Published in Methods Enzymol on January 01, 1982
Structural similarity of bovine lung prostaglandin F synthase to lens epsilon-crystallin of the European common frog. Proc Natl Acad Sci U S A (1988) 1.39
Major differences exist in the function and tissue-specific expression of human aflatoxin B1 aldehyde reductase and the principal human aldo-keto reductase AKR1 family members. Biochem J (1999) 1.26
Human class II (pi) alcohol dehydrogenase has a redox-specific function in norepinephrine metabolism. Proc Natl Acad Sci U S A (1986) 0.87
Effects of long-acting somatostatin analogues on redox systems in rat lens in experimental diabetes. Int J Exp Pathol (2014) 0.75
The aldo-keto reductase superfamily. cDNAs and deduced amino acid sequences of human aldehyde and aldose reductases. J Biol Chem (1989) 2.59
Purification and properties of an NADPH-dependent carbonyl reductase from human brain. Relationship to prostaglandin 9-ketoreductase and xenobiotic ketone reductase. J Biol Chem (1981) 1.72
Human carbonyl reductase. Nucleotide sequence analysis of a cDNA and amino acid sequence of the encoded protein. J Biol Chem (1988) 1.23
Purification and characterization of human-brain aldose reductase. Eur J Biochem (1982) 1.22
Carbonyl reductase provides the enzymatic basis of quinone detoxication in man. Biochem Pharmacol (1986) 1.20
An atypical human alcohol dehydrogenase. Can J Biochem (1965) 1.18
Prophylaxis and reversal of ifosfamide encephalopathy with methylene-blue. Lancet (1994) 1.15
Heterogeneity of erythrocyte catalase. Correlations between sulfhydryl group content, chromatographic and electrophoretic properties. Eur J Biochem (1969) 1.15
Purification and properties of NADPH-dependent aldehyde reductase from human liver. J Biol Chem (1977) 1.15
Mutation of ornithine transcarbamylase (H136R) in a girl with severe intermittent orotic aciduria but normal enzyme activity. J Inherit Metab Dis (1997) 1.08
Heterogeneity of NADPH-dependent aldehyde reductase from human and rat brain. Eur J Biochem (1973) 1.06
Kinetics of carbonyl reductase from human brain. Biochem J (1987) 1.01
Human carbonyl and aldose reductases: new catalytic functions in tetrahydrobiopterin biosynthesis. Biochem Biophys Res Commun (1991) 1.01
N-Acetylglutamate synthetase deficiency responding to carbamylglutamate. J Inherit Metab Dis (1997) 1.01
Human gastric alcohol dehydrogenase activity: effect of age, sex, and alcoholism. Gut (1993) 0.97
Identification of the reactive cysteine residue (Cys227) in human carbonyl reductase. Eur J Biochem (1999) 0.97
Human brain aldehyde reductases: relationship to succinic semialdehyde reductase and aldose reductase. J Neurochem (1980) 0.96
Kinetics of chlormethiazole in patients with alcohol withdrawal manifestations. Clin Pharmacol Ther (1978) 0.95
Human liver alcohol dehydrogenase. 1. The primary structure of the beta 1 beta 1 isoenzyme. Eur J Biochem (1984) 0.94
Reevaluation of the disulfiram-alcohol reaction in man. J Stud Alcohol (1977) 0.94
Aldose and aldehyde reductase exhibit isocorticosteroid reductase activity. Eur J Biochem (1983) 0.94
A novel two-nucleotide deletion in the ornithine transcarbamylase gene causing fatal hyperammonia in early pregnancy. Hepatology (1996) 0.93
Biology of disease. Alcoholism and aldehydism: new biomedical concepts. Lab Invest (1984) 0.93
[Heterogeneity and organ distribution of alcohol dehydrogenase in various species]. Enzymol Biol Clin (Basel) (1968) 0.93
Structural studies of human-liver alcohol-dehydrogenase isoenzymes. Eur J Biochem (1974) 0.93
Heterogeneity of horse liver alcohol dehydrogenase. Purification and characterization of multiple molecular forms. Eur J Biochem (1970) 0.92
Immunohistochemical localization of alcohol dehydrogenase in the human gastrointestinal tract. Gastroenterology (1983) 0.92
Active-site-specific zinc-depleted and reconstituted cobalt(II) human-liver alcohol dehydrogenase. Preparation, characterization and complexation with NADH and trans-4-(N,N-dimethylamino)-cinnamaldehyde. Eur J Biochem (1988) 0.91
Ornithine transcarbamylase deficiency: new sites with increased probability of mutation. Hum Genet (1995) 0.91
Ornithine transcarbamylase deficiency: characterization of gene mutations and polymorphisms. Hum Mutat (1996) 0.90
Human liver alcohol dehydrogenase. 2. The primary structure of the gamma 1 protein chain. Eur J Biochem (1984) 0.90
Pyridine nucleotide transhydrogenase from Pseudomonas aeruginosa: purification by affinity chromatography and physicochemical properties. Arch Biochem Biophys (1976) 0.89
Cloning and expression of succinic semialdehyde reductase from human brain. Identity with aflatoxin B1 aldehyde reductase. Eur J Biochem (1999) 0.89
Expression, crystallization and preliminary crystallographic analysis of human carbonyl reductase. J Mol Biol (1994) 0.88
Gene structure of human carbamylphosphate synthetase 1 and novel mutations in patients with neonatal onset. Hum Mutat (2003) 0.88
Primary structure of aldehyde reductase from human liver. Prog Clin Biol Res (1987) 0.87
Antioxidant and thyroid hormone status in selenium-deficient phenylketonuric and hyperphenylalaninemic patients. Am J Clin Nutr (2000) 0.87
Aldo-keto reductases. Prog Clin Biol Res (1985) 0.87
Determination of acetaldehyde in human blood. Experientia (1979) 0.87
Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome. J Inherit Metab Dis (1992) 0.86
Misleading diagnosis of partial N-acetylglutamate synthase deficiency based on enzyme measurement corrected by mutation analysis. Acta Paediatr (2005) 0.86
Human liver 6-pyruvoyl tetrahydropterin reductase is biochemically and immunologically indistinguishable from aldose reductase. Biochem Biophys Res Commun (1989) 0.85
Atypical human liver alcohol dehydrogenase. Ann N Y Acad Sci (1968) 0.85
Genetic analysis of carbamoylphosphate synthetase I and ornithine transcarbamylase deficiency using fibroblasts. Eur J Pediatr (2001) 0.85
Immunohistochemical localization of carbonyl reductase in human tissues. J Histochem Cytochem (1992) 0.84
Immunohistochemical localisation of aldehyde and aldose reductase in human tissues. Prog Clin Biol Res (1985) 0.84
Partial N-acetyl-glutamate synthetase deficiency masquerading as a valproic acid-induced Reye-like syndrome. Acta Paediatr (1999) 0.84
Combined 3-methylglutaconic and 3-hydroxy-3-methylglutaric aciduria with endocardial fibroelastosis and dilatative cardiomyopathy in male and female siblings with partial deficiency of complex II/III in fibroblasts. Enzyme Protein (1996) 0.83
Human carbonyl reductases. Prog Clin Biol Res (1982) 0.83
Separation of aldehyde reductases and alcohol dehydrogenase from brain by affinity chromatography: metabolism of succinic semialdehyde and ethanol. Biochem Biophys Res Commun (1975) 0.83
Human alcohol dehydrogenase: structural differences between the beta and gamma subunits suggest parallel duplications in isoenzyme evolution and predominant expression of separate gene descendants in livers of different mammals. Proc Natl Acad Sci U S A (1984) 0.82
Purification and substrate specificities of three human liver alcohol dehydrogenase isoenzymes. FEBS Lett (1982) 0.82
Characterization of a mitochondrial NADH-dependent nitro reductase from rat brain. Biochim Biophys Acta (1980) 0.82
Partial N-acetylglutamate synthetase deficiency in a 13-year-old girl: diagnosis and response to treatment with N-carbamylglutamate. Eur J Pediatr (1998) 0.82
Fibrinogen Milano V: a congenital dysfibrinogenaemia with a gamma 275 Arg-->Cys substitution. Blood Coagul Fibrinolysis (1994) 0.81
Partial N-acetylglutamate synthetase deficiency: a new case with uncontrollable movement disorders. J Inherit Metab Dis (1992) 0.81
Characterization and kinetics of native and chemically acitvated human liver alcohol dehydrogenases. J Biol Chem (1977) 0.81
Aldose reductase from human tissues. Methods Enzymol (1982) 0.81
Determination of human alcohol dehydrogenase and acetaldehyde dehydrogenase genotypes by single strand conformation polymorphism in discontinuous buffer electrophoresis. Electrophoresis (1993) 0.81
8-(6-Aminohexyl)-amino-adenine nucleotide derivatives for affinity chromatography. Arch Biochem Biophys (1974) 0.80
Mutation of threonine-241 to proline eliminates autocatalytic modification of human carbonyl reductase. Biochem J (2000) 0.80
A new substitution, gamma 358 Ser-->Cys, in fibrinogen Milano VII causes defective fibrin polymerization. Blood (1994) 0.79
Kinetic studies on NADPH-linked aldehyde reductase from human liver. Adv Exp Med Biol (1980) 0.79
Influence of genetic variation in alcohol and aldehyde dehydrogenase on serotonin metabolism. Life Sci (1994) 0.79
Increased plasma amylase in the family of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency. Clin Chem (1992) 0.78
Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codon. Clin Genet (2001) 0.78
Studies on the subcellular localization of monoamine oxidase types A and B and its importance for the deamination of dopamine in the rat brain. Biochem Pharmacol (1980) 0.78
The fate of the ethanol analogue 1,3-butanediol in the dog. An in vivo-in vitro comparison. Biochem Pharmacol (1981) 0.78
Coenzyme specificity of human monomeric carbonyl reductase: contribution of Lys-15, Ala-37 and Arg-38. Chem Biol Interact (2001) 0.78
Immunochemical characterization of aldo-keto reductases from human tissues. FEBS Lett (1985) 0.78
Reduction of biogenic aldehydes by aldehyde reductase and alcohol dehydrogenase from human liver. Biochem Pharmacol (1979) 0.78
Interaction of proflavine and acriflavine with acetylcholinesterase. Eur J Biochem (1973) 0.78
Mutational spectrum and linkage disequilibrium patterns at the ornithine transcarbamylase gene (OTC). Ann Hum Genet (2006) 0.77
Circulating ionized and total magnesium in end-stage kidney disease. Nephron (1998) 0.77
Effect of increasing dietary threonine intakes on amino acid metabolism of the central nervous system and peripheral tissues in growing rats. Pediatr Res (1998) 0.77
Stereospecificity of hydrogen transfer of aldehyde reductase. Experientia (1979) 0.77
Biologic aspects of alcohol: an introduction. Ann N Y Acad Sci (1976) 0.77
Metabolism of ethanol and fructose in the perfused rat liver. Enzymol Biol Clin (Basel) (1970) 0.77
Identification of four novel splice site mutations in the ornithine transcarbamylase gene. Hum Genet (1996) 0.77
A rapid behavioral treatment for needle phobics. J Nerv Ment Dis (1978) 0.76
Carbonyl reductase from human testis: purification and comparison with carbonyl reductase from human brain and rat testis. Biochim Biophys Acta (1992) 0.76
Application of general ligand affinity chromatography for the mutual separation of deoxyribonclease and ribonuclease free of protease contamination. Anal Biochem (1976) 0.76
Aminoglycosides and renal magnesium homeostasis in humans. Nephrol Dial Transplant (2000) 0.76
Alcohol metabolism and alcoholism--pharmacogenetic considerations. Acta Psychiatr Scand Suppl (1980) 0.75
Metabolic stroke in carbamyl phosphate synthetase deficiency. Neuropediatrics (1997) 0.75
Permanently reduced plasma ionized magnesium among renal transplant recipients on cyclosporine. Transpl Int (1999) 0.75
Degradation of aliphatic alcohols by human liver alcohol dehydrogenase: effect of ethanol and pharmacokinetic implications. Alcohol Clin Exp Res (1988) 0.75
[Considering the psychotropic effect of alcohol]. Ther Umsch (1990) 0.75
Fibrinogen Bern I: substitution gamma 337 Asn-->Lys is responsible for defective fibrin monomer polymerization. Blood (1993) 0.75
Polycyclic aromatic hydrocarbons and phenolic antioxidants do not significantly induce carbonyl reductase in human cell lines. Adv Exp Med Biol (1993) 0.75
Methionine lowers circulating levels of acetaldehyde after ethanol ingestion. Alcohol Clin Exp Res (1989) 0.75