about
Molecular cloning of human ABPL, an actin-binding protein homologueProcessing of von Willebrand factor by ADAMTS-13.High-density lipoprotein modulates thrombosis by preventing von Willebrand factor self-association and subsequent platelet adhesion.Complex changes in von Willebrand factor-associated parameters are acquired during uncomplicated pregnancy.Second international collaborative study evaluating performance characteristics of methods measuring the von Willebrand factor cleaving protease (ADAMTS-13).von Willebrand factor is a cofactor in complement regulation.Hypochlorous acid generated by neutrophils inactivates ADAMTS13: an oxidative mechanism for regulating ADAMTS13 proteolytic activity during inflammation.Characterization of a core binding site for ADAMTS-13 in the A2 domain of von Willebrand factor.Shear stress-induced unfolding of VWF accelerates oxidation of key methionine residues in the A1A2A3 region.Variable content of von Willebrand factor mutant monomer drives the phenotypic variability in a family with von Willebrand diseaseFibrin clot structure and mechanics associated with specific oxidation of methionine residues in fibrinogen.Post-translational oxidative modification of fibrinogen is associated with coagulopathy after traumatic injury.Endothelial Activation and Blood-Brain Barrier Disruption in Neurotoxicity after Adoptive Immunotherapy with CD19 CAR-T Cells.The polymerization pocket "a" within the carboxyl-terminal region of the gamma chain of human fibrinogen is adjacent to but independent from the calcium-binding siteVWF self-association: more bands for the buckPolymerized fibrin activates glycoprotein VIInflammation, von Willebrand factor, and ADAMTS13
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description
researcher
@en
name
D W Chung
@en
D W Chung
@nl
type
label
D W Chung
@en
D W Chung
@nl
prefLabel
D W Chung
@en
D W Chung
@nl
P106
P31
P496
0000-0002-2645-5703