Disruption of Mouse Cenpj, a Regulator of Centriole Biogenesis, Phenocopies Seckel Syndrome

Disruption of the centromere protein J gene, CENPJ (CPAP, MCPH6, SCKL4), which is a highly conserved and ubiquitiously expressed centrosomal protein, has been associated with primary microcephaly and the microcephalic primordial dwarfism disorder Seckel syndrome. The mechanism by which disruption of...

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Detalles Bibliográficos
Autores principales: McIntyre, Rebecca E., Lakshminarasimhan Chavali, Pavithra, Ismail, Ozama, Carragher, Damian M., Sanchez-Andrade, Gabriela, Forment, Josep V., Fu, Beiyuan, Del Castillo Velasco-Herrera, Martin, Edwards, Andrew, van der Weyden, Louise, Yang, Fengtang, Ramirez-Solis, Ramiro, Estabel, Jeanne, Gallagher, Ferdia A., Logan, Darren W., Arends, Mark J., Tsang, Stephen H., Mahajan, Vinit B., Scudamore, Cheryl L., White, Jacqueline K., Jackson, Stephen P., Gergely, Fanni, Adams, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499256/
https://www.ncbi.nlm.nih.gov/pubmed/23166506
http://dx.doi.org/10.1371/journal.pgen.1003022

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499256/
https://www.ncbi.nlm.nih.gov/pubmed/23166506
http://dx.doi.org/10.1371/journal.pgen.1003022

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