about
Human cholesterol 7alpha-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype.Variants in the promoter region of CYP7A1 are associated with neuromyelitis optica but not with multiple sclerosis in the Han Chinese population.Membrane binding and substrate access merge in cytochrome P450 7A1, a key enzyme in degradation of cholesterol.
P2860
description
1992 nî lūn-bûn
@nan
1992 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Polymorphisms of human cholesterol 7 alpha-hydroxylase.
@ast
Polymorphisms of human cholesterol 7 alpha-hydroxylase.
@en
type
label
Polymorphisms of human cholesterol 7 alpha-hydroxylase.
@ast
Polymorphisms of human cholesterol 7 alpha-hydroxylase.
@en
prefLabel
Polymorphisms of human cholesterol 7 alpha-hydroxylase.
@ast
Polymorphisms of human cholesterol 7 alpha-hydroxylase.
@en
P1476
Polymorphisms of human cholesterol 7 alpha-hydroxylase
@en
P2093
P304
P356
10.1016/0006-291X(92)91665-D
P407
P50
P577
1992-06-01T00:00:00Z