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Journal Abstract Search

228 related items for PubMed ID: 22898599

  • 1.
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  • 2. MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.
    Antony-Debré I, Bluteau D, Itzykson R, Baccini V, Renneville A, Boehlen F, Morabito M, Droin N, Deswarte C, Chang Y, Leverger G, Solary E, Vainchenker W, Favier R, Raslova H.
    Blood; 2012 Sep 27; 120(13):2719-22. PubMed ID: 22677128
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  • 5. 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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  • 6. Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency.
    Jalagadugula G, Mao G, Kaur G, Goldfinger LE, Dhanasekaran DN, Rao AK.
    Blood; 2010 Dec 23; 116(26):6037-45. PubMed ID: 20876458
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  • 9. In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis.
    Michaud J, Wu F, Osato M, Cottles GM, Yanagida M, Asou N, Shigesada K, Ito Y, Benson KF, Raskind WH, Rossier C, Antonarakis SE, Israels S, McNicol A, Weiss H, Horwitz M, Scott HS.
    Blood; 2002 Feb 15; 99(4):1364-72. PubMed ID: 11830488
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  • 10. 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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  • 11. 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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  • 12. 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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  • 14. 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 26; 23(2):166-75. PubMed ID: 10508512
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  • 15. 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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  • 17. [A new form of familial platelet disorder caused by germline mutations in RUNX1 in a pedigree].
    Guan J, Wang LL, Wang CY, Zhu XM, Shuai HZ, Yi X, Zou L, Yu D, Cheng H.
    Zhonghua Nei Ke Za Zhi; 2023 Apr 01; 62(4):393-400. PubMed ID: 37032134
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