(Q35724824)

English

Mutation of the androgen receptor (R840S) in an Egyptian patient with partial androgen insensitivity syndrome: review of the literature on the clinical expression of different R840 substitutions

scientific article published on January 2004

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scholarly article

1 reference

Europe PubMed Central

9 August 2017

1 reference

Europe PubMed Central

Mutation of the androgen receptor (R840S) in an Egyptian patient with partial androgen insensitivity syndrome: review of the literature on the clinical expression of different R840 substitutions (English)

1 reference

Europe PubMed Central

9 August 2017

partial androgen insensitivity syndrome

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

androgen insensitivity syndrome

1 reference

based on heuristic

inferred from title

author name string

Mazen I

1

1 reference

Europe PubMed Central

9 August 2017

Lumbroso S

2

1 reference

Europe PubMed Central

9 August 2017

Abdel Ghaffar S

3

1 reference

Europe PubMed Central

9 August 2017

Salah N

4

1 reference

Europe PubMed Central

9 August 2017

Sultan C

5

1 reference

Europe PubMed Central

9 August 2017

publication date

1 January 2004

1 reference

Europe PubMed Central

9 August 2017

Journal of Endocrinological Investigation

1 reference

Europe PubMed Central

9 August 2017

27

1 reference

Europe PubMed Central

9 August 2017

1

1 reference

Europe PubMed Central

9 August 2017

57-60

1 reference

Europe PubMed Central

9 August 2017

https://scigraph.springernature.com/pub.10.1007/bf03350912

0 references

Novel amino acid substitutional mutation, tyrosine-739-aspartic acid, in the androgen receptor gene in complete androgen insensitivity syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

Androgen receptor (AR) coregulators: an overview

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

Response to local dihydrotestosterone treatment in a patient with partial androgen-insensitivity syndrome due to a novel mutation in the androgen receptor gene

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

Phenotypic diversity in siblings with partial androgen insensitivity syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

Genotype versus phenotype in families with androgen insensitivity syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

Substitution of arginine-839 by cysteine or histidine in the androgen receptor causes different receptor phenotypes in cultured cells and coordinate degrees of clinical androgen resistance

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

Mutations in the ligand-binding domain of the androgen receptor gene cluster in two regions of the gene

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

Amino acid substitutions in the hormone-binding domain of the human androgen receptor alter the stability of the hormone receptor complex

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

Clinical and biochemical investigations and molecular analysis of subjects with mutations in the androgen receptor gene

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

Is the human testis still an organ at risk?

1 reference

https://api.crossref.org/works/10.1007%2FBF03350912

21 January 2018

[Perfect male external genital development and salt-loss syndrome in girls with congenital adrenogenital syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional characterisation of mutations in the ligand-binding domain of the androgen receptor gene in patients with androgen insensitivity syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Androgen receptor defects: historical, clinical, and molecular perspectives

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single amino acid substitution (840Arg-->His) in the hormone-binding domain of the androgen receptor leads to incomplete androgen insensitivity syndrome associated with a thermolabile androgen receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of androgen insensitivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Male pseudohermaphroditism due to disorder of androgen receptor function]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Environmentally persistent alkylphenolic compounds are estrogenic

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of mutant androgen receptors causing partial androgen insensitivity syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcription of androgen receptor and 5alpha-reductase II in genital fibroblasts from patients with androgen insensitivity syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel substitution (Leu707Arg) in exon 4 of the androgen receptor gene causes complete androgen resistance

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Familial form of partial androgen insensitivity (Reifenstein syndrome): arginine-histidine mutation in position 840 in the androgen receptor]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Androgen Receptor Gene Mutations Database

1 reference

https://pubmed.ncbi.nlm.nih.gov/15053245

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF03350912

1 reference

Europe PubMed Central

9 August 2017

1 reference

Europe PubMed Central

9 August 2017

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