CYP27A1チトクロムP450
- 関
- sterol 27-hydroxylase
WordNet
- the 16th letter of the Roman alphabet (同)p
- (biochemistry) a class of hemoprotein whose principal biological function is electron transfer (especially in cellular respiration)
- a river in western Thailand; a major tributary of the Chao Phraya (同)Ping River
PrepTutorEJDIC
- parking
- phosphorusの化学記号
- palladiumの化学記号
UpToDate Contents
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English Journal
- 25-Hydroxyvitamin D in pregnancy and genome wide cord blood DNA methylation in two pregnancy cohorts (MoBa and ALSPAC).
- Suderman M1, Stene LC2, Bohlin J3, Page CM2, Holvik K2, Parr CL2, Magnus MC2, Håberg SE2, Joubert BR4, Wu MC5, London SJ4, Relton C6, Nystad W2.
- The Journal of steroid biochemistry and molecular biology.J Steroid Biochem Mol Biol.2016 May;159:102-9. doi: 10.1016/j.jsbmb.2016.03.005. Epub 2016 Mar 4.
- The aim of the study was to investigate whether maternal mid-pregnancy 25-hydroxyvitamin D concentrations are associated with cord blood DNA methylation. DNA methylation was assessed using the Illumina HumanMethylation450 BeadChip, and maternal plasma 25-hydroxyvitamin D was measured in 819 mothers/
- PMID 26953979
- Motor neuron-like NSC-34 cells as a new model for the study of vitamin D metabolism in the brain.
- Almokhtar M1, Wikvall K1, Ubhayasekera SJ2, Bergquist J2, Norlin M3.
- The Journal of steroid biochemistry and molecular biology.J Steroid Biochem Mol Biol.2016 Apr;158:178-88. doi: 10.1016/j.jsbmb.2015.12.010. Epub 2015 Dec 15.
- Vitamin D3 is a pro-hormone, which is sequentially activated by 25- and 1α-hydroxylation to form 25-hydroxyvitamin D3 [25(OH)D3] and 1α,25-dihydroxyvitamin D3 [1α,25(OH)2D3], respectively. Subsequent inactivation is performed by 24-hydroxylation. These reactions are carried out by a series of CYP
- PMID 26704532
- Late-onset spinal form xanthomatosis without brain lesion: a case report.
- Yanagihashi M1, Kano O2, Terashima T3, Kawase Y4, Hanashiro S5, Sawada M6, Ishikawa Y7, Shiraga N8, Ikeda K9, Iwasaki Y10.
- BMC neurology.BMC Neurol.2016 Feb 9;16:21. doi: 10.1186/s12883-016-0542-2.
- BACKGROUND: Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive sterol storage disease caused by a mutated sterol 27-hydroxylase (CYP27A1) gene. Patients with typical CTX show neurological dysfunction including bilateral cataracts, paresis, cerebral ataxia, dementia, and psychiatric d
- PMID 26861945
Related Links
- Mutation in Cytochrome P-450 CYP27A1 is associated with cerebrotendinous xanthomatosis ...
- Consumer-friendly information about human genetics from the U.S. National Library of Medicine. ... The CYP27A1 gene is a member of the cytochrome P450 gene family. Enzymes produced from the cytochrome P450 genes are ...
Related Pictures
★リンクテーブル★
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- 英
- cytochrome P-450 CYP27A1
- 関
- ステロール27-水酸化酵素
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- 10の-12乗
- 関
- pico
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パラジウム palladium
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シトクロムP450 CYP