coenzyme a has been researched along with Acidosis in 39 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 39 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
WEISS, L; WIELAND, O | 1 |
HIBBITT, KG | 1 |
Isselbacher, KJ; Tanaka, K | 1 |
Bussman, YL; DeVivo, DC; Haymond, MW; Leckie, MP; McDougal, DB; Pagliara, AS | 1 |
Ando, T; Kilroy, A; Nyhan, WL; Sweetman, L; Wadlington, WB | 1 |
Marsac, C; Stansbie, D; Wallace, SJ | 1 |
Dugan, RE; Gilles, BA; Hoganson, GE; Schmidt, MJ; Shug, AL; Steele, J | 1 |
Goldstein, L; Tullson, PC | 1 |
Callaghan, P; Newman, CG; Wilson, BD; Young, L | 1 |
Hsia, YE; Rosenberg, LE; Scully, KJ | 1 |
Bau, DC; Gompertz, D; Hughes, EA; Peters, TJ; Storrs, CN | 1 |
Cornblath, M; Tildon, JT | 1 |
Ackermann, RH; Bässler, KH; Schönerstedt, B; Wagner, K | 1 |
Erfle, JD; Sauer, F | 1 |
Lemieux, G; Lussier, Y; Martin, P; Plante, GE; Robitaille, P; Vinay, P | 1 |
Dierich, C; Huth, W; Seubert, W; von Oeynhausen, V | 1 |
Gerald, PS; Kang, ES; Snodgrass, PJ | 1 |
Hillman, RE; Keating, JP | 1 |
Brandt, IK; Clement, DH; Hsia, YE; Provence, SA | 1 |
Cunningham, NF; Patterson, DS | 1 |
David, M | 1 |
Assan, R | 1 |
Williamson, DH | 1 |
Boisse, J; Charpentier, C; Perelman, R; Pousset, JP; Rudler, JC | 1 |
Blass, JP; Schulman, JD | 1 |
Bressler, R; Katz, R; Wittels, B | 1 |
Budd, MA; Efron, ML; Isselbacher, KJ; Tanaka, K | 1 |
Isselbacher, KJ; Miller, EM; Tanaka, K | 1 |
Bremer, J | 2 |
Binns, MR; Erfle, JD; Sauer, F | 1 |
Hsia, YE; Lilljeqvist, AC; Rosenberg, LE | 2 |
Ando, T; Barnes, ND; Donnell, GN; Nyhan, WL; Rasmussen, K | 1 |
Hsia, YE; Lilljeqvist, A; Rosenberg, LE | 1 |
Lynen, F; Young, DL | 1 |
5 review(s) available for coenzyme a and Acidosis
Article | Year |
---|---|
Disorders of the pyruvate dehydrogenase complex.
Topics: Acetyl Coenzyme A; Acetyltransferases; Acidosis; Brain; Carbon Dioxide; Child; Child, Preschool; Coenzyme A; Cranial Nerves; Dihydrolipoamide Dehydrogenase; Dihydrolipoyllysine-Residue Acetyltransferase; Facial Bones; Feedback; Humans; Lactates; Lactic Acid; Leigh Disease; Molecular Weight; Movement Disorders; NAD; Nervous System Diseases; Phosphoric Monoester Hydrolases; Pyruvate Decarboxylase; Pyruvate Dehydrogenase Complex; Pyruvate Dehydrogenase Complex Deficiency Disease; Pyruvates; Pyruvic Acid; Spectrophotometry | 1986 |
Acetoacetate production in starvation ketosis.
Topics: Acetoacetates; Acidosis; Animals; Coenzyme A; Fatty Acids; Liver; Oxidation-Reduction; Rats; Starvation | 1968 |
Nutritional disorders of ruminants.
Topics: Acidosis; Adrenal Cortex Hormones; Animals; Cattle; Cattle Diseases; Coenzyme A; Epinephrine; Female; Gluconeogenesis; Growth Hormone; Insulin; Lipid Metabolism; Liver; Pre-Eclampsia; Pregnancy; Sheep; Sheep Diseases | 1969 |
[Methylmalonyl acidemia].
Topics: Acidosis; Coenzyme A; Enzyme Repression; Humans; Isomerases; Malonates | 1968 |
Physiological ketosis, or why ketone bodies?
Topics: Acidosis; Acyltransferases; Animals; Brain; Coenzyme A; Fatty Acids, Nonesterified; Humans; Hydroxybutyrate Dehydrogenase; Ketone Bodies; Organ Specificity; Physical Exertion; Rats; Triglycerides | 1971 |
34 other study(ies) available for coenzyme a and Acidosis
Article | Year |
---|---|
Increase in liver acetyl-coenzyme A during ketosis.
Topics: Acetyl Coenzyme A; Acidosis; Animals; Coenzyme A; Diabetes Mellitus, Experimental; Humans; Ketosis; Liver | 1963 |
LEVELS OF COENZYME A IN THE LIVER OF NORMAL COWS AND OF COWS SUFFERING FROM PRIMARY KETOSIS.
Topics: Acidosis; Animals; Cattle; Cattle Diseases; Coenzyme A; Female; Glutarates; Humans; Ketosis; Lactation; Liver; Proteins; Pyruvates | 1964 |
The isolation and identification of N-isovalerylglycine from urine of patients with isovaleric acidemia.
Topics: Acidosis; Amino Acids; Chemistry, Clinical; Child; Child, Preschool; Chromatography, Gas; Coenzyme A; Female; Humans; In Vitro Techniques; Leucine; Magnetic Resonance Spectroscopy; Male; Spectrum Analysis; Valerates | 1967 |
The clinical and biochemical implications of pyruvate carboxylase deficiency.
Topics: Acidosis; Amino Acids; Bicarbonates; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Citrates; Citric Acid Cycle; Coenzyme A; Female; Fibroblasts; Humans; Infant; Lactates; Liver; Muscles; Pyruvate Carboxylase Deficiency Disease | 1977 |
Hyperglycinemia and propionyl coA carboxylase deficiency and episodic severe illness without consistent ketosis.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Citrates; Coenzyme A; Creatinine; Crotonates; Glutamates; Glutamine; Glycine; Humans; Infant; Ketone Bodies; Ketosis; Ligases; Male; Propionates; Pyrrolidonecarboxylic Acid | 1975 |
High-performance liquid chromatography of coenzyme A esters formed by transesterification of short-chain acylcarnitines: diagnosis of acidemias by urinary analysis.
Topics: Acidosis; Carnitine; Chromatography, High Pressure Liquid; Coenzyme A; Esterification; Humans | 1987 |
Effects of acute acid-base changes on rat renal pyruvate dehydrogenase. Renal pyruvate dehydrogenase during acid-base alterations.
Topics: Acid-Base Imbalance; Acidosis; Acidosis, Respiratory; Adenine Nucleotides; Alkalosis; Animals; Coenzyme A; Kidney; Male; NAD; Pyruvate Dehydrogenase Complex; Rats; Rats, Inbred Strains | 1987 |
Neonatal death associated with isovalericacidaemia.
Topics: Acidosis; Bicarbonates; Chromatography; Chromatography, Gas; Coenzyme A; Electrolytes; Fatty Acids; Fatty Acids, Nonesterified; Glucose; Hemorrhage; Humans; Hypocalcemia; Infant Mortality; Infant, Newborn; Leucine; Male; Metabolism, Inborn Errors; Valerates | 1967 |
Defective propionate carboxylation in ketotic hyperglycinaemia.
Topics: Acidosis; Carbon Isotopes; Child; Coenzyme A; Female; Glycine; Humans; Infant, Newborn; Leukocytes; Malonates; Propionates; Succinates | 1969 |
Localisation of enzymic defect in propionicacidaemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Citric Acid Cycle; Coenzyme A; Consanguinity; Erythrocytes; Esters; Fatty Acids; Glycine; Humans; Hyperglycemia; Infant, Newborn; Ketones; Ligases; Male; Malonates; Mitochondria; Pedigree; Propionates | 1970 |
Succinyl-CoA: 3-ketoacid CoA-transferase deficiency. A cause for ketoacidosis in infancy.
Topics: Acidosis; Acyltransferases; Adipates; Autopsy; Brain; Cell Fractionation; Coenzyme A; Culture Techniques; Fibroblasts; Glucose; Glyceraldehyde-3-Phosphate Dehydrogenases; Glycolysis; Humans; Infant, Newborn; Keto Acids; Kidney; Male; Metabolism, Inborn Errors; Muscles; Phosphofructokinase-1; Phosphopyruvate Hydratase; Pyruvate Kinase; Skin; Succinates; Sulfurtransferases | 1972 |
Enzymatic changes associated with ketosis in long standing diabetes and prolonged starvation of rats.
Topics: Acetoacetates; Acidosis; Animals; Blood Glucose; Coenzyme A; Diabetes Mellitus; Hydroxybutyrate Dehydrogenase; Insulin; Ketone Bodies; Ketosis; Ligases; Male; Manometry; Mitochondria, Muscle; Oxygen Consumption; Rats; Starvation; Streptozocin; Succinates; Sulfurtransferases; Time Factors | 1973 |
Acetyl coenzyme A and acetylcarnitine concentration and turnover rates in muscle and liver of the ketotic rat and guinea pig.
Topics: Acetates; Acidosis; Acyltransferases; Animals; Carbon Dioxide; Carbon Isotopes; Carnitine; Coenzyme A; Fasting; Guinea Pigs; In Vitro Techniques; Liver; Malate Dehydrogenase; Malates; Muscles; NAD; Oxaloacetates; Pyruvates; Rats | 1967 |
The effect of ketone bodies on renal ammoniogenesis.
Topics: Acetoacetates; Acidosis; Ammonia; Ammonium Chloride; Animals; Bicarbonates; Citric Acid Cycle; Coenzyme A; Depression, Chemical; Dogs; Female; Glutamates; Glutamine; Hydrogen-Ion Concentration; Hydroxybutyrates; Ketoglutaric Acids; Ketone Bodies; Kidney; Kidney Tubules; Lactates; Mannitol; Mitochondria; NAD; Oxaloacetates; Urine | 1971 |
[Mechanism of ketogenesis in various situations of metabolism].
Topics: Acetoacetates; Acetyltransferases; Acidosis; Animals; Carbon Isotopes; Carbon Monoxide; Coenzyme A; Diabetic Ketoacidosis; Fatty Acids; Rats | 1972 |
Methylmalonyl coenzyme A racemase defect: another cause of methylmalonic aciduria.
Topics: Acidosis; Ammonia; Carbon Isotopes; Cells, Cultured; Cobamides; Coenzyme A; Fibroblasts; Humans; Infant, Newborn; Isomerases; Liver; Male; Malonates; Metabolism, Inborn Errors; Mitochondria, Liver; Propionates; Succinates; Tritium | 1972 |
Beta-ketothiolase deficiency as a cause of the "ketotic hyperglycinemia syndrome".
Topics: Acetoacetates; Acidosis; Acyltransferases; Amino Acid Metabolism, Inborn Errors; Butanones; Carbon Radioisotopes; Child; Chromatography, Thin Layer; Coenzyme A; Dinitrophenols; Fibroblasts; Glycine; Humans; Hydrazones; Hydroxybutyrates; Isoleucine; Malonates; Propionates | 1974 |
Propionicacidemia (ketotic hyperglycinemia): dietary treatment resulting in normal growth and development.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Body Height; Body Weight; Carboxy-Lyases; Child; Coenzyme A; Diet Therapy; Dietary Carbohydrates; Dietary Proteins; Female; Follow-Up Studies; Glycine; Humans; Intelligence; Ketone Bodies; Propionates | 1974 |
[Ketogenesis: mechanism, regulation, metabolic repercussions].
Topics: Acetoacetates; Acetone; Acidosis; Animals; Cattle; Citric Acid Cycle; Coenzyme A; Fatty Acids; Fatty Acids, Nonesterified; Female; Gluconeogenesis; Glucose; Hormones; Humans; Hydroxybutyrates; Insulin; Ketone Bodies; Lipid Metabolism; Liver; Mice; Prostaglandins; Rabbits; Rats; Uric Acid | 1970 |
Lipid biosynthesis and increase in isovaleric acid of plasma.
Topics: Acidosis; Coenzyme A; Humans; Lipids; Valerates | 1972 |
[Methylmalonic acidemia. A new cause of severe ketoacidosis. Study of a case].
Topics: Acidosis; Child, Preschool; Coenzyme A; Coma; Humans; Seizures | 1971 |
Measurement of citrate synthase activity in human fibroblasts.
Topics: Acidosis; Adenosine Triphosphate; Carbon Isotopes; Cell Line; Chromatography, Paper; Citrates; Coenzyme A; Fibroblasts; Humans; Kinetics; Lactates; Lyases; Methods; Oxaloacetates | 1971 |
The role of carnitine in the intracellular translocation of acyl coenzyme-a derivatives.
Topics: Acetoacetates; Acidosis; Adipose Tissue; Animals; Carnitine; Cholesterol; Citrates; Coenzyme A; Diphtheria Toxin; Fatty Acids; Guinea Pigs; In Vitro Techniques; Liver; Mitochondria; Myocardium; Palmitic Acids; Pyruvates | 1965 |
Isovaleric acidemia: a new genetic defect of leucine metabolism.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Butyrates; Caproates; Child, Preschool; Chromatography, Gas; Coenzyme A; Fatty Acids; Female; Humans; Leucine; Male; Propionates; Valerates | 1966 |
Hypoglycin A: a specific inhibitor of isovaleryl CoA dehydrogenase.
Topics: Acidosis; Alanine; Amino Acid Metabolism, Inborn Errors; Animals; Butyrates; Caproates; Carbon Dioxide; Carbon Isotopes; Carnitine; Chromatography, Gas; Coenzyme A; Cyclopropanes; In Vitro Techniques; Isoleucine; Leucine; Male; Oxidoreductases; Plant Poisoning; Rats; Valerates; Vomiting | 1971 |
Pathogenesis of ketonemia.
Topics: Acetoacetates; Acidosis; Animals; Carnitine; Coenzyme A; Diabetes Mellitus; Fasting; Gluconeogenesis; Ketone Bodies; Liver; Mitochondria, Liver; Oxaloacetates; Rats | 1969 |
[Enzyme system in diabetes].
Topics: Acidosis; Adipose Tissue; Coenzyme A; Diabetes Mellitus; Fatty Acids; Humans; Hyperglycemia; Insulin; Liver | 1970 |
Turnover rates and intracellular pool size distribution of citrate cycle intermediates in normal, diabetic and fat-fed rats estimated by computer analysis from specific activity decay data of 14C-labeled citrate cycle acids.
Topics: Acetates; Acetoacetates; Acidosis; Animals; Aspartic Acid; Carbon Isotopes; Carnitine; Chromatography, Gas; Citrates; Coenzyme A; Computers; Cytoplasm; Diabetes Mellitus, Experimental; Dietary Fats | 1970 |
Vitamin B12-dependent methylmalonicaciduria: amino acid toxicity, long chain ketonuria, and protective effect of vitamin B12.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Coenzyme A; Diet Therapy; Dietary Proteins; Humans; Isoleucine; Ketones; Leucine; Leukocytes; Male; Malonates; Methionine; Nutritional Requirements; Propionates; Threonine; Valine; Vitamin B 12 | 1970 |
Propionic acidemia in patients with ketotic hyperglycinemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Gas; Coenzyme A; Female; Glycine; Humans; Infant; Ligases; Male; Propionates; Remission, Spontaneous | 1971 |
Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Chromatography, Thin Layer; Coenzyme A; Dietary Proteins; Glycine; Humans; Infant; Intellectual Disability; Isomerases; Ketone Bodies; Ligases; Male; Malonates; Vitamin B 12 | 1968 |
Importance of the single case.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Coenzyme A; Glycine; Humans; Infant; Intellectual Disability; Ketone Bodies; Male; Malonates; Vitamin B 12 | 1968 |
Methylmalonic aciduria: metabolic block localization and vitamin B 12 dependency.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Carbon Dioxide; Carbon Isotopes; Coenzyme A; Humans; Hydro-Lyases; Infant; Isomerases; Leukocytes; Malonates; Metabolism, Inborn Errors; Molecular Biology; Mutation; Propionates; Pyridoxal Phosphate; Succinates; Vitamin B 12; Xanthurenates | 1968 |
Enzymatic regulation of 3-sn-phosphatidylcholine and triacylglycerol synthesis in states of altered lipid metabolism.
Topics: Acidosis; Acyltransferases; Animals; Carbon Isotopes; Choline; Chromatography, Ion Exchange; Coenzyme A; Diabetes Mellitus, Experimental; Glycerides; Glycerol; Lipid Metabolism; Lipoproteins; Liver; Male; Methods; Microsomes; Palmitic Acids; Phosphatidylcholines; Phosphotransferases; Propylthiouracil; Rats; Triiodothyronine | 1969 |