메뉴 건너뛰기




Volumn 40, Issue 1, 2004, Pages 78-83

Identification of a Novel Gene, FGFR1OP2, Fused to FGFR1 in 8p11 Myeloproliferative Syndrome

Author keywords

[No Author keywords available]

Indexed keywords

BCR ABL PROTEIN; COMPLEMENTARY DNA; FIBROBLAST GROWTH FACTOR RECEPTOR 1; MESSENGER RNA;

EID: 1942422114     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/gcc.20023     Document Type: Article
Times cited : (87)

References (19)
  • 1
    • 0036045381 scopus 로고    scopus 로고
    • Tyrosine kinase fusion genes in chronic myeloproliferative diseases
    • Cross NCP, Reiter A. 2002. Tyrosine kinase fusion genes in chronic myeloproliferative diseases. Leukemia 16:1207-1212.
    • (2002) Leukemia , vol.16 , pp. 1207-1212
    • Cross, N.C.P.1    Reiter, A.2
  • 2
    • 0028153771 scopus 로고
    • An optimized multiplex polymerase chain reaction (PCR) for detection of BCR-ABL fusion mRNAs in haematological disorders
    • Cross NCP, Melo JV, Feng L, Goldman JM. 1994. An optimized multiplex polymerase chain reaction (PCR) for detection of BCR-ABL fusion mRNAs in haematological disorders. Leukemia 8:186-189.
    • (1994) Leukemia , vol.8 , pp. 186-189
    • Cross, N.C.P.1    Melo, J.V.2    Feng, L.3    Goldman, J.M.4
  • 4
    • 0035159831 scopus 로고    scopus 로고
    • 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 T, Panagopoulos I, Lassen C, Swedin A, Billstrom R, Isaksson M, Strombeck B, Olofsson T, Mitelman F, Johansson B. 2001. 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. Genes Chromosomes Cancer 32:302-310.
    • (2001) Genes Chromosomes Cancer , vol.32 , pp. 302-310
    • Fioretos, T.1    Panagopoulos, I.2    Lassen, C.3    Swedin, A.4    Billstrom, R.5    Isaksson, M.6    Strombeck, B.7    Olofsson, T.8    Mitelman, F.9    Johansson, B.10
  • 5
    • 0034161335 scopus 로고    scopus 로고
    • FGFR1 is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33)
    • Guasch G, Mack GJ, Popovici C, Dastugue N, Birnbaum D, Rattner JB, Pebusque MJ. 2000. FGFR1 is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33). Blood 95:1788-1796.
    • (2000) Blood , vol.95 , pp. 1788-1796
    • Guasch, G.1    Mack, G.J.2    Popovici, C.3    Dastugue, N.4    Birnbaum, D.5    Rattner, J.B.6    Pebusque, M.J.7
  • 6
    • 0037216062 scopus 로고    scopus 로고
    • Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3)
    • Guasch G, Popovici C, Mugneret F, Chaffanet M, Pontarotti P, Birnbaum D, Pebusque MJ. 2003. Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3). Blood 101:286-288.
    • (2003) Blood , vol.101 , pp. 286-288
    • Guasch, G.1    Popovici, C.2    Mugneret, F.3    Chaffanet, M.4    Pontarotti, P.5    Birnbaum, D.6    Pebusque, M.J.7
  • 7
    • 0026356891 scopus 로고
    • Predicting coiled coils from protein sequences
    • Lupas A, Van Dyke M, Stock J. 1991. Predicting coiled coils from protein sequences. Science 252:1162-1164.
    • (1991) Science , vol.252 , pp. 1162-1164
    • Lupas, A.1    Van Dyke, M.2    Stock, J.3
  • 8
    • 0036202064 scopus 로고    scopus 로고
    • The 8p11 myeloproliferative syndrome: A distinct clinical entity caused by constitutive activation of FGFR1
    • Macdonald D, Reiter A, Cross NCP. 2002. The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1. Acta Haematol 107:101-107.
    • (2002) Acta Haematol , vol.107 , pp. 101-107
    • Macdonald, D.1    Reiter, A.2    Cross, N.C.P.3
  • 9
    • 0033503450 scopus 로고    scopus 로고
    • Congenital acute megakaryoblastic leukaemia (M7) with chromosomal t(1;22)(p13; q13) translocation in a set of identical twins
    • Ng KC, Tan AM, Chong YY, Lau LC, Lou J. 1999. Congenital acute megakaryoblastic leukaemia (M7) with chromosomal t(1;22)(p13; q13) translocation in a set of identical twins. J Pediatr Hematol Oncol 21:428-430.
    • (1999) J Pediatr Hematol Oncol , vol.21 , pp. 428-430
    • Ng, K.C.1    Tan, A.M.2    Chong, Y.Y.3    Lau, L.C.4    Lou, J.5
  • 10
    • 0031873337 scopus 로고    scopus 로고
    • Abnormalities of the ETV6 gene occur in the majority of patients with aberrations of the short arm of chromosome 12: A combined PCR and Southern blotting analysis
    • O'Connor HE, Butler TA, Clark R, Swanton S, Harrison CJ, Secker-Walker LM, Foroni L. 1998. Abnormalities of the ETV6 gene occur in the majority of patients with aberrations of the short arm of chromosome 12: a combined PCR and Southern blotting analysis. Leukaemia 12:1099-1106.
    • (1998) Leukaemia , vol.12 , pp. 1099-1106
    • O'Connor, H.E.1    Butler, T.A.2    Clark, R.3    Swanton, S.4    Harrison, C.J.5    Secker-Walker, L.M.6    Foroni, L.7
  • 12
    • 0033558253 scopus 로고    scopus 로고
    • 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, Zhang B, Gregoire MJ, Jonveaux P, Lafage-Pochilatoff M, Birnbaum D, Pebusque MJ. 1999. The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1. Blood 93:1381-1389.
    • (1999) Blood , vol.93 , pp. 1381-1389
    • Popovici, C.1    Zhang, B.2    Gregoire, M.J.3    Jonveaux, P.4    Lafage-Pochilatoff, M.5    Birnbaum, D.6    Pebusque, M.J.7
  • 14
    • 0033817222 scopus 로고    scopus 로고
    • The FGFR1 inhibitor PD 173074 selectively and potently antagonizes FGF-2 neurotrophic and neurotropic effects
    • Skaper SD, Kee WJ, Facci L, Macdonald G, Doherty P, Walsh FS. 2000. The FGFR1 inhibitor PD 173074 selectively and potently antagonizes FGF-2 neurotrophic and neurotropic effects. J Neurochem 75:1520-1527.
    • (2000) J Neurochem , vol.75 , pp. 1520-1527
    • Skaper, S.D.1    Kee, W.J.2    Facci, L.3    Macdonald, G.4    Doherty, P.5    Walsh, F.S.6
  • 15
    • 6844255886 scopus 로고    scopus 로고
    • 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, Hamoudi R, Clark J, Warren W, Abdul-Rauf M, Somers G, Venter D, Fagan K, Cooper C, Shipley J. 1998 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. Hum Mol Genet 7:637-642.
    • (1998) Hum Mol Genet , vol.7 , pp. 637-642
    • Smedley, D.1    Hamoudi, R.2    Clark, J.3    Warren, W.4    Abdul-Rauf, M.5    Somers, G.6    Venter, D.7    Fagan, K.8    Cooper, C.9    Shipley, J.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.