Ristocetin-dependent, but not botrocetin-dependent, binding of von Willebrand factor to the platelet glycoprotein Ib-IX-V complex correlates with shear-dependent interactions.
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ADAMTS-13 metalloprotease interacts with the endothelial cell-derived ultra-large von Willebrand factorMicrofluidics and coagulation biologyVon Willebrand factor-A1 domain binds platelet glycoprotein Ibα in multiple states with distinctive force-dependent dissociation kineticsStructural Basis of Regulation of von Willebrand Factor Binding to Glycoprotein IbGlycoprotein IIb-IIIa-dependent aggregation by glycoprotein Ibalpha is reinforced by a Src family kinase inhibitor (PP1)-sensitive signalling pathwayPlatelet glycoprotein Ibalpha forms catch bonds with human WT vWF but not with type 2B von Willebrand disease vWF.Platelet FcgammaRIIA His131Arg polymorphism and platelet function: antibodies to platelet-bound fibrinogen induce platelet activation.Primary and secondary hemostatic functionalities of rehydrated, lyophilized platelets.Force-induced cleavage of single VWFA1A2A3 tridomains by ADAMTS-13.von Willebrand factor, Jedi knight of the bloodstreamKinetics of GPIbalpha-vWF-A1 tether bond under flow: effect of GPIbalpha mutations on the association and dissociation rates.Exploiting the kinetic interplay between GPIbα-VWF binding interfaces to regulate hemostasis and thrombosisEchicetin coated polystyrene beads: a novel tool to investigate GPIb-specific platelet activation and aggregationCloning of porcine platelet glycoprotein Ibα and comparison with the human homolog.Direct observation of von Willebrand factor elongation and fiber formation on collagen during acute whole blood exposure to pathological flow.Differential surface activation of the A1 domain of von Willebrand factor.Cooperative unfolding of distinctive mechanoreceptor domains transduces force into signals.Platelet interaction with von Willebrand factor is enhanced by shear-induced clustering of glycoprotein Ibα.Platelet clearance via shear-induced unfolding of a membrane mechanoreceptor.Biology and physics of von Willebrand factor concatamers.Novel antiplatelet agents: ALX-0081, a Nanobody directed towards von Willebrand factor.Purified A2 domain of von Willebrand factor binds to the active conformation of von Willebrand factor and blocks the interaction with platelet glycoprotein Ibalpha.Shielding of the A1 domain by the D'D3 domains of von Willebrand factor modulates its interaction with platelet glycoprotein Ib-IX-V.A biophysical view on von Willebrand factor activation.A mechanically stabilized receptor-ligand flex-bond important in the vasculature.Tyrosine sulfation of glycoprotein I(b)alpha. Role of electrostatic interactions in von Willebrand factor binding.A factor VIII-derived peptide enables von Willebrand factor (VWF)-binding of artificial platelet nanoconstructs without interfering with VWF-adhesion of natural platelets.Enhanced shear-induced platelet aggregation due to low-temperature storage.Covalent regulation of ULVWF string formation and elongation on endothelial cells under flow conditionsCloning of the cDNA for murine von Willebrand factor and identification of orthologous genes reveals the extent of conservation among diverse species.GPIbalpha-selective activation of platelets induces platelet signaling events comparable to GPVI activation events.Convulxin binds to native, human glycoprotein Ib alpha.Differences and similarities in tyrosine phosphorylation of proteins in platelets from human and pig species.The interaction of von Willebrand factor-A1 domain with collagen: mutation G1324S (type 2M von Willebrand disease) impairs the conformational change in A1 domain induced by collagen.Shear-induced disulfide bond formation regulates adhesion activity of von Willebrand factor.A template-assembled synthetic protein surface mimetic of the von Willebrand factor A1 domain inhibits botrocetin-induced platelet aggregation.Von Willebrand factor present in fibrillar collagen enhances platelet adhesion to collagen and collagen-induced platelet aggregation.The contribution of von Willebrand factor-GPIbα interactions to persistent aggregate formation in apheresis platelet concentrates.A discontinuous autoinhibitory module masks the A1 domain of von Willebrand factor.The Von Willebrand Factor A1-Collagen III Interaction Is Independent of Conformation and Type 2 Von Willebrand Disease Phenotype.
P2860
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P2860
Ristocetin-dependent, but not botrocetin-dependent, binding of von Willebrand factor to the platelet glycoprotein Ib-IX-V complex correlates with shear-dependent interactions.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Ristocetin-dependent, but not ...... shear-dependent interactions.
@en
Ristocetin-dependent, but not ...... shear-dependent interactions.
@nl
type
label
Ristocetin-dependent, but not ...... shear-dependent interactions.
@en
Ristocetin-dependent, but not ...... shear-dependent interactions.
@nl
prefLabel
Ristocetin-dependent, but not ...... shear-dependent interactions.
@en
Ristocetin-dependent, but not ...... shear-dependent interactions.
@nl
P2093
P356
P1433
P1476
Ristocetin-dependent, but not ...... shear-dependent interactions.
@en
P2093
P304
P356
10.1182/BLOOD.V97.1.162
P407
P577
2001-01-01T00:00:00Z