The t(6;8)(q27;p11) Translocation in a Stem Cell Myeloproliferative Disorder Fuses a Novel Gene, FOP, to Fibroblast Growth Factor Receptor 1
- 15 February 1999
- journal article
- Published by American Society of Hematology in Blood
- Vol. 93 (4) , 1381-1389
- https://doi.org/10.1182/blood.v93.4.1381
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Structural diversity of leucine-rich repeat proteins 1 1Edited by F. CohenJournal of Molecular Biology, 1998
- FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndromeNature Genetics, 1998
- Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3Nature Genetics, 1997
- The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding proteinNature Genetics, 1996
- Identification of a YAC spanning the translocation breakpoint t(8;22) associated with acute monocytic leukemiaGenes, Chromosomes and Cancer, 1996
- Chromosomal translocations in human cancerNature, 1994
- Identification of protein coding regions by database similarity searchNature Genetics, 1993
- Fibroblast Growth Factor Receptors from Liver Vary in Three Structural DomainsScience, 1991
- Basic local alignment search toolJournal of Molecular Biology, 1990
- A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemiaBritish Journal of Haematology, 1987