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

[Association of FOXE1 gene polymorphism with idiopathic premature ovarian failure].

Zhonghua fu chan ke za zhi - 1 Feb 2015

Qin Chunrong, Yao Jilong, Yuan Zhen, Ren Xiaohui, Xie Jiansheng, Wu Weiqing

Abstract excerpt

OBJECTIVE: To assess the influence of length of the alanine tract of forkhead box E1 (FOXE1) gene on genetic susceptibility to idiopathic premature ovarian failure (POF). METHODS: Totally 110 patients with idiopathic POF were recruited between February 2009 and December 2012 at the Affiliated She...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Case-Control Studies
Share to Forkhead Transcription Factors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Multiplex Polymerase Chain Reaction

Share to Peptides

Share to Polymorphism, Genetic

Share to Primary Ovarian Insufficiency

Source

Identifiers

PMID: 25877608

Genes

FOXE1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25877608-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Association of FOXE1 gene polymorphism with idiopathic premature ovarian failure].PMID 25877608Read ↗

FOXE1 polyalanine tract length screening by MLPA in idiopathic premature ovarian failure.Semantic proximity Read ↗

An investigation into FOXE1 polyalanine tract length in premature ovarian failure.Semantic proximity Read ↗

[Role of FOXL2 impairment in syndromic and non-syndromic premature ovarian failure (POF)].Semantic proximity Read ↗

Identification of novel mutations in FOXL2 associated with premature ovarian failure.Semantic proximity Read ↗

A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus.Semantic proximity Read ↗

Recent advances in the study of genes involved in non-syndromic premature ovarian failure.Semantic proximity Read ↗

New candidate gene POU5F1 associated with premature ovarian failure in Chinese patients.Semantic proximity Read ↗

Analysis of LHX8 mutation in premature ovarian failure.Semantic proximity Read ↗

Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure.Semantic proximity Read ↗

[Genetic analysis of premature ovarian failure: role of forkhead and TGF-beta genes].Semantic proximity Read ↗

The combination of polyalanine expansion mutation and a novel missense substitution in transcription factor FOXL2 leads to different ovarian phenotypes in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) patients.Semantic proximity Read ↗

The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles.Semantic proximity Read ↗

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