PRC2 alterations in NF1-associated malignant peripheral nerve sheath tumors: Schwann cells with no complex;Altérations du PRC2 au sein des tumeurs malignes associées à la neurofibromatose de type 1: des cellules de Schwann sans aucun complexe !
NF1 molecular characterization and neurofibromatosis type i genotype-phenotype correlation: The French experience
Sabbagh A, Pasmant E, Imbard A, et al. NF1 molecular characterization and neurofibromatosis type I genotype-phenotype correlation: the French experience. Hum Mutat 2013; 34: 1510-1518.
Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1
Sabbagh A, Pasmant E, Laurendeau I, et al. Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1. Hum Mol Genet 2009; 18: 2768-2778.
Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1
Pasmant E, Sabbagh A, Masliah-Planchon J, et al. Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1. J Natl Cancer Inst 2011; 103: 1713-1722.
Genetic inactivation of the polycomb repressive complex 2 in T cell acute lymphoblastic leukemia
Ntziachristos P, Tsirigos A, Van Vlierberghe P, et al. Genetic inactivation of the polycomb repressive complex 2 in T cell acute lymphoblastic leukemia. Nat Med 2012; 18: 298-301.
PRC2 loss amplifies Ras-driven transcription and sensitizes cancers to epigenetic-based therapies
(sous presse).
De Raedt T, Beert E, Pasmant E, et al. PRC2 loss amplifies Ras-driven transcription and sensitizes cancers to epigenetic-based therapies. Nature 2014. (sous presse).