Light chain of factor VIII is sufficient for accelerating cleavage of von Willebrand factor by ADAMTS13 metalloprotease (Q36294654)

13 August 2017

Light chain of factor VIII is sufficient for accelerating cleavage of von Willebrand factor by ADAMTS13 metalloprotease (English)

1 reference

13 August 2017

Wenjing Cao

1

1 reference

13 August 2017

Denise E Sabatino

2

1 reference

13 August 2017

Ekaterina Altynova

3

1 reference

13 August 2017

Amy M Lange

4

1 reference

13 August 2017

Veronica C Casina

5

1 reference

13 August 2017

Rodney M Camire

6

1 reference

13 August 2017

X Long Zheng

7

1 reference

13 August 2017

language of work or name

English

0 references

publication date

1 August 2012

1 reference

Journal of Biological Chemistry

13 August 2017

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13 August 2017

287

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13 August 2017

39

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13 August 2017

32459-32466

1 reference

describes a project that uses

13 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3463299/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Essential domains of a disintegrin and metalloprotease with thrombospondin type 1 repeats-13 metalloprotease required for modulation of arterial thrombosis.

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Efficacy and safety of long-term prophylaxis in severe hemophilia A dogs following liver gene therapy using AAV vectors

30 September 2017

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Factor VIII and platelets synergistically accelerate cleavage of von Willebrand factor by ADAMTS13 under fluid shear stress

30 September 2017

1 reference

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Recombinant canine B-domain-deleted FVIII exhibits high specific activity and is safe in the canine hemophilia A model

30 September 2017

1 reference

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von Willebrand factor-cleaving protease ADAMTS13 reduces ischemic brain injury in experimental stroke

30 September 2017

1 reference

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Correction of ADAMTS13 deficiency by in utero gene transfer of lentiviral vector encoding ADAMTS13 genes

30 September 2017

1 reference

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Factor VIII accelerates proteolytic cleavage of von Willebrand factor by ADAMTS13.

30 September 2017

1 reference

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Pathogenesis of thrombotic microangiopathies

30 September 2017

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Evidence that high von Willebrand factor and low ADAMTS-13 levels independently increase the risk of a non-fatal heart attack

30 September 2017

1 reference

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Hydrodynamic gene delivery: its principles and applications

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Platelet-VWF complexes are preferred substrates of ADAMTS13 under fluid shear stress

30 September 2017

1 reference

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Serial changes in von Willebrand factor-cleaving protease (ADAMTS13) and prognosis after acute myocardial infarction

30 September 2017

1 reference

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The enhancing effects of the light chain on heavy chain secretion in split delivery of factor VIII gene

30 September 2017

1 reference

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The cooperative activity between the carboxyl-terminal TSP1 repeats and the CUB domains of ADAMTS13 is crucial for recognition of von Willebrand factor under flow

30 September 2017

1 reference

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High von Willebrand Factor Levels Increase the Risk of First Ischemic Stroke: Influence of ADAMTS13, Inflammation, and Genetic Variability

30 September 2017

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Size regulation of von Willebrand factor-mediated platelet thrombi by ADAMTS13 in flowing blood

30 September 2017

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Binding of platelet glycoprotein Ibalpha to von Willebrand factor domain A1 stimulates the cleavage of the adjacent domain A2 by ADAMTS13.

30 September 2017

1 reference

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Cleavage of von Willebrand factor requires the spacer domain of the metalloprotease ADAMTS13.

30 September 2017

1 reference

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ADAMTS-13 metalloprotease interacts with the endothelial cell-derived ultra-large von Willebrand factor

30 September 2017

1 reference

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The molecular basis of hemophilia A: genotype-phenotype relationships and inhibitor development

30 September 2017

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ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions

30 September 2017

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30 September 2017

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Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura

30 September 2017

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von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome

30 September 2017

1 reference

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Shear stress enhances the proteolysis of von Willebrand factor in normal plasma

30 September 2017

1 reference

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Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura

30 September 2017

1 reference

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Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion.

30 September 2017

1 reference

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Paradoxical hyperfibrinolysis is associated with a more intensely haemorrhagic phenotype in severe congenital haemophilia

29 June 2018

1 reference

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Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis.

22 September 2018

1 reference

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Targeted disruption of the mouse factor VIII gene produces a model of haemophilia A

22 September 2018

1 reference

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Reduced von Willebrand factor-cleaving protease (ADAMTS13) activity in acute myocardial infarction

22 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22854959

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Changes in plasma von Willebrand factor-cleaving protease (ADAMTS13) levels in patients with unstable angina

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22854959

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1074/JBC.M112.390690

1 reference

13 August 2017

1 reference

13 August 2017

PubMed publication ID

22854959

1 reference