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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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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2007
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| Assuntos: | |
| Acesso em linha: | 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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