9 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
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 |