Results 121 to 130 of about 577,308 (213)
Activating mutations in signaling molecules, such as JAK2-V617F, have been associated with myeloproliferative neoplasms (MPNs). Mice lacking the inhibitory adaptor protein Lnk display deregulation of thrombopoietin/thrombopoietin receptor signaling ...
Bruno Cassinat +16 more
core +1 more source
Neutrophilia and the JAK2 V617F Mutation
Stephen E, Langabeer, Karl, Haslam
openaire +2 more sources
Rescue balloon pulmonary angioplasty for worsening chronic thromboembolic pulmonary hypertension with essential thrombocythaemia and the JAK2-V617F mutation: a case report. [PDF]
Tamura H, Hosokawa S, Yuba K, Kishi K.
europepmc +1 more source
Essential thrombocythemia (ET) is a kind of myeloproliferative neoplasms. Thrombosis is one of the common symptoms, however, the incidence of thrombosis in ET with JAK2, CALR, MPL gene mutations varies greatly, and the underlying mechanism is unclear ...
Xueya Zhang, Xizhe Guo
doaj +1 more source
Detection of JAK2 V617F mutation among donors with erythrocytosis
Introduction: It is mandatory that every blood donor must have their haemoglobin (Hb) values measured before blood donation. High Hb may indicate an underlying hidden pathological condition.
Nur Elida Mohd Kamil
core
We identified 13 new gene expression markers that were elevated and one marker, ANKRD15, that was down-regulated in patients with polycythemia vera (PV).
CAZZOLA, MARIO +11 more
core +1 more source
Somatic mutations in the Jak2 allele that lead to constitutive kinase activation of the protein have been identified in human disease conditions such as the myeloproliferative neoplasms (MPNs).
Peter P. Sayeski (395099) +2 more
core +1 more source
Detection of JAK2 V617F Mutation among Donors with Erythrocytosis / Siti Fatimah Mohamed Kamaruzzaman … [et al.] [PDF]
Introduction: It is mandatory that every blood donor must have their haemoglobin (Hb) values measured before blood donation. High Hb may indicate an underlying hidden pathological condition.
Mohamed Kamaruzzaman, Siti Fatimah +4 more
core
Low-level somatic JAK2 V617F mutation in myelodysplastic/myeloproliferative neoplasm with ring sideroblasts, and thrombocytosis with co-mutated SF3B1 and CALR. [PDF]
Ji YS, Park SK, Jeon BR, Jang MA.
europepmc +1 more source
Twenty-five patients with myeloproliferative diseases were treated with pegylated interferon alpha-2b. Prior to therapy, 15/25 patients had a JAK2(V617F) mutation.
J Samuelsson +5 more
doaj

