Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mutation analysis of the WNT-4 gene in patients with polycystic ovary syndrome.

Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology - 1 Sept 2006

Canto Patricia, Söderlund Daniela, Carranza-Lira Sebastián, Méndez Juan Pablo

Abstract excerpt

Polycystic ovary syndrome (PCOS) is one of the most common endocrinopathies in women of childbearing age and is characterized by chronic anovulation with either oligomenorrhea or amenorrhea and hyperandrogenism. The etiology of this entity remains unknown. It has been suggested that genomic variants in genes related to the regulation of androgen biosynthesis and function could be involved in genetic...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polycystic Ovary Syndrome

Share to Proto-Oncogene Proteins

Share to Wnt Proteins

Share to Wnt4 Protein

Source

Identifiers

PMID: 17071531
DOI: 10.1080/09513590600911698

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation analysis of the WNT-4 gene in patients with polycystic ovary syndrome.PMID 17071531Read ↗

Mutation analysis of the WNT4 gene in Han Chinese women with premature ovarian failure.Semantic proximity Read ↗

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.Semantic proximity Read ↗

WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report.Semantic proximity Read ↗

Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome).Semantic proximity Read ↗

A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman.Semantic proximity Read ↗

Characterization and expression of the human WNT4; lack of associated germline mutations in high--to moderate--risk breast and ovarian cancer.Semantic proximity Read ↗

Mutations in WNT4 are not responsible for Müllerian duct abnormalities in Chinese women.Semantic proximity Read ↗

Study on the zona pellucida 4 (ZP4) gene sequence and its expression in the ovaries of patients with polycystic ovary syndrome.Semantic proximity Read ↗

Mutational analysis of the WNT gene family in women with Mayer-Rokitansky-Kuster-Hauser syndrome.Semantic proximity Read ↗

Molecular analysis of the WNT4 gene in 6 patients with Mayer-Rokitansky-Küster-Hauser syndrome.Semantic proximity Read ↗

Association of genetic markers within the BMP15 gene with anovulation and infertility in women with polycystic ovary syndrome.Semantic proximity Read ↗

Screening for mutations in the WNT-4 gene in patients with 46,XX true hermaphroditism.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.