Phenylalanine

cytochrome P450 family 17 subfamily A member 1 ; Homo sapiens







7 Article(s)
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1 12706306 A complex heterozygous mutation of His373Leu and Asp487-Ser488-Phe489 deletion in human cytochrome P450c17 causes 17alpha-hydroxylase/17,20-lyase deficiency in three Chinese sisters. 2003 Mar 28 1
2 11836339 Combined 17alpha-Hydroxylase/17,20-lyase deficiency caused by Phe93Cys mutation in the CYP17 gene. 2002 Feb 1
3 10620365 The use of random chimeragenesis to study structure/function properties of rat and human P450c17. 2000 Jan 15 1
4 10856480 Induction of endometrial cycles and ovulation in a woman with combined 17alpha-hydroxylase/17,20-lyase deficiency due to compound heterozygous mutations on the p45017alpha gene. 2000 Jun 1
5 8855840 Mutation of cytochrome P-45017 alpha gene (CYP17) in a Japanese patient previously reported as having glucocorticoid-responsive hyperaldosteronism: with a review of Japanese patients with mutations of CYP17. 1996 Oct 2
6 8345056 Deletion of amino acids Asp487-Ser488-Phe489 in human cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency. 1993 Aug 1
7 2808364 Deletion of a phenylalanine in the N-terminal region of human cytochrome P-450(17 alpha) results in partial combined 17 alpha-hydroxylase/17,20-lyase deficiency. 1989 Oct 25 1