Differential Apoptotic and Proliferative Activities of Wild-type FOXL2 and Blepharophimosis-ptosis-epicanthus Inversus Syndrome (BPES)-associated Mutant FOXL2 Proteins

FOXL2 is an essential transcription factor that is required for proper development of the ovary and eyelid. Mutations in FOXL2 cause an autosomal dominant genetic disorder, blepharophimosis-ptosis-epicanthus inversus syndrome (BPES). BPES type I patients have eyelid malformation and premature ovaria...

Descripción completa

Detalles Bibliográficos
Autores principales: KIM, Jae-Hong, BAE, Jeehyeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Society for Reproduction and Development 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958583/
https://www.ncbi.nlm.nih.gov/pubmed/24240106
http://dx.doi.org/10.1262/jrd.2013-090

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958583/
https://www.ncbi.nlm.nih.gov/pubmed/24240106
http://dx.doi.org/10.1262/jrd.2013-090

Ejemplares similares