Activating CBL mutations are associated with a distinct MDS/MPN phenotype
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Title
Activating CBL mutations are associated with a distinct MDS/MPN phenotype
Authors
Keywords
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Journal
ANNALS OF HEMATOLOGY
Volume 91, Issue 11, Pages 1713-1720
Publisher
Springer Nature
Online
2012-08-09
DOI
10.1007/s00277-012-1521-3
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- (2010) Ulrike Bacher et al. CANCER TREATMENT REVIEWS
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- (2009) F. H. Grand et al. BLOOD
- CBL Exon 8/9 Mutants Activate the FLT3 Pathway and Cluster in Core Binding Factor/11q Deletion Acute Myeloid Leukemia/Myelodysplastic Syndrome Subtypes
- (2009) C. Reindl et al. CLINICAL CANCER RESEARCH
- Mutations of E3 Ubiquitin Ligase Cbl Family Members Constitute a Novel Common Pathogenic Lesion in Myeloid Malignancies
- (2009) Hideki Makishima et al. JOURNAL OF CLINICAL ONCOLOGY
- Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms
- (2009) Masashi Sanada et al. NATURE
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- (2008) S. Abbas et al. HAEMATOLOGICA
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