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Journal Abstract Search

251 related items for PubMed ID: 29666006

  • 1. Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia.
    Cavalcante de Andrade Silva M, Krepischi ACV, Kulikowski LD, Zanardo EA, Nardinelli L, Leal AM, Costa SS, Muto NH, Rocha V, Velloso EDRP.
    Cancer Genet; 2018 Apr; 222-223():32-37. PubMed ID: 29666006
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  • 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. 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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  • 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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  • 9. 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 15; 23(2):166-75. PubMed ID: 10508512
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  • 13. [Familial platelet disorder with predisposition to myeloid leukemia (FPD/AML): a case report and literature review].
    Zhang RR, Chen XJ, Ren YY, Yang WY, Zhu XF.
    Zhonghua Xue Ye Xue Za Zhi; 2021 Apr 14; 42(4):308-312. PubMed ID: 33979975
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  • 15. A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder.
    Almazni I, Chudakou P, Dawson-Meadows A, Downes K, Freson K, Mason J, Page P, Reay K, Myers B, Morgan NV, UK GAPP Study Group.
    Platelets; 2022 Feb 17; 33(2):320-323. PubMed ID: 33616470
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  • 19. 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 17; 28(12):2344-54. PubMed ID: 24732596
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