Associated Papers
A novel complex mutation affecting two codons in the exon 10 hotspot region of the MPL gene.
Iaquinta G et al.
Current Research in Translational Medicine, 2025
Non-MPL-W515K/L mutations in myeloproliferative neoplasms: Insights from two case reports and a review of the literature.
Tønne Nesse AS et al.
Expert Review of Hematology, 2025
Diagnosis- and Prognosis-Related Gene Alterations in BCR::ABL1-Negative Myeloproliferative Neoplasms.
Morishita S et al.
International Journal of Molecular Sciences, 2023
37629188 (PubMed )
Supplement: ijms-24-13008-s001.zip › ijms-2555672-supplementary.pdf
Thrombocytosis in children and adolescents-classification, diagnostic approach, and clinical management.
Stockklausner C et al.
Annals of Hematology, 2021
A Rare Case of Essential Thrombocythemia with Coexisting JAK2 and MPL Driver Mutations.
Jang MA et al.
Journal of Korean Medical Science, 2020
Two activating mutations of MPL in triple-negative myeloproliferative neoplasms.
Xie J et al.
Cancer Medicine, 2019
Mutation status of essential thrombocythemia and primary myelofibrosis defines clinical outcome.
Asp J et al.
Haematologica, 2016
Acquired copy-neutral loss of heterozygosity of chromosome 1p as a molecular event associated with marrow fibrosis in MPL-mutated myeloproliferative neoplasms.
Rumi E et al.
Blood, 2013
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