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PUBMED FOR HANDHELDS

Journal Abstract Search


328 related items for PubMed ID: 22773603

  • 21. Spectrum of molecular defects in juvenile myelomonocytic leukaemia includes ASXL1 mutations.
    Sugimoto Y, Muramatsu H, Makishima H, Prince C, Jankowska AM, Yoshida N, Xu Y, Nishio N, Hama A, Yagasaki H, Takahashi Y, Kato K, Manabe A, Kojima S, Maciejewski JP.
    Br J Haematol; 2010 Jul; 150(1):83-7. PubMed ID: 20408841
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  • 22. SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML).
    Meggendorfer M, Roller A, Haferlach T, Eder C, Dicker F, Grossmann V, Kohlmann A, Alpermann T, Yoshida K, Ogawa S, Koeffler HP, Kern W, Haferlach C, Schnittger S.
    Blood; 2012 Oct 11; 120(15):3080-8. PubMed ID: 22919025
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  • 23. Srsf2P95H/+ co-operates with loss of TET2 to promote myeloid bias and initiate a chronic myelomonocytic leukemia-like disease in mice.
    Xu JJ, Chalk AM, Wall M, Langdon WY, Smeets MF, Walkley CR.
    Leukemia; 2022 Dec 11; 36(12):2883-2893. PubMed ID: 36271153
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  • 24. Cytogenetic and molecular abnormalities in chronic myelomonocytic leukemia.
    Patnaik MM, Tefferi A.
    Blood Cancer J; 2016 Feb 05; 6(2):e393. PubMed ID: 26849014
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  • 25. Mutational landscape of chronic myelomonocytic leukemia in Chinese patients.
    Nie Y, Shao L, Zhang H, He CK, Li H, Zou J, Chen L, Ji H, Tan H, Lin Y, Ru K.
    Exp Hematol Oncol; 2022 May 24; 11(1):32. PubMed ID: 35610628
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  • 26. Targeted Next-Generation Sequencing in Myelodysplastic Syndrome and Chronic Myelomonocytic Leukemia Aids Diagnosis in Challenging Cases and Identifies Frequent Spliceosome Mutations in Transformed Acute Myeloid Leukemia.
    Reinig E, Yang F, Traer E, Arora R, Brown S, Rattray R, Braziel R, Fan G, Press R, Dunlap J.
    Am J Clin Pathol; 2016 Apr 24; 145(4):497-506. PubMed ID: 27124934
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  • 28. Genomic Landscape and Risk Stratification in Chronic Myelomonocytic Leukemia.
    Hunter A, Padron E.
    Curr Hematol Malig Rep; 2021 Jun 24; 16(3):247-255. PubMed ID: 33660195
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  • 31. Single nucleotide polymorphism array lesions, TET2, DNMT3A, ASXL1 and CBL mutations are present in systemic mastocytosis.
    Traina F, Visconte V, Jankowska AM, Makishima H, O'Keefe CL, Elson P, Han Y, Hsieh FH, Sekeres MA, Mali RS, Kalaycio M, Lichtin AE, Advani AS, Duong HK, Copelan E, Kapur R, Olalla Saad ST, Maciejewski JP, Tiu RV.
    PLoS One; 2012 Jun 24; 7(8):e43090. PubMed ID: 22905207
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  • 33. Morphologic and Immunophenotypic Differences in Juvenile Myelomonocytic Leukemias With CBL and Other Canonical RAS-pathway Gene Mutations: A Single Institutional Experience.
    Mariani RA, Jennings L, Zhang S, Bhat R, Gong S.
    J Pediatr Hematol Oncol; 2021 Aug 01; 43(6):e819-e825. PubMed ID: 33769390
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  • 34. CBL mutations in chronic myelomonocytic leukemia often occur in the RING domain with multiple subclones per patient: Implications for targeting.
    Lim K, Kan WL, Nair PC, Kutyna M, Lopez AF, Hercus T, Ross DM, Lane S, Fong CY, Brown A, Yong A, Yeung D, Hughes T, Hiwase D, Thomas D.
    PLoS One; 2024 Aug 01; 19(9):e0310641. PubMed ID: 39298477
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  • 35. Mutational landscape of chronic myelomonocytic leukemia and its potential clinical significance.
    Han W, Zhou F, Wang Z, Hua H, Qin W, Jia Z, Cai X, Chen M, Liu J, Chao H, Lu X.
    Int J Hematol; 2022 Jan 01; 115(1):21-32. PubMed ID: 34449040
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  • 38. Molecular similarity between myelodysplastic form of chronic myelomonocytic leukemia and refractory anemia with ring sideroblasts.
    Gelsi-Boyer V, Cervera N, Bertucci F, Brecqueville M, Finetti P, Murati A, Arnoulet C, Mozziconacci MJ, Mills KI, Cross NC, Vey N, Birnbaum D.
    Haematologica; 2013 Apr 01; 98(4):576-83. PubMed ID: 23065512
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