JAK2V617F and the evolving paradigm of polycythemia vera

JAK2 V617F and the evolving paradigm of polycythemia vera

Polycythemia vera (PV) was first described nearly 120 years ago. In the subsequent century, the clinical syndrome of PV, its natural history, its treatment, and many critical pathogenetic features of the disease were characterized. The discovery of the Janus-associated kinase - 2 mutation JAK2 V617F and the characterization of its role in myeloproliferative neoplasms have substantially changed ...

The JAK2V617F mutation in polycythemia vera and other myeloproliferative disorders: one mutation for three diseases?

The discovery of the JAK2V617F mutation has made the diagnosis of polycythemia vera (PV) much easier, but the pathogenesis of PV is still incompletely understood. In particular, it is not yet elucidated how a single mutation can be found in multiple myeloproliferative disorders (MPD) and myelodysplastic syndromes with ring sideroblasts and whether the sole JAK2V617F is sufficient to induce a MP...

Enhanced calreticulin expression in red cells of polycythemia vera patients harboring the JAK2V617F mutation.

Involvement of various hematopoietic-cell lineages by the JAK2V617F mutation in polycythemia vera.

The JAK2(V617F) mutation has been shown to occur in the overwhelming majority of patients with polycythemia vera (PV). To study the role of the mutation in the excessive production of differentiated hematopoietic cells in PV, CD19+, CD3+, CD34+, CD33+, and glycophorin A+ cells and granulocytes were isolated from the peripheral blood (PB) of 8 patients with PV and 3 healthy donors mobilized with...

Congenital JAK2V617F polycythemia vera: where does the genotype-phenotype diversity end?

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