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Journal Abstract Search

377 related items for PubMed ID: 29703722

  • 1. MYD88 L265P Mutation in Lymphoid Malignancies.
    Yu X, Li W, Deng Q, Li L, Hsi ED, Young KH, Zhang M, Li Y.
    Cancer Res; 2018 May 15; 78(10):2457-2462. PubMed ID: 29703722
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  • 3. Detection of MYD88 L265P and WHIM-like CXCR4 mutation in patients with IgM monoclonal gammopathy related disease.
    Cao XX, Meng Q, Cai H, He TH, Zhang CL, Su W, Sun J, Li Y, Xu W, Zhou DB, Li J.
    Ann Hematol; 2017 Jun 15; 96(6):971-976. PubMed ID: 28280994
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  • 10. Significances of MYD88L265P and CXCR4WHIM Mutations in Waldenstrom Macroglobulinemia.
    Meng Q, Cao XX, Li J.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2017 Aug 20; 39(4):578-582. PubMed ID: 28877839
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  • 11. [Lymphoplasmacytic lymphoma accompanied by transformed diffuse large B-cell lymphoma with the MYD88L265P mutation].
    Kida T, Tanimura A, Ono A, Matsui T, Honma K, Fujita J, Maeda T, Shibayama H, Oritani K, Morii E, Kanakura Y.
    Rinsho Ketsueki; 2017 Aug 20; 58(2):155-160. PubMed ID: 28321094
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  • 12. MYD88 Mutations: Transforming the Landscape of IgM Monoclonal Gammopathies.
    Alcoceba M, García-Álvarez M, Medina A, Maldonado R, González-Calle V, Chillón MC, Sarasquete ME, González M, García-Sanz R, Jiménez C.
    Int J Mol Sci; 2022 May 16; 23(10):. PubMed ID: 35628381
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  • 13. Prognostic impact of MYD88 and CXCR4 mutations assessed by droplet digital polymerase chain reaction in IgM monoclonal gammopathy of undetermined significance and smouldering Waldenström macroglobulinaemia.
    Moreno DF, López-Guerra M, Paz S, Oliver-Caldés A, Mena MP, Correa JG, Battram AM, Osuna M, Rivas-Delgado A, Rodríguez-Lobato LG, Cardús O, Tovar N, Cibeira MT, Jiménez-Segura R, Bladé J, Rosiñol L, Colomer D, Fernández de Larrea C.
    Br J Haematol; 2023 Jan 16; 200(2):187-196. PubMed ID: 36210485
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  • 14. A mutation in MYD88 (L265P) supports the survival of lymphoplasmacytic cells by activation of Bruton tyrosine kinase in Waldenström macroglobulinemia.
    Yang G, Zhou Y, Liu X, Xu L, Cao Y, Manning RJ, Patterson CJ, Buhrlage SJ, Gray N, Tai YT, Anderson KC, Hunter ZR, Treon SP.
    Blood; 2013 Aug 15; 122(7):1222-32. PubMed ID: 23836557
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  • 15. Clonal architecture of CXCR4 WHIM-like mutations in Waldenström Macroglobulinaemia.
    Xu L, Hunter ZR, Tsakmaklis N, Cao Y, Yang G, Chen J, Liu X, Kanan S, Castillo JJ, Tai YT, Zehnder JL, Brown JR, Carrasco RD, Advani R, Sabile JM, Argyropoulos K, Lia Palomba M, Morra E, Trojani A, Greco A, Tedeschi A, Varettoni M, Arcaini L, Munshi NM, Anderson KC, Treon SP.
    Br J Haematol; 2016 Mar 15; 172(5):735-44. PubMed ID: 26659815
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  • 17. MYD88 L265P somatic mutation in Waldenström's macroglobulinemia.
    Treon SP, Xu L, Yang G, Zhou Y, Liu X, Cao Y, Sheehy P, Manning RJ, Patterson CJ, Tripsas C, Arcaini L, Pinkus GS, Rodig SJ, Sohani AR, Harris NL, Laramie JM, Skifter DA, Lincoln SE, Hunter ZR.
    N Engl J Med; 2012 Aug 30; 367(9):826-33. PubMed ID: 22931316
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