Cloning of human 25-hydroxyvitamin D-1 alpha-hydroxylase and mutations causing vitamin D-dependent rickets type 1.

Fu, G K; Lin, D; Zhang, M Y; Bikle, D D; Shackleton, C H; Miller, W L; Portale, A A

Fu, G K; Lin, D; Zhang, M Y; Bikle, D D; Shackleton, C H; Miller, W L; Portale, A A.

Affiliation

Fu GK; Department of Pediatrics, Child Health Research Center, San Francisco, California 94121, USA.

Mol Endocrinol ; 11(13): 1961-70, 1997 Dec.

Article in En | MEDLINE | ID: mdl-9415400

Subject(s)

25-Hydroxyvitamin D3 1-alpha-Hydroxylase/genetics; Chronic Kidney Disease-Mineral and Bone Disorder/enzymology; Chronic Kidney Disease-Mineral and Bone Disorder/genetics; Cloning, Molecular; Mutation; 25-Hydroxyvitamin D3 1-alpha-Hydroxylase/physiology; Amino Acid Sequence; Animals; Base Sequence; Cell Line; Cells, Cultured; Chronic Kidney Disease-Mineral and Bone Disorder/congenital; DNA, Complementary/biosynthesis; DNA, Complementary/isolation & purification; Female; Humans; Infant; Keratinocytes; Leydig Cells; Male; Mice; Molecular Sequence Data; Organ Specificity/genetics; RNA, Messenger/biosynthesis

Key words

Non-programmatic

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Collection: 01-internacional Database: MEDLINE Main subject: Chronic Kidney Disease-Mineral and Bone Disorder / Cloning, Molecular / 25-Hydroxyvitamin D3 1-alpha-Hydroxylase / Mutation Limits: Animals / Female / Humans / Infant / Male Language: En Journal: Mol Endocrinol Journal subject: BIOLOGIA MOLECULAR / ENDOCRINOLOGIA Year: 1997 Document type: Article Affiliation country: United States

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