FOXL2 drives the differentiation of supporting gonadal cells in early ovarian development
Abstract Background Forkhead box L2 (FOXL2) is a transcription factor from the forkhead box family primarily expressed in the pituitary, ovaries, and eyelids. Human mutations in FOXL2 cause blepharophimosis, ptosis, epicanthus and inversus syndrome (BPES), which can be associated with primary ovaria...
Kaydedildi:
| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMC
2025-03-01
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| Seri Bilgileri: | Reproductive Biology and Endocrinology |
| Konular: | |
| Online Erişim: | https://doi.org/10.1186/s12958-025-01377-0 |
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