טוען...

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...

תיאור מלא

שמור ב:

מידע ביבליוגרפי
Main Authors:	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
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	BioMed Central 2010
נושאים:	Research Article
גישה מקוונת:	https://ncbi.nlm.nih.gov/pmc/articles/PMC2988714/ https://ncbi.nlm.nih.gov/pubmed/21044324 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2121-11-85
תגים:	הוספת תג אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!

Human ASPM participates in spindle organisation, spindle orientation and cytokinesis

פריטים דומים