2005BloodRequires access

The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders

Linda M. Scott, Peter J. Campbell, E. Joanna Baxter, Tony Todd, Philip Stephens, Sarah Edkins, Richard Wooster, Michael R. Stratton, P. Andrew Futreal, Anthony R. Green

Open publisher page 156 citations

Abstract

Four groups recently reported the existence of an activating mutation of JAK2 in many patients with one of the classic myeloproliferative disorders (MPDs).[1][1]-[4][2] Mutant Janus kinase 2 (JAK2) has increased kinase activity, renders BaF3 cells cytokine independent, and produces erythrocytosis in

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What this paper is about

Four groups recently reported the existence of an activating mutation of JAK2 in many patients with one of the classic myeloproliferative disorders (MPDs).[1][1]-[4][2] Mutant Janus kinase 2 (JAK2) has increased kinase activity, renders BaF3 cells cytokine independent, and produces erythrocytosis in

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OpenAlex reports 156 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Four groups recently reported the existence of an activating mutation of JAK2 in many patients with one of the classic myeloproliferative disorders (MPDs).[1][1]-[4][2] Mutant Janus kinase 2 (JAK2) has increased kinase activity, renders BaF3 cells cytokine independent, and produces erythrocytosis in

Key concepts: Myeloproliferative Disorders, Janus kinase 2, JAK2 V617F, Cancer research, Mutation, Polycythemia vera, Myeloid, Medicine

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The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders — Research Paper | ScholarLens