Nonsense mutation causing steroid 21-hydroxylase deficiency (Q34556991)

3 August 2017

title

Nonsense mutation causing steroid 21-hydroxylase deficiency (English)

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3 August 2017

H Globerman

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3 August 2017

M Amor

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3 August 2017

K L Parker

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3 August 2017

M I New

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3 August 2017

P C White

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3 August 2017

language of work or name

English

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publication date

1 July 1988

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Journal of Clinical Investigation

3 August 2017

published in

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3 August 2017

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3 August 2017

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3 August 2017

page(s)

139-144

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A highly polymorphic locus in human DNA

3 August 2017

cites work

1 reference

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Buffer gradient gels and 35S label as an aid to rapid DNA sequence determination

7 July 2018

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

7 July 2018

1 reference

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Lambda replacement vectors carrying polylinker sequences

7 July 2018

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2 New M13 vectors for cloning

7 July 2018

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Cloning and characterization of the bovine gene for steroid 21-hydroxylase (P-450c21).

7 July 2018

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Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

7 July 2018

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Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries

7 July 2018

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Nucleotide sequence analysis of murine 21-hydroxylase genes: mutations affecting gene expression

7 July 2018

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Frequent deletion and duplication of the steroid 21-hydroxylase genes

7 July 2018

1 reference

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Structure of human steroid 21-hydroxylase genes

7 July 2018

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Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia

7 July 2018

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Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene

7 July 2018

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Gene conversion in a cytochrome P-450 gene family

7 July 2018

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Congenital adrenal hyperplasia (2).

7 July 2018

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

7 July 2018

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Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia

7 July 2018

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Structural analysis of cloned cDNA for mRNA of microsomal cytochrome P-450(C21) which catalyzes steroid 21-hydroxylation in bovine adrenal cortex

7 July 2018

1 reference

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Expression of murine 21-hydroxylase in mouse adrenal glands and in transfected Y1 adrenocortical tumor cells

7 July 2018

1 reference

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

7 July 2018

1 reference

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In vitro RNA synthesis with SP6 RNA polymerase

7 July 2018

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

7 July 2018

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7 July 2018

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Screening λgt Recombinant Clones by Hybridization to Single Plaques in Situ

7 July 2018

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DNA sequencing with chain-terminating inhibitors

7 July 2018

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19 In Vitro packaging of λ and cosmid DNA

7 July 2018

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beta 0 thalassemia, a nonsense mutation in man

7 July 2018

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A reliable method for the recovery of DNA fragments from agarose and acrylamide gels

7 July 2018

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12 December 2020

α1-Antitrypsin deficiency detection by direct analysis of the mutation in the gene

1 reference

12 December 2020

Two steroid 21-hydroxylase genes are located in the murine S region

1 reference

12 December 2020

Pharmacologic suppression of the fetal adrenal gland in utero. Attempted prevention of abnormal external genital masculinization in suspected congenital adrenal hyperplasia

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12 December 2020

Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia

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12 December 2020

Is salt-wasting in congenital adrenal hyperplasia due to the same gene as the fasciculata defect?

1 reference

12 December 2020

First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination

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12 December 2020

Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI113562

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3 August 2017

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3 August 2017

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