scholarly article | Q13442814 |
P356 | DOI | 10.1074/JBC.M513314200 |
P698 | PubMed publication ID | 16373331 |
P50 | author | Hans Deckmyn | Q37829138 |
P2093 | author name string | Karen Vanhoorelbeke | |
Peter J Lenting | |||
Inge Pareyn | |||
Nele Vandeputte | |||
Hans Ulrichts | |||
Miklós Udvardy | |||
P2860 | cites work | Identification of the regulatory elements of the human von Willebrand factor for binding to platelet GPIb. Importance of structural integrity of the regions flanked by the CYS1272-CYS1458 disulfide bond | Q24293697 |
Structures of glycoprotein Ibalpha and its complex with von Willebrand factor A1 domain | Q24304907 | ||
Crystal structure of the wild-type von Willebrand factor A1-glycoprotein Ibalpha complex reveals conformation differences with a complex bearing von Willebrand disease mutations | Q24319306 | ||
Crystal structure of the von Willebrand Factor A1 domain and implications for the binding of platelet glycoprotein Ib | Q27749469 | ||
A consensus tetrapeptide selected by phage display adopts the conformation of a dominant discontinuous epitope of a monoclonal anti-VWF antibody that inhibits the von Willebrand factor-collagen interaction | Q30961540 | ||
Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function | Q34423491 | ||
Platelets in atherothrombosis | Q34986345 | ||
A definitive set of oligonucleotide primers for amplifying human V regions | Q36896019 | ||
Expression of the mouse dihydrofolate reductase complementary deoxyribonucleic acid in simian virus 40 vectors | Q36957553 | ||
A monomeric von Willebrand factor fragment, Leu-504--Lys-728, inhibits von Willebrand factor interaction with glycoprotein Ib-IX [corrected] | Q37168874 | ||
Effect of deletion of the A1 domain of von Willebrand factor on its binding to heparin, collagen and platelets in the presence of ristocetin | Q38336125 | ||
A monoclonal antibody recognizes a von Willebrand factor domain within the amino-terminal portion of the subunit that modulates the function of the glycoprotein IB- and IIB/IIIA-binding domains | Q40512752 | ||
An experimental model to study the in vivo survival of von Willebrand factor. Basic aspects and application to the R1205H mutation. | Q40616991 | ||
Identification of amino acid residues essential for von Willebrand factor binding to platelet glycoprotein Ib. Charged-to-alanine scanning mutagenesis of the A1 domain of human von Willebrand factor | Q41336486 | ||
Ristocetin-dependent, but not botrocetin-dependent, binding of von Willebrand factor to the platelet glycoprotein Ib-IX-V complex correlates with shear-dependent interactions | Q43513939 | ||
Isolation and chemical characterization of two structurally and functionally distinct forms of botrocetin, the platelet coagglutinin isolated from the venom of Bothrops jararaca | Q43916499 | ||
von Willebrand factor but not alpha-thrombin binding to platelet glycoprotein Ibalpha is influenced by the HPA-2 polymorphism | Q44459167 | ||
Functional modulation of the isolated glycoprotein Ib binding domain of von Willebrand factor expressed in Escherichia coli | Q44699205 | ||
A monoclonal antibody directed against human von Willebrand factor induces type 2B-like alterations | Q45033734 | ||
Impact of O-linked glycosylation of the VWF-A1-domain flanking regions on platelet interaction | Q45192183 | ||
Specific synergy of multiple substrate-receptor interactions in platelet thrombus formation under flow. | Q45967882 | ||
The von Willebrand factor self-association is modulated by a multiple domain interaction | Q58481460 | ||
Shear-dependent morphology of von Willebrand factor bound to immobilized collagen | Q58481474 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 4699-4707 | |
P577 | publication date | 2005-12-22 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Shielding of the A1 domain by the D'D3 domains of von Willebrand factor modulates its interaction with platelet glycoprotein Ib-IX-V. | |
P478 | volume | 281 |
Q52330622 | 14-3-3 proteins in platelet biology and glycoprotein Ib-IX signaling. |
Q27658166 | A Structural Explanation for the Antithrombotic Activity of ARC1172, a DNA Aptamer that Binds von Willebrand Factor Domain A1 |
Q39159765 | A biophysical view on von Willebrand factor activation. |
Q34351167 | A common variant in the Von Willebrand factor gene is associated with multiple functional consequences. |
Q48152338 | A discontinuous autoinhibitory module masks the A1 domain of von Willebrand factor. |
Q39665373 | A mechanically stabilized receptor-ligand flex-bond important in the vasculature. |
Q37168411 | A mechanism for localized dynamics-driven affinity regulation of the binding of von Willebrand factor to platelet glycoprotein Ibα. |
Q34448727 | An integrated fragment based screening approach for the discovery of small molecule modulators of the VWF-GPIbα interaction. |
Q34170382 | Analysis of the role of von Willebrand factor, platelet glycoprotein VI-, and α2β1-mediated collagen binding in thrombus formation |
Q52672840 | Autoregulation of von Willebrand factor function by a disulfide bond switch. |
Q37903936 | Biology and physics of von Willebrand factor concatamers |
Q37293577 | Catch-bond mechanism of force-enhanced adhesion: counterintuitive, elusive, but ... widespread? |
Q34016608 | Cleavage of von Willebrand factor by granzyme M destroys its factor VIII binding capacity |
Q90572410 | Delimiting the autoinhibitory module of von Willebrand factor |
Q34003816 | Destabilization of the A1 domain in von Willebrand factor dissociates the A1A2A3 tri-domain and provokes spontaneous binding to glycoprotein Ibalpha and platelet activation under shear stress |
Q91856606 | Electrostatic Steering Enables Flow-Activated Von Willebrand Factor to Bind Platelet Glycoprotein, Revealed by Single-Molecule Stretching and Imaging |
Q53394850 | Examining platelet adhesion via Stokes flow simulations and microfluidic experiments. |
Q34684020 | Exploiting the kinetic interplay between GPIbα-VWF binding interfaces to regulate hemostasis and thrombosis |
Q41490553 | Flow-induced elongation of von Willebrand factor precedes tension-dependent activation |
Q37279293 | Fluid shear induces conformation change in human blood protein von Willebrand factor in solution. |
Q40382861 | Force-sensitive autoinhibition of the von Willebrand factor is mediated by interdomain interactions |
Q30353471 | Functional display of platelet-binding VWF fragments on filamentous bacteriophage |
Q34122627 | Identification of a small molecule that modulates platelet glycoprotein Ib-von Willebrand factor interaction |
Q34278082 | In vivo analysis of the role of O-glycosylations of von Willebrand factor. |
Q56883323 | Interaction of the cysteine-rich domain of snake venom metalloproteinases with the A1 domain of von Willebrand factor promotes site-specific proteolysis of von Willebrand factor and inhibition of von Willebrand factor-mediated platelet aggregation |
Q52579774 | Interdomain interaction in the FimH adhesin of Escherichia coli regulates the affinity to mannose. |
Q39905838 | Internal tension in a collapsed polymer under shear flow and the connection to enzymatic cleavage of von Willebrand factor |
Q35922561 | N-terminal flanking region of A1 domain in von Willebrand factor stabilizes structure of A1A2A3 complex and modulates platelet activation under shear stress. |
Q98156926 | Noncanonical type 2B von Willebrand disease associated with mutations in the VWF D'D3 and D4 domains |
Q33624852 | Pannexin- and Connexin-Mediated Intercellular Communication in Platelet Function. |
Q45865145 | Plasma levels of active Von Willebrand factor are increased in patients with first ST-segment elevation myocardial infarction: a multicenter and multiethnic study. |
Q30620128 | Platelet GpIba binding to von Willebrand Factor under fluid shear:contributions of the D′D3-domain, A1-domain flanking peptide and O-linked glycans |
Q37824742 | Platelet adhesion to collagen |
Q30483148 | Platelet glycoprotein Ibalpha forms catch bonds with human WT vWF but not with type 2B von Willebrand disease vWF. |
Q38303337 | Purified A2 domain of von Willebrand factor binds to the active conformation of von Willebrand factor and blocks the interaction with platelet glycoprotein Ibalpha |
Q47625174 | Receptor-mediated cell mechanosensing. |
Q38645643 | Role of fluid shear stress in regulating VWF structure, function and related blood disorders |
Q37540219 | Rolling cell adhesion |
Q34206072 | Shear-stabilized rolling behavior of E. coli examined with simulations. |
Q90516261 | Structure of von Willebrand factor A1 on polystyrene determined from experimental and calculated sum frequency generation spectra |
Q37289199 | The N-terminal flanking region of the A1 domain regulates the force-dependent binding of von Willebrand factor to platelet glycoprotein Ibα. |
Q53073825 | The O-linked glycans of human von Willebrand factor modulate its interaction with ADAMTS-13. |
Q30557410 | The linker between the D3 and A1 domains of vWF suppresses A1-GPIbα catch bonds by site-specific binding to the A1 domain. |
Q47239922 | The physical spacing between the von willebrand factor d'd3- and a1- domains regulates platelet adhesion in vitro and in vivo |
Q26852187 | The unfolded von Willebrand factor response in bloodstream: the self-association perspective |
Q33775630 | Visualization of allostery in P-selectin lectin domain using MD simulations |
Q27303207 | Von Willebrand factor-A1 domain binds platelet glycoprotein Ibα in multiple states with distinctive force-dependent dissociation kinetics |
Q36010217 | von Willebrand factor (VWF) propeptide binding to VWF D'D3 domain attenuates platelet activation and adhesion |
Q34310946 | von Willebrand factor self-association on platelet GpIbalpha under hydrodynamic shear: effect on shear-induced platelet activation |
Q34106824 | von Willebrand factor, Jedi knight of the bloodstream |
Q37903943 | von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein |
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