Please use this identifier to cite or link to this item: https://doi.org/10.1111/j.1365-2141.2005.05793.x
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dc.titleHaploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice
dc.contributor.authorIto, Y.
dc.contributor.authorYamashita, N.
dc.contributor.authorOsato, M.
dc.contributor.authorYanagida, M.
dc.contributor.authorShigesada, K.
dc.contributor.authorHuang, L.
dc.contributor.authorKogan, S.C.
dc.contributor.authorIwasaki, M.
dc.contributor.authorNakamura, T.
dc.contributor.authorAsou, N.
dc.date.accessioned2011-09-27T05:43:46Z
dc.date.available2011-09-27T05:43:46Z
dc.date.issued2005
dc.identifier.citationIto, Y., Yamashita, N., Osato, M., Yanagida, M., Shigesada, K., Huang, L., Kogan, S.C., Iwasaki, M., Nakamura, T., Asou, N. (2005). Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice. British Journal of Haematology 131 (4) : 495-507. ScholarBank@NUS Repository. https://doi.org/10.1111/j.1365-2141.2005.05793.x
dc.identifier.issn00071048
dc.identifier.issn13652141
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/27012
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1111/j.1365-2141.2005.05793.x
dc.sourceScopus
dc.subjectAML1
dc.subjectCBF
dc.subjectFamilial platelet disorder
dc.subjectMutagenesis
dc.subjectRunx
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.contributor.departmentNATIONAL UNIVERSITY MEDICAL INSTITUTES
dc.description.doi10.1111/j.1365-2141.2005.05793.x
dc.description.sourcetitleBritish Journal of Haematology
dc.description.volume131
dc.description.issue4
dc.description.page495-507
dc.identifier.isiut000232978300011
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