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FOXL2 gene

Known as: PITUITARY FORKHEAD FACTOR, MOUSE, HOMOLOG OF, BPES1, FOXL2 
This gene plays a role in ovarian function.
National Institutes of Health

Related topics

Related topics

9 relations
ApoptosisCell Differentiation processForkhead Box Protein L2Homo sapiens

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FOXL2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2014
Review
2014
The role of FOXL2 in the pathogenesis of adult ovarian granulosa cell tumours.
Highly Cited
2014
Highly Cited
2014
Molecular signatures in rainbow darter (Etheostoma caeruleum) inhabiting an urbanized river reach receiving wastewater effluents.
2014
2014
Intragenic and extragenic disruptions of FOXL2 mapped by whole genome low-coverage sequencing in two BPES families with chromosome reciprocal translocation.
2012
2012
FOXL2 Is Regulated During the Bovine Estrous Cycle and Its Expression in the Endometrium Is Independent of Conceptus-Derived Interferon Tau1
ABSTRACT FOXL2, a winged-helix/forkhead domain transcription factor, is a key gene involved in the differentiation and biological… 
Review
2011
Review
2011
FOXL2 C402G mutation detection using MALDI-TOF-MS in DNA extracted from Israeli granulosa cell tumors.
Highly Cited
2010
Highly Cited
2010
FOXL2 mutations lead to different ovarian phenotypes in BPES patients: Case Report.
FOXL2 mutations cause the autosomal dominant Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) that may be associated… 
Review
2010
Review
2010
The forkhead factor FOXL2: a novel tumor suppressor?
2005
2005
A new heterozygous mutation of the FOXL2 gene is associated with a large ovarian cyst and ovarian dysfunction in an adolescent girl with blepharophimosis/ptosis/epicanthus inversus syndrome.
Blepharophimosis/ptosis/epicanthus inversus syndrome (BPES), an autosomal dominant syndrome in which eyelid malformation is… 
2005
2005
Blepharophimosis and bilateral Duane syndrome associated with a FOXL2 mutation
This case describes the novel coexistence of sporadic blepharophimosis–ptosis–epicanthus inversus syndrome (BPES) and bilateral… 
2002
2002
Mutations in FOXL2 underlying BPES (types 1 and 2) in Colombian families.
We report the genetic characterization of one family with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) type 1 and… 
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