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Loss of Sip1 leads to migration defects and retention of ectodermal markers during lens development
SIP1 encodes a DNA-binding transcription factor that regulates multiple developmental processes, as highlighted by the pleiotropic defects observed in Mowat-Wilson Syndrome, which results from mutations in this gene. Further, in adults, dysregulated SIP1 expression has been implicated in both cancer...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4144920/ https://ncbi.nlm.nih.gov/pubmed/24161570 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mod.2013.09.005 |
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