Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.
about
Extensive conjugation of dopamine (3,4-dihydroxyphenethylamine) metabolites in cultured human skin fibroblasts and rat hepatoma cellsSeven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiencyLens fringe in homocystinuria.Total homocysteine and cardiovascular disease.Inborn errors of metabolism. Vitamin-responsive genetic disease.Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase.Long term treatment with betaine in methylenetetrahydrofolate reductase deficiency.Changing incidence of neonatal hypermethioninaemia: implications for the detection of homocystinuriaMechanisms of cardiovascular remodeling in hyperhomocysteinemiaIntermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutations.Betaine for treatment of homocystinuria caused by methylenetetrahydrofolate reductase deficiencyClinical Implications of Methylenetetrahydrofolate Reductase Mutations and Plasma Homocysteine Levels in Patients with Thromboembolic Occlusion.Structural perturbations in the Ala --> Val polymorphism of methylenetetrahydrofolate reductase: how binding of folates may protect against inactivationElevation of total homocysteine in the serum of patients with cobalamin or folate deficiency detected by capillary gas chromatography-mass spectrometry.Homocysteine concentrations in patients with diabetes mellitus--relationship to microvascular and macrovascular disease.Recurrent unprovoked venous thromboembolism in a young female patient with high levels of homocysteine.Valproic acid increases expression of methylenetetrahydrofolate reductase (MTHFR) and induces lower teratogenicity in MTHFR deficiencyDecreased rates of methionine synthesis by methylene tetrahydrofolate reductase-deficient fibroblasts and lymphoblasts.Activation of Nrf2-Antioxidant Response Element Mediated Glutamate Cysteine Ligase Expression in Hepatoma Cell line by HomocysteineHas folate a role in the developing nervous system after birth and not just during embryogenesis and gestation?Homocysteine Metabolism, Atherosclerosis, and Diseases of Aging.Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency.MTHFR: Addressing Genetic Counseling Dilemmas Using Evidence-Based Literature.The dietary treatment of inborn errors of metabolism.Folate distribution in cultured human cells. Studies on 5,10-CH2-H4PteGlu reductase deficiency.Folate metabolism genetic polymorphisms and meningioma and glioma susceptibility in adults.Hyperhomocyst(e)inemia and atherothrombosis.Homocystinuria due to cystathionine beta-synthase deficiency associated with megaloblastic anaemia.Metabolic etiologies in West syndrome.VitaminsMethylenetetrahydrofolate reductase, MTHFR, polymorphisms and predisposition to different multifactorial disorders
P2860
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P2860
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.
description
1972 nî lūn-bûn
@nan
1972年の論文
@ja
1972年学术文章
@wuu
1972年学术文章
@zh
1972年学术文章
@zh-cn
1972年学术文章
@zh-hans
1972年学术文章
@zh-my
1972年学术文章
@zh-sg
1972年學術文章
@yue
1972年學術文章
@zh-hant
name
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.
@en
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.
@nl
type
label
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.
@en
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.
@nl
prefLabel
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.
@en
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.
@nl
P2093
P1476
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.
@en
P2093
B W Uhlendorf
J D Finkelstein
J M Freeman
P304
P356
10.1016/S0006-291X(72)80227-4
P407
P577
1972-01-01T00:00:00Z