SETBP1 mutations in 415 patients with primary myelofibrosis or chronic myelomonocytic leukemia: independent prognostic impact in CMML

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Veröffentlicht in:	Leukemia 2013-10, Vol.27 (10), p.2100-2102
Hauptverfasser:	Laborde, R R, Patnaik, M M, Lasho, T L, Finke, C M, Hanson, C A, Knudson, R A, Ketterling, R P, Pardanani, A, Tefferi, A
Format:	Artikel
Sprache:	eng
Schlagworte:	631/208/737 692/699/67/1990/2331 692/699/67/1990/283/1896 692/700/1750 Aged Binding proteins Cancer Research Carrier Proteins - genetics Cell growth Chronic myelomonocytic leukemia Critical Care Medicine DNA Mutational Analysis Female Follow-Up Studies Genetic aspects Health aspects Hematology Humans Intensive Internal Medicine Letter to the Editor Letters to the editor Leukemia Leukemia, Myelomonocytic, Chronic - genetics Leukemia, Myelomonocytic, Chronic - mortality Localization Male Medicine Medicine & Public Health Mutation Mutation (Biology) Mutation - genetics Myelofibrosis Nuclear Proteins - genetics Oncogenes Oncology Physiological aspects Primary Myelofibrosis - genetics Primary Myelofibrosis - mortality Prognosis Proteins Real-Time Polymerase Chain Reaction Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - genetics Survival Rate Transcription factors
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