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Anti‐PF4 disorders: Pathogenesis, diagnosis and treatment
Anti‐platelet factor 4 (PF4) disorders include heparin‐induced thrombocytopenia (HIT) and vaccine‐induced immune thrombocytopenia and thrombosis (VITT)/VITT‐like disorders. The formation of immunoglobulin G (IgG)/PF4 immune complexes facilitates uncontrolled activation of platelets, neutrophils and monocytes via IgG‐mediated Fcγ receptor binding.
Megan V. Preece+3 more
wiley +1 more source
Improved Instrumentation for the Determination of Prothrombin Activity [PDF]
Rex E. Sterling+3 more
openalex +1 more source
Tumor endothelial cells (TECs) promote the polarization of macrophages to M2 subtype by secreting IL‐4. Downregulation of IL‐4 in TECs suppressed M2 polarization and tumor progression. A high abundance of both TECs and M2 macrophages in HCC specimens is associated with poor prognosis.
Daijiro Matoba+17 more
wiley +1 more source
Enoxaparin Failure in Patient With Cerebral Venous Sinus Thrombosis and Prothrombin G20210A Mutation: Case Report. [PDF]
Polavarapu A+4 more
europepmc +1 more source
THE CONVERSION OF PROTHROMBIN TO THROMBIN, FOLLOWED BY MEANS OF THE RADIOACTIVE PHOSPHORUS ISOTOPE
Erwin Chargaff+2 more
openalex +1 more source
RNA Analysis Uncovers Pathogenic PARN Variant in Dyskeratosis Congenita
Using WGS and RNA analysis, we identified a branch point‐disrupting variant in the PARN gene and elucidated its pathogenic molecular mechanism in a child with atypical dyskeratosis congenita presentation. ABSTRACT Dyskeratosis congenita (DC) is a rare genetic disorder caused by impaired telomere maintenance, leading to diverse clinical manifestations ...
Daria Akimova+3 more
wiley +1 more source