Mutation of the CYP2R1 vitamin D 25-hydroxylase in a Saudi Arabian family with severe vitamin D deficiency.
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Vitamin D: Metabolism, Molecular Mechanism of Action, and Pleiotropic Effects.Quantitation of CYP24A1 enzymatic activity with a simple two-hybrid system.Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A.CYP2R1 Mutations Impair Generation of 25-hydroxyvitamin D and Cause an Atypical Form of Vitamin D Deficiency.Cytochromes p450: roles in diseasesHypovitaminosis D in the Middle East and North Africa: Prevalence, risk factors and impact on outcomes.CYP2R1 is a major, but not exclusive, contributor to 25-hydroxyvitamin D production in vivoThe clinical use of vitamin D metabolites and their potential developments: a position statement from the European Society for Clinical and Economic Aspects of Osteoporosis and Osteoarthritis (ESCEO) and the International Osteoporosis Foundation (IOVitamin D-Dependent Rickets Type 1B (25-Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition?Accumulation of the Vitamin D Precursor Cholecalciferol Antagonizes Hedgehog Signaling to Impair Hemogenic Endothelium Formation.Vitamin D3 dose requirement to raise 25-hydroxyvitamin D to desirable levels in adolescents: results from a randomized controlled trial.The cellular selection between apoptosis and autophagy: roles of vitamin D, glucose and immune response in diabetic nephropathy.CYP2R1 polymorphisms are important modulators of circulating 25-hydroxyvitamin D levels in elderly females with vitamin insufficiency, but not of the response to vitamin D supplementation.Biology and Mechanisms of Action of the Vitamin D Hormone.Properties of purified CYP2R1 in a reconstituted membrane environment and its 25-hydroxylation of 20-hydroxyvitamin D3.Triangular relationship between single nucleotide polymorphisms in the CYP2R1 gene (rs10741657 and rs12794714), 25-hydroxyvitamin d levels, and coronary artery disease incidence.The genetic determinants of circulating C3-epimers of 25-hydroxyvitamin D.
P2860
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P2860
Mutation of the CYP2R1 vitamin D 25-hydroxylase in a Saudi Arabian family with severe vitamin D deficiency.
description
2012 nî lūn-bûn
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2012年の論文
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name
Mutation of the CYP2R1 vitamin ...... h severe vitamin D deficiency.
@ast
Mutation of the CYP2R1 vitamin ...... h severe vitamin D deficiency.
@en
type
label
Mutation of the CYP2R1 vitamin ...... h severe vitamin D deficiency.
@ast
Mutation of the CYP2R1 vitamin ...... h severe vitamin D deficiency.
@en
prefLabel
Mutation of the CYP2R1 vitamin ...... h severe vitamin D deficiency.
@ast
Mutation of the CYP2R1 vitamin ...... h severe vitamin D deficiency.
@en
P2860
P921
P356
P1476
Mutation of the CYP2R1 vitamin ...... h severe vitamin D deficiency.
@en
P2093
Angham N Al Mutair
Ghada H Nasrat
P2860
P304
P356
10.1210/JC.2012-1340
P407
P577
2012-08-01T00:00:00Z