Fusion gene-mediated truncation ofRUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome
Author:
Publisher
Wiley
Subject
Cancer Research,Genetics
Reference44 articles.
1. 8p11 myeloproliferative syndrome with a novel t(7;8) translocation leading to fusion of theFGFR1 andTIF1 genes
2. Molecular genetics of acute myeloid leukaemia
3. The t(8;22) in chronic myeloid leukemia fuses BCR to FGFR1: transforming activity and specific inhibition of FGFR1 fusion proteins
4. Identification of breakpoints in t(8;21) acute myelogenous leukemia and isolation of a fusion transcript, AML1/ETO, with similarity to Drosophila segmentation gene, runt
5. Fusion of theBCRand the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: The first fusion gene involvingBCRbut notABL
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2. A case mimicking chronic myeloid leukemia with t(8;22)(p11;q11)/BCR-FGFR1 and sequential transformation to B-acute lymphoblastic leukemia and acute myeloid leukemia;Journal of Hematopathology;2021-01-08
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