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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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Библиографические подробности
Главные авторы: Chung, Jacky, Grant, R. Ian, Kaplan, David R., Irwin, Meredith S.
Формат: Artigo
Язык:Inglês
Опубликовано: American Society for Biochemistry and Molecular Biology 2011
Предметы:
Online-ссылка: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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