HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation (Q37579085)

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scientific article published on December 1, 1984

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English	HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation	scientific article published on December 1, 1984

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instance of

scholarly article

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stated in

Europe PubMed Central

PMC publication ID

392175

retrieved

21 August 2017

title

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

1 reference

stated in

Europe PubMed Central

PMC publication ID

392175

retrieved

21 August 2017

main subject

congenital disorder

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cell line

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congenital adrenal hyperplasia

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based on heuristic

inferred from title

author name string

P. C. White

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6334310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6334310

retrieved

1 October 2023

M. I. New

series ordinal

2

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stated in

Europe PubMed Central

PubMed publication ID

6334310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6334310

retrieved

1 October 2023

B. Dupont

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6334310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6334310

retrieved

1 October 2023

language of work or name

English

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publication date

1 December 1984

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stated in

Europe PubMed Central

PMC publication ID

392175

retrieved

21 August 2017

full work available at URL

https://europepmc.org/articles/pmc392175?pdf=render

file format

Portable Document Format

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6334310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6334310

retrieved

1 October 2023

https://europepmc.org/articles/PMC392175

file format

HTML

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6334310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6334310

retrieved

1 October 2023

https://europepmc.org/articles/PMC392175?pdf=render

file format

Portable Document Format

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6334310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6334310

retrieved

1 October 2023

https://pnas.org/doi/pdf/10.1073/pnas.81.23.7505

1 reference

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Crossref

DOI

10.1073/PNAS.81.23.7505

reference URL

https://api.crossref.org/works/10.1073/PNAS.81.23.7505

retrieved

1 October 2023

published in

Proceedings of the National Academy of Sciences of the United States of America

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stated in

Europe PubMed Central

PMC publication ID

392175

retrieved

21 August 2017

volume

81

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stated in

Europe PubMed Central

PMC publication ID

392175

retrieved

21 August 2017

issue

23

1 reference

stated in

Europe PubMed Central

PMC publication ID

392175

retrieved

21 August 2017

page(s)

7505-7509

1 reference

stated in

Europe PubMed Central

PMC publication ID

392175

retrieved

21 August 2017

describes a project that uses

PLH

0 references

cites work

Deoxycorticosterone biosynthesis in human kidney: potential for formation of a potent mineralocorticosteroid in its site of action

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392175

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23 August 2017

A highly polymorphic locus in human DNA

1 reference

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PubMed Central

reference URL

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retrieved

23 August 2017

HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392175

retrieved

23 August 2017

Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392175

retrieved

23 August 2017

Use of a cDNA clone for the fourth component of human complement (C4) for analysis of a genetic deficiency of C4 in guinea pig

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392175

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23 August 2017

Molecular map of the murine S region

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23 August 2017

A rapid boiling method for the preparation of bacterial plasmids

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PubMed Central

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23 August 2017

Detection of specific sequences among DNA fragments separated by gel electrophoresis

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PubMed Central

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23 August 2017

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392175

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23 August 2017

Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392175

retrieved

9 September 2017

Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392175

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9 September 2017

Improved B Cell Typing for HLA-DR Using Nylon Wool Column Enriched B Lymphocyte Preparations

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PubMed Central

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14 September 2017

The traditional and a new version of the mouse H-2 complex

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14 September 2017

Genes of the Major Histocompatibility Complex in Mouse and Man

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14 September 2017

Inborn errors of steroid biosynthesis

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392175

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14 September 2017

The 21-Hydroxylase Activity in the Glomerulosa and Fasciculata of the Adrenal Cortex in Congenital Adrenal Hyperplasia*

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392175

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25 June 2018

Comparison of one-dimensional IEF patterns for serologically detectable HLA-A and B allotypes

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=392175

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25 June 2018

Studies of the C-21 and C-19 Steroids and HLA Genotyping in Siblings and Parents of Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency*

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6334310

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on the steroid hydroxylation system in adrenal cortex microsomes. Purification and characterization of cytochrome P-450 specific for steroid C-21 hydroxylation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6334310

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of rabbit microsomal cytochrome P-450 isozyme, form 1, as a hepatic progesterone 21-hydroxylase

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6334310

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6334310

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antenatal diagnosis of the haemoglobin disorders by analysis of foetal DNA

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6334310

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.81.23.7505

1 reference

stated in

Europe PubMed Central

PMC publication ID

392175

retrieved

21 August 2017

ADS bibcode

1984PNAS...81.7505W

0 references

PMC publication ID

392175

1 reference

stated in

Europe PubMed Central

PMC publication ID

392175

retrieved

21 August 2017

PubMed publication ID

6334310

1 reference

stated in

Europe PubMed Central

PMC publication ID

392175

retrieved

21 August 2017

ResearchGate publication ID

16862599

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