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The regulation of 17,20 lyase activity

Data up to Jan 2025

Published1997
Citations236
References82

Total Citations Per Year

Abstract

References (82)

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Regulation of steroidogenesis in NCI-H295 cells: a cellular model of the human fetal adrenal

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Identification and location of .alpha.-helices in mammalian cytochromes P450

1989 • 83 citations

Proteins from eight eukaryotic cytochrome P-450 families share a segmented region of sequence similarity.

1988 • 80 citations

Deletion of amino acids Asp487-Ser488-Phe489 in human cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency.

1993 • 72 citations

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1986 • 64 citations

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1990 • 64 citations

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1991 • 64 citations

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1994 • 62 citations

Male Pseudohermaphroditism Consistent with 17,20-Desmolase Deficiency

1976 • 62 citations

Point mutation of Arg440 to His in cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency.

1994 • 62 citations

Two Types of Male Pseudohermaphroditism due to 17,20-Desmolase Deficiency*

1982 • 61 citations

Human Proopiomelanocortin-(79–96), a Proposed Androgen Stimulatory Hormone, Does not Affect Steroidogenesis in Cultured Human Fetal Adrenal Cells*

1991 • 60 citations

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Human Proopiomelanocortin-(79–96), a Proposed Cortical Androgen- Stimulating Hormone, Does not Affect Steroidogenesis in Cultured Human Adult Adrenal Cells*

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

Steroid 17 alpha-hydroxylase and 17,20-lyase activities of P450c17: contributions of serine106 and P450 reductase

1993 • 45 citations

The molecular basis of isolated 17,20 lyase deficiency

1998 • 35 citations

Conversion from pure 17,20-desmolase- to combined 17,20-desmolase/17α-hydroxylase deficiency with age

1992 • 34 citations

The MIDAS database system

1988 • 30 citations

Modeling and mutagenesis of the active site of human P450c17

1994 • 29 citations

TESTICULAR FUNCTION IN POST PUBERTAL MALE PSEUDOHERMAPHRODITISM

1979 • 26 citations

Isolation and Characterization of Three Forms of Joining Peptide from Adult Human Pituitaries: Lack of Adrenal Androgen-Stimulating Activity*

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

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