Comparison of Folic Acid Coenzyme Distribution Patterns in Patients with Methylenetetrahydrofolate Reductase and Methionine Synthetase Deficiencies
暂无分享,去创建一个
[1] D. Rosenblatt,et al. Differences in Liver Folate Enzyme Patterns in Premature and Full Term Infants , 1982, Pediatric Research.
[2] E. Eger,et al. Nitrous Oxide Inactivates Methionine Synthetase in Human Liver , 1982, Anesthesia and analgesia.
[3] T. Brody,et al. Folate pentaglutamate and folate hexaglutamate mediated one-carbon metabolism. , 1982, Biochemistry.
[4] R. Chalmers,et al. Disorders of propionate and methylmalonate metabolism , 1982 .
[5] G. Boss,et al. Decreased rates of methionine synthesis by methylene tetrahydrofolate reductase-deficient fibroblasts and lymphoblasts. , 1981, The Journal of clinical investigation.
[6] J. Harpey,et al. Homocystinuria caused by 5,10-methylenetetrahydrofolate reductase deficiency: a case in an infant responding to methionine, folinic acid, pyridoxine, and vitamin B12 therapy. , 1981, The Journal of pediatrics.
[7] E. Stokstad,et al. Metabolic responses of folic acid and related compounds to thyroxine in rats. , 1980, Biochimica et biophysica acta.
[8] R. Carmel,et al. Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression test. , 1980, Blood.
[9] D. Rosenblatt,et al. Folate distribution in cultured human cells. Studies on 5,10-CH2-H4PteGlu reductase deficiency. , 1979, The Journal of clinical investigation.
[10] E. R. Baumgartner,et al. Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology. , 1979, Helvetica paediatrica acta.
[11] E. R. Baumgartner,et al. Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigations. , 1979, Helvetica paediatrica acta.
[12] W. Nyhan,et al. A syndrome of methylmalonic aciduria, homocystinuria, megaloblastic anemia and neurologic abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian. , 1978, The New England journal of medicine.
[13] P. Wong,et al. Folic acid nonresponsive homocystinuria due to methylenetetrahydrofolate reductase deficiency. , 1977, Pediatrics.
[14] Y. Wada,et al. Infantile type of homocystinuria with N5,10-methylenetetrahydrofolate reductase defect. , 1977, The Tohoku journal of experimental medicine.
[15] Y. Kanwar,et al. Morphologic Studies in a Patient with Homocystinuria due to 5,10-Methylenetetrahydrofolate Reductase Deficiency , 1976, Pediatric Research.
[16] J. Finkelstein,et al. Folate-responsive homocystinuria and "schizophrenia". A defect in methylation due to deficient 5,10-methylenetetrahydrofolate reductase activity. , 1975, The New England journal of medicine.
[17] E. Stokstad,et al. Urinary excretion of 5-methyltetrahydrofolate and liver S-adenosylmethionine levels of rats fed a vitamin B 12-deficient diet. , 1974, Biochimica et biophysica acta.
[18] H. Sauer,et al. Bedeutung und Regulation der Cobalamin-abhängigen Methionin-Synthetase und der Betain: Homocystein-Methyltransferase im Stoffwechsel des Methionins und der Tetrahydrofolsäure bei der Ratte , 1973 .
[19] E. Stokstad,et al. Lactobacillus casei response to pteroylpolyglutamates. , 1972, Analytical biochemistry.
[20] J. Finkelstein,et al. Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity. , 1972, Biochemical and biophysical research communications.
[21] J. Schulman,et al. A derangement in B12 metabolism associated with homocystinemia, cystathioninemia, hypomethioninemia and methylmalonic aciduria. , 1970, The American journal of medicine.
[22] V. Herbert,et al. Interrelations of vitamin B12 and folic acid metabolism: folic acid clearance studies. , 1962, The Journal of clinical investigation.