(Q24305984)

English

Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18182450%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18182450%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

0 references

Wnt family member 4

1 reference

GOA release 2020-03-11

paramesonephric duct development

1 reference

GOA release 2020-03-11

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

primary amenorrhea

0 references

Pascal Philibert

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18182450%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

3

1 reference

Europe PubMed Central

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31 December 2019

6

1 reference

Europe PubMed Central

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31 December 2019

author name string

Anna Biason-Lauber

2

1 reference

Europe PubMed Central

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31 December 2019

Catherine Pienkowski

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18182450%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Françoise Paris

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18182450%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Eugene Schoenle

7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18182450%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Charles Sultan

8

1 reference

Europe PubMed Central

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31 December 2019

language of work or name

0 references

publication date

8 January 2008

1 reference

Europe PubMed Central

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31 December 2019

The Journal of Clinical Endocrinology and Metabolism

1 reference

Europe PubMed Central

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31 December 2019

93

1 reference

Europe PubMed Central

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31 December 2019

3

1 reference

Europe PubMed Central

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31 December 2019

895-900

1 reference

Europe PubMed Central

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31 December 2019

Exclusion ofWNT4 as a major gene in Rokitansky-Küster-Hauser anomaly

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

Female development in mammals is regulated by Wnt-4 signalling

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormal sexual development in transgenic mice chronically expressing Müllerian inhibiting substance

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

Wnt proteins are lipid-modified and can act as stem cell growth factors

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

Wnt4 overexpression disrupts normal testicular vasculature and inhibits testosterone synthesis by repressing steroidogenic factor 1/beta-catenin synergy

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

Ontogeny of reproductive abnormalities induced by deregulation of anti-müllerian hormone expression in transgenic mice.

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

The partial female to male sex reversal in Wnt-4-deficient females involves induced expression of testosterone biosynthetic genes and testosterone production, and depends on androgen action.

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad.

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

Specificity of WNT-receptor interactions

1 reference

https://api.crossref.org/works/10.1210%2FJC.2007-2023

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1210/JC.2007-2023

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18182450%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18182450%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

ResearchGate publication ID

0 references

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