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Journal Abstract Search

347 related items for PubMed ID: 18295660

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  • 3. Identification of four new translocations involving FGFR1 in myeloid disorders.
    Sohal J, Chase A, Mould S, Corcoran M, Oscier D, Iqbal S, Parker S, Welborn J, Harris RI, Martinelli G, Montefusco V, Sinclair P, Wilkins BS, van den Berg H, Vanstraelen D, Goldman JM, Cross NC.
    Genes Chromosomes Cancer; 2001 Oct; 32(2):155-63. PubMed ID: 11550283
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  • 4. Myeloproliferative neoplasms with t(8;22)(p11.2;q11.2)/BCR-FGFR1: a meta-analysis of 20 cases shows cytogenetic progression with B-lymphoid blast phase.
    Montenegro-Garreaud X, Miranda RN, Reynolds A, Tang G, Wang SA, Yabe M, Wang W, Fang L, Bueso-Ramos CE, Lin P, Medeiros LJ, Lu X.
    Hum Pathol; 2017 Jul; 65():147-156. PubMed ID: 28551329
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  • 5. Hematologic malignancies with PCM1-JAK2 gene fusion share characteristics with myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1.
    Patterer V, Schnittger S, Kern W, Haferlach T, Haferlach C.
    Ann Hematol; 2013 Jun; 92(6):759-69. PubMed ID: 23400675
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  • 6. Myeloid/lymphoid neoplasm with CEP110-FGFR1 fusion: An analysis of 16 cases show common features and poor prognosis.
    Chen M, Wang K, Cai X, Zhang X, Chao H, Chen S, Shen H, Wang Q, Zhang R.
    Hematology; 2021 Dec; 26(1):153-159. PubMed ID: 33491601
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  • 7. A biphenotypic transformation of 8p11 myeloproliferative syndrome with CEP1/FGFR1 fusion gene.
    Yamamoto K, Kawano H, Nishikawa S, Yakushijin K, Okamura A, Matsui T.
    Eur J Haematol; 2006 Oct; 77(4):349-54. PubMed ID: 16879608
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  • 10. Molecular identification of a TPR-FGFR1 fusion transcript in an adult with myeloproliferative neoplasm, T-lymphoblastic lymphoma, and a t(1;8)(q25;p11.2).
    Kim SY, Kim JE, Park S, Kim HK.
    Cancer Genet; 2014 Jun; 207(6):258-62. PubMed ID: 25037443
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  • 11. [Clinical pathological features of the 8p11 myeloproliferative syndrome].
    Yan Z, Yang B, Wang QS, Wang LL, Han XP, Ren F, Yu L.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Oct; 18(5):1321-6. PubMed ID: 21129285
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  • 13. Identification of a novel partner gene, TPR, fused to FGFR1 in 8p11 myeloproliferative syndrome.
    Li F, Zhai YP, Tang YM, Wang LP, Wan PJ.
    Genes Chromosomes Cancer; 2012 Sep; 51(9):890-7. PubMed ID: 22619110
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  • 14. 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; 1998 Jan; 18(1):84-7. PubMed ID: 9425908
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  • 15. Chromosome 8p11.2 translocations: prevalence, FISH analysis for FGFR1 and MYST3, and clinicopathologic correlates in a consecutive cohort of 13 cases from a single institution.
    Patnaik MM, Gangat N, Knudson RA, Keefe JG, Hanson CA, Pardanani A, Ketterling RP, Tefferi A.
    Am J Hematol; 2010 Apr; 85(4):238-42. PubMed ID: 20143402
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  • 16. The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1.
    Macdonald D, Reiter A, Cross NC.
    Acta Haematol; 2002 Apr; 107(2):101-7. PubMed ID: 11919391
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  • 17. 8p11 myeloproliferative syndrome with t(1;8)(q25;p11.2): a case report and review of the literature.
    Kim WS, Park SG, Park G, Jang SJ, Moon DS, Kang SH.
    Acta Haematol; 2015 Apr; 133(1):101-5. PubMed ID: 25227135
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  • 18. Myeloid and lymphoid neoplasm with abnormalities of FGFR1 presenting with trilineage blasts and RUNX1 rearrangement: a case report and review of literature.
    Kumar KR, Chen W, Koduru PR, Luu HS.
    Am J Clin Pathol; 2015 May; 143(5):738-48. PubMed ID: 25873510
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  • 20. Myeloproliferative disorders with t(8;9)(p12;q33): a case report and review of the literature.
    Hu S, He Y, Zhu X, Li J, He H.
    Pediatr Hematol Oncol; 2011 Mar; 28(2):140-6. PubMed ID: 21214407
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