Loss of Gsx1 and Gsx2 Function Rescues Distinct Phenotypes in Dlx1/2 Mutants

Mice lacking the Dlx1 and Dlx2 homeobox genes (Dlx1/2 mutants) have severe deficits in subpallial differentiation, including overexpression of the Gsx1 and Gsx2 homeobox genes. To investigate whether Gsx overexpression contributes to the Dlx1/2 mutant phenotypes, we made compound loss-of-function mu...

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Detalles Bibliográficos
Autores principales: Wang, Bei, Long, Jason E, Flandin, Pierre, Pla, Ramon, Waclaw, Ronald R, Campbell, Kenneth, Rubenstein, John LR
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Subscription Services, Inc., A Wiley Company 2013
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615175/
https://www.ncbi.nlm.nih.gov/pubmed/23042297
http://dx.doi.org/10.1002/cne.23242

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615175/
https://www.ncbi.nlm.nih.gov/pubmed/23042297
http://dx.doi.org/10.1002/cne.23242

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