(Q24302509)

cortisol biosynthetic process

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

P C White

1

P C

White

1 reference

20 October 2023

J Dupont

2

J

Dupont

1 reference

20 October 2023

M I New

3

M I

New

1 reference

20 October 2023

E Leiberman

4

E

Leiberman

1 reference

20 October 2023

Z Hochberg

5

Z

Hochberg

1 reference

20 October 2023

A Rösler

6

A

Rösler

1 reference

Journal of Clinical Investigation

20 October 2023

language of work or name

English

0 references

publication date

May 1991

0 references

published in

0 references

volume

87

0 references

issue

5

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page(s)

1664-7

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cites work

Cloning of cDNA encoding steroid 11 beta-hydroxylase (P450c11)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

DNA sequence analysis with a modified bacteriophage T7 DNA polymerase

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

The CpG dinucleotide and human genetic disease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta)

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

Molecular cloning and expression of cDNAS encoding rat aldosterone synthase: variants of cytochrome P-450(11 beta)

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

Supercoil sequencing: a fast and simple method for sequencing plasmid DNA

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

Congenital adrenal hyperplasia (2).

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

Site-directed mutageneses of rat liver cytochrome P-450d: axial ligand and heme incorporation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

The P450 superfamily: updated listing of all genes and recommended nomenclature for the chromosomal loci

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

Molecular pathology of congenital adrenal hyperplasia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

Molecular basis of base substitution hotspots in Escherichia coli

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

An inherited defect in aldosterone biosynthesis caused by a mutation in or near the gene for steroid 11-hydroxylase

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

Clinical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295260

11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis

30 May 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/2022736

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1172/JCI115182

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Fatcat ID

release_dvd4syxhznb4xk7hlkhh2f7mm4

0 references

PMC publication ID

295260

0 references