BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

382 related articles for article (PubMed ID: 20226962)

  • 41. Distinct stem cell myeloproliferative/T lymphoma syndromes induced by ZNF198-FGFR1 and BCR-FGFR1 fusion genes from 8p11 translocations.
    Roumiantsev S; Krause DS; Neumann CA; Dimitri CA; Asiedu F; Cross NC; Van Etten RA
    Cancer Cell; 2004 Mar; 5(3):287-98. PubMed ID: 15050920
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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; Gonçalves C; Hernandez JM; Jennings BA; Goldman JM; Cross NC
    Blood; 1998 Sep; 92(5):1735-42. PubMed ID: 9716603
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Myeloproliferative Syndrome With Eosinophilia Associated With Translocation t(8; 13) and T-cell Lymphoblastic Lymphoma: A Case Report and Review of the Literature.
    Urrea Pineda LY; Perilla O; Santiago-Pacheco V; Trujillo Montoya S
    Cureus; 2022 Mar; 14(3):e22734. PubMed ID: 35386486
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 45. A chronic myelogenous leukemia-like myeloproliferative disorder accompanied by T-cell lymphoblastic lymphoma with chromosome translocation t(8;13)(p11;q12): a Japanese case.
    Matsumoto K; Morita K; Takada S; Sakura T; Shiozaki H; Murakami H; Miyawaki S
    Int J Hematol; 1999 Dec; 70(4):278-82. PubMed ID: 10643154
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [8p11 myeloproliferative syndrome with CEP110-FGFR1 fusion in a patient].
    Chao H; Chen S; Zhou M; Lu X; Zhang X; Pan J; Wu C; Zhang R
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct; 32(5):679-82. PubMed ID: 26418991
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [The 8p11 myeloproliferative syndrome].
    Reither A; Hehlmann R; Goldman JM; Cross NC
    Med Klin (Munich); 1999 Apr; 94(4):207-10. PubMed ID: 10373756
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Dual lympho-myeloproliferative disorder in a patient with t(8;22) with BCR-FGFR1 gene fusion.
    Murati A; Arnoulet C; Lafage-Pochitaloff M; Adélaide J; Derré M; Slama B; Delaval B; Popovici C; Vey N; Xerri L; Mozziconacci MJ; Boulat O; Sainty D; Birnbaum D; Chaffanet M
    Int J Oncol; 2005 Jun; 26(6):1485-92. PubMed ID: 15870860
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome.
    Agerstam H; Lilljebjörn H; Lassen C; Swedin A; Richter J; Vandenberghe P; Johansson B; Fioretos T
    Genes Chromosomes Cancer; 2007 Jul; 46(7):635-43. PubMed ID: 17394134
    [TBL] [Abstract][Full Text] [Related]  

  • 50. t(8;22)/BCR-FGFR1 myeloproliferative disorder presenting as B-acute lymphoblastic leukemia: report of a case treated with sorafenib and review of the literature.
    Wakim JJ; Tirado CA; Chen W; Collins R
    Leuk Res; 2011 Sep; 35(9):e151-3. PubMed ID: 21628071
    [No Abstract]   [Full Text] [Related]  

  • 51. 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; Grégoire MJ; Jonveaux P; Lafage-Pochitaloff M; Birnbaum D; Pébusque MJ
    Blood; 1999 Feb; 93(4):1381-9. PubMed ID: 9949182
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A further case of myeloproliferative syndrome with reciprocal translocation (8;13)(p11;q12).
    Invernizzi R; Benatti C; Travaglino E; Girino M; Bernasconi P; Loni C; Ascari E
    Haematologica; 2004 Feb; 89(2):239-41. PubMed ID: 15003903
    [No Abstract]   [Full Text] [Related]  

  • 53. Myeloid and lymphoid neoplasm with FGFR1 abnormality.
    Keane C; Henden A; Mills T; Wood P
    Br J Haematol; 2009 May; 145(4):440. PubMed ID: 19076174
    [No Abstract]   [Full Text] [Related]  

  • 54. Prevalence of chromosome 8p11.2 translocations and correlation with myeloid and lymphoid neoplasms associated with FGFR1 abnormalities in a consecutive cohort from nine institutions in Japan.
    Usuki K; Kameda T; Kawano N; Ito T; Hashimoto Y; Shide K; Kawano H; Sekine M; Toyama T; Iizuka H; Sato S; Takeuchi M; Ishizaki J; Maeda K; Nakai M; Yamashita K; Kubuki Y; Shimoda K
    Int J Hematol; 2024 Jun; 119(6):722-727. PubMed ID: 38457113
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Myeloproliferative disorders.
    Bench AJ; Cross NC; Huntly BJ; Nacheva EP; Green AR
    Best Pract Res Clin Haematol; 2001 Sep; 14(3):531-51. PubMed ID: 11640868
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [The 8p11 myeloproliferative syndrome: a review of recent literature].
    Kirito K
    Rinsho Ketsueki; 2019; 60(9):1157-1165. PubMed ID: 31597839
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Clinical and gene involved of one case of 8p11 myeloproliferative syndrome with ins(13;8)(q12;p11p23)].
    Zhou F; Chen S; Chao H; Zhang R; Zhou M; Pan J
    Zhonghua Xue Ye Xue Za Zhi; 2015 Apr; 36(4):291-6. PubMed ID: 25916288
    [TBL] [Abstract][Full Text] [Related]  

  • 59. The 8p11 myeloproliferative syndrome: Genotypic and phenotypic classification and targeted therapy.
    Li T; Zhang G; Zhang X; Lin H; Liu Q
    Front Oncol; 2022; 12():1015792. PubMed ID: 36408177
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Systemic mastocytosis with associated myeloproliferative disease and precursor B lymphoblastic leukaemia with t(13;13)(q12;q22) involving FLT3.
    Tzankov A; Sotlar K; Muhlematter D; Theocharides A; Went P; Jotterand M; Horny HP; Dirnhofer S
    J Clin Pathol; 2008 Aug; 61(8):958-61. PubMed ID: 18663058
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.