Disease: Familial myelofibrosis
- A TET2 rs3733609 C/T genotype is associated with predisposition to the myeloproliferative neoplasms harboring JAK2(V617F) and confers a proliferative potential on erythroid lineages
- Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhage
- BOREAS: a global, phase III study of the MDM2 inhibitor navtemadlin (KRT-232) in relapsed/refractory myelofibrosis
- Budd-Chiari syndrome in myeloproliferative neoplasms: A review of literature
- Characterization of myeloproliferative neoplasms in the paediatric and young adult population
- Chronic Myeloproliferative Neoplasms Treatment (PDQ®): Patient Version
- Familial myelofibrosis
- First Approval of Pacritinib as a Selective Janus Associated Kinase-2 Inhibitor for the Treatment of Patients with Myelofibrosis
- Janus kinase (JAK) inhibitors in the treatment of neoplastic and inflammatory disorders
- Primary Hypertrophic Osteoarthropathy With Myelofibrosis
- Pro106Leu MPL mutation is associated with thrombocytosis and a low risk of thrombosis, splenomegaly and marrow fibrosis
- Properties of FDA-approved small molecule protein kinase inhibitors: A 2023 update
- Recent knowledge of NFATc4 in oncogenesis and cancer prognosis
- The emerging importance of immunophilins in fibrosis development
- The Outcome of Fatherhood in Patients With Philadelphia-Negative Myeloproliferative Neoplasms: A Single-Institution Experience
- The Role of JAK/STAT Pathway in Fibrotic Diseases: Molecular and Cellular Mechanisms
- Treatment of congenital thrombocytopenia and decreased collagen reactivity in G6b-B-deficient mice