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Potential targets of FOXL2, a transcription factor involved in craniofacial and follicular development, identified by transcriptomics

FOXL2 is a gene encoding a forkhead transcription factor, whose mutations are responsible for the blepharophimosis-ptosis-epicanthus inversus syndrome that often involves premature ovarian failure. FOXL2 is one of the earliest ovarian markers and it offers, along with its targets, an excellent model...

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Autors principals: Batista, Frank, Vaiman, Daniel, Dausset, Jean, Fellous, Marc, Veitia, Reiner A.
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2007
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1805535/
https://ncbi.nlm.nih.gov/pubmed/17360647
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0611326104
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