Cystathionine synthase in tissue culture derived from human skin: enzyme defect in homocystinuria.
about
Familial hypercholesterolemia: identification of a defect in the regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity associated with overproduction of cholesterolTissue culture techniques as an aid to prenatal diagnosis and genetic counselling in homocystinuria.Diseases of the collagen moleculeThe 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.Cystathionine synthase activity in human lymphocytes: induction by phytohemagglutinin.Homocystinuria: heterozygote detection using phytohemagglutinin-stimulated lymphocytes.Homocystinuria. Evidence for three distinct classes of cystathionine beta-synthase mutants in cultured fibroblasts.Immunochemical studies on cultured fibroblasts from patients with homocystinuria due to cystathionine beta-synthase deficiency.Effect of chronologic age on induction of cystathionine synthase, uroporphyrinogen I synthase, and glucose-6-phosphate dehydrogenase activities in lymphocytes.The growth and development of human genetics as a clinical discipline.Homocystinuria due to cystathionine synthase deficiency: the effect of pyridoxine.Antenatal detection of genetic enzyme defectsHomocystine-induced arteriosclerosis. The role of endothelial cell injury and platelet response in its genesisTreatment of homocystinuria with pyridoxine. A preliminary study.Importance of homocysteine-induced abnormalities of proteoglycan structure in arteriosclerosis.The Jeremiah Metzger lecture of The American Clinical and Climatological Association 1975. New genetic insight into old diseasesSulphur metabolism in relation to cutaneous disease.Fibroblast culture and inherited neurological diseases.Electrophoresis of platelet monoamine oxidase in schizophrenia and manic-depressive illness.Molecular and clinical characterisation of homocystinuria in two Austrian families with cystathionine beta-synthase deficiency.
P2860
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P2860
Cystathionine synthase in tissue culture derived from human skin: enzyme defect in homocystinuria.
description
1968 nî lūn-bûn
@nan
1968 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1968 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1968年の論文
@ja
1968年論文
@yue
1968年論文
@zh-hant
1968年論文
@zh-hk
1968年論文
@zh-mo
1968年論文
@zh-tw
1968年论文
@wuu
name
Cystathionine synthase in tiss ...... zyme defect in homocystinuria.
@ast
Cystathionine synthase in tiss ...... zyme defect in homocystinuria.
@en
Cystathionine synthase in tiss ...... zyme defect in homocystinuria.
@nl
type
label
Cystathionine synthase in tiss ...... zyme defect in homocystinuria.
@ast
Cystathionine synthase in tiss ...... zyme defect in homocystinuria.
@en
Cystathionine synthase in tiss ...... zyme defect in homocystinuria.
@nl
prefLabel
Cystathionine synthase in tiss ...... zyme defect in homocystinuria.
@ast
Cystathionine synthase in tiss ...... zyme defect in homocystinuria.
@en
Cystathionine synthase in tiss ...... zyme defect in homocystinuria.
@nl
P1433
P1476
Cystathionine synthase in tiss ...... zyme defect in homocystinuria.
@en
P2093
P304
P356
10.1126/SCIENCE.160.3831.1007
P407
P577
1968-05-01T00:00:00Z