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Article

Foxl2 function in ovarian development.

Molecular genetics and metabolism - 1 Jul 2006

Uhlenhaut Nina Henriette, Treier Mathias

Abstract excerpt

Foxl2 is a forkhead transcription factor essential for proper reproductive function in females. Human patients carrying mutations in the FOXL2 gene display blepharophimosis/ptosis/epicanthus inversus syndrome (BPES), an autosomal dominant disease associated with eyelid defects and premature ovari...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16647286
DOI: 10.1016/j.ymgme.2006.03.005

Genes

FOXL2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16647286-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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FOXL2 mutations lead to different ovarian phenotypes in BPES patients: Case Report.Semantic proximity Read ↗

The mutations and potential targets of the forkhead transcription factor FOXL2.Semantic proximity Read ↗

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Structure, evolution and expression of the FOXL2 transcription unitSemantic proximity Read ↗

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome.Semantic proximity Read ↗

FOXL2: a gene central to ovarian function.Semantic proximity Read ↗

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