NOTCH1 mutations identify a genetic subgroup of chronic lymphocytic leukemia patients with high risk of transformation and poor outcome-Reference-Cited by-同舟云学术

NOTCH1 mutations identify a genetic subgroup of chronic lymphocytic leukemia patients with high risk of transformation and poor outcome

Published:2012-12-06 Issue:5 Volume:27 Page:1100-1106
ISSN:0887-6924
Container-title:Leukemia
language:en
Short-container-title:Leukemia

Author:

Villamor N,Conde L,Martínez-Trillos A,Cazorla M,Navarro A,Beà S,López C,Colomer D,Pinyol M,Aymerich M,Rozman M,Abrisqueta P,Baumann T,Delgado J,Giné E,González-Díaz M,Hernández J M,Colado E,Payer A R,Rayon C,Navarro B,José Terol M,Bosch F,Quesada V,Puente X S,López-Otín C,Jares P,Pereira A,Campo E,López-Guillermo A

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Link

http://www.nature.com/articles/leu2012357.pdf

Reference38 articles.

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3. Zenz T, Mertens D, Kuppers R, Dohner H, Stilgenbauer S . From pathogenesis to treatment of chronic lymphocytic leukaemia. Nat Rev Cancer 2010; 10: 37–50.

4. Puente XS, Pinyol M, Quesada V, Conde L, Ordonez GR, Villamor N et al. Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia. Nature 2011; 475: 101–105.

5. Quesada V, Conde L, Villamor N, Ordonez GR, Jares P, Bassaganyas L et al. Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia. Nat Genet 2012; 44: 47–52.

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