Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia-Reference-Cited by-同舟云学术

Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia

Published:2015-08-28 Issue:4 Volume:30 Page:999-1002
ISSN:0887-6924
Container-title:Leukemia
language:en
Short-container-title:Leukemia

Author:

Antony-Debré I,Duployez N,Bucci M,Geffroy S,Micol J-B,Renneville A,Boissel N,Dhédin N,Réa D,Nelken B,Berthon C,Leblanc T,Mozziconacci M-J,Favier R,Heller P G,Abdel-Wahab O,Raslova H,Latger-Cannard V,Preudhomme C

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Link

http://www.nature.com/articles/leu2015236.pdf

Reference14 articles.

1. Preudhomme C, Renneville A, Bourdon V, Philippe N, Roche-Lestienne C, Boissel N et al. High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder. Blood 2009; 113: 5583–5587.

2. Yoshimi A, Toya T, Kawazu M, Ueno T, Tsukamoto A, Iizuka H et al. Recurrent CDC25C mutations drive malignant transformation in FPD/AML. Nat Commun 2014; 5: 4770.

3. Micol JB, Duployez N, Boissel N, Petit A, Geffroy S, Nibourel O et al. Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations. Blood 2014; 124: 1445–1449.

4. Prebet T, Carbuccia N, Raslova H, Favier R, Rey J, Arnoulet C et al. Concomitant germ-line RUNX1 and acquired ASXL1 mutations in a T-cell acute lymphoblastic leukemia. Eur J Haematol 2013; 91: 277–279.

5. Boissel N, Leroy H, Brethon B, Philippe N, de Botton S, Auvrignon A et al. Incidence and prognostic impact of c-Kit, FLT3, and Ras gene mutations in core binding factor acute myeloid leukemia (CBF-AML). Leukemia 2006; 20: 965–970.

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