Mechanism of degradation of the steroid side chain in the formation of bile acids.
about
Bile salts of vertebrates: structural variation and possible evolutionary significanceCross-talk between bile acids and intestinal microbiota in host metabolism and healthFine-mapping, mutation analyses, and structural mapping of cerebrotendinous xanthomatosis in U.S. pedigreesSuppression of sterol 27-hydroxylase mRNA and transcriptional activity by bile acids in cultured rat hepatocytesAtherosclerosis and sterol 27-hydroxylase: evidence for a role of this enzyme in elimination of cholesterol from human macrophagesDisturbed cholesterol homeostasis in a peroxisome-deficient PEX2 knockout mouse modelIntegrated metabolic modelling reveals cell-type specific epigenetic control points of the macrophage metabolic networkCholesterol homeostasis in human brain: evidence for an age-dependent flux of 24S-hydroxycholesterol from the brain into the circulationEffect of Cyp27A1 gene dosage on atherosclerosis development in ApoE-knockout mice.Disruption of cholesterol 7alpha-hydroxylase gene in mice. II. Bile acid deficiency is overcome by induction of oxysterol 7alpha-hydroxylase.Medical bioremediation of age-related diseases.Regulation of bile acid and cholesterol metabolism by PPARsDe novo synthesis of steroids and oxysterols in adipocytesMetabolism of a novel side chain modified Delta8(14)-15-ketosterol, a potential cholesterol lowering drug: 28-hydroxylation by CYP27A1.Increasing dietary cholesterol induces different regulation of classic and alternative bile acid synthesis.Heterogeneous expression of cholesterol 7 alpha-hydroxylase and sterol 27-hydroxylase genes in the rat liver lobulusSelective inhibition of mitochondrial 27-hydroxylation of bile acid intermediates and 25-hydroxylation of vitamin D3 by cyclosporin A.Parenteral Nutrition-Associated Liver Disease: The Role of the Gut MicrobiotaBile acid formation in primary human hepatocytes.Sterol 27-hydroxylase gene dosage and the antiatherosclerotic effect of Rifampicin in mice.miR-204 functions as a tumor suppressor gene, at least partly by suppressing CYP27A1 in glioblastoma.
P2860
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P2860
Mechanism of degradation of the steroid side chain in the formation of bile acids.
description
1992 nî lūn-bûn
@nan
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
1992年论文
@zh
1992年论文
@zh-cn
name
Mechanism of degradation of the steroid side chain in the formation of bile acids.
@ast
Mechanism of degradation of the steroid side chain in the formation of bile acids.
@en
type
label
Mechanism of degradation of the steroid side chain in the formation of bile acids.
@ast
Mechanism of degradation of the steroid side chain in the formation of bile acids.
@en
prefLabel
Mechanism of degradation of the steroid side chain in the formation of bile acids.
@ast
Mechanism of degradation of the steroid side chain in the formation of bile acids.
@en
P1476
Mechanism of degradation of the steroid side chain in the formation of bile acids.
@en
P304
P577
1992-04-01T00:00:00Z