Human ASPM participates in spindle organisation, spindle orientation and cytokinesis

BACKGROUND: Mutations in the Abnormal Spindle Microcephaly related gene (ASPM) are the commonest cause of autosomal recessive primary microcephaly (MCPH) a disorder characterised by a small brain and associated mental retardation. ASPM encodes a mitotic spindle pole associated protein. It is suggest...

Descripción completa

Detalles Bibliográficos
Autores principales: Higgins, Julie, Midgley, Carol, Bergh, Anna-Maria, Bell, Sandra M, Askham, Jonathan M, Roberts, Emma, Binns, Ruth K, Sharif, Saghira M, Bennett, Christopher, Glover, David M, Woods, C Geoffrey, Morrison, Ewan E, Bond, Jacquelyn
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2988714/
https://www.ncbi.nlm.nih.gov/pubmed/21044324
http://dx.doi.org/10.1186/1471-2121-11-85

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2988714/
https://www.ncbi.nlm.nih.gov/pubmed/21044324
http://dx.doi.org/10.1186/1471-2121-11-85

Ejemplares similares