Citations for
1FGFR1, SCLLS, ZMYM2
Constitutive Notch pathway activation in murine ZMYM2-FGFR1-induced T-cell lymphomas associated with atypical myeloproliferative disease.
Ren M, Cowell JK.
Blood Jun 23;117(25):6837-47. doi: 10.1182/blood-2010-07-295725. Epub 2011 Apr 28 2011
2FGFR1, SCLLS, ZMYM2
The 8p11 myeloproliferative syndrome: review of literature and an illustrative case report.
Goradia A, Bayerl M, Cornfield D.
Int J Clin Exp Pathol 1(5):448-56.PMID: 18787627 2008
3FGFR1, SCLLS, ZMYM2
The genomic structure of ZNF198 and location of breakpoints in the t(8;13) myeloproliferative syndrome.
Kulkarni S, et al.
Genomics 55 : 118-121. 1999
4 FGFR1OP, SCLLS
The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1.
Popovici C, et al.
Blood 93(4):1381-9. 1999
5AMLT3, SCLLS
Characterization of a t(8;13)(p11;q11-12) in an atypical myeloproliferative disorder.
Smedley D, Somers G, Venter D, Chow CW, Cooper C, Shipley J.
Genes Chromosomes Cancer 21(1):70-3. 1998
6FGFR1, SCLLS, ZMYM2
FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome.
Xiao S, Nalabolu SR, Aster JC, Ma J, Abruzzo L, Jaffe ES, Stone R, Weissman SM, Hudson TJ, Fletcher JA.
Nat Genet 18(1):84-7. 1998
7FGFR1, SCLLS, ZMYM2
The t(8;13)(p11;q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP.
Smedley D, et al.
Hum Mol Genet 7 : 637-642. 1998
8FGFR1, SCLLS, ZMYM2
Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)(p12;q12).
Popovici C, et al.
Proc Natl Acad Sci U S A 95 : 5712-5717. 1998
9FGFR1, SCLLS, ZMYM2
t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12.
Chaffanet M, et al.
Oncogene 16 : 945-949. 1998
10FGFR1, SCLLS, ZMYM2
Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome.
Reiter A, Sohal J, Kulkarni S, Chase A, Macdonald DH, Aguiar RC, Goncalves C, Hernandez JM, Jennings BA, Goldman JM, Cross NC.
Blood 92 : 1735-1742. 1998
11AMLT3, SCLLS
Molecular characterization of the t(8;13)(p11;q12) translocation associated with an atypical myeloproliferative disorder: evidence for three discrete loci involved in myeloid leukemias on 8p11.
Still IH, Chernova O, Hurd D, Stone RM, Cowell JK.
Blood 90(8):3136-41. 1997