A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy

Haploinsufficiency for the transcription factor SOX10 is associated with the pigmentary deficiencies of Waardenburg syndrome (WS) and is modeled in Sox10 haploinsufficient mice (Sox10(LacZ)(/+)). As genetic background affects WS severity in both humans and mice, we established an N-ethyl-N-nitrosour...

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Main Authors: Matera, Ivana, Watkins-Chow, Dawn E., Loftus, Stacie K., Hou, Ling, Incao, Arturo, Silver, Debra L., Rivas, Cecelia, Elliott, Eugene C., Baxter, Laura L., Pavan, William J.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2008
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2902284/
https://ncbi.nlm.nih.gov/pubmed/18397875
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn110
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