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Journal Abstract Search

422 related items for PubMed ID: 11830488

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  • 4. Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
    Song WJ, Sullivan MG, Legare RD, Hutchings S, Tan X, Kufrin D, Ratajczak J, Resende IC, Haworth C, Hock R, Loh M, Felix C, Roy DC, Busque L, Kurnit D, Willman C, Gewirtz AM, Speck NA, Bushweller JH, Li FP, Gardiner K, Poncz M, Maris JM, Gilliland DG.
    Nat Genet; 1999 Oct; 23(2):166-75. PubMed ID: 10508512
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  • 5. 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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  • 6. CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML).
    Shiba N, Hasegawa D, Park MJ, Murata C, Sato-Otsubo A, Ogawa C, Manabe A, Arakawa H, Ogawa S, Hayashi Y.
    Blood; 2012 Mar 15; 119(11):2612-4. PubMed ID: 22138511
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  • 7. Point mutations of the RUNx1/AML1 gene in sporadic and familial myeloid leukemias.
    Osato M, Yanagida M, Shigesada K, Ito Y.
    Int J Hematol; 2001 Oct 15; 74(3):245-51. PubMed ID: 11721958
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  • 8. Familial mutations of the transcription factor RUNX1 (AML1, CBFA2) predispose to acute myeloid leukemia.
    Ganly P, Walker LC, Morris CM.
    Leuk Lymphoma; 2004 Jan 15; 45(1):1-10. PubMed ID: 15061191
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  • 9. 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
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  • 10. High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder.
    Preudhomme C, Renneville A, Bourdon V, Philippe N, Roche-Lestienne C, Boissel N, Dhedin N, André JM, Cornillet-Lefebvre P, Baruchel A, Mozziconacci MJ, Sobol H.
    Blood; 2009 May 28; 113(22):5583-7. PubMed ID: 19357396
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  • 14. Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia.
    Harada H, Harada Y, Tanaka H, Kimura A, Inaba T.
    Blood; 2003 Jan 15; 101(2):673-80. PubMed ID: 12393679
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  • 17. Myeloid neoplasms with germ line RUNX1 mutation.
    Hayashi Y, Harada Y, Huang G, Harada H.
    Int J Hematol; 2017 Aug 15; 106(2):183-188. PubMed ID: 28534116
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  • 18. High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21.
    Preudhomme C, Warot-Loze D, Roumier C, Grardel-Duflos N, Garand R, Lai JL, Dastugue N, Macintyre E, Denis C, Bauters F, Kerckaert JP, Cosson A, Fenaux P.
    Blood; 2000 Oct 15; 96(8):2862-9. PubMed ID: 11023523
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  • 19. [Familial leukemia due to germline RUNX1 mutations: lessons learned from two decades of research and unsolved problems].
    Osato M, Nambu A.
    Rinsho Ketsueki; 2020 Oct 15; 61(6):687-696. PubMed ID: 32624544
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  • 20. Unrelated hematopoietic stem cell transplantation for familial platelet disorder/acute myeloid leukemia with germline RUNX1 mutations.
    Toratani K, Watanabe M, Kanda J, Oka T, Hyuga M, Arai Y, Iwasaki M, Sakurada M, Nannya Y, Ogawa S, Yamada T, Takaori-Kondo A.
    Int J Hematol; 2023 Sep 15; 118(3):400-405. PubMed ID: 36897502
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