about
Blood lead is a predictor of homocysteine levels in a population-based study of older adultsThe localization and interactions of huntingtinRare Diseases Leading to Childhood Glaucoma: Epidemiology, Pathophysiogenesis, and ManagementHybrid sequencing approach applied to human fecal metagenomic clone libraries revealed clones with potential biotechnological applicationsInduction of hyperhomocysteinemia models vascular dementia by induction of cerebral microhemorrhages and neuroinflammation.Homocystinuria: an observation on the inheritance of cystathionine synthase deficiency.The skin in genetically-controlled metabolic disordersTissue culture techniques as an aid to prenatal diagnosis and genetic counselling in homocystinuria.Lens fringe in homocystinuria.Effects of hyperhomocysteinemia on arterial pressure and nitric oxide production in pregnant ratsThe nutrigenetics of hyperhomocysteinemia: quantitative proteomics reveals differences in the methionine cycle enzymes of gene-induced versus diet-induced hyperhomocysteinemia.Total homocysteine and cardiovascular disease.Corrective effects of hepatotoxicity by hepatic Dyrk1a gene delivery in mice with intermediate hyperhomocysteinemia.Homocystinuria. Review of four cases.A revisit to the natural history of homocystinuria due to cystathionine beta-synthase deficiency.Homocysteine: an emergent cardiovascular risk factor?Homocystinuria due to cystathionine synthase deficiency: the metabolism of L-methionine.Hyperhomocysteinemia: a new risk factor for central retinal vein occlusion.Methionine-deficient diet induces post-transcriptional downregulation of cystathionine β-synthase.Roles of homocysteine in cell metabolism: old and new functions.The molecular basis of cystathionine beta-synthase deficiency in Dutch patients with homocystinuria: effect of CBS genotype on biochemical and clinical phenotype and on response to treatment.Vascular dysfunction in hyperhomocyst(e)inemia. Implications for atherothrombotic disease.Homocystinuria due to cystathionine synthase deficiency. Studies of nitrogen balance and sulfur excretionCystathionine synthase activity in human lymphocytes: induction by phytohemagglutinin.Homocystinuria: heterozygote detection using phytohemagglutinin-stimulated lymphocytes.Disposition of homocysteine in subjects heterozygous for homocystinuria due to cystathionine beta-synthase deficiency: relationship between genotype and phenotype.Vascular presentation of cystathionine beta-synthase deficiency in adulthood.The natural history of homocystinuria due to cystathionine beta-synthase deficiency.Homocystinuria. Evidence for three distinct classes of cystathionine beta-synthase mutants in cultured fibroblasts.Homocystinuria in New South WalesMechanisms of hyperhomocysteinemia induced skeletal muscle myopathy after ischemia in the CBS-/+ mouse model.Inherited trombophilic states and pulmonary embolism.On the mechanism of pyridoxine responsive homocystinuria. II. Properties of normal and mutant cystathionine beta-synthase from cultured fibroblasts.Homocystinuria. Reduced folate levels during pyridoxine treatmentHomocystinuria: biogenesis of cystathionine beta-synthase subunits in cultured fibroblasts and in an in vitro translation system programmed with fibroblast messenger RNAAdenosine kinase deficiency disrupts the methionine cycle and causes hypermethioninemia, encephalopathy, and abnormal liver functionPromotion of vascular smooth muscle cell growth by homocysteine: a link to atherosclerosis.Homocystinuria due to cystathionine synthase deficiency: the effect of pyridoxine.Neurodevelopmental and Cognitive Outcomes of Classical Homocystinuria: Experience from Qatar.Hyperhomocysteinemia, endoplasmic reticulum stress, and alcoholic liver injury.
P2860
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P2860
description
1964 nî lūn-bûn
@nan
1964 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1964 թվականի մարտին հրատարակված գիտական հոդված
@hy
1964年の論文
@ja
1964年論文
@yue
1964年論文
@zh-hant
1964年論文
@zh-hk
1964年論文
@zh-mo
1964年論文
@zh-tw
1964年论文
@wuu
name
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.
@ast
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.
@en
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.
@nl
type
label
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.
@ast
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.
@en
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.
@nl
prefLabel
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.
@ast
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.
@en
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.
@nl
P2093
P1433
P1476
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.
@en
P2093
FINKELSTEIN JD
IRREVERRE F
P304
P356
10.1126/SCIENCE.143.3613.1443
P407
P577
1964-03-01T00:00:00Z