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Special AT-rich Binding Protein-2 (SATB2) Differentially Affects Disease-causing p63 Mutant Proteins

p63, a p53 family member, is critical for proper skin and limb development and directly regulates gene expression in the ectoderm. Mice lacking p63 exhibit skin and craniofacial defects including cleft palate. In humans p63 mutations are associated with several distinct developmental syndromes. p63...

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Detalles Bibliográficos
Main Authors: Chung, Jacky, Grant, R. Ian, Kaplan, David R., Irwin, Meredith S.
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Biochemistry and Molecular Biology 2011
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3220488/
https://ncbi.nlm.nih.gov/pubmed/21965674
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M111.271189
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