Characterization of the H-kininogen-binding site on factor XI: a comparison of factor XI and plasma prekallikrein.
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Defective thrombus formation in mice lacking coagulation factor XIIThe factor XIIa blocking antibody 3F7: a safe anticoagulant with anti-inflammatory activitiesThe hyaluronan-binding serine protease from human plasma cleaves HMW and LMW kininogen and releases bradykininDomain V of beta2-glycoprotein I binds factor XI/XIa and is cleaved at Lys317-Thr318A role for factor XIIa-mediated factor XI activation in thrombus formation in vivoActivated factor V is a cofactor for the activation of factor XI by thrombin in plasma.Structure and function of factor XIIn vivo roles of factor XII.Do platelets synthesize factor XI?Productive recognition of factor IX by factor XIa exosites requires disulfide linkage between heavy and light chains of factor XIa.A novel DFP tripeptide motif interacts with the coagulation factor XI apple 2 domainKininogen deficiency protects from ischemic neurodegeneration in mice by reducing thrombosis, blood-brain barrier damage, and inflammation.Beta 2-Glycoprotein I binds factor XI and inhibits its activation by thrombin and factor XIIa: loss of inhibition by clipped beta 2-glycoprotein I.Neutralizing blood-borne polyphosphate in vivo provides safe thromboprotection.Structural and functional features of factor XI.The procoagulant and proinflammatory plasma contact system.Factor XII-Driven Inflammatory Reactions with Implications for Anaphylaxis.Ferritin binds to light chain of human H-kininogen and inhibits kallikrein-mediated bradykinin release.High-molecular-weight kininogen and the risk of a myocardial infarction and ischemic stroke in young women: the RATIO case-control study.The relative priority of prekallikrein and factors XI/XIa assembly on cultured endothelial cells.Factor XI apple domains and protein dimerization.Interaction of insulin-like growth factor II (IGF-II) with multiple plasma proteins: high affinity binding of plasminogen to IGF-II and IGF-binding protein-3.An update on factor XI structure and function.Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation.Factor XI, but not prekallikrein, blocks high molecular weight kininogen binding to human umbilical vein endothelial cells.Identification of a Binding Site for Glycoprotein Ibα in the Apple 3 Domain of Factor XI
P2860
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P2860
Characterization of the H-kininogen-binding site on factor XI: a comparison of factor XI and plasma prekallikrein.
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
Characterization of the H-kini ...... r XI and plasma prekallikrein.
@en
type
label
Characterization of the H-kini ...... r XI and plasma prekallikrein.
@en
prefLabel
Characterization of the H-kini ...... r XI and plasma prekallikrein.
@en
P2093
P2860
P356
P1476
Characterization of the H-kini ...... r XI and plasma prekallikrein.
@en
P2093
David Gailani
Joost C M Meijers
Thomas Renné
P2860
P304
P356
10.1074/JBC.M105221200
P407
P577
2001-11-30T00:00:00Z