Unveiling Baryon Charge Carriers through Charge Stopping in Isobar Collisions.

Utilizing a comprehensive (3+1)D relativistic hydrodynamic framework with multiple conserved charge currents and charge-dependent lattice-QCD-based equation of state, we study the baryon and electric charge number deposition at midrapidity in isobar Ru+Ru and Zr+Zr collisions at the center of mass energy sqrt[s_{NN}]=200  GeV. Comparing our predictions with upcoming experimental data from the Relativistic Heavy Ion Collider will shed light on the existence of baryon junctions.

Runx1-R188Q germ line mutation induces inflammation and predisposition to hematologic malignancies in mice.

Germ line mutations in the RUNX1 gene cause familial platelet disorder (FPD), an inherited disease associated with lifetime risk to hematopoietic malignancies (HM). Patients with FPD frequently show clonal expansion of premalignant cells preceding HM onset. Despite the extensive studies on the role of RUNX1 in hematopoiesis, its function in the premalignant bone marrow (BM) is not well-understood.

Myeloid sarcoma with mutation may be clinically and genetically distinct from AML with mutation: a study from the Bone Marrow Pathology Group.

Myeloid sarcoma (MS) is currently considered equivalent to de novo acute myeloid leukemia (AML); however, the relationship between these entities is poorly understood. This retrospective multi-institutional cohort study compared 43 MS with mutation to 106 AML with mutation. Compared to AML, MS had more frequent cytogenetic abnormalities including complex karyotype ( = .