Rare translocations involving chromosome band 8p11 in myeloid neoplasms
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference9 articles.
1. The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1;Macdonald;Acta Haematol,2002
2. NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15) [Erratum in: Blood 2002;100:1132];Rosati;Blood,2002
3. Fusion of the BCR and 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 involving BCR but not ABL;Fioretos;Genes Chromosomes Cancer,2001
4. The t(8;22) in chronic myeloid leukemia fuses BCR to FGFR1: transforming activity and specific inhibition of FGFR1 fusion proteins;Demiroglu;Blood,2001
5. A fourth case of BCR–FGFR1 positive CML-like disease with t(8;22) translocation showing an extensive deletion on the derivative chromosome 8p;Pini;Hematol J,2002
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1. Clinical whole-genome sequencing and FISH identify two different fusion partners for NUP98 in a patient with acute myeloid leukemia: A case report;Cancer Genetics;2024-01
2. Myeloid/lymphoid neoplasms with eosinophilia and tyrosine kinase gene fusions: reevaluation of the defining characteristics in a registry-based cohort;Leukemia;2023-07-15
3. The 8p11 myeloproliferative syndrome: Genotypic and phenotypic classification and targeted therapy;Frontiers in Oncology;2022-11-03
4. Myeloid/lymphoid neoplasm with CEP110-FGFR1 fusion: An analysis of 16 cases show common features and poor prognosis;Hematology;2021-01-01
5. Functional characterization of two rare BCR–FGFR1+ leukemias;Molecular Case Studies;2020-01-24
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