about
New developments in the management of moderate-to-severe hemophilia BThe regulation of factor IXa by supersulfated low molecular weight heparin.Molecular mapping of the heparin-binding exosite of thrombin.Low molecular weight heparin inhibits plasma thrombin generation via direct targeting of factor IXa: contribution of the serpin-independent mechanismIncreased Red Blood Cell Stiffness Increases Pulmonary Vascular Resistance and Pulmonary Arterial PressureFactor XI anion-binding sites are required for productive interactions with polyphosphate.Heparin inhibits the intrinsic tenase complex by interacting with an exosite on factor IXa.Tissue factor-factor VIIa complex triggers protease activated receptor 2-dependent growth factor release and migration in ovarian cancer.The factor IXa heparin-binding exosite is a cofactor interactive site: mechanism for antithrombin-independent inhibition of intrinsic tenase by heparin.Zebrafish factor 10 and the life aquatic.Selective disruption of heparin and antithrombin-mediated regulation of human factor IX.Elevated Plasma Factor IXa Activity in Premenopausal Women on Hormonal Contraception.Anticoagulant Protein S Targets the Factor IXa Heparin-Binding Exosite to Prevent Thrombosis.Identification and characterization of zebrafish thrombocytesAnalysis of hemostasis in the zebrafishThe heparin-binding exosite is critical to allosteric activation of factor IXa in the intrinsic tenase complex: the role of arginine 165 and factor X
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description
researcher ORCID ID = 0000-0002-4328-2613
@en
wetenschapper
@nl
name
J P Sheehan
@ast
J P Sheehan
@en
J P Sheehan
@es
J P Sheehan
@nl
type
label
J P Sheehan
@ast
J P Sheehan
@en
J P Sheehan
@es
J P Sheehan
@nl
prefLabel
J P Sheehan
@ast
J P Sheehan
@en
J P Sheehan
@es
J P Sheehan
@nl
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0000-0002-4328-2613