Steroid 21-hydroxylase expression and activity in human lymphocytes (Q41120926)

27 September 2017

title

Steroid 21-hydroxylase expression and activity in human lymphocytes (English)

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27 September 2017

Z Zhou

1

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27 September 2017

V R Agarwal

2

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27 September 2017

N Dixit

3

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27 September 2017

P White

4

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27 September 2017

P W Speiser

5

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27 September 2017

publication date

1 March 1997

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Molecular and Cellular Endocrinology

27 September 2017

published in

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27 September 2017

volume

127

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27 September 2017

issue

1

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27 September 2017

page(s)

11-18

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Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

27 September 2017

cites work

1 reference

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7 January 2021

Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations

1 reference

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7 January 2021

Molecular analysis of patient and carrier genes with congenital steroid 21-hydroxylase deficiency by using polymerase chain reaction and single strand conformation polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylase

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7 January 2021

Screening of CYP21 gene mutations in 129 French patients affected by steroid 21-hydroxylase deficiency

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https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

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https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21B

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7 January 2021

Effects of individual mutations in the P-450(C21) pseudogene on the P-450(C21) activity and their distribution in the patient genomes of congenital steroid 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Further evidence that there is more than one adrenal 21-hydroxylase system

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Conversion of plasma progesterone to deoxycorticosterone in men, nonpregnant and pregnant women, and adrenalectomized subjects

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Extraadrenal steroid 21-hydroxylation is not mediated by P450c21

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7 January 2021

Extraadrenal formation of a mineralocorticosteroid: deoxycorticosterone and deoxycorticosterone sulfate biosynthesis and metabolism

1 reference

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7 January 2021

Conversion of progesterone to deoxycorticosterone in the human fetus: steroid 21-hydroxylase activity in fetal tissues

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7 January 2021

Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data*

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7 January 2021

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Detection of steroid 21-hydroxylase alleles using gene-specific PCR and a multiplexed ligation detection reaction

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https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Cell interactions and the control of gene activity during early development of Xenopus laevis

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7 January 2021

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Androstenedione metabolism by human lymphocytes

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7 January 2021

Steroid production in the thymus: implications for thymocyte selection.

1 reference

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7 January 2021

A paradox: elevated 21-hydroxypregnenolone production in newborns with 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Constitutive human steroid 21-hydroxylase promoter gene and pseudogene activity in steroidogenic and nonsteroidogenic cells with the luciferase gene as a reporter

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Neurosteroids Biosynthesis and function.

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https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

The immune-hypothalamic-pituitary-adrenal axis

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Effects of selective type I and II adrenal steroid agonists on immune cell distribution

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903997-4

7 January 2021

10.1016/S0303-7207(96)03997-4

Identifiers

DOI

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27 September 2017

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