Cargando…
Angelman Syndrome Protein UBE3A Interacts with Primary Microcephaly Protein ASPM, Localizes to Centrosomes and Regulates Chromosome Segregation
Many proteins associated with the phenotype microcephaly have been localized to the centrosome or linked to it functionally. All the seven autosomal recessive primary microcephaly (MCPH) proteins localize at the centrosome. Microcephalic osteodysplastic primordial dwarfism type II protein PCNT and S...
Autores principales: | Singhmar, Pooja, Kumar, Arun |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102111/ https://www.ncbi.nlm.nih.gov/pubmed/21633703 http://dx.doi.org/10.1371/journal.pone.0020397 |
Ejemplares similares
-
The Multiple Mitotic Roles of the ASPM Orthologous Proteins: Insight into the Etiology of ASPM-Dependent Microcephaly
por: Razuvaeva, Alyona V., et al.
Publicado: (2023) -
The neurological and non-neurological roles of the primary microcephaly-associated protein ASPM
por: Wu, Xingxuan, et al.
Publicado: (2023) -
The molecular landscape of ASPM mutations in primary microcephaly
por: Nicholas, A K, et al.
Publicado: (2009) -
Primary microcephaly caused by novel compound heterozygous mutations in ASPM
por: Okamoto, Nobuhiko, et al.
Publicado: (2018) -
Excessive Laughter-like Vocalizations, Microcephaly, and Translational Outcomes in the Ube3a Deletion Rat Model of Angelman Syndrome
por: Berg, Elizabeth L., et al.
Publicado: (2021)