scholarly article | Q13442814 |
P50 | author | X. Long Zheng | Q56808910 |
P2093 | author name string | Christopher G Skipwith | |
Sandra L Haberichter | |||
Ashley Gehrand | |||
P2860 | cites work | von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome | Q33504463 |
Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor | Q33998293 | ||
Factor VIII and platelets synergistically accelerate cleavage of von Willebrand factor by ADAMTS13 under fluid shear stress | Q34121211 | ||
Exosite interactions contribute to tension-induced cleavage of von Willebrand factor by the antithrombotic ADAMTS13 metalloprotease | Q35193294 | ||
von Willebrand factor (VWF) propeptide binding to VWF D'D3 domain attenuates platelet activation and adhesion | Q36010217 | ||
Light chain of factor VIII is sufficient for accelerating cleavage of von Willebrand factor by ADAMTS13 metalloprotease | Q36294654 | ||
Factor VIII accelerates proteolytic cleavage of von Willebrand factor by ADAMTS13. | Q36677173 | ||
The genetic basis of von Willebrand disease | Q37735428 | ||
An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant | Q40694998 | ||
The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor. | Q41235952 | ||
Abnormal binding of factor VIII is linked with the substitution of glutamine for arginine 91 in von Willebrand factor in a variant form of von Willebrand disease | Q41660891 | ||
Validation of the first commercial ELISA for type 2N von Willebrand's disease diagnosis | Q45867954 | ||
Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor | Q59511738 | ||
Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization | Q80234430 | ||
P433 | issue | 1 | |
P304 | page(s) | 202-204 | |
P577 | publication date | 2013-05-02 | |
P1433 | published in | Thrombosis and Haemostasis | Q15724413 |
P1476 | title | Compromised shear-dependent cleavage of type 2N von Willebrand factor variants by ADAMTS13 in the presence of factor VIII | |
P478 | volume | 110 |
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