Related references
Note: Only part of the references are listed.Identification of Coagulation Factor XI as a Ligand for Platelet Apolipoprotein E Receptor 2 (ApoER2)
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Macromolecular substrate-binding exosites on both the heavy and light chains of factor XIa mediate the formation of the Michaelis complex required for factor IX-Activation
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BIOCHEMISTRY (2007)
A new type of plasma prekallikrein deficiency associated with homozygosity for Gly104Arg and Asn124Ser in apple domain 2 of the heavy-chain region
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The central role of thrombin in hemostasis
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Dimer dissociation and unfolding mechanism of coagulation factor XI apple 4 domain: Spectroscopic and mutational analysis
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Platelet adhesion to dimeric β2-glycoprotein I under conditions of flow is mediated by at least two receptors:: glycoprotein Ibα and apolipoprotein E receptor 2′
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Levels of intrinsic coagulation factors and the risk of myocardial infarction among men: opposite and synergistic effects of factors XI and YII
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Regulation of fibrinolysis by thrombin activatable fibrinolysis inhibitor, an unstable carboxypeptidase B that unites the pathways of coagulation and fibrinolysis
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Targeting coagulation factor XII provides protection from pathological thrombosis in cerebral ischemia without interfering with hemostasis
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Structural and mutational analyses of the molecular interactions between the catalytic domain of factor XIa and the Kunitz protease inhibitor domain of protease nexin 2
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JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
The discovery of TAFI
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JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2005)
Mutation of surface residues to promote crystallization of activated factor XI as a complex with benzamidine: an essential step for the iterative structure-based design of factor XI inhibitors
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Defective thrombus formation in mice lacking coagulation factor XII
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Exosite-mediated substrate recognition of factor IX by factor XIa - The factor XIa heavy chain is required for initial recognition of factor IX
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JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
A classification system for cross-reactive material-negative factor XI deficiency
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BLOOD (2005)
Effects of factor IX or factor XI deficiency on ferric chloride-induced carotid artery occlusion in mice
X Wang et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2005)
Crystal structures of the FXIa catalytic domain in complex with ecotin mutants reveal substrate-like interactions
L Jin et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Structural interpretation of 42 mutations causing factor XI deficiency using homology modeling
NM O'Connell et al.
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Dominant factor XI deficiency caused by mutations in the factor XI catalytic domain
DV Kravtsov et al.
BLOOD (2004)
Factor XI interacts with the leucine-rich repeats of glycoprotein Ibα on the activated platelet
FA Baglia et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Identification of a binding site for glycoprotein Ibα in the Apple 3 domain of factor XI
FA Baglia et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
New insights into factors affecting clot stability: A role for thrombin activatable fibrinolysis inhibitor (TAFI; Plasma procarboxypeptidase B, plasma procarboxypeptidase U, procarboxypeptidase R)
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SEMINARS IN HEMATOLOGY (2004)
被撤回的出版物: Thrombin activation of factor XI on activated platelets requires the interaction of factor XI and platelet glycoprotein Ibα with thrombin anion-binding exosites I and II, respectively (Retracted Article. See vol 282, pg 29067, 2007)
TH Yun et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Factor XI apple domains and protein dimerization
Q Cheng et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2003)
Eighteen unrelated patients with factor XI deficiency, four novel mutations and a 100% detection rate by denaturing high-performance liquid chromatography
M Mitchell et al.
BRITISH JOURNAL OF HAEMATOLOGY (2003)
The factor IX γ-carboxyglutamic acid (Gla) domain is involved in interactions between factor IX and factor XIa
A Aktimur et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Structure-function relationships in factor IX and factor IXa
AE Schmidt et al.
TRENDS IN CARDIOVASCULAR MEDICINE (2003)
Fine mapping of the H-kininogen binding site in plasma prekallikrein apple domain 2
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INTERNATIONAL IMMUNOPHARMACOLOGY (2002)
Characterization of the H-kininogen-binding site on factor XI -: A comparison of factor XI and plasma prekallikrein
T Renné et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Type I von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers:: a possible general mechanism for dominant mutations of oligomeric proteins
I Bodó et al.
BLOOD (2001)
The structure of leech anti-platelet protein, an inhibitor of haemostasis
EG Huizinga et al.
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY (2001)
被撤回的出版物: Defective binding of factor XI-N248 to activated human platelets (Retracted Article. See vol 110, pg 4164, 2007)
MF Sun et al.
BLOOD (2001)
Localization of a heparin binding site in the catalytic domain of factor XIa
KO Badellino et al.
BIOCHEMISTRY (2001)
Domains of invasion organelle proteins from apicomplexan parasites are homologous with the Apple domains of blood coagulation factor XI and plasma pre-kallikrein and are members of the PAN module superfamily
PJ Brown et al.
FEBS LETTERS (2001)
Noncovalent interactions of the apple 4 domain that mediate coagulation factor XI homodimerization
R Dorfman et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
SERPIN regulation of factor XIa - The novel observation that protease nexin 1 in the presence of heparin is a more potent inhibitor of factor XIa than C1 inhibitor
DJ Knauer et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
The role of high molecular weight kininogen and prothrombin as cofactors in the binding of factor XI A3 domain to the platelet surface
DH Ho et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Fibrinogen brescia -: Hepatic endoplasmic reticulum storage and hypofibrinogenemia because of a γ284 Gly→Arg mutation
SO Brennan et al.
AMERICAN JOURNAL OF PATHOLOGY (2000)
High levels of coagulation factor XI as a risk factor for venous thrombosis.
JCM Meijers et al.
NEW ENGLAND JOURNAL OF MEDICINE (2000)