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Journal Abstract Search

631 related items for PubMed ID: 10508512

  • 1.
    ; . PubMed ID:
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  • 2. Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies.
    Minelli A, Maserati E, Rossi G, Bernardo ME, De Stefano P, Cecchini MP, Valli R, Albano V, Pierani P, Leszl A, Sainati L, Lo Curto F, Danesino C, Locatelli F, Pasquali F.
    Genes Chromosomes Cancer; 2004 Jul; 40(3):165-71. PubMed ID: 15138996
    [Abstract] [Full Text] [Related]

  • 3. Low Mpl receptor expression in a pedigree with familial platelet disorder with predisposition to acute myelogenous leukemia and a novel AML1 mutation.
    Heller PG, Glembotsky AC, Gandhi MJ, Cummings CL, Pirola CJ, Marta RF, Kornblihtt LI, Drachman JG, Molinas FC.
    Blood; 2005 Jun 15; 105(12):4664-70. PubMed ID: 15741216
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  • 5. Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions.
    Béri-Dexheimer M, Latger-Cannard V, Philippe C, Bonnet C, Chambon P, Roth V, Grégoire MJ, Bordigoni P, Lecompte T, Leheup B, Jonveaux P.
    Eur J Hum Genet; 2008 Aug 15; 16(8):1014-8. PubMed ID: 18478040
    [Abstract] [Full Text] [Related]

  • 6. AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies.
    Taketani T, Taki T, Takita J, Tsuchida M, Hanada R, Hongo T, Kaneko T, Manabe A, Ida K, Hayashi Y.
    Genes Chromosomes Cancer; 2003 Sep 15; 38(1):1-7. PubMed ID: 12874780
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  • 7. 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 15; 125(6):709-19. PubMed ID: 15180860
    [Abstract] [Full Text] [Related]

  • 8. A novel RUNX1 mutation in familial platelet disorder with propensity to develop myeloid malignancies.
    Kirito K, Sakoe K, Shinoda D, Takiyama Y, Kaushansky K, Komatsu N.
    Haematologica; 2008 Jan 15; 93(1):155-6. PubMed ID: 18166807
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  • 9. A novel CBFA2 single-nucleotide mutation in familial platelet disorder with propensity to develop myeloid malignancies.
    Buijs A, Poddighe P, van Wijk R, van Solinge W, Borst E, Verdonck L, Hagenbeek A, Pearson P, Lokhorst H.
    Blood; 2001 Nov 01; 98(9):2856-8. PubMed ID: 11675361
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  • 10. AML1 haploinsufficiency, gene dosage, and the predisposition to acute leukemia.
    Barton K, Nucifora G.
    Bioessays; 2000 Mar 01; 22(3):214-8. PubMed ID: 10684580
    [Abstract] [Full Text] [Related]

  • 11. Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.
    Latger-Cannard V, Philippe C, Bouquet A, Baccini V, Alessi MC, Ankri A, Bauters A, Bayart S, Cornillet-Lefebvre P, Daliphard S, Mozziconacci MJ, Renneville A, Ballerini P, Leverger G, Sobol H, Jonveaux P, Preudhomme C, Nurden P, Lecompte T, Favier R.
    Orphanet J Rare Dis; 2016 Apr 26; 11():49. PubMed ID: 27112265
    [Abstract] [Full Text] [Related]

  • 12. Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice.
    Yamashita N, Osato M, Huang L, Yanagida M, Kogan SC, Iwasaki M, Nakamura T, Shigesada K, Asou N, Ito Y.
    Br J Haematol; 2005 Nov 26; 131(4):495-507. PubMed ID: 16281942
    [Abstract] [Full Text] [Related]

  • 13. Familial myelodysplasia and acute myeloid leukaemia--a review.
    Owen C, Barnett M, Fitzgibbon J.
    Br J Haematol; 2008 Jan 26; 140(2):123-32. PubMed ID: 18173751
    [Abstract] [Full Text] [Related]

  • 14. Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis.
    Ruiz-Perez VL, Ide SE, Strom TM, Lorenz B, Wilson D, Woods K, King L, Francomano C, Freisinger P, Spranger S, Marino B, Dallapiccola B, Wright M, Meitinger T, Polymeropoulos MH, Goodship J.
    Nat Genet; 2000 Mar 26; 24(3):283-6. PubMed ID: 10700184
    [Abstract] [Full Text] [Related]

  • 15. A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia.
    Walker LC, Stevens J, Campbell H, Corbett R, Spearing R, Heaton D, Macdonald DH, Morris CM, Ganly P.
    Br J Haematol; 2002 Jun 26; 117(4):878-81. PubMed ID: 12060124
    [Abstract] [Full Text] [Related]

  • 16. Recurrent CDC25C mutations drive malignant transformation in FPD/AML.
    Yoshimi A, Toya T, Kawazu M, Ueno T, Tsukamoto A, Iizuka H, Nakagawa M, Nannya Y, Arai S, Harada H, Usuki K, Hayashi Y, Ito E, Kirito K, Nakajima H, Ichikawa M, Mano H, Kurokawa M.
    Nat Commun; 2014 Aug 27; 5():4770. PubMed ID: 25159113
    [Abstract] [Full Text] [Related]

  • 17. Impaired hematopoietic differentiation of RUNX1-mutated induced pluripotent stem cells derived from FPD/AML patients.
    Sakurai M, Kunimoto H, Watanabe N, Fukuchi Y, Yuasa S, Yamazaki S, Nishimura T, Sadahira K, Fukuda K, Okano H, Nakauchi H, Morita Y, Matsumura I, Kudo K, Ito E, Ebihara Y, Tsuji K, Harada Y, Harada H, Okamoto S, Nakajima H.
    Leukemia; 2014 Dec 27; 28(12):2344-54. PubMed ID: 24732596
    [Abstract] [Full Text] [Related]

  • 18. Familial mutations of the transcription factor RUNX1 (AML1, CBFA2) predispose to acute myeloid leukemia.
    Ganly P, Walker LC, Morris CM.
    Leuk Lymphoma; 2004 Jan 27; 45(1):1-10. PubMed ID: 15061191
    [Abstract] [Full Text] [Related]

  • 19. Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia.
    Steensma DP, Gibbons RJ, Mesa RA, Tefferi A, Higgs DR.
    Eur J Haematol; 2005 Jan 27; 74(1):47-53. PubMed ID: 15613106
    [Abstract] [Full Text] [Related]

  • 20. Identification of an alternatively spliced form of the mouse AML1/RUNX1 gene transcript AML1c and its expression in early hematopoietic development.
    Fujita Y, Nishimura M, Taniwaki M, Abe T, Okuda T.
    Biochem Biophys Res Commun; 2001 Mar 27; 281(5):1248-55. PubMed ID: 11243869
    [Abstract] [Full Text] [Related]

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