A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q(−) syndrome

The identification of the genes associated with chromosomal translocation breakpoints has fundamentally changed our understanding of the molecular basis of hematological malignancies. By contrast, the study of chromosomal deletions has been hampered by the large number of genes deleted and the compl...

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Bibliografiska uppgifter
Huvudupphovsmän: Barlow, Jillian L., Drynan, Lesley F., Hewett, Duncan R., Holmes, Luke R., Lorenzo-Abalde, Silvia, Lane, Alison L., Jolin, Helen E., Pannell, Richard, Middleton, Angela J., Wong, See Heng, Warren, Alan J, Wainscoat, James S., Boultwood, Jacqueline, McKenzie, Andrew N.J.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2009
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2803774/
https://ncbi.nlm.nih.gov/pubmed/19966810
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nm.2063
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