(Q24646466)

English

Deletion of the steroid-binding domain of the human androgen receptor gene in one family with complete androgen insensitivity syndrome: evidence for further genetic heterogeneity in this syndrome

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scholarly article

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Deletion of the steroid-binding domain of the human androgen receptor gene in one family with complete androgen insensitivity syndrome: evidence for further genetic heterogeneity in this syndrome (English)

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complete androgen insensitivity syndrome

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1 reference

based on heuristic

inferred from title

6

object named as

C J Migeon

author given names

C J

author last names

Migeon

1 reference

19 October 2023

author name string

T R Brown

1

author given names

T R

author last names

Brown

1 reference

19 October 2023

D B Lubahn

2

author given names

D B

author last names

Lubahn

1 reference

19 October 2023

E M Wilson

3

author given names

E M

author last names

Wilson

1 reference

19 October 2023

D R Joseph

4

author given names

D R

author last names

Joseph

1 reference

19 October 2023

F S French

5

author given names

F S

author last names

French

1 reference

19 October 2023

language of work or name

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publication date

November 1988

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

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85

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8151-5

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21

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"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

7 April 2017

The steroid and thyroid hormone receptor superfamily

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

7 April 2017

Molecular Cloning of Human and Rat Complementary DNA Encoding Androgen Receptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

7 April 2017

Cloning of Human Androgen Receptor Complementary DNA and Localization to the X Chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

7 April 2017

X-linked Gene for Testicular Feminization in the Mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

7 April 2017

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

7 April 2017

Cultured human skin fibroblasts: a model for the study of androgen action

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

27 September 2017

Regulation of the androgen receptor in human genital skin fibroblasts, with a review of sex steroid receptor regulation by homologous and heterologous steroids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

27 September 2017

Genetic Disorders of Male Sexual Differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

27 September 2017

Plasma concentration of testosterone, dihydrotestosterone, testosterone-oestradiol binding globulin, and pituitary gonadotrophins in the syndrome of male pseudo-hermaphroditism with testicular feminization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

27 September 2017

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

27 September 2017

Androgen insensitivity as a cause of infertility in otherwise normal men

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

27 September 2017

Male pseudohermaphroditism presumably due to target organ unresponsiveness to androgens. Deficient 5alpha-dihydrotestosterone binding in cultured skin fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

27 September 2017

Dihydrotestosterone binding by cultured human fibroblasts. Comparison of cells from control subjects and from patients with hereditary male pseudohermaphroditism due to androgen resistance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

27 September 2017

Androgen insensitivity in man: evidence for genetic heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

27 September 2017

Locus on human X chromosome for dihydrotestosterone receptor and androgen insensitivity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

27 September 2017

Gene deletions in patients with haemophilia B and anti-factor IX antibodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

30 May 2018

Syndrome of androgen insensitivity in man: absence of 5 alpha-dihydrotestosterone binding protein in skin fibroblasts.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

30 May 2018

Studies of androgens in the syndrome of male pseudohermaphroditism with testicular feminization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

30 May 2018

Complete androgen insensitivity syndrome characterized by increased concentration of a normal androgen receptor in genital skin fibroblasts.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

30 May 2018

Hemophilia A. Detection of molecular defects and of carriers by DNA analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=282385

30 May 2018

Part I. Male Pseudohermaphroditism in the Laboratory Norway Rat

1 reference

https://pubmed.ncbi.nlm.nih.gov/3186717

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete androgen insensitivity with a normal amount of 5α-dihydrotestosterone-binding activity in labium majus skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/3186717

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human complete androgen insensitivity with normal dihydrotestosterone receptor binding capacity in cultured genital skin fibroblasts: evidence for a qualitative abnormality of the receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/3186717

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinical syndrome of mild androgen insensitivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/3186717

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/3186717

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segment

1 reference

https://pubmed.ncbi.nlm.nih.gov/3186717

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion in the gene for the low-density-lipoprotein receptor in a majority of French Canadians with familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3186717

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.85.21.8151

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1988PNAS...85.8151B

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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