load in patients with cirrhosis. | 5(6) | 515-20 | 21 patients with cirrhosis of the liver and 24 control patients were studied before and after a protein load (120 g protein per day during one week). An EEG was recorded and a visual assessment of frequency pattern was performed. Venous admixture was estimated during hyperoxia. According to the EEG frequency pattern the patient group with cirrhosis was subdivided into those with EEG slowing after the protein load (n = 7) and those without (n = 14). The following results were obtained: 1) Resting arterial blood gases did not change in either group. 2) There was a significant increase of the AaD02 (difference between alveolar p02 and peripheral arterial p02) in cirrhotics and controls. 3) The increase in AaD02 was significantly larger in those cirrhotics showing EEG slowing compared to those without EEG - slowing or to the controls. 4) Fractional venous admisture increased significantly in those cirrhotics showing EEG slowing. There was no significant change in those patients who did not show EEG changes or in the controls. | European journal of clinical investigation | [
{
"affiliation": "",
"forename": "H",
"identifier": "",
"initials": "H",
"lastname": "Schomerus"
},
{
"affiliation": "",
"forename": "I",
"identifier": "",
"initials": "I",
"lastname": "Buchta"
},
{
"affiliation": "",
"forename": "H",
"identifier": "",
"initials": "H",
"lastname": "Arndt"
}
] | 1975-11-21 | 241 | D001794:Blood Pressure; D002245:Carbon Dioxide / Q000097:blood; D004044:Dietary Proteins; D004569:Electroencephalography; D006801:Humans; D006863:Hydrogen-Ion Concentration; D008103:Liver Cirrhosis / Q000503:physiopathology*; D010100:Oxygen / Q000097:blood; D010313:Partial Pressure | D016428:Journal Article | D004044:Dietary Proteins; D002245:Carbon Dioxide; D010100:Oxygen | 10.1111/j.1365-2362.1975.tb00484.x | [] | false | eng | Eur J Clin Invest | 0245331 | 0014-2972 | England | [] | "2024-08-13T15:33:32.682762Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Formation of fertilization acid by sea urchin eggs does not require specific cations. | 94(1) | 1-6 | Experimental cell research | [
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Paul"
},
{
"affiliation": "",
"forename": "D",
"identifier": "",
"initials": "D",
"lastname": "Epel"
}
] | 1975-08 | 242 | D000143:Acids / Q000378:metabolism*; D000818:Animals; D000001:Calcimycin / Q000494:pharmacology; D002118:Calcium / Q000378:metabolism / Q000494:pharmacology*; D004533:Egtazic Acid / Q000494:pharmacology; D005260:Female; D005306:Fertilization; D006863:Hydrogen-Ion Concentration; D008274:Magnesium / Q000494:pharmacology; D010063:Ovum / Q000187:drug effects / Q000378:metabolism*; D011188:Potassium / Q000494:pharmacology; D011189:Potassium Chloride / Q000494:pharmacology; D012617:Sea Urchins; D012965:Sodium Chloride / Q000494:pharmacology | D016428:Journal Article; D013486:Research Support, U.S. Gov't, Non-P.H.S. | D000143:Acids; D000001:Calcimycin; D012965:Sodium Chloride; D004533:Egtazic Acid; D011189:Potassium Chloride; D008274:Magnesium; D011188:Potassium; D002118:Calcium | 10.1016/0014-4827(75)90524-8 | [] | false | eng | Exp Cell Res | 0373226 | 0014-4827 | United States | [] | "2024-08-13T15:33:32.683657Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Primary culture of parenchymal liver cells on collagen membranes. Morphological and biochemical observations. | 94(1) | 70-8 | Experimental cell research | [
{
"affiliation": "",
"forename": "G",
"identifier": "",
"initials": "G",
"lastname": "Michalopoulos"
},
{
"affiliation": "",
"forename": "H C",
"identifier": "",
"initials": "HC",
"lastname": "Pitot"
}
] | 1975-08 | 243 | D003994:Bucladesine / Q000494:pharmacology; D002449:Cell Aggregation; D002467:Cell Nucleus / Q000648:ultrastructure; D002470:Cell Survival; D002478:Cells, Cultured / Q000201:enzymology / Q000648:ultrastructure; D003094:Collagen; D003594:Cytoplasmic Granules / Q000648:ultrastructure; D004790:Enzyme Induction / Q000187:drug effects; D005934:Glucagon / Q000494:pharmacology; D005947:Glucose / Q000494:pharmacology; D006854:Hydrocortisone / Q000494:pharmacology; D007328:Insulin / Q000494:pharmacology; D007365:Intercellular Junctions / Q000648:ultrastructure; D008099:Liver / Q000166:cytology*; D014444:Tyrosine Transaminase / Q000096:biosynthesis | D003160:Comparative Study; D016428:Journal Article; D013487:Research Support, U.S. Gov't, P.H.S. | D007328:Insulin; D003994:Bucladesine; D003094:Collagen; D005934:Glucagon; D014444:Tyrosine Transaminase; D005947:Glucose; D006854:Hydrocortisone | 10.1016/0014-4827(75)90532-7 | [] | false | eng | Exp Cell Res | 0373226 | 0014-4827 | United States | [] | "2024-08-13T15:33:32.684672Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Cell transformation in isolated striated muscle of hydromedusae independent of DNA synthesis. | 94(2) | 401-8 | Experimental cell research | [
{
"affiliation": "",
"forename": "V",
"identifier": "",
"initials": "V",
"lastname": "Schmid"
}
] | 1975-09 | 244 | D000818:Animals; D002454:Cell Differentiation; D003063:Cnidaria; D004247:DNA / Q000096:biosynthesis*; D004305:Dose-Response Relationship, Drug; D005407:Flagella / Q000648:ultrastructure; D008937:Mitomycins / Q000494:pharmacology; D009132:Muscles / Q000166:cytology* / Q000378:metabolism / Q000648:ultrastructure | D016428:Journal Article | D008937:Mitomycins; D004247:DNA | 10.1016/0014-4827(75)90506-6 | [
{
"citation": "Cochrane Database Syst Rev. 2007 Jul 18;(3):CD005542",
"pmid": "17636806"
},
{
"citation": "Diabet Med. 2008 Jul;25(7):765-74",
"pmid": "18644063"
},
{
"citation": "Cochrane Database Syst Rev. 2010 Jan 20;(1):CD005103",
"pmid": "20091571"
},
{
"citation": "J Diabetes Sci Technol. 2012 Jan 01;6(1):184-90",
"pmid": "22401338"
},
{
"citation": "Br Med J. 1978 Jan 28;1(6107):204-7",
"pmid": "340000"
}
] | false | eng | Exp Cell Res | 0373226 | 0014-4827 | United States | [
{
"agency": "Wellcome Trust",
"country": "United Kingdom",
"grant_acronym": "",
"grant_id": "090441"
}
] | "2024-08-13T15:33:32.685609Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Induction of DNA synthesis by dichloroisoproterenol without initial rise of the cAMP level in the parotid gland of mouse. | 94(2) | 431-4 | Experimental cell research | [
{
"affiliation": "",
"forename": "I",
"identifier": "",
"initials": "I",
"lastname": "Furuno"
},
{
"affiliation": "",
"forename": "H",
"identifier": "",
"initials": "H",
"lastname": "Matsudaira"
}
] | 1975-09 | 245 | D000818:Animals; D000242:Cyclic AMP / Q000378:metabolism*; D003513:Cycloheximide / Q000494:pharmacology; D004247:DNA / Q000096:biosynthesis*; D003609:Dactinomycin / Q000494:pharmacology; D004305:Dose-Response Relationship, Drug; D007545:Isoproterenol / Q000494:pharmacology*; D008297:Male; D051379:Mice; D008815:Mice, Inbred Strains; D010306:Parotid Gland / Q000378:metabolism* / Q000528:radiation effects; D011830:Radiation Effects; D014965:X-Rays | D016428:Journal Article | D003609:Dactinomycin; D004247:DNA; D003513:Cycloheximide; D000242:Cyclic AMP; D007545:Isoproterenol | 10.1016/0014-4827(75)90509-1 | [] | false | eng | Exp Cell Res | 0373226 | 0014-4827 | United States | [] | "2024-08-13T15:33:32.686449Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Cell density-dependent stimulation of glutamine synthetase activity in cultured mouse teratoma cells. | 94(2) | 459-64 | Experimental cell research | [
{
"affiliation": "",
"forename": "D T",
"identifier": "",
"initials": "DT",
"lastname": "Connolly"
},
{
"affiliation": "",
"forename": "S B",
"identifier": "",
"initials": "SB",
"lastname": "Oppenheimer"
}
] | 1975-09 | 246 | D003994:Bucladesine / Q000494:pharmacology; D002452:Cell Count; D002455:Cell Division; D002478:Cells, Cultured; D003470:Culture Media; D003513:Cycloheximide / Q000494:pharmacology; D003609:Dactinomycin / Q000494:pharmacology; D005974:Glutamate-Ammonia Ligase / Q000378:metabolism*; D005973:Glutamine / Q000494:pharmacology; D006854:Hydrocortisone / Q000494:pharmacology; D013806:Theophylline / Q000494:pharmacology | D016428:Journal Article; D013487:Research Support, U.S. Gov't, P.H.S. | D003470:Culture Media; D005973:Glutamine; D003609:Dactinomycin; D003994:Bucladesine; D003513:Cycloheximide; D013806:Theophylline; D005974:Glutamate-Ammonia Ligase; D006854:Hydrocortisone | 10.1016/0014-4827(75)90518-2 | [] | false | eng | Exp Cell Res | 0373226 | 0014-4827 | United States | [] | "2024-08-13T15:33:32.689875Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Polyadenylation of nascent RNA during the embryogenesis of Ilyanassa obsoleta. | 95(2) | 263-8 | Experimental cell research | [
{
"affiliation": "",
"forename": "J R",
"identifier": "",
"initials": "JR",
"lastname": "Collier"
}
] | 1975-10-15 | 247 | D000818:Animals; D002455:Cell Division; D003609:Dactinomycin / Q000494:pharmacology; D006863:Hydrogen-Ion Concentration; D011061:Poly A / Q000378:metabolism*; D012313:RNA / Q000096:biosynthesis*; D012335:RNA, Ribosomal / Q000096:biosynthesis; D012908:Snails / Q000196:embryology* / Q000378:metabolism | D016428:Journal Article; D013486:Research Support, U.S. Gov't, Non-P.H.S. | D012335:RNA, Ribosomal; D003609:Dactinomycin; D011061:Poly A; D012313:RNA | 10.1016/0014-4827(75)90550-9 | [] | false | eng | Exp Cell Res | 0373226 | 0014-4827 | United States | [] | "2024-08-13T15:33:32.690644Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
The effect of environmental pH upon acid hydrolase activities of cultured human diploid fibroblasts. | 96(2) | 317-20 | Experimental cell research | [
{
"affiliation": "",
"forename": "S",
"identifier": "",
"initials": "S",
"lastname": "Wood"
}
] | 1975-12 | 248 | D002478:Cells, Cultured; D003470:Culture Media; D005696:Galactosidases / Q000378:metabolism; D005959:Glucosidases / Q000378:metabolism; D005966:Glucuronidase / Q000378:metabolism; D006026:Glycoside Hydrolases / Q000378:metabolism*; D006596:Hexosaminidases / Q000378:metabolism; D006863:Hydrogen-Ion Concentration | D003160:Comparative Study; D016428:Journal Article | D003470:Culture Media; D005696:Galactosidases; D005959:Glucosidases; D006026:Glycoside Hydrolases; D006596:Hexosaminidases; D005966:Glucuronidase | 10.1016/0014-4827(75)90263-3 | [] | false | eng | Exp Cell Res | 0373226 | 0014-4827 | United States | [] | "2024-08-13T15:33:32.691390Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Enucleation of cells by density gradient centrifugation. | 96(2) | 360-6 | Experimental cell research | [
{
"affiliation": "",
"forename": "W",
"identifier": "",
"initials": "W",
"lastname": "Bossart"
},
{
"affiliation": "",
"forename": "H",
"identifier": "",
"initials": "H",
"lastname": "Loeffler"
},
{
"affiliation": "",
"forename": "K",
"identifier": "",
"initials": "K",
"lastname": "Bienz"
}
] | 1975-12 | 249 | D002458:Cell Fractionation / Q000379:methods*; D002460:Cell Line; D002467:Cell Nucleus; D002470:Cell Survival; D002499:Centrifugation, Density Gradient / Q000379:methods*; D003571:Cytochalasin B; D006863:Hydrogen-Ion Concentration; D013696:Temperature | D016428:Journal Article | D003571:Cytochalasin B | 10.1016/0014-4827(75)90268-2 | [] | false | eng | Exp Cell Res | 0373226 | 0014-4827 | United States | [] | "2024-08-13T15:33:32.692347Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
An evaluation of factors affecting the in vitro bioassay for erythropoietin. | 3(6) | 362-74 | Two main aspects of the in vitro mouse foetal liver cell assay for Erythroid Stimulating Factor (ESF) in human sera have been investigated. The haem extraction process has been shown to give specific and quantitative recovery of 59Fe labelled haem from haemoglobin thus confirming that the material assayed in human sera is stimulating the synthesis of this protein. The extraction procedure can be simplified considerably by prior mixing of the reagents without significantly influencing the results. Several serum constituents (citrate, testosterone, B12, folic acid and iron) have been investigated over a range of concentrations for possible effects on the cultures. Generally only small effects on haem synthesis were observed. It is concluded that variations in the levels of these factors in sera from treated patients will not produce any significant alterations in the estimated ESF concentrations. | Experimental hematology | [
{
"affiliation": "",
"forename": "C D",
"identifier": "",
"initials": "CD",
"lastname": "Dunn"
},
{
"affiliation": "",
"forename": "J A",
"identifier": "",
"initials": "JA",
"lastname": "Napier"
}
] | 1975-11 | 250 | D000818:Animals; D001681:Biological Assay; D002478:Cells, Cultured; D002951:Citrates / Q000097:blood; D003470:Culture Media; D004921:Erythropoietin / Q000378:metabolism*; D005069:Evaluation Studies as Topic; D005333:Fetus; D005492:Folic Acid / Q000097:blood; D006418:Heme / Q000378:metabolism; D006454:Hemoglobins / Q000096:biosynthesis; D006461:Hemolysis; D006863:Hydrogen-Ion Concentration; D066298:In Vitro Techniques; D007501:Iron / Q000097:blood; D008099:Liver / Q000196:embryology / Q000378:metabolism*; D051379:Mice; D013739:Testosterone / Q000097:blood; D014805:Vitamin B 12 / Q000097:blood | D016428:Journal Article | D002951:Citrates; D003470:Culture Media; D006454:Hemoglobins; D004921:Erythropoietin; D013739:Testosterone; D006418:Heme; D005492:Folic Acid; D007501:Iron; D014805:Vitamin B 12 | [] | false | eng | 76066375 | Exp Hematol | 0402313 | 0301-472X | Netherlands | [] | "2024-08-13T15:33:32.693279Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
[Cryptorchism]. | 40(10) | 23-6 | Fel'dsher i akusherka | [
{
"affiliation": "",
"forename": "S I",
"identifier": "",
"initials": "SI",
"lastname": "Volozhin"
}
] | 1975-10 | 252 | D003456:Cryptorchidism; D006801:Humans; D008297:Male | D016428:Journal Article | [] | false | rus | Kriptorkhizm | Feldsher Akush | 16930040R | 0014-9772 | Russia (Federation) | [] | "2024-08-13T15:33:32.694119Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
[Synthesis of N-substituted isoindolines]. | 30(11) | 884-90 | Some derivatives of isoindoline were prepared in order to test their cardiovascular activity. Pharmacological tests showed that some of the compounds had moderate alpha-blocking and coronarodilatory activity whereas others had some local anesthetic activity. | Il Farmaco; edizione scientifica | [
{
"affiliation": "",
"forename": "F",
"identifier": "",
"initials": "F",
"lastname": "Chimenti"
},
{
"affiliation": "",
"forename": "S",
"identifier": "",
"initials": "S",
"lastname": "Vomero"
}
] | 1975-11 | 251 | D000319:Adrenergic beta-Antagonists / Q000138:chemical synthesis*; D000779:Anesthetics, Local / Q000138:chemical synthesis*; D001562:Benzimidazoles; D007211:Indoles / Q000138:chemical synthesis*; D014665:Vasodilator Agents / Q000138:chemical synthesis* | D004740:English Abstract; D016428:Journal Article | D000319:Adrenergic beta-Antagonists; D000779:Anesthetics, Local; D001562:Benzimidazoles; D007211:Indoles; D014665:Vasodilator Agents | [] | false | ita | Sintesi di isoindoline N-sostituite | Farmaco Sci | 0370716 | 0430-0920 | Italy | [
{
"agency": "Wellcome Trust",
"country": "United Kingdom",
"grant_acronym": "",
"grant_id": "101784"
}
] | "2024-08-13T15:33:32.700796Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
[Elements of scientific work organization in ambulance feldshers' functions]. | 40(10) | 32-4 | Fel'dsher i akusherka | [
{
"affiliation": "",
"forename": "N N",
"identifier": "",
"initials": "NN",
"lastname": "Sorokin"
}
] | 1975-10 | 253 | D004632:Emergency Medical Services; D010823:Physician Assistants; D013597:Systems Analysis; D014187:Transportation of Patients | D016428:Journal Article | [] | false | rus | Elementy not v rabote fel'dshera skoroĭ pomoshchi | Feldsher Akush | 16930040R | 0014-9772 | Russia (Federation) | [] | "2024-08-13T15:33:32.701439Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
[Participation of feldshers and midwives in the secret and partisan activities during the great patriotic war]. | 40(9) | 3-6 | Fel'dsher i akusherka | [
{
"affiliation": "",
"forename": "A F",
"identifier": "",
"initials": "AF",
"lastname": "Kiselev"
}
] | 1975-09 | 254 | D006676:History of Nursing; D049673:History, 20th Century; D008880:Midwifery / Q000266:history*; D010823:Physician Assistants / Q000266:history*; D014586:USSR | D016456:Historical Article; D016428:Journal Article | [] | false | rus | Uchastie fel'dsherov i akusherok nikolaevskoĭ oblasti v podpol'nom i partizanskom dvizhenii v gody velikoĭ otechestvennoĭ voĭny | Feldsher Akush | 16930040R | 0014-9772 | Russia (Federation) | [] | "2024-08-13T15:33:32.702047Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
[The organization of health education meetings, verbal reports, carnivals, reader's conferences]. | 40(9) | 31-4 | Fel'dsher i akusherka | [
{
"affiliation": "",
"forename": "A N",
"identifier": "",
"initials": "AN",
"lastname": "Shibaeva"
}
] | 1975-09 | 255 | D003226:Congresses as Topic; D005085:Exhibitions as Topic; D006266:Health Education; D008722:Methods; D014586:USSR | D016423:Congress | [] | false | rus | Organizatsiia sanitarno-prosvetitel'nykh vecherov, ustnykh zhurnalov, karnavalov, chitatel'skikh konferentsiĭ | Feldsher Akush | 16930040R | 0014-9772 | Russia (Federation) | [] | "2024-08-13T15:33:32.702697Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
[Problems concerning the training of feldshers in foreign countries]. | 40(9) | 37-41 | Fel'dsher i akusherka | [
{
"affiliation": "",
"forename": "E V",
"identifier": "",
"initials": "EV",
"lastname": "Galakhov"
},
{
"affiliation": "",
"forename": "E P",
"identifier": "",
"initials": "EP",
"lastname": "Zhiliaeva"
}
] | 1975-09 | 256 | D010823:Physician Assistants / Q000193:education* | D016428:Journal Article | [] | false | rus | Problemy podgotovki fel'dsherov za rubezhom | Feldsher Akush | 16930040R | 0014-9772 | Russia (Federation) | [] | "2024-08-13T15:33:32.703509Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
[Mechanisms of the thermogenic action of noradrenaline during adaptation to cold]. | 61(11) | 1709-14 | In white rats both adapted and unadapted to cold, the RQ dynamics during cold exposure, noradrenaline and ganglion blocking agent administration, were studied. The adapted animals' RQ in thermoneutral conditions was shown to be a little higher than in the control rats; 0.5 mg/kg noradrenaline injections induced a clear RQ decrease in the former and did not influence the latters' RQ. Cold exposure was followed by a RQ decrease in both. Ganglion blocking agent administration decreased the RQ in the adapted animals and prevented it from falling in the control those. Noradrenaline is supposed to be the main but not the only factor activating lipolysis in the cold adapted animals. | Fiziologicheskii zhurnal SSSR imeni I. M. Sechenova | [
{
"affiliation": "",
"forename": "V I",
"identifier": "",
"initials": "VI",
"lastname": "Sobolev"
},
{
"affiliation": "",
"forename": "S A",
"identifier": "",
"initials": "SA",
"lastname": "Pevnyĭ"
}
] | 1975-11 | 257 | D000222:Adaptation, Physiological / Q000187:drug effects*; D000818:Animals; D001831:Body Temperature / Q000187:drug effects; D003080:Cold Temperature; D003864:Depression, Chemical; D005730:Ganglionic Blockers / Q000494:pharmacology; D008297:Male; D009638:Norepinephrine / Q000494:pharmacology*; D010101:Oxygen Consumption / Q000187:drug effects*; D051381:Rats | D004740:English Abstract; D016428:Journal Article | D005730:Ganglionic Blockers; D009638:Norepinephrine | [] | false | rus | O mekhanizmakh termogennogo deĭstviia noradrenaline pri adaptatsii k kholodu | Fiziol Zh SSSR Im I M Sechenova | 0427673 | 0015-329X | Russia (Federation) | [] | "2024-08-13T15:33:32.704210Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Response to exogenous gonadotropins in the unresponsive ovary syndrome. | 13(1) | 23-8 | International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics | [
{
"affiliation": "",
"forename": "P A",
"identifier": "",
"initials": "PA",
"lastname": "Zourlas"
}
] | 1975 | 258 | D015068:17-Ketosteroids / Q000652:urine; D000328:Adult; D000568:Amenorrhea / Q000188:drug therapy*; D001831:Body Temperature; D006063:Chorionic Gonadotropin / Q000494:pharmacology / Q000627:therapeutic use*; D004967:Estrogens / Q000652:urine; D005260:Female; D005640:Follicle Stimulating Hormone / Q000652:urine; D006801:Humans; D008596:Menotropins / Q000494:pharmacology / Q000627:therapeutic use*; D010053:Ovary / Q000187:drug effects; D011276:Pregnanediol / Q000652:urine | D016428:Journal Article | D015068:17-Ketosteroids; D006063:Chorionic Gonadotropin; D004967:Estrogens; D008596:Menotropins; D005640:Follicle Stimulating Hormone; D011276:Pregnanediol | 10.1002/j.1879-3479.1975.tb00329.x | [] | false | eng | Int J Gynaecol Obstet | 0210174 | 0020-7292 | United States | [] | "2024-08-13T15:33:32.705017Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
A comparative study of metal and plastic (Karman) cannulae for first trimester abortion by suction curettage. | 13(1) | 33-8 | International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics | [
{
"affiliation": "",
"forename": "L",
"identifier": "",
"initials": "L",
"lastname": "Antonovski"
},
{
"affiliation": "",
"forename": "K",
"identifier": "",
"initials": "K",
"lastname": "Ljatkova"
},
{
"affiliation": "",
"forename": "L L",
"identifier": "",
"initials": "LL",
"lastname": "Sukarov"
},
{
"affiliation": "",
"forename": "W E",
"identifier": "",
"initials": "WE",
"lastname": "Brenner"
},
{
"affiliation": "",
"forename": "D A",
"identifier": "",
"initials": "DA",
"lastname": "Edelman"
},
{
"affiliation": "",
"forename": "R P",
"identifier": "",
"initials": "RP",
"lastname": "Bernard"
}
] | 1975 | 259 | D000028:Abortion, Induced / Q000379:methods*; D000328:Adult; D004107:Dilatation and Curettage; D005260:Female; D006801:Humans; D010298:Parity; D011247:Pregnancy; D011261:Pregnancy Trimester, First; D013997:Time Factors; D014619:Vacuum Curettage | D003160:Comparative Study; D016428:Journal Article | 10.1002/j.1879-3479.1975.tb00331.x | [] | false | eng | Int J Gynaecol Obstet | 0210174 | 0020-7292 | United States | [] | "2024-08-13T15:33:32.706978Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
Acute bacterial myositis following septic abortion. An unusual complication. | 13(1) | 6-8 | International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics | [
{
"affiliation": "",
"forename": "W F",
"identifier": "",
"initials": "WF",
"lastname": "Chan"
},
{
"affiliation": "",
"forename": "H C",
"identifier": "",
"initials": "HC",
"lastname": "Ong"
},
{
"affiliation": "",
"forename": "W P",
"identifier": "",
"initials": "WP",
"lastname": "Wong"
}
] | 1975 | 260 | D000031:Abortion, Septic / Q000150:complications*; D000328:Adult; D005260:Female; D005734:Gangrene / Q000209:etiology*; D006801:Humans; D009220:Myositis / Q000209:etiology* / Q000382:microbiology; D011247:Pregnancy; D013290:Streptococcal Infections; D013291:Streptococcus / Q000302:isolation & purification | D002363:Case Reports; D016428:Journal Article | 10.1002/j.1879-3479.1975.tb00325.x | [] | false | eng | Int J Gynaecol Obstet | 0210174 | 0020-7292 | United States | [] | "2024-08-13T15:33:32.707662Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
The binding of substrates and inhibitors to dihydrofolate reductase. | 3(5) | 630-1 | Biochemical Society transactions | [
{
"affiliation": "",
"forename": "G C",
"identifier": "",
"initials": "GC",
"lastname": "Roberts"
}
] | 1975 | 261 | D001665:Binding Sites; D005492:Folic Acid; D005493:Folic Acid Antagonists; D006863:Hydrogen-Ion Concentration; D007700:Kinetics; D008024:Ligands; D009243:NAD; D011485:Protein Binding; D011487:Protein Conformation; D013762:Tetrahydrofolate Dehydrogenase / Q000378:metabolism | D016428:Journal Article | D005493:Folic Acid Antagonists; D008024:Ligands; D009243:NAD; D005492:Folic Acid; D013762:Tetrahydrofolate Dehydrogenase | 10.1042/bst0030630 | [] | false | eng | Biochem Soc Trans | 7506897 | 0300-5127 | England | [] | "2024-08-13T15:33:32.708253Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Euglena gracilis deoxyribonucleic acid polymerases: subcellular locations and variations during the cell cycle. | 3(5) | 652 | Biochemical Society transactions | [
{
"affiliation": "",
"forename": "A G",
"identifier": "",
"initials": "AG",
"lastname": "McLennan"
},
{
"affiliation": "",
"forename": "H M",
"identifier": "",
"initials": "HM",
"lastname": "Keir"
}
] | 1975 | 262 | D000818:Animals; D002455:Cell Division; D002736:Chloroplasts / Q000201:enzymology; D004254:DNA Nucleotidyltransferases / Q000378:metabolism*; D004789:Enzyme Activation / Q000187:drug effects; D005056:Euglena gracilis / Q000201:enzymology*; D006863:Hydrogen-Ion Concentration; D007527:Isoenzymes / Q000378:metabolism; D008274:Magnesium / Q000494:pharmacology; D013347:Subcellular Fractions / Q000201:enzymology; D013997:Time Factors | D016428:Journal Article | D007527:Isoenzymes; D004254:DNA Nucleotidyltransferases; D008274:Magnesium | 10.1042/bst0030652 | [] | false | eng | Biochem Soc Trans | 7506897 | 0300-5127 | England | [] | "2024-08-13T15:33:32.708850Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Monomer complexes of polyadenylic acid. | 3(5) | 655-6 | Biochemical Society transactions | [
{
"affiliation": "",
"forename": "R",
"identifier": "",
"initials": "R",
"lastname": "Jeremy"
},
{
"affiliation": "",
"forename": "H",
"identifier": "",
"initials": "H",
"lastname": "Davies"
}
] | 1975 | 263 | D001665:Binding Sites; D006863:Hydrogen-Ion Concentration; D009690:Nucleic Acid Conformation; D009905:Optical Rotatory Dispersion; D011061:Poly A; D013329:Structure-Activity Relationship; D014970:Xanthines | D016428:Journal Article | D014970:Xanthines; D011061:Poly A | 10.1042/bst0030655 | [] | false | eng | Biochem Soc Trans | 7506897 | 0300-5127 | England | [] | "2024-08-13T15:33:32.709684Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
5-Carbamoylmethyluridine: a new minor nucleoside of transfer ribonucleic acid. | 3(5) | 656-9 | Biochemical Society transactions | [
{
"affiliation": "",
"forename": "D B",
"identifier": "",
"initials": "DB",
"lastname": "Dunn"
},
{
"affiliation": "",
"forename": "M M",
"identifier": "",
"initials": "MM",
"lastname": "Trigg"
}
] | 1975 | 264 | D006863:Hydrogen-Ion Concentration; D010944:Plants / Q000032:analysis; D012343:RNA, Transfer / Q000032:analysis*; D012441:Saccharomyces cerevisiae / Q000032:analysis; D013045:Species Specificity; D013056:Spectrophotometry, Ultraviolet; D014908:Triticum / Q000032:analysis; D014529:Uridine / Q000031:analogs & derivatives* / Q000032:analysis | D016428:Journal Article | D012343:RNA, Transfer; D014529:Uridine | 10.1042/bst0030656 | [] | false | eng | Biochem Soc Trans | 7506897 | 0300-5127 | England | [] | "2024-08-13T15:33:32.710588Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
The protective effects of cephaloridine on rat kidney lysosomes in vitro. | 3(5) | 736-8 | Biochemical Society transactions | [
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Fry"
},
{
"affiliation": "",
"forename": "E O",
"identifier": "",
"initials": "EO",
"lastname": "Ngaha"
},
{
"affiliation": "",
"forename": "D T",
"identifier": "",
"initials": "DT",
"lastname": "Plummer"
}
] | 1975 | 265 | D000135:Acid Phosphatase / Q000032:analysis; D000818:Animals; D001192:Arylsulfatases / Q000032:analysis; D002509:Cephaloridine / Q000494:pharmacology*; D003605:D-Amino-Acid Oxidase / Q000032:analysis; D005952:Glucose-6-Phosphatase / Q000032:analysis; D005969:Glutamate Dehydrogenase / Q000032:analysis; D007668:Kidney / Q000201:enzymology*; D008247:Lysosomes / Q000187:drug effects / Q000201:enzymology / Q000648:ultrastructure*; D008297:Male; D008856:Microscopy, Fluorescence; D051381:Rats | D016428:Journal Article | D005969:Glutamate Dehydrogenase; D003605:D-Amino-Acid Oxidase; D000135:Acid Phosphatase; D005952:Glucose-6-Phosphatase; D001192:Arylsulfatases; D002509:Cephaloridine | 10.1042/bst0030736 | [] | false | eng | Biochem Soc Trans | 7506897 | 0300-5127 | England | [] | "2024-08-13T15:33:32.711396Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[In vitro studies on human ovarian contractility (author's transl)]. | 20(4) | 38-43 | Nihon Funin Gakkai zasshi | [
{
"affiliation": "",
"forename": "H",
"identifier": "",
"initials": "H",
"lastname": "Okamura"
},
{
"affiliation": "",
"forename": "T",
"identifier": "",
"initials": "T",
"lastname": "Okazaki"
},
{
"affiliation": "",
"forename": "A",
"identifier": "",
"initials": "A",
"lastname": "Nakajima"
}
] | 1975-10 | 266 | D000109:Acetylcholine / Q000494:pharmacology; D000318:Adrenergic beta-Agonists / Q000494:pharmacology*; D003338:Corpus Luteum / Q000187:drug effects; D004558:Electric Stimulation; D005260:Female; D006801:Humans; D066298:In Vitro Techniques; D007556:Isoxsuprine / Q000494:pharmacology; D009119:Muscle Contraction / Q000187:drug effects; D009130:Muscle, Smooth / Q000187:drug effects; D009638:Norepinephrine / Q000494:pharmacology; D006080:Ovarian Follicle / Q000187:drug effects; D010053:Ovary / Q000187:drug effects / Q000502:physiology*; D010643:Phenoxybenzamine / Q000494:pharmacology; D011453:Prostaglandins / Q000494:pharmacology*; D011458:Prostaglandins E / Q000494:pharmacology; D011460:Prostaglandins F / Q000494:pharmacology | D003160:Comparative Study; D004740:English Abstract; D016428:Journal Article | D000318:Adrenergic beta-Agonists; D011453:Prostaglandins; D011458:Prostaglandins E; D011460:Prostaglandins F; D010643:Phenoxybenzamine; D000109:Acetylcholine; D007556:Isoxsuprine; D009638:Norepinephrine | [
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] | false | jpn | Nihon Funin Gakkai Zasshi | 7505712 | 0029-0629 | Japan | [] | "2024-08-13T15:33:32.713710Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
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[Studies on the energy for sperm motility (author's transl)]. | 20(4) | 6-13 | Nihon Funin Gakkai zasshi | [
{
"affiliation": "",
"forename": "K",
"identifier": "",
"initials": "K",
"lastname": "Imamura"
}
] | 1975-10 | 267 | D000251:Adenosine Triphosphatases / Q000378:metabolism; D000255:Adenosine Triphosphate / Q000378:metabolism; D006801:Humans; D006863:Hydrogen-Ion Concentration; D008297:Male; D010101:Oxygen Consumption; D013081:Sperm Motility; D013094:Spermatozoa / Q000378:metabolism* | D004740:English Abstract; D016428:Journal Article | D000255:Adenosine Triphosphate; D000251:Adenosine Triphosphatases | [] | false | jpn | Nihon Funin Gakkai Zasshi | 7505712 | 0029-0629 | Japan | [] | "2024-08-13T15:33:32.714523Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
Properties of urophysial proteins (urophysins) from the white sucker, Catostomus commersoni. | 3(4) | 297-307 | Molecular and cellular endocrinology | [
{
"affiliation": "",
"forename": "G",
"identifier": "",
"initials": "G",
"lastname": "Moore"
},
{
"affiliation": "",
"forename": "G",
"identifier": "",
"initials": "G",
"lastname": "Burford"
},
{
"affiliation": "",
"forename": "K",
"identifier": "",
"initials": "K",
"lastname": "Lederis"
}
] | 1975-10 | 268 | D000818:Animals; D002352:Carrier Proteins / Q000032:analysis* / Q000302:isolation & purification; D003956:Dialysis; D004591:Electrophoresis, Polyacrylamide Gel; D005399:Fishes; D006863:Hydrogen-Ion Concentration; D007525:Isoelectric Focusing; D009490:Neurosecretory Systems / Q000032:analysis* | D016428:Journal Article | D002352:Carrier Proteins | 10.1016/0303-7207(75)90011-8 | [] | false | eng | Mol Cell Endocrinol | 7500844 | 0303-7207 | Ireland | [] | "2024-08-13T15:33:32.715372Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
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Glutamine synthetase in newborn mice homozygous for lethal albino alleles. | 45(2) | 369-71 | Developmental biology | [
{
"affiliation": "",
"forename": "S",
"identifier": "",
"initials": "S",
"lastname": "Gluecksohn-Waelsch"
},
{
"affiliation": "",
"forename": "M B",
"identifier": "",
"initials": "MB",
"lastname": "Schiffman"
}
] | 1975-08 | 269 | D000417:Albinism / Q000235:genetics*; D000483:Alleles; D000818:Animals; D001921:Brain / Q000201:enzymology; D005123:Eye / Q000201:enzymology; D005260:Female; D005804:Genes, Lethal; D005974:Glutamate-Ammonia Ligase / Q000032:analysis*; D006579:Heterozygote; D006720:Homozygote; D008099:Liver / Q000201:enzymology*; D008297:Male; D051379:Mice; D009206:Myocardium / Q000201:enzymology; D011506:Proteins / Q000032:analysis | D016428:Journal Article; D013487:Research Support, U.S. Gov't, P.H.S. | D011506:Proteins; D005974:Glutamate-Ammonia Ligase | 10.1016/0012-1606(75)90075-5 | [] | false | eng | Dev Biol | 0372762 | 0012-1606 | United States | [] | "2024-08-13T15:33:32.716216Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Chromosomal basis of the merozygosity in a partially deploid mutant of Pneumococcus. | 80(4) | 667-78 | A sulfonamide-resistant mutant of pneumococcus, sulr-c, displays a genetic instability, regularly segregating to wild type. DNA extracts of derivatives of the strain possess transforming activities for both the mutant and wild-type alleles, establishing that the strain is a partial diploid. The linkage of sulr-c to strr-61, a stable chromosomal marker, was established, thus defining a chromosomal locus for sulr-c. DNA isolated from sulr-c cells transforms two mutant recipient strains at the same low efficiency as it does a wild-type recipient, although the mutant property of these strains makes them capable of integrating classical "low-efficiency" donor markers equally as efficiently as "high efficiency" markers. Hence sulr-c must have a different basis for its low efficiency than do classical low efficiency point mutations. We suggest that the DNA in the region of the sulr-c mutation has a structural abnormality which leads both to its frequent segregation during growth and its difficulty in efficiently mediating genetic transformation. | Genetics | [
{
"affiliation": "",
"forename": "M L",
"identifier": "",
"initials": "ML",
"lastname": "Ledbetter"
},
{
"affiliation": "",
"forename": "R D",
"identifier": "",
"initials": "RD",
"lastname": "Hotchkiss"
}
] | 1975-08 | 270 | D002874:Chromosome Mapping; D002876:Chromosomes, Bacterial; D003433:Crosses, Genetic; D004261:DNA Replication; D004171:Diploidy; D004352:Drug Resistance, Microbial; D008040:Genetic Linkage; D006238:Haploidy; D009154:Mutation; D013296:Streptococcus pneumoniae / Q000187:drug effects*; D013449:Sulfonamides / Q000494:pharmacology; D014170:Transformation, Genetic | D016428:Journal Article; D013487:Research Support, U.S. Gov't, P.H.S. | D013449:Sulfonamides | 10.1093/genetics/80.4.667 | [
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] | false | eng | Genetics | 0374636 | 0016-6731 | United States | [] | "2024-08-13T15:33:32.717753Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Recombination as a requirement for segregation of a partially diploid mutant of Pneumococcus. | 80(4) | 679-94 | Conditions are described in which the pneumococcal mutant strain sulr-c, resistant to the drug sulfanilamide, gives rise to sensitive segregants resistant to nitrobenzoic acid at a frequency constant with time. This segregant frequency is markedly enhanced upon exposure of the cells to doses of ultraviolet light or mitomycin C that permit survival of 50% to 90% of the cells. Treatment with acridine orange diminishes the segregant frequency. From the known influences of these three agents on genetic recombination, we propose that a recombination event is necessary in the generation of segregants.--During a period of incubation following treatment with ultraviolet light or mitomycin C, cell division resumes and the original segregant frequency is restored. Thus potential segregants are either unable to replicate in the absence of selection, or they are under-represented among the cells dividing soon after treatment.--If the sulr-c mutation is introduced into a mutant pneumococcal strain lacking an ATP-dependent exonuclease activity and deficient in recombination with transforming DNA, segregant frequencies are unaffected. This fact may indicate limits upon the type of recombination event responsible for segregation. | Genetics | [
{
"affiliation": "",
"forename": "M L",
"identifier": "",
"initials": "ML",
"lastname": "Ledbetter"
},
{
"affiliation": "",
"forename": "R D",
"identifier": "",
"initials": "RD",
"lastname": "Hotchkiss"
}
] | 1975-08 | 271 | D000166:Acridines / Q000494:pharmacology; D002455:Cell Division; D004171:Diploidy; D004352:Drug Resistance, Microbial; D008540:Meiosis / Q000187:drug effects / Q000528:radiation effects; D008937:Mitomycins / Q000494:pharmacology; D009154:Mutation; D009579:Nitrobenzoates / Q000494:pharmacology; D011815:R Factors; D011831:Radiation Genetics; D011995:Recombination, Genetic; D012459:Salicylates / Q000494:pharmacology; D013296:Streptococcus pneumoniae / Q000187:drug effects*; D013449:Sulfonamides / Q000494:pharmacology; D013997:Time Factors; D014466:Ultraviolet Rays | D016428:Journal Article; D013487:Research Support, U.S. Gov't, P.H.S. | D000166:Acridines; D008937:Mitomycins; D009579:Nitrobenzoates; D012459:Salicylates; D013449:Sulfonamides | 10.1093/genetics/80.4.679 | [
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] | false | eng | Genetics | 0374636 | 0016-6731 | United States | [] | "2024-08-13T15:33:32.720120Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
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[Extrabronchial effects of Bronchodilat in patients with asthma and chronic asthmatic bronchitis]. | 43(11) | 995-1000 | Gruzlica i choroby pluc; tuberculosis et pneumonologia | [
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "Rozniecki"
},
{
"affiliation": "",
"forename": "W",
"identifier": "",
"initials": "W",
"lastname": "Grabski"
}
] | 1975-11 | 272 | D000293:Adolescent; D000328:Adult; D000628:Aminophylline / Q000494:pharmacology / Q000627:therapeutic use; D000779:Anesthetics, Local / Q000494:pharmacology* / Q000627:therapeutic use; D001249:Asthma / Q000188:drug therapy; D001980:Bronchi / Q000187:drug effects; D001991:Bronchitis / Q000188:drug therapy; D002908:Chronic Disease; D004338:Drug Combinations; D006321:Heart / Q000187:drug effects*; D006634:Histamine H1 Antagonists / Q000494:pharmacology* / Q000627:therapeutic use; D006801:Humans; D008875:Middle Aged; D010627:Phenethylamines / Q000494:pharmacology* / Q000627:therapeutic use; D011437:Propylamines / Q000494:pharmacology* / Q000627:therapeutic use | D003160:Comparative Study; D016428:Journal Article | D000779:Anesthetics, Local; D004338:Drug Combinations; D006634:Histamine H1 Antagonists; D010627:Phenethylamines; D011437:Propylamines; D000628:Aminophylline; C011412:bronchodilat | [] | false | pol | Ocena bronchospasmolitycznego i pozaoskrzelowego działania brondilatu u chorych na astme oskrzelowa lub przewlekłe astmatyczne zapalenie oskrzeli | Gruzlica | 0167652 | 0017-4955 | Poland | [] | "2024-08-13T15:33:32.721268Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Involvement of the small intestine in systemic mast cell disease. | 16(11) | 918-24 | A patient is reported with mast cell infiltration of the small intestine in the absence of the skin involvement characteristic of mast cell disease. She also had subtotal villous atrophy responsive to a gluten-free diet. Criteria for diagnosing mast cell disease of the small intestine are proposed. The literature of small intestinal mast cell disease is reviewed and the relationship to coeliac disease is discussed. | Gut | [
{
"affiliation": "",
"forename": "B B",
"identifier": "",
"initials": "BB",
"lastname": "Scott"
},
{
"affiliation": "",
"forename": "G J",
"identifier": "",
"initials": "GJ",
"lastname": "Hardy"
},
{
"affiliation": "",
"forename": "M S",
"identifier": "",
"initials": "MS",
"lastname": "Losowsky"
}
] | 1975-11 | 273 | D000328:Adult; D002446:Celiac Disease / Q000150:complications / Q000178:diet therapy / Q000473:pathology; D005260:Female; D006634:Histamine H1 Antagonists / Q000627:therapeutic use; D006801:Humans; D007413:Intestinal Mucosa / Q000473:pathology; D007421:Intestine, Small / Q000473:pathology*; D007583:Jejunum / Q000473:pathology; D008286:Malabsorption Syndromes / Q000150:complications; D008875:Middle Aged; D014582:Urticaria Pigmentosa / Q000175:diagnosis / Q000188:drug therapy / Q000473:pathology* | D002363:Case Reports; D016428:Journal Article | D006634:Histamine H1 Antagonists | 10.1136/gut.16.11.918 | [
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] | false | eng | Gut | 2985108R | 0017-5749 | England | [] | "2024-08-13T15:33:32.723171Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Gastric pH and microflora of normal and diarrhoeic infants. | 16(9) | 719-26 | The microflora and pH of gastric contents were determined in breast-fed and in bottle-fed normal infants, in well nourished infants with acute diarrhoea and in infants with chronic diarrhoea and protein-calorie malnutrition. The last group of infants was reevaluated after recovery from diarrhoea and protein-calorie malnutrition. A bactericidal pH effect below 2-5 was observed. Bottle-fed controls had low pH values and low bacterial concentrations, whereas infants with chronic diarrhoea and protein-calorie malnutrition had high pH values and bacterial overgrowth, essentially of Gram-negative bacilli. After recovery, the only remaining alteration was the frequent isolation of yeast-like fungi in low concentrations. Infants with acute diarrhoea, except for the isolation more frequently of yeast-like fungi, presented no alterations; this seems to indicate that pH alterations and Gram-negative bacilli overgrowth occurred during the evolution of the disease to a chronic state. Breast-fed normal infants had hydrogen-ion concentrations similar to those of the chronic diarrhoea group, but without Gram-negative bacilli overgrowth, suggesting that other factors, besides pH, regulate bacterial growth in the gastric contents of these groups of infants. | Gut | [
{
"affiliation": "",
"forename": "H V",
"identifier": "",
"initials": "HV",
"lastname": "Maffei"
},
{
"affiliation": "",
"forename": "F J",
"identifier": "",
"initials": "FJ",
"lastname": "Nóbrega"
}
] | 1975-09 | 274 | D000208:Acute Disease; D001419:Bacteria / Q000302:isolation & purification*; D001942:Breast Feeding; D002176:Candida albicans / Q000302:isolation & purification; D002908:Chronic Disease; D003968:Diarrhea, Infantile / Q000382:microbiology*; D004755:Enterobacteriaceae / Q000302:isolation & purification; D005750:Gastric Juice / Q000378:metabolism*; D006801:Humans; D006863:Hydrogen-Ion Concentration; D007223:Infant; D010614:Pharynx / Q000382:microbiology; D011502:Protein-Energy Malnutrition / Q000382:microbiology; D011549:Pseudomonas / Q000302:isolation & purification; D013210:Staphylococcus / Q000302:isolation & purification; D013270:Stomach / Q000382:microbiology*; D013291:Streptococcus / Q000302:isolation & purification | D003160:Comparative Study; D016428:Journal Article | 10.1136/gut.16.9.719 | [
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] | false | eng | Gut | 2985108R | 0017-5749 | England | [] | "2024-08-13T15:33:32.725983Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Allogenic bone marrow transplantation in men]. | 16() | 306-29 | Hamatologie und Bluttransfusion | [
{
"affiliation": "",
"forename": "K A",
"identifier": "",
"initials": "KA",
"lastname": "Dicker"
},
{
"affiliation": "",
"forename": "B",
"identifier": "",
"initials": "B",
"lastname": "Löwenberg"
},
{
"affiliation": "",
"forename": "U W",
"identifier": "",
"initials": "UW",
"lastname": "Schaefer"
},
{
"affiliation": "",
"forename": "D W",
"identifier": "",
"initials": "DW",
"lastname": "van Bekkum"
}
] | 1975 | 275 | D000367:Age Factors; D000741:Anemia, Aplastic / Q000601:surgery; D000818:Animals; D001854:Bone Marrow Cells; D016026:Bone Marrow Transplantation; D002470:Cell Survival; D006087:Graft vs Host Reaction; D006680:HLA Antigens; D018380:Hematopoietic Stem Cell Transplantation; D006801:Humans; D051379:Mice; D011832:Radiation Injuries / Q000601:surgery; D014019:Tissue Donors; D014184:Transplantation, Homologous | D016428:Journal Article | D006680:HLA Antigens | [] | false | ger | Allogene knochenmarktransplantation beim menschen | Hamatol Bluttransfus | 7804332 | 0440-0607 | Germany | [] | "2024-08-13T15:33:32.726947Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Bone marrow transplantation in patients with aplastic anemia]. | 16() | 330-51 | Hamatologie und Bluttransfusion | [
{
"affiliation": "",
"forename": "L J",
"identifier": "",
"initials": "LJ",
"lastname": "Dooren"
},
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "de Koning"
},
{
"affiliation": "",
"forename": "R P",
"identifier": "",
"initials": "RP",
"lastname": "Kamphuis"
},
{
"affiliation": "",
"forename": "C H",
"identifier": "",
"initials": "CH",
"lastname": "Uittenbogaart"
},
{
"affiliation": "",
"forename": "A M",
"identifier": "",
"initials": "AM",
"lastname": "Brubakk"
},
{
"affiliation": "",
"forename": "J M",
"identifier": "",
"initials": "JM",
"lastname": "Vossen"
}
] | 1975 | 276 | D000293:Adolescent; D000328:Adult; D000741:Anemia, Aplastic / Q000601:surgery*; D001854:Bone Marrow Cells; D016026:Bone Marrow Transplantation; D002648:Child; D002675:Child, Preschool; D005260:Female; D006087:Graft vs Host Reaction; D006680:HLA Antigens; D006801:Humans; D008297:Male; D008875:Middle Aged; D014019:Tissue Donors; D014184:Transplantation, Homologous | D016428:Journal Article | D006680:HLA Antigens | [] | false | ger | Knochenmarktransplantation bei patienten mit aplastischer anämie | Hamatol Bluttransfus | 7804332 | 0440-0607 | Germany | [] | "2024-08-13T15:33:32.727975Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Analysis of clinical phenomena and changes in physico-chemical properties of the blood in mentally ill children]. | 17(3) | 313-28 | Folia medica Cracoviensia | [
{
"affiliation": "",
"forename": "R",
"identifier": "",
"initials": "R",
"lastname": "Bichoński"
}
] | 1975 | 277 | D000293:Adolescent; D000367:Age Factors; D001809:Blood Viscosity; D002648:Child; D002675:Child, Preschool; D006801:Humans; D006863:Hydrogen-Ion Concentration; D001523:Mental Disorders / Q000097:blood*; D013500:Surface Tension | D004740:English Abstract; D016428:Journal Article | [] | false | pol | Analiza zjawisk klinicznych oraz zmian właściwości fizykochemicznych krwi u dzieci psychicznie chorych | Folia Med Cracov | 0374617 | 0015-5616 | Poland | [] | "2024-08-13T15:33:32.728638Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
[Biphasic (ulcer-forming and ulcer-preventing) effect of adrenaline in rats]. | 71(5) | 405-14 | Adrenaline-induced gastric ulceration was studied in rats. Adrenaline in high doses caused gastric ulcer, which was completely blocked by pretreatment with alpha-blockers (phenoxybenzamine, dibenamine), but not by pretreatment with propranolol or atropine, nor by vagotomy, hypophysectomy or adrenalectomy. After successive administration of adrenaline, once daily for 7 days, however, no gastric ulcer was observed. Recovery from the ulcerogenic action of adrenaline was seen after 4 weeks withdrawal. Pretreatment with a small dose of adrenaline inhibited the ulcerogenic action of a high dose of adrenaline. Pretreatment with reserpine, pyrogallol or iproniazid inhibited the action of adrenaline. It is concluded that adrenaline has a biphasic effect on gastric ulceration, the ulcerogenic action is due to its alpha-action and antiulcerogenic effect is due to development of tachyphylaxis. | Nihon yakurigaku zasshi. Folia pharmacologica Japonica | [
{
"affiliation": "",
"forename": "T",
"identifier": "",
"initials": "T",
"lastname": "Dozaki"
},
{
"affiliation": "",
"forename": "K",
"identifier": "",
"initials": "K",
"lastname": "Imai"
},
{
"affiliation": "",
"forename": "S",
"identifier": "",
"initials": "S",
"lastname": "Mizukami"
}
] | 1975-07 | 278 | D000315:Adrenalectomy; D000317:Adrenergic alpha-Antagonists / Q000494:pharmacology; D000319:Adrenergic beta-Antagonists / Q000494:pharmacology; D000818:Animals; D001285:Atropine / Q000494:pharmacology; D002395:Catecholamines / Q000494:pharmacology; D004305:Dose-Response Relationship, Drug; D004837:Epinephrine / Q000008:administration & dosage / Q000037:antagonists & inhibitors* / Q000494:pharmacology*; D006634:Histamine H1 Antagonists / Q000494:pharmacology; D007016:Hypophysectomy; D007490:Iproniazid / Q000494:pharmacology; D008297:Male; D011748:Pyrogallol / Q000494:pharmacology; D051381:Rats; D012110:Reserpine / Q000494:pharmacology; D013276:Stomach Ulcer / Q000139:chemically induced / Q000517:prevention & control; D014628:Vagotomy | D004740:English Abstract; D016428:Journal Article | D000317:Adrenergic alpha-Antagonists; D000319:Adrenergic beta-Antagonists; D002395:Catecholamines; D006634:Histamine H1 Antagonists; D011748:Pyrogallol; D001285:Atropine; D012110:Reserpine; D007490:Iproniazid; D004837:Epinephrine | [] | false | jpn | Nihon Yakurigaku Zasshi | 0420550 | 0015-5691 | Japan | [] | "2024-08-13T15:33:32.730802Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Comparison of drug effects on the isolated rat colon and duodenum]. | 71(5) | 415-26 | Adrenaline and isoproterenol elicited nearly maximal relaxation of the colon even in small doses, whereas increase in the doses caused greater relaxation in the duodenum. In the colon, these drugs prevented, to a great extent the contraction induced by acetylcholine (ACh) and serotonin but in the duodenum were totally ineffective. Dibenamine and propranolol reduced adrenaline- and isoproterenol-induced relaxation in the duodenum, though propranolol decreased the relaxation caused by isoproterenol. Atropine prevented ACh-induced contraction in both the colon and duodenum in the same way. After 2-bromolysergic acid diethylamide, duodenal contraction caused by ACh or serotonin decreased by over 70%; however, the contraction of the colon was not significantly inhibited. Methysergide had similar effects, but to a lesser degree. In calcium-free bathing fluid without addition of Na2EDTA, ACh and prostaglandin E1 elicited contraction in the colon, but not in the duodenum. | Nihon yakurigaku zasshi. Folia pharmacologica Japonica | [
{
"affiliation": "",
"forename": "H",
"identifier": "",
"initials": "H",
"lastname": "Koshiba"
}
] | 1975-07 | 279 | D000109:Acetylcholine / Q000494:pharmacology; D000818:Animals; D001285:Atropine / Q000494:pharmacology; D003106:Colon / Q000187:drug effects*; D003404:Creatinine / Q000494:pharmacology; D003983:Dibenzylchlorethamine / Q000494:pharmacology; D004386:Duodenum / Q000187:drug effects*; D004492:Edetic Acid / Q000494:pharmacology; D004837:Epinephrine / Q000494:pharmacology; D005260:Female; D066298:In Vitro Techniques; D007545:Isoproterenol / Q000494:pharmacology; D008238:Lysergic Acid Diethylamide / Q000494:pharmacology; D008297:Male; D008784:Methysergide / Q000494:pharmacology; D011433:Propranolol / Q000494:pharmacology; D011458:Prostaglandins E / Q000494:pharmacology; D051381:Rats; D012701:Serotonin / Q000494:pharmacology | D003160:Comparative Study; D004740:English Abstract; D016428:Journal Article | D011458:Prostaglandins E; D012701:Serotonin; D003983:Dibenzylchlorethamine; D001285:Atropine; D008238:Lysergic Acid Diethylamide; D004492:Edetic Acid; D011433:Propranolol; D003404:Creatinine; D007545:Isoproterenol; D000109:Acetylcholine; D008784:Methysergide; D004837:Epinephrine | [
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{
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] | false | jpn | Nihon Yakurigaku Zasshi | 0420550 | 0015-5691 | Japan | [] | "2024-08-13T15:33:32.731961Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Monoamine oxidase (XXXVI). Characteristics of benzylamine oxidase in the dog serum]. | 71(5) | 457-62 | Enzymic properties of monoamine oxidase (MAO) in dog serum were studied and the following results were obtained. Some of enzymic properties of MAO in dog serum differed from that of mitochondrial MAO. When dog serum was fractionated by ammonium sulfate, proteins were concentrated in two fractions, such as 25 approximately 33% and 67 approximately 80% of saturated ammonium sulfate fraction, while MAO activity was concentrated in 40 approximately 50% of saturated ammonium sulfate fraction. The reaction rate of MAO in dog serum was found to be proportional to enzyme concentration. The optimum pH of MAO in dog serum was 7.0 which differed from that of MAO in rabbit serum (pH 8.0). Tris-HCl buffer strongly inhibited MAO activity in dog serum. When benzylamine was used as substrate, the highest activity was obtained compared with the other substrate used. The activities with butylamine, amylamine, beta-phenylethylamine and tyramine showed about 30% while tryptamine and serotonin showed 3 approximately 10% compared to that with benzymlamine as substrate. The value of pI50 of catron was about 3 X 10(-6) M and that of harmaline was about 3 X 10(-5) M, but pargyline did not inhibit MAO activity in dog serum at the concentration of 1 X 10(-4) M. | Nihon yakurigaku zasshi. Folia pharmacologica Japonica | [
{
"affiliation": "",
"forename": "T",
"identifier": "",
"initials": "T",
"lastname": "Fukushima"
}
] | 1975-07 | 280 | D000645:Ammonium Sulfate; D000818:Animals; D001595:Benzylamine Oxidase / Q000097:blood*; D001798:Blood Proteins / Q000032:analysis; D004285:Dogs; D006863:Hydrogen-Ion Concentration; D008995:Monoamine Oxidase / Q000097:blood* | D004740:English Abstract; D016428:Journal Article | D001798:Blood Proteins; D001595:Benzylamine Oxidase; D008995:Monoamine Oxidase; D000645:Ammonium Sulfate | [] | false | jpn | Nihon Yakurigaku Zasshi | 0420550 | 0015-5691 | Japan | [] | "2024-08-13T15:33:32.732949Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Combined use of bucolome and pyrazolone derivatives (1). Pharmacological activities and blood concentration]. | 71(6) | 609-29 | A combination of two or more drugs may exert a drug-drug interaction, in which case the effect can be potentiated or antagonized. Such synergistic effects are well known in the case of pyrabital (barbital + aminopyrine) or irgapyrine (phenylbutazone + aminopyrine). Bucolome (BCP), a non-steroidal anti-inflammatory agent, has the chemical structure of a barbiturate and also resembles the formula of pheylbutazone. Thus the influence of BCP combination on the pharmacological activities of various pyrazolone derivatives was examined. BCP potentiated the analgesic and antipyretic effects of 4-aminoantipyrine (4A), methylaminoantipyrine (MA), aminopyrine (AM) and isopropylaminoantipyrine (IPA), which were substituted by the alkylamino group at 4-position of the pyrazolone ring. This potentiation occurred when the dose of BCP exceeded that of the pyrazolones, and was especially marked when combination ratio of BCP exceeded that of the pyrazolones, and was especially marked when combination ratio of BCP and pyrazolone was 2:1 mola. The analgesic effects of antipyrine (AN), isopropylantipyrine (IP) and aminopropylone (AP), which were substituted by alkyl group or aminoacylamino group at 4-position, were not potentiated by BCP in any combination ratio. Most pyrazolones showed additive acute toxicity in their combination with BCP, but acute toxicities of 4A and AM, which were potentiated in analgesic effects, were decreased and antagonized when combined with BCP. The plasma concentration of AM was increased and prolonged by BCP, while that of IP remained much the same. These results suggest that the pharmacological activities are associated with certain molecular interactions between BCP and pyrazolones, which are substituted by the alkylamino group at 4-position of the pyrazolone ring. | Nihon yakurigaku zasshi. Folia pharmacologica Japonica | [
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Nozaki"
}
] | 1975-09 | 281 | D000700:Analgesics / Q000494:pharmacology; D000818:Animals; D001463:Barbiturates / Q000097:blood / Q000494:pharmacology / Q000633:toxicity; D001831:Body Temperature / Q000187:drug effects; D004338:Drug Combinations; D004347:Drug Interactions; D008297:Male; D051379:Mice; D011720:Pyrazoles / Q000097:blood / Q000494:pharmacology / Q000633:toxicity; D011817:Rabbits | D004740:English Abstract; D016428:Journal Article | D000700:Analgesics; D001463:Barbiturates; D004338:Drug Combinations; D011720:Pyrazoles | [] | false | jpn | Nihon Yakurigaku Zasshi | 0420550 | 0015-5691 | Japan | [] | "2024-08-13T15:33:32.733821Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Combined use of bucolome and pyrazolone derivatives (II). Complex formation due to interaction between bucolome and pyrazolones]. | 71(6) | 631-9 | We have already reported that bucolome (BCP), a non-steroidal anti-inflammatory agent, potentiates significantly the analgesic and antipyretic effects of pyrazolones which are substituted by alkylamino group at 4-position of the pyrazolone ring. Physical and quantum chemistry were applied to the mechanism of this synergistic action. The solubility of BCP was markedly increased in proportion to elevation of aminopyrine (AM) concentration, but not by a combination with isopropylantipyrine (IP). The binding of BCP to bovine serum albumin was slightly inhibited by AM, but not by IP. The mixture of AM and BCP in aqueous media generated optical absorption in the ultraviolet differential spectrum, due to the charge transfer interaction. The results of the infrared or NMR spectrum demonstrated the formation of a hydrogen binding in non-aqueous media between BCP and AM. From the calculation of the charge on an atom, the energy of the highest occupied molecular orbital and the frontier electron density, BCP is considered to be a good electron acceptor. The beta-units of Mho of pyrazolones were found to correlate with the potentiation coefficient of analgesic activity in combination drugs. These results suggest that the complex formation between BCP and pyrazolones is an important factor for the synergism of action and is due to the charge transfer interaction and the hydrogen binding of both molecules. | Nihon yakurigaku zasshi. Folia pharmacologica Japonica | [
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Nozaki"
}
] | 1975-09 | 282 | D001463:Barbiturates / Q000097:blood / Q000494:pharmacology; D055598:Chemical Phenomena; D002621:Chemistry; D004338:Drug Combinations; D004347:Drug Interactions; D011485:Protein Binding / Q000187:drug effects; D011720:Pyrazoles / Q000494:pharmacology; D012709:Serum Albumin / Q000378:metabolism | D004740:English Abstract; D016428:Journal Article | D001463:Barbiturates; D004338:Drug Combinations; D011720:Pyrazoles; D012709:Serum Albumin | [] | false | jpn | Nihon Yakurigaku Zasshi | 0420550 | 0015-5691 | Japan | [] | "2024-08-13T15:33:32.735746Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Fructose 1,6-bisphosphate aldolase activity of Rhizobium species. | 20(5) | 412-7 | FDP aldolase was found to be present in the cell-free extracts of Rhizobium leguminosarum, Rhizobium phaseoli, Rhizobium trifolii, Rhizobium meliloti, Rhizobium lupini, Rhizobium japonicum and Rhizobium species from Arachis hypogaea and Sesbania cannabina. The enzyme in 3 representative species has optimal activity at pH 8.4 in 0.2M veronal buffer. The enzyme activity was completely lost by treatment at 60 degrees C for 15 min. The Km values were in the range from 2.38 to 4.55 X 10(-6)M FDP. Metal chelating agents inhibited enzyme activity, but monovalent or bivalent metal ions failed to stimulate the activity. Bivalent metal ions in general were rather inhibitory. | Folia microbiologica | [
{
"affiliation": "",
"forename": "K A",
"identifier": "",
"initials": "KA",
"lastname": "Siddiqui"
},
{
"affiliation": "",
"forename": "A K",
"identifier": "",
"initials": "AK",
"lastname": "Banerjee"
}
] | 1975 | 283 | D002474:Cell-Free System; D002614:Chelating Agents / Q000494:pharmacology; D003545:Cysteine / Q000494:pharmacology; D005634:Fructose-Bisphosphate Aldolase / Q000378:metabolism*; D006358:Hot Temperature; D006863:Hydrogen-Ion Concentration; D008670:Metals / Q000494:pharmacology; D012231:Rhizobium / Q000201:enzymology*; D013045:Species Specificity | D016428:Journal Article | D002614:Chelating Agents; D008670:Metals; D005634:Fructose-Bisphosphate Aldolase; D003545:Cysteine | 10.1007/BF02877044 | [
{
"citation": "J Bacteriol. 1970 Mar;101(3):698-704",
"pmid": "5438044"
},
{
"citation": "Can J Microbiol. 1957 Oct;3(6):879-84",
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},
{
"citation": "Nature. 1955 Mar 26;175(4456):551-2",
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},
{
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},
{
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},
{
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},
{
"citation": "Biochem J. 1956 May;63(1):94-105",
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},
{
"citation": "J Bacteriol. 1969 Mar;97(3):1184-91",
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},
{
"citation": "J Bacteriol. 1962 Oct;84:694-700",
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},
{
"citation": "Plant Physiol. 1966 Oct;41(8):1330-6",
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},
{
"citation": "Fed Proc. 1964 Nov-Dec;23:1248-57",
"pmid": "14236133"
}
] | false | eng | Folia Microbiol (Praha) | 0376757 | 0015-5632 | United States | [] | "2024-08-13T15:33:32.736628Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Prevention of cell agglutination and competence in a genetically transformable strain of Pneumococcus by D-glucosamine and D-galactosamine. | 20(6) | 443-51 | In the presence of amino sugars D-glucosamine and D-galactosamine no spontaneous competence could be observed in the highly transformable R6bd strain of Pneumococcus or it was decreased by several orders of magnitude. The highest inhibition of competence was detected when the amino sugar at a concentration 5 mg/ml of the medium was added not only to the transformation but also to the pretransformation medium. After a 150 min growth in the transformation medium in the presence of the amino sugar a 3--4-fold greater number of cells (as a viable count) could be detected as compared with the control without the amino sugar. It was found microscopically that the amino sugar prevents natural agglutination, which normally occurs in the competent culture. The role of specific amino sugar determinants for binding of the competence factor on the cell surface and the resulting inhibitory effect of these sugars on the development of competence are discussed. | Folia microbiologica | [
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Kohoutová"
}
] | 1975 | 284 | D000371:Agglutination / Q000187:drug effects*; D000606:Amino Sugars / Q000494:pharmacology; D004269:DNA, Bacterial; D003864:Depression, Chemical; D005688:Galactosamine / Q000494:pharmacology*; D005944:Glucosamine / Q000494:pharmacology*; D008358:Mannose; D013237:Stereoisomerism; D013296:Streptococcus pneumoniae / Q000187:drug effects* / Q000276:immunology; D014170:Transformation, Genetic / Q000187:drug effects* | D016428:Journal Article | D000606:Amino Sugars; D004269:DNA, Bacterial; D005688:Galactosamine; D005944:Glucosamine; D008358:Mannose | 10.1007/BF02891702 | [
{
"citation": "J Bacteriol. 1971 Nov;108(2):668-79",
"pmid": "5001867"
},
{
"citation": "Nature. 1974 Feb 1;247(5439):277-9",
"pmid": "4150438"
},
{
"citation": "Folia Microbiol (Praha). 1975;20(3):212-8",
"pmid": "237807"
},
{
"citation": "J Biol Chem. 1963 Jun;238:1928-34",
"pmid": "13931034"
},
{
"citation": "Folia Microbiol (Praha). 1973;18(6):499-505",
"pmid": "4149534"
},
{
"citation": "J Bacteriol. 1974 Dec;120(3):1478-80",
"pmid": "4154936"
},
{
"citation": "Biochim Biophys Acta. 1955 Dec;18(4):467-81",
"pmid": "13304028"
},
{
"citation": "J Bacteriol. 1972 Feb;109(2):652-8",
"pmid": "4621684"
},
{
"citation": "J Bacteriol. 1972 Apr;110(1):273-80",
"pmid": "5018023"
},
{
"citation": "J Biol Chem. 1967 Feb 10;242(3):463-70",
"pmid": "4381522"
},
{
"citation": "Can J Microbiol. 1970 May;16(5):345-50",
"pmid": "5463244"
},
{
"citation": "J Bacteriol. 1966 Mar;91(3):1050-61",
"pmid": "4379672"
},
{
"citation": "Science. 1972 Sep 15;177(4053):949-59",
"pmid": "5055944"
},
{
"citation": "J Gen Microbiol. 1965 Feb;38:211-9",
"pmid": "14287199"
},
{
"citation": "Folia Microbiol (Praha). 1973;18(6):506-13",
"pmid": "4775441"
},
{
"citation": "J Bacteriol. 1971 Mar;105(3):1213-5",
"pmid": "4396142"
},
{
"citation": "Proc Natl Acad Sci U S A. 1954 Feb;40(2):49-55",
"pmid": "16589433"
}
] | false | eng | Folia Microbiol (Praha) | 0376757 | 0015-5632 | United States | [] | "2024-08-13T15:33:32.737817Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Effect of some aldoses on growth of Saccharomyces cerevisiae inhibited with molybdenum. | 20(6) | 467-9 | The inhibitory effect of molybdenum ions on growth of yeasts at pH 5.5 was found to be decreased by aldoses in the following order: D-talose greater than L-mannose greater than L-ribose greater than D-lyxose greater than L-galactose greater than L-arabinose greater than L-glucose greater than L-xylose. Increased concentrations of molybdenum brought about morphological changes of yeast cells. Cells grown under these conditions were smaller, had thicker walls and formed clusters. | Folia microbiologica | [
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "Zemek"
},
{
"affiliation": "",
"forename": "V",
"identifier": "",
"initials": "V",
"lastname": "Bílik"
},
{
"affiliation": "",
"forename": "L",
"identifier": "",
"initials": "L",
"lastname": "Zákutná"
}
] | 1975 | 285 | D001089:Arabinose / Q000494:pharmacology; D002241:Carbohydrates / Q000494:pharmacology*; D002473:Cell Wall / Q000648:ultrastructure; D005690:Galactose / Q000494:pharmacology; D005947:Glucose / Q000494:pharmacology; D006863:Hydrogen-Ion Concentration; D008358:Mannose / Q000494:pharmacology; D008982:Molybdenum / Q000494:pharmacology*; D012266:Ribose / Q000494:pharmacology; D012441:Saccharomyces cerevisiae / Q000187:drug effects / Q000254:growth & development* / Q000648:ultrastructure; D013237:Stereoisomerism; D014994:Xylose / Q000494:pharmacology | D016428:Journal Article | D002241:Carbohydrates; D012266:Ribose; D008982:Molybdenum; D014994:Xylose; D001089:Arabinose; D005947:Glucose; D008358:Mannose; D005690:Galactose | 10.1007/BF02891705 | [] | false | eng | Folia Microbiol (Praha) | 0376757 | 0015-5632 | United States | [] | "2024-08-13T15:33:32.751149Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Transport properties of membrane vesicles from Acholeplasma laidlawii. II. Kinetic characteristics and specificity of glucose transport system. | 20(6) | 480-7 | The glucose transport system of membrane vesicles isolated from Acholeplasma laidlawii is saturable, with a Km of 21.2 mum and V of 0.68 nmol min-1 (mg protein)-1. The process is pH-dependent and a break occurs in the Arrhenius plot at 15 degrees C. Exogenous substrates did not stimulate glucose transport probably due to their inability to penetrate into membrane vesicles. 3-O-Methylglucose and 6-deoxyglucose competitively inhibited glucose transport. Maltose inhibited transport of glucose noncompetitively. These sugars also elicited glucose efflux from preloaded membrane vesicles. | Folia microbiologica | [
{
"affiliation": "",
"forename": "L F",
"identifier": "",
"initials": "LF",
"lastname": "Panchenko"
},
{
"affiliation": "",
"forename": "N S",
"identifier": "",
"initials": "NS",
"lastname": "Fedotov"
},
{
"affiliation": "",
"forename": "M A",
"identifier": "",
"initials": "MA",
"lastname": "Tarshis"
}
] | 1975 | 286 | D000128:Acholeplasma laidlawii / Q000378:metabolism*; D001693:Biological Transport, Active; D002462:Cell Membrane / Q000378:metabolism; D003847:Deoxyglucose / Q000378:metabolism; D005947:Glucose / Q000378:metabolism*; D006863:Hydrogen-Ion Concentration; D007700:Kinetics; D008320:Maltose / Q000378:metabolism; D008757:Methylglucosides / Q000378:metabolism; D013347:Subcellular Fractions; D013696:Temperature | D016428:Journal Article | D008757:Methylglucosides; D008320:Maltose; D003847:Deoxyglucose; D005947:Glucose | 10.1007/BF02891707 | [
{
"citation": "Biochim Biophys Acta. 1969 Jul 15;183(2):295-303",
"pmid": "5792242"
},
{
"citation": "J Bacteriol. 1974 Feb;117(2):888-99",
"pmid": "4590489"
},
{
"citation": "J Bacteriol. 1972 Aug;111(2):454-8",
"pmid": "5053467"
},
{
"citation": "Biochem Biophys Res Commun. 1972 May 26;47(4):838-45",
"pmid": "4337324"
},
{
"citation": "J Bacteriol. 1969 Feb;97(2):787-92",
"pmid": "5773029"
},
{
"citation": "Folia Microbiol (Praha). 1975;20(6):470-9",
"pmid": "127739"
},
{
"citation": "Biochim Biophys Acta. 1973 Oct 25;323(3):429-40",
"pmid": "4271263"
},
{
"citation": "J Bacteriol. 1973 Jan;113(1):212-7",
"pmid": "4688137"
},
{
"citation": "J Biol Chem. 1951 Nov;193(1):265-75",
"pmid": "14907713"
},
{
"citation": "Eur J Biochem. 1973 Dec 3;40(1):171-5",
"pmid": "4772677"
},
{
"citation": "Proc Natl Acad Sci U S A. 1973 Dec;70(12):3376-81",
"pmid": "4587250"
}
] | false | eng | Folia Microbiol (Praha) | 0376757 | 0015-5632 | United States | [] | "2024-08-13T15:33:32.753435Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Transport of 4-deoxy- and 6-deoxy-D-glucose in baker's yeast. | 20(6) | 496-503 | Tritium-labelled 4-deoxy-D-glucose (4-dglc) and 6-deoxy-D-glucose (6-dgcl) were prepared by catalytic hydrogenolysis of the corresponding deoxyiodo derivatives with gaseous tritium. The two sugars are transported into Saccharomyces cerevisiae by both the constitutive glucose and the inducible galactose carrier. Uranyl ions are powerful inhibitors. The pH optimum in uninduced cells lies at 5.5 for both sugars, the apparent activation energies (between 15 and 35 degrees C) are 25.1 kJ/mol and 16.5 kJ/mol, respectively. The steady-state intracellular concentration of both sugars is less than the extracellular one (no uphill transport). Neither of them is a substrate of yeast hexokinase. 4-Deoxy-D-glucose undergoes a dinitrophenol-sensitive conversion to an unknown metabolite which is not phosphorylated and may represent one of its oxidation products. | Folia microbiologica | [
{
"affiliation": "",
"forename": "A",
"identifier": "",
"initials": "A",
"lastname": "Kotyk"
},
{
"affiliation": "",
"forename": "D",
"identifier": "",
"initials": "D",
"lastname": "Michaljanicová"
},
{
"affiliation": "",
"forename": "K",
"identifier": "",
"initials": "K",
"lastname": "Veres"
},
{
"affiliation": "",
"forename": "V",
"identifier": "",
"initials": "V",
"lastname": "Soukupová"
}
] | 1975 | 287 | D003837:Deoxy Sugars / Q000378:metabolism*; D003847:Deoxyglucose / Q000138:chemical synthesis / Q000378:metabolism*; D004140:Dinitrophenols / Q000494:pharmacology; D004579:Electron Transport; D005632:Fructose / Q000378:metabolism; D005947:Glucose / Q000378:metabolism; D006593:Hexokinase / Q000378:metabolism; D006863:Hydrogen-Ion Concentration; D007460:Iodoacetamide / Q000494:pharmacology; D012441:Saccharomyces cerevisiae / Q000201:enzymology / Q000378:metabolism*; D013696:Temperature; D014501:Uranium / Q000494:pharmacology | D016428:Journal Article | D003837:Deoxy Sugars; D004140:Dinitrophenols; D005632:Fructose; D014501:Uranium; D003847:Deoxyglucose; D006593:Hexokinase; D005947:Glucose; D007460:Iodoacetamide | 10.1007/BF02891709 | [
{
"citation": "J Theor Biol. 1972 Apr;35(1):113-8",
"pmid": "5044826"
},
{
"citation": "Folia Microbiol (Praha). 1968;13(3):212-20",
"pmid": "5672582"
},
{
"citation": "Eur J Biochem. 1968 Aug;5(3):321-9",
"pmid": "5680352"
},
{
"citation": "Folia Microbiol (Praha). 1971;16(6):432-44",
"pmid": "4947177"
},
{
"citation": "Folia Microbiol (Praha). 1968;13(1):12-9",
"pmid": "5642682"
},
{
"citation": "Folia Microbiol (Praha). 1967;12(2):121-31",
"pmid": "6047678"
},
{
"citation": "J Bacteriol. 1968 Feb;95(2):603-11",
"pmid": "5640385"
}
] | false | eng | Folia Microbiol (Praha) | 0376757 | 0015-5632 | United States | [] | "2024-08-13T15:33:32.754467Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Gluconic acid production by Penicillium puberulum. | 20(6) | 504-8 | Twenty-five Penicillium species isolated from Egyptian soil were examined for their ability to produce gluconic acid in surface culture. Of the eight species capable of producing gluconic acid, Penicillium puberulum gave the maximum yield (91% gluconic acid from glucose after 7 days of fermentation with 3% CaCO3). Peptone was the best nitrogen source for acid fermentation and glucose was superior to sucrose. Addition of low concentrations of KH2PO4 and MgSO4 - 7 H2O stimulated acid production. An initial pH of 6.1 was most favourable for acid accumulation and addition of CaCO3 was necessary for maximum acid production. | Folia microbiologica | [
{
"affiliation": "",
"forename": "M A",
"identifier": "",
"initials": "MA",
"lastname": "Elnaghy"
},
{
"affiliation": "",
"forename": "S E",
"identifier": "",
"initials": "SE",
"lastname": "Megalla"
}
] | 1975 | 288 | D002119:Calcium Carbonate / Q000378:metabolism; D004534:Egypt; D005285:Fermentation; D005942:Gluconates / Q000096:biosynthesis*; D005947:Glucose / Q000378:metabolism; D006863:Hydrogen-Ion Concentration; D008278:Magnesium Sulfate / Q000494:pharmacology; D010407:Penicillium / Q000378:metabolism*; D010461:Peptones / Q000378:metabolism; D010710:Phosphates / Q000494:pharmacology; D012988:Soil Microbiology; D013045:Species Specificity; D013395:Sucrose / Q000378:metabolism | D016428:Journal Article | D005942:Gluconates; D010461:Peptones; D010710:Phosphates; D013395:Sucrose; D008278:Magnesium Sulfate; D002119:Calcium Carbonate; D005947:Glucose | 10.1007/BF02891710 | [
{
"citation": "Folia Microbiol (Praha). 1963 Jul;8:203-14",
"pmid": "13936632"
},
{
"citation": "Can J Microbiol. 1955 Jun;1(6):470-2",
"pmid": "14390024"
},
{
"citation": "Appl Microbiol. 1965 Sep;13(5):713-9",
"pmid": "5325935"
}
] | false | eng | Folia Microbiol (Praha) | 0376757 | 0015-5632 | United States | [] | "2024-08-13T15:33:32.755797Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
A simple method of isolation and purification of cultures of wood-rotting fungi. | 20(6) | 519-20 | A simple method of isolation and purification of cultures of higher fungi, mainly wood-rotting fungi, without special requirements for the presence of nitrogencontaining nutrients is described. Parts of fruiting bodies, spores or infected wood is inoculated on Petri dishes with an agar medium of the following composition: 1.0 g KH2PO4, 0.2 g MgSO4 - 7 H2O, 0.1 g caSO4, 0.01 g Fe2(SO4)3, 10.0 g glucose, tap water to 1 litre; 20.0 g agar. This medium does not suit most of the contaminants but fungal hyphae overgrow the whole surface of the dish so that a purified culture can be obtained from parts distant from the inoculation site. | Folia microbiologica | [
{
"affiliation": "",
"forename": "A",
"identifier": "",
"initials": "A",
"lastname": "Ginterová"
},
{
"affiliation": "",
"forename": "O",
"identifier": "",
"initials": "O",
"lastname": "Janotková"
}
] | 1975 | 289 | D000362:Agar; D003470:Culture Media; D005658:Fungi / Q000302:isolation & purification* / Q000378:metabolism; D006863:Hydrogen-Ion Concentration; D009584:Nitrogen / Q000378:metabolism; D014934:Wood | D016428:Journal Article | D003470:Culture Media; D000362:Agar; D009584:Nitrogen | 10.1007/BF02891714 | [
{
"citation": "Folia Microbiol (Praha). 1966;11(2):146-54",
"pmid": "5916361"
}
] | false | eng | Folia Microbiol (Praha) | 0376757 | 0015-5632 | United States | [] | "2024-08-13T15:33:32.756508Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
The effect of CTAB, a cationic surfactant, on the absorption rate of [14C]tripalmitate from a test meal in the rat. | 13(5) | 517-20 | Food and cosmetics toxicology | [
{
"affiliation": "",
"forename": "B",
"identifier": "",
"initials": "B",
"lastname": "Isomaa"
},
{
"affiliation": "",
"forename": "G",
"identifier": "",
"initials": "G",
"lastname": "Sjöblom"
}
] | 1975-10 | 290 | D000821:Animal Feed; D000818:Animals; D002593:Cetrimonium Compounds / Q000494:pharmacology*; D004032:Diet; D005750:Gastric Juice / Q000378:metabolism; D005753:Gastric Mucosa / Q000187:drug effects / Q000378:metabolism; D006863:Hydrogen-Ion Concentration; D007408:Intestinal Absorption / Q000187:drug effects*; D008297:Male; D010168:Palmitates / Q000378:metabolism*; D010169:Palmitic Acids / Q000378:metabolism*; D000644:Quaternary Ammonium Compounds / Q000494:pharmacology*; D051381:Rats; D013268:Stimulation, Chemical | D016428:Journal Article | D002593:Cetrimonium Compounds; D010168:Palmitates; D010169:Palmitic Acids; D000644:Quaternary Ammonium Compounds | 10.1016/0015-6264(75)90005-x | [] | false | eng | Food Cosmet Toxicol | 0374623 | 0015-6264 | England | [] | "2024-08-13T15:33:32.757576Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Language of the other]. | 93(34) | 1708-11 | Fortschritte der Medizin | [
{
"affiliation": "",
"forename": "L",
"identifier": "",
"initials": "L",
"lastname": "von Ferber"
}
] | 1975-12-04 | 291 | D003226:Congresses as Topic; D006233:Disabled Persons; D005260:Female; D005860:Germany, West; D006801:Humans; D007802:Language; D007804:Language Development; D008297:Male; D009034:Mother-Child Relations; D009497:Neurotic Disorders / Q000150:complications; D011618:Psychotic Disorders / Q000150:complications; D012564:Schizophrenic Language; D013064:Speech Disorders / Q000209:etiology*; D014705:Verbal Behavior | D016423:Congress | [] | false | ger | Die Sprache des Anderen | Fortschr Med | 2984763R | 0015-8178 | Germany | [] | "2024-08-13T15:33:32.759535Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||||
[Studies on low volume priming heart lung bypass (author's transl)]. | 50(2) | 137-67 | This report concerns the feasibility of low volume priming extracorporeal circulation. Through this study, the bubble oxygenator with Zuhdi's heat exchange was used. Moderate hypothermia with surface cooling and hemodilution perfusion with 5 per cent D/W was evaluated in 32 mongrel dogs and 16 clinical open heart cases. The results obtained here were as follow: 1) Body temperature reduction by surface cooling before bypass provided more even cooling than did core cooling by low flow partial bypass alone. 2) In regard to cardiac loading on returning the whole perfusate of the circuit to patient, approximately 20 ml/kg of 5 per cent D/W was feasible as a priming solution. 3) To reduce the blood visicosity, hemodilution technique with 5 per cent D/W was superior, and hemodilution effect during postoperative periods was temporaly. 4) The excess lactate volume postulated by Huckabee was a available index to evaluate metabolic acidosis during the extracorporeal circulation. 5) With aid of surface cooling, the acid-base balance during perfusion was kept to lesser extent than that of core cooling only. 6) This study indicated that the low priming perfusion in conjunction with surface cooling hypothermia was a reliable technique for the open heart operation and may be applied in more prolonged perfusion. | [Hokkaido igaku zasshi] The Hokkaido journal of medical science | [
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Kawamura"
}
] | 1975-03 | 292 | D000136:Acid-Base Equilibrium; D000293:Adolescent; D000328:Adult; D000818:Animals; D001772:Blood Cell Count; D001809:Blood Viscosity; D001810:Blood Volume; D001831:Body Temperature; D002648:Child; D002675:Child, Preschool; D004285:Dogs; D004573:Electrolytes / Q000097:blood; D005112:Extracorporeal Circulation / Q000379:methods*; D005260:Female; D006355:Heart-Lung Machine; D006400:Hematocrit; D006801:Humans; D006863:Hydrogen-Ion Concentration; D007036:Hypothermia, Induced / Q000379:methods*; D007773:Lactates / Q000097:blood; D008297:Male; D010477:Perfusion | D004740:English Abstract; D016428:Journal Article; D016454:Review | D004573:Electrolytes; D007773:Lactates | [] | false | jpn | Hokkaido Igaku Zasshi | 17410290R | 0367-6102 | Japan | [] | "2024-08-13T15:33:32.760364Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Studies on extracorporeal circulation with large volume hemodilution using lactate ringer's solution and low molecular weight dextran: alterations of acid-base balance associated with intentional hemodilution (author's transl)]. | 50(2) | 169-96 | Twenty mongrel dogs, weighing between 7.5 and 13.0 kg were used to investigate the percentage limits permissible for hemodilution using a double-helical reservoir heart-lung machine which has a 1,100 ml of priming volume. In both 40 and 50 per cent groups of intentional hemodilution by 30 minute extracorporeal circulation, remarkable anemia was inevitable and recovery was extremely slow, especially in the 50 per cent dilution group. In both 40 and 50 per cent groups of intentional hemodilutions by 30 minute extracorporeal circulation, metabolic acidosis was observed. In 50 per cent group of intentional hemodilution, no improvement of metabolic acidosis was observed even after perfusion. When sodium bicarbonate was administered to 40 per cent hemodilution group, minimum alterations of acid-base balance and of serum electrolytes were observed during and after extracorporeal perfusion. When sodium bicarbonate was administered to 50 per cent hemodilution group, metabolic acidosis was more evident than in 40 per cent hemodilution group accompanied with an increase in serum sodium concentration and a decrease in serum chloride concentration. These data qualify the use of 40 per cent intentional hemodilution using Lactate Ringer's solution or low molecular weight dextran for 30 minute extracorporeal circulation when sodium bicarbonate is administered in adequate amounts. | [Hokkaido igaku zasshi] The Hokkaido journal of medical science | [
{
"affiliation": "",
"forename": "T",
"identifier": "",
"initials": "T",
"lastname": "Yamada"
}
] | 1975-03 | 293 | D000136:Acid-Base Equilibrium / Q000187:drug effects*; D000138:Acidosis / Q000209:etiology; D000740:Anemia / Q000209:etiology; D000818:Animals; D001639:Bicarbonates / Q000097:blood; D001810:Blood Volume; D003911:Dextrans / Q000494:pharmacology*; D004285:Dogs; D004573:Electrolytes / Q000097:blood; D005112:Extracorporeal Circulation / Q000379:methods*; D006400:Hematocrit; D006454:Hemoglobins / Q000032:analysis; D006863:Hydrogen-Ion Concentration; D007552:Isotonic Solutions; D007773:Lactates / Q000097:blood / Q000494:pharmacology*; D010100:Oxygen / Q000097:blood; D010952:Plasma Substitutes | D016428:Journal Article; D016454:Review | D001639:Bicarbonates; D003911:Dextrans; D004573:Electrolytes; D006454:Hemoglobins; D007552:Isotonic Solutions; D007773:Lactates; D010952:Plasma Substitutes; D010100:Oxygen | [] | false | jpn | Hokkaido Igaku Zasshi | 17410290R | 0367-6102 | Japan | [] | "2024-08-13T15:33:32.761469Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
[Malignant rheumatoid arthritis]. | 50(3) | 278-80 | [Hokkaido igaku zasshi] The Hokkaido journal of medical science | [
{
"affiliation": "",
"forename": "M",
"identifier": "",
"initials": "M",
"lastname": "Nakahara"
}
] | 1975-05 | 294 | D000328:Adult; D001172:Arthritis, Rheumatoid / Q000150:complications / Q000175:diagnosis; D005260:Female; D006801:Humans; D008297:Male; D008875:Middle Aged; D010493:Pericarditis / Q000150:complications; D010488:Polyarteritis Nodosa / Q000150:complications; D011115:Polyneuropathies / Q000150:complications | D016428:Journal Article | [] | false | jpn | Hokkaido Igaku Zasshi | 17410290R | 0367-6102 | Japan | [] | "2024-08-13T15:33:32.762118Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||||
Purification and characterization of phosphodiesterase from Crotalus venom. | 356(7) | 1085-96 | A procedure for the purification of phosphodiesterase from Crotalus venom on DEAE-cellulose at alkaline pH is described. The enzyme gives a single band in polyacrylamide gels and is free of contaminating nucleolytic enzymes. The molecular weight is about 115000. Concentration in an Amicon ultrafiltrator gave a highly concentrated active enzyme. Phosphodiesterase is relatively stable and can be stored at 4 degrees C in the presence of Mg2 and serum albumin for years. For the detection of contaminating endonuclease, an assay was used in which tRNA was the substrate and possible internal breaks were detected in polyacrylamide gel after denaturation. With bis(p-nitrophenyl) phosphate as substrate, 15mM Mg2 was necessary for optimal activity. The reaction remained linear for at least 15 min at 22 degrees C. At 45 degrees C, the liberation of p-nitrophenol was highest within 25 min of incubation. At 75 degrees C, inactivation of the enzyme occurred after 4 min. | Hoppe-Seyler's Zeitschrift fur physiologische Chemie | [
{
"affiliation": "",
"forename": "G R",
"identifier": "",
"initials": "GR",
"lastname": "Philipps"
}
] | 1975-07 | 295 | D000818:Animals; D002848:Chromatography, DEAE-Cellulose; D004591:Electrophoresis, Polyacrylamide Gel; D004720:Endonucleases; D006863:Hydrogen-Ion Concentration; D008274:Magnesium / Q000494:pharmacology; D008722:Methods; D008970:Molecular Weight; D010727:Phosphoric Diester Hydrolases / Q000302:isolation & purification* / Q000378:metabolism; D012343:RNA, Transfer / Q000378:metabolism; D012910:Snake Venoms / Q000032:analysis* / Q000378:metabolism; D013696:Temperature; D014462:Ultrafiltration | D016428:Journal Article | D012910:Snake Venoms; D012343:RNA, Transfer; D004720:Endonucleases; D010727:Phosphoric Diester Hydrolases; D008274:Magnesium | 10.1515/bchm2.1975.356.2.1085 | [] | false | eng | Hoppe Seylers Z Physiol Chem | 2985060R | 0018-4888 | Germany | [] | "2024-08-13T15:33:32.767616Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Limited hydrolysis of tRNA by phosphodiesterase. | 356(7) | 1097-104 | Digestion of tRNA by electrophoretically pure phosphodiesterase is limited to a short sequence of nucleotides at the 3'-terminus. On the average, four percent of all nucleotides can be released from tRNA. The optimum Mg2 concentration is 10mM and the optimum pH 9.2. The mode of action is a random attack by the enzyme on the substrate. The terminal AMP is completely removed at 15 degrees C after short incubation; about 400 mol of AMP were removed per min by 1 mol of enzyme. The following CMP residues are released much more slowly; at 15 degrees C incompletely, and at 37 degrees C more or less completely in 1 h. In about 50% of the tRNA molecules, the fourth nucleotide could be removed in very long incubations or with very high enzyme concentrations. | Hoppe-Seyler's Zeitschrift fur physiologische Chemie | [
{
"affiliation": "",
"forename": "G R",
"identifier": "",
"initials": "GR",
"lastname": "Philipps"
},
{
"affiliation": "",
"forename": "T",
"identifier": "",
"initials": "T",
"lastname": "Chiemprasert"
}
] | 1975-07 | 296 | D000249:Adenosine Monophosphate / Q000378:metabolism; D001483:Base Sequence; D003568:Cytidine Monophosphate / Q000378:metabolism; D004926:Escherichia coli / Q000201:enzymology; D006863:Hydrogen-Ion Concentration; D006868:Hydrolysis; D008274:Magnesium / Q000494:pharmacology; D009713:Nucleotidyltransferases / Q000378:metabolism; D010727:Phosphoric Diester Hydrolases / Q000378:metabolism*; D012343:RNA, Transfer / Q000378:metabolism* | D016428:Journal Article | D000249:Adenosine Monophosphate; D012343:RNA, Transfer; D009713:Nucleotidyltransferases; D010727:Phosphoric Diester Hydrolases; D003568:Cytidine Monophosphate; D008274:Magnesium | 10.1515/bchm2.1975.356.2.1097 | [] | false | eng | Hoppe Seylers Z Physiol Chem | 2985060R | 0018-4888 | Germany | [] | "2024-08-13T15:33:32.769697Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Ecdysone Oxidase, an enzyme from the blowfly Calliphora erythrocephala (Meigen). | 356(7) | 1131-8 | In the blowfly, the formation of 3-dehydroecdysone from the insect molting hormone ecdysone is catalyzed by an enzyme which carries hydrogen from ecdysone and ecdysterone to oxygen. The enzyme is therefore called "ecdysone oxidase". Two methods are described for the detection of ecdysone oxidase activity, one using a radiolabelled substrate which is separated from the product by thin-layer chromatography after the reaction, and the other using dichloroindophenol, which is discoloured by the redox reaction. The ecdysone oxidase is purified by a factor of 2200 from prepupae of Calliphora erythrocephala using salt precipitation and ion exchange chromatography. The ecdysone oxidase has a Km value for ecdysone of 42muM. The pH optimum is 6.5. The temperature optimum lies at 45 degrees C. The ecdysone oxidase has a molecular weight of 240000. | Hoppe-Seyler's Zeitschrift fur physiologische Chemie | [
{
"affiliation": "",
"forename": "J",
"identifier": "",
"initials": "J",
"lastname": "Koolman"
},
{
"affiliation": "",
"forename": "P",
"identifier": "",
"initials": "P",
"lastname": "Karlson"
}
] | 1975-07 | 297 | D015086:2,6-Dichloroindophenol; D000818:Animals; D002852:Chromatography, Ion Exchange; D002855:Chromatography, Thin Layer; D004175:Diptera / Q000201:enzymology*; D004440:Ecdysone / Q000378:metabolism*; D004441:Ecdysterone / Q000378:metabolism; D006863:Hydrogen-Ion Concentration; D007700:Kinetics; D008970:Molecular Weight; D010084:Oxidation-Reduction; D010088:Oxidoreductases / Q000302:isolation & purification / Q000378:metabolism* | D016428:Journal Article | D004440:Ecdysone; D004441:Ecdysterone; D015086:2,6-Dichloroindophenol; D010088:Oxidoreductases | 10.1515/bchm2.1975.356.2.1131 | [] | false | eng | Hoppe Seylers Z Physiol Chem | 2985060R | 0018-4888 | Germany | [] | "2024-08-13T15:33:32.770624Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
||||
Using a hospital for desensitization of an outpatient's illness-related fears. | 26(10) | 675-7 | An outpatient with phobias related to enclosed places, hospitals, doctors, and cancer was treated by systematic desensitization; the facilities of a general hospital were used for part of the process. Steps in treatment included securing a complete psychiatric and social history, teaching the patient relaxation therapy techniques, and establishing a hierarchy of anxiety-provoking stimuli specifically related to the patient's fears. After desensitization the patient was able to enter the hospital for tests for a physical ailment and showed a general decrease in her fears. | Hospital & community psychiatry | [
{
"affiliation": "",
"forename": "P S",
"identifier": "",
"initials": "PS",
"lastname": "Powers"
},
{
"affiliation": "",
"forename": "H P",
"identifier": "",
"initials": "HP",
"lastname": "Powers"
}
] | 1975-10 | 298 | D000328:Adult; D001521:Behavior Therapy; D003863:Depression / Q000628:therapy; D003887:Desensitization, Psychologic; D005260:Female; D006769:Hospitals, General; D006801:Humans; D010698:Phobic Disorders / Q000628:therapy*; D012064:Relaxation Therapy | D002363:Case Reports; D016428:Journal Article | 10.1176/ps.26.10.675 | [] | false | eng | Hosp Community Psychiatry | 0040250 | 0022-1597 | United States | [] | "2024-08-13T15:33:32.771358Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Analog computer for base excess and HCO3-from pH and PCO2 electrodes. | 23(1) | 77-81 | IEEE transactions on bio-medical engineering | [
{
"affiliation": "",
"forename": "J W",
"identifier": "",
"initials": "JW",
"lastname": "Severinghaus"
}
] | 1976-01 | 299 | D000136:Acid-Base Equilibrium; D001639:Bicarbonates / Q000097:blood*; D002245:Carbon Dioxide / Q000097:blood*; D003202:Computers, Analog; D004566:Electrodes; D005110:Extracellular Space / Q000032:analysis; D006801:Humans; D006863:Hydrogen-Ion Concentration; D010313:Partial Pressure | D016428:Journal Article | D001639:Bicarbonates; D002245:Carbon Dioxide | 10.1109/tbme.1976.324622 | [] | false | eng | IEEE Trans Biomed Eng | 0012737 | 0018-9294 | United States | [] | "2024-08-13T15:33:32.772204Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |
|||||
Alcohol-related problems in a general hospital emergency room. | 148(5) | 509-10 | IMJ. Illinois medical journal | [
{
"affiliation": "",
"forename": "M A",
"identifier": "",
"initials": "MA",
"lastname": "Amdur"
}
] | 1975-11 | 300 | D000435:Alcoholic Intoxication / Q000453:epidemiology*; D000437:Alcoholism / Q000453:epidemiology*; D004636:Emergency Service, Hospital; D005260:Female; D006769:Hospitals, General; D006801:Humans; D007087:Illinois; D008297:Male | D003160:Comparative Study; D016428:Journal Article | [] | false | eng | IMJ Ill Med J | 7703940 | United States | [] | "2024-08-13T15:33:32.772787Z" | https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0001.xml.gz |