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Deletion of Cdc42 in embryonic cardiomyocytes results in right ventricle hypoplasia
BACKGROUND: Cdc42 is a member of the Rho GTPase family and functions as a molecular switch in regulating cytoskeleton remodeling and cell polarity establishment. Inactivating Cdc42 in cardiomyocytes resulted in embryonic lethality with heart developmental defects, including ventricular septum defect...
Autores principales: | Liu, Yang, Wang, Jian, Li, Jieli, Wang, Rui, Tharakan, Binu, Zhang, Shenyuan L., Tong, Carl W., Peng, Xu |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670094/ https://www.ncbi.nlm.nih.gov/pubmed/29101495 http://dx.doi.org/10.1186/s40169-017-0171-4 |
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