Arginine

cytochrome P450 family 17 subfamily A member 1 ; Homo sapiens







9 Article(s)
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Pub. Year
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1 32820515 [Clinical and genetic analysis of a patient with 17-hydroxylase/17,20-lyase deficiency]. 2020 Sep 10 1
2 28992603 Sex steroid hormones and sex hormone binding globulin levels, CYP17 MSP AI (-34T:C) and CYP19 codon 39 (Trp:Arg) variants in children with developmental stuttering. 2017 Dec 1
3 19636199 A novel mutation in the N-terminal region of the CYP17A1 gene in a patient with 17 alpha-hydroxylase/17,20-lyase deficiency. 2009 Apr 1
4 16569739 A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiency. 2006 Jun 1
5 16176874 Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-hydroxylase/17,20-lyase deficiency: demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling. 2005 Nov 1
6 15555906 The cationic charges on Arg347, Arg358 and Arg449 of human cytochrome P450c17 (CYP17) are essential for the enzyme's cytochrome b5-dependent acyl-carbon cleavage activities. 2004 Oct 6
7 12446594 Molecular evolution of adrenarche: structural and functional analysis of p450c17 from four primate species. 2002 Dec 2
8 10455016 Lysine mutagenesis identifies cationic charges of human CYP17 that interact with cytochrome b5 to promote male sex-hormone biosynthesis. 1999 Sep 1 6
9 8027220 Point mutation of Arg440 to His in cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency. 1994 Jul 1