The regulation of 17,20 lyase activity
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Abstract
References (82)
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Two Types of Male Pseudohermaphroditism due to 17,20-Desmolase Deficiency*
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1991 • 55 citations
Mutation R96W in cytochrome P450c17 gene causes combined 17 alpha-hydroxylase/17-20-lyase deficiency in two French Canadian patients.
1996 • 51 citations
Molecular basis of apparent isolated 17,20-lyase deficiency: compound heterozygous mutations in the C-terminal region (Arg(496) → Cys, Gln(461) → Stop) actually cause combined 17α-hydroxylase/17,20-lyase deficiency
1992 • 48 citations
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1993 • 45 citations
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1998 • 35 citations
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1992 • 34 citations
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1988 • 30 citations
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1991 • 22 citations
Use of aromatase metabolite ratios to characterize electron transfer from NADPH-cytochrome P450 reductase
1993 • 21 citations
Point mutation of Arg440 to His in cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency
1994 • 20 citations
Mutation R96W in cytochrome P450c17 gene causes combined 17 alpha- hydroxylase/17-20-lyase deficiency in two French Canadian patients
1996 • 18 citations
Demethylation of Specific Sites in the 5′-Flanking Region of theCYP17Genes When Bovine Adrenocortical Cells Are Placed in Culture
1992 • 18 citations
Deletion of amino acids Asp487-Ser488-Phe489 in human cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency
1993 • 17 citations
THE MOLECULAR BASIS OF ISOLATED 17,20 LYASE DEFICIENCY. • 519
1996 • 3 citations