KRAS, NRAS, and BRAF mutations are highly enriched in trisomy 12 chronic lymphocytic leukemia and are associated with shorter treatment-free survival.
第一作者:
Elena,Vendramini
第一单位:
Clinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano (PN), Italy.
作者:
主题词
成年人(Adult);老年人(Aged);染色体, 人, 12对(Chromosomes, Human, Pair 12);女(雌)性(Female);GTP磷酸水解酶类(GTP Phosphohydrolases);人类(Humans);白血病, 淋巴细胞, 慢性, B细胞(Leukemia, Lymphocytic, Chronic, B-Cell);男(雄)性(Male);膜蛋白质类(Membrane Proteins);中年人(Middle Aged);突变(Mutation);原癌基因蛋白质B-raf(Proto-Oncogene Proteins B-raf);原癌基因蛋白质类p21(ras)(Proto-Oncogene Proteins p21(ras));三体性(Trisomy)
DOI
10.1038/s41375-019-0444-6
PMID
30872781
发布时间
2021-01-09
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Leukemia
2111-2115页
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