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Steroid 21-Monooxygenase
Known as:
Cytochrome P 450 CYP21
, hydroxylase 21
, 21-hydroxylase
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An adrenal microsomal cytochrome P450 enzyme that catalyzes the 21-hydroxylation of steroids in the presence of molecular oxygen and NADPH…
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National Institutes of Health
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Related topics
Related topics
13 relations
21-Hydroxylase Ab:ACnc:Pt:Ser:Qn
CYP21A2 gene
Congenital adrenal hyperplasia
In Blood
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Narrower (2)
CYP21A2 protein, human
CYP2C5 protein, Oryctolagus cuniculus
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2008
Review
2008
Sexual Orientation in Women with Classical or Non-classical Congenital Adrenal Hyperplasia as a Function of Degree of Prenatal Androgen Excess
H. Meyer-Bahlburg
,
C. Dolezal
,
S. Baker
,
M. New
Archives of Sexual Behavior
2008
Corpus ID: 7545303
Abstract46,XX individuals with classical congenital adrenal hyperplasia (CAH) due to deficiency of the enzyme, 21-hydroxylase…
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Highly Cited
2004
Highly Cited
2004
Prevalence and clinical associations of 10 defined autoantibodies in autoimmune polyendocrine syndrome type I.
A. Söderbergh
,
A. Myhre
,
+15 authors
T. Nilsson
Journal of Clinical Endocrinology and Metabolism
2004
Corpus ID: 21921881
The prevalence of autoantibodies against nine intracellular enzyme autoantigens, namely 21-hydroxylase, side-chain cleavage…
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Highly Cited
2003
Highly Cited
2003
Glucocorticoid-induced increase in lymphocytic FKBP51 messenger ribonucleic acid expression: a potential marker for glucocorticoid sensitivity, potency, and bioavailability.
H. Vermeer
,
B. I. Hendriks-Stegeman
,
B. van der Burg
,
S. V. van Buul-Offers
,
M. Jansen
Journal of Clinical Endocrinology and Metabolism
2003
Corpus ID: 27304531
To reduce the side effects of corticosteroid treatment, the administered dose of glucocorticoids (GCs) should be kept to a…
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Highly Cited
1999
Highly Cited
1999
Screening for 21-hydroxylase-deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study.
R. Azziz
,
L. A. Hincapié
,
E. Knochenhauer
,
D. Dewailly
,
L. Fox
,
L. Boots
Fertility and Sterility
1999
Corpus ID: 38583109
Highly Cited
1993
Highly Cited
1993
Characterization of the mouse FTZ-F1 gene, which encodes a key regulator of steroid hydroxylase gene expression.
Y. Ikeda
,
D. Lala
,
Xunrong Luo
,
Edward Kim
,
M. Moisan
,
K. Parker
Molecular Endocrinology
1993
Corpus ID: 22141412
The cytochrome P450 steroid hydroxylases are coordinately regulated by steroidogenic factor 1 (SF-1), a protein expressed…
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Highly Cited
1992
Highly Cited
1992
Steroidogenic factor I, a key regulator of steroidogenic enzyme expression, is the mouse homolog of fushi tarazu-factor I.
D. Lala
,
D. Rice
,
K. Parker
Molecular Endocrinology
1992
Corpus ID: 43014706
We proposed that a cell-selective regulatory protein coordinately regulates the expression of three enzymes that are required for…
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Highly Cited
1991
Highly Cited
1991
A shared promoter element regulates the expression of three steroidogenic enzymes.
D. A. Rice
,
Andréa
,
+5 authors
Parker
Molecular Endocrinology
1991
Corpus ID: 19765623
The adrenal cortex of the mouse coordinately expresses three cytochrome P450 enzymes that are required for the biosynthesis of…
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Highly Cited
1988
Highly Cited
1988
Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
S. Pang
,
M. Wallace
,
+7 authors
S. Suwa
Pediatrics
1988
Corpus ID: 35925898
Highly Cited
1988
Highly Cited
1988
Aberrant splicing and missense mutations cause steroid 21-hydroxylase [P-450(C21)] deficiency in humans: possible gene conversion products.
Yujiro Higashi
,
Ayako Tanae
,
H. Inoue
,
Takako Hiromasa
,
Yoshiaki Fujii-Kuriyama
Proceedings of the National Academy of Sciences…
1988
Corpus ID: 12066947
Four steroid 21-hydroxylase B [P-450(C21)B] genes (designated P.7, P.10-1, P.10-2, and P.3) from three P-450(C21)-deficient…
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Highly Cited
1984
Highly Cited
1984
HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.
P. White
,
M. New
,
B. DuPont
1984
Corpus ID: 30048681
We have determined the molecular genetic basis of congenital adrenal hyperplasia due to 21-hydroxylase (21-OHase) deficiency…
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