Please use this identifier to cite or link to this item: https://doi.org/10.1111/j.1365-2141.2005.05793.x
DC FieldValue
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
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

37
checked on Aug 13, 2019

WEB OF SCIENCETM
Citations

35
checked on Aug 13, 2019

Page view(s)

137
checked on Aug 19, 2019

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.