SET Nuclear Oncogene Associates with Microcephalin/MCPH1 and Regulates Chromosome Condensation

Primary microcephaly is an autosomal recessive disorder characterized by marked reduction in human brain size. Microcephalin (MCPH1), one of the genes mutated in primary microcephaly, plays an important role in DNA damage checkpoint control and mitotic entry. Additionally, MCPH1 ensures the proper t...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Leung, Justin W., Leitch, Andrea, Wood, Jamie L., Shaw-Smith, Charles, Metcalfe, Kay, Bicknell, Louise S., Jackson, Andrew P., Chen, Junjie
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society for Biochemistry and Molecular Biology 2011
Aiheet:
DNA and Chromosomes
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3122199/
https://ncbi.nlm.nih.gov/pubmed/21515671
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M110.208793
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