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

FOXE1 polyalanine tract length screening by MLPA in idiopathic premature ovarian failure.

Reproductive biology and endocrinology : RB&E - 16 Dec 2011

Qin Chun-rong, Yao Ji-long, Zhu Wen-jie, Wu Wei-qing, Xie Jian-sheng

Abstract excerpt

BACKGROUND: FOXE1 is one of the candidate genes for genetic predisposition to premature ovarian failure (POF) and it contains an alanine tract. Our purpose is to assess the influence of length of the alanine tract of FOXE1 on genetic susceptibility to POF. METHODS: The group studied consisted of 110 Chinese patients with idiopathic POF and 110 women from normal controls. The polyalanine tract and flanking...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to DNA Repeat Expansion
Share to Forkhead Transcription Factors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to FOXE1 gene

Share to Genetic Testing

Share to Genotype

Share to Peptides

Share to Primary Ovarian Insufficiency

Source

Open in PubMed Open full text

Identifiers

PMID: 22177572
DOI: 10.1186/1477-7827-9-158
PMCID: PMC3286416

Genes

FOXE1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

FOXE1 polyalanine tract length screening by MLPA in idiopathic premature ovarian failure.PMID 22177572Read ↗

[Association of FOXE1 gene polymorphism with idiopathic premature ovarian failure].Semantic proximity Read ↗

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

Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis.Semantic proximity Read ↗

Association of FOXE1 polyalanine repeat region with papillary thyroid cancer.Semantic proximity Read ↗

Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure.Semantic proximity Read ↗

Genetic investigation of FOXE1 polyalanine tract in thyroid diseases: new insight on the role of FOXE1 in thyroid carcinoma.Semantic proximity Read ↗

FOXE1 polyalanine tract length polymorphism in patients with thyroid hemiagenesis and subjects with normal thyroid.Semantic proximity Read ↗

Association of FOXE1 polyalanine repeat region with thyroid cancer is dependent on tumour size.Semantic proximity Read ↗

Genotype Analyses in the Japanese and Belarusian Populations Reveal Independent Effects of rs965513 and rs1867277 but Do Not Support the Role of FOXE1 Polyalanine Tract Length in Conferring Risk for Papillary Thyroid Carcinoma.Semantic proximity Read ↗

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