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Details on Person Russell, David W
| Class:Id | Person:192138 |
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| _displayName | Russell, David W |
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| _timestamp | 2015-12-08 23:13:31 |
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| firstname | David W |
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| initial | DW |
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| modified | [InstanceEdit:193476] D'Eustachio, P, 2007-02-19 17:36:33
[InstanceEdit:538689] D'Eustachio, P, 2010-03-08
[InstanceEdit:8848498] D'Eustachio, Peter, 2015-12-08 |
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| surname | Russell |
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| (author) | [LiteratureReference:191396] Cholesterol biosynthesis and metabolism
[LiteratureReference:191969] Expression cloning of an oxysterol 7alpha-hydroxylase selective for 24-hydroxycholesterol
[LiteratureReference:192002] cDNA cloning of cholesterol 24-hydroxylase, a mediator of cholesterol homeostasis in the brain
[LiteratureReference:192080] The enzymes, regulation, and genetics of bile acid synthesis
[LiteratureReference:192168] cDNA cloning of mouse and human cholesterol 25-hydroxylases, polytopic membrane proteins that synthesize a potent oxysterol regulator of lipid metabolism
[LiteratureReference:192197] Characterization of human sterol 27-hydroxylase. A mitochondrial cytochrome P-450 that catalyzes multiple oxidation reaction in bile acid biosynthesis.
[LiteratureReference:193374] Molecular genetics of 3beta-hydroxy-Delta5-C27-steroid oxidoreductase deficiency in 16 patients with loss of bile acid synthesis and liver disease
[LiteratureReference:193487] Mutations in the bile acid biosynthetic enzyme sterol 27-hydroxylase underlie cerebrotendinous xanthomatosis
[LiteratureReference:193532] The bile acid synthetic gene 3beta-hydroxy-Delta(5)-C(27)-steroid oxidoreductase is mutated in progressive intrahepatic cholestasis
[LiteratureReference:193828] Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease |
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No pathways have been reviewed or authored by Russell, David W (192138)
