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Journal Abstract Search

250 related items for PubMed ID: 17330262

  • 21. Acute myeloid leukemia in an adult Noonan syndrome patient with PTPN11 mutation.
    Matsubara K, Yabe H, Ogata T, Yoshida R, Fukaya T.
    Am J Hematol; 2005 Jun; 79(2):171-2. PubMed ID: 15929108
    [No Abstract] [Full Text] [Related]

  • 22. PTPN11 mutations in pediatric patients with acute myeloid leukemia: results from the Children's Cancer Group.
    Loh ML, Reynolds MG, Vattikuti S, Gerbing RB, Alonzo TA, Carlson E, Cheng JW, Lee CM, Lange BJ, Meshinchi S, Children's Cancer Group.
    Leukemia; 2004 Nov; 18(11):1831-4. PubMed ID: 15385933
    [Abstract] [Full Text] [Related]

  • 23. PTPN11, RAS and FLT3 mutations in childhood acute lymphoblastic leukemia.
    Yamamoto T, Isomura M, Xu Y, Liang J, Yagasaki H, Kamachi Y, Kudo K, Kiyoi H, Naoe T, Kojma S.
    Leuk Res; 2006 Sep; 30(9):1085-9. PubMed ID: 16533526
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  • 24.
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  • 25. Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML.
    Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, De Braekeleer M.
    Eur J Haematol; 2007 Jun; 78(6):457-67. PubMed ID: 17391336
    [Abstract] [Full Text] [Related]

  • 26. Mutation screening of the PTPN11 gene in hypertrophic cardiomyopathy.
    Limongelli G, Hawkes L, Calabro R, McKenna WJ, Syrris P.
    Eur J Med Genet; 2006 Jun; 49(5):426-30. PubMed ID: 16488201
    [Abstract] [Full Text] [Related]

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  • 28. Methylation status of the p15 and p16 genes in paediatric myelodysplastic syndrome and juvenile myelomonocytic leukaemia.
    Hasegawa D, Manabe A, Kubota T, Kawasaki H, Hirose I, Ohtsuka Y, Tsuruta T, Ebihara Y, Goto Y, Zhao XY, Sakashita K, Koike K, Isomura M, Kojima S, Hoshika A, Tsuji K, Nakahata T.
    Br J Haematol; 2005 Mar; 128(6):805-12. PubMed ID: 15755284
    [Abstract] [Full Text] [Related]

  • 29. Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ?
    Lessard M, Hélias C, Struski S, Perrusson N, Uettwiller F, Mozziconacci MJ, Lafage-Pochitaloff M, Dastugue N, Terré C, Brizard F, Cornillet-Lefebvre P, Mugneret F, Barin C, Herry A, Luquet I, Desangles F, Michaux L, Verellen-Dumoulin C, Perrot C, Van den Akker J, Lespinasse J, Eclache V, Berger R, Groupe Francophone de Cytogénétique Hématologique.
    Cancer Genet Cytogenet; 2007 Jul 01; 176(1):1-21. PubMed ID: 17574959
    [Abstract] [Full Text] [Related]

  • 30. [Abnormalities of chromosome 17 in myeloid malignancies with complex chromosomal abnormalities].
    Zhu Y, Xu W, Liu Q, Pan J, Qiu H, Wang R, Qiao C, Jiang Y, Zhang S, Fan L, Zhang J, Shen Y, Xue Y, Li J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct 01; 25(5):579-82. PubMed ID: 18841577
    [Abstract] [Full Text] [Related]

  • 31. Two novel translocations disrupt the RUNX1 gene in acute myeloid leukemia.
    Dai H, Xue Y, Pan J, Wu Y, Wang Y, Shen J, Zhang J.
    Cancer Genet Cytogenet; 2007 Sep 01; 177(2):120-4. PubMed ID: 17854666
    [Abstract] [Full Text] [Related]

  • 32. Heterogeneous patterns of CEBPalpha mutation status in the progression of myelodysplastic syndrome and chronic myelomonocytic leukemia to acute myelogenous leukemia.
    Shih LY, Huang CF, Lin TL, Wu JH, Wang PN, Dunn P, Kuo MC, Tang TC.
    Clin Cancer Res; 2005 Mar 01; 11(5):1821-6. PubMed ID: 15756005
    [Abstract] [Full Text] [Related]

  • 33. Novel loss-of-function mutations of the haematopoiesis-related transcription factor, acute myeloid leukaemia 1/runt-related transcription factor 1, detected in acute myeloblastic leukaemia and myelodysplastic syndrome.
    Nakao M, Horiike S, Fukushima-Nakase Y, Nishimura M, Fujita Y, Taniwaki M, Okuda T.
    Br J Haematol; 2004 Jun 01; 125(6):709-19. PubMed ID: 15180860
    [Abstract] [Full Text] [Related]

  • 34. Rearrangement and expression of the p53 gene in myelodysplastic syndrome and acute myeloid leukemia.
    Fenaux P, Collyn d'Hooghe M, Jonveaux P, Lai JL, Bauters F, Loucheux MH, Kerckaert JP.
    Nouv Rev Fr Hematol (1978); 1990 Jun 01; 32(5):341-4. PubMed ID: 2099408
    [Abstract] [Full Text] [Related]

  • 35. CEBPA polymorphisms and mutations in patients with acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin's lymphoma.
    Fuchs O, Provaznikova D, Kocova M, Kostecka A, Cvekova P, Neuwirtova R, Kobylka P, Cermak J, Brezinova J, Schwarz J, Markova J, Salaj P, Klamova H, Maaloufova J, Lemez P, Novakova L, Benesova K.
    Blood Cells Mol Dis; 2008 Jun 01; 40(3):401-5. PubMed ID: 18182175
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  • 36.
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  • 37. Genetics of therapy-related myelodysplasia and acute myeloid leukemia.
    Pedersen-Bjergaard J, Andersen MK, Andersen MT, Christiansen DH.
    Leukemia; 2008 Feb 01; 22(2):240-8. PubMed ID: 18200041
    [Abstract] [Full Text] [Related]

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  • 39. Molecular mechanisms that produce secondary MDS/AML by RUNX1/AML1 point mutations.
    Harada Y, Harada H.
    J Cell Biochem; 2011 Feb 01; 112(2):425-32. PubMed ID: 21268063
    [Abstract] [Full Text] [Related]

  • 40. NPM1 mutations in myelodysplastic syndromes and acute myeloid leukemia with normal karyotype.
    Zhang Y, Zhang M, Yang L, Xiao Z.
    Leuk Res; 2007 Jan 01; 31(1):109-11. PubMed ID: 16678898
    [Abstract] [Full Text] [Related]

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