Cleavage of von Willebrand factor requires the spacer domain of the metalloprotease ADAMTS13. (Q40641838)

22 September 2017

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

1 reference

22 September 2017

Xinglong Zheng

1

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author name string

Kenji Nishio

series ordinal

2

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22 September 2017

Elaine M Majerus

series ordinal

3

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22 September 2017

J Evan Sadler

series ordinal

4

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22 September 2017

language of work or name

English

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publication date

5 June 2003

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Journal of Biological Chemistry

22 September 2017

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22 September 2017

278

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22 September 2017

30136-30141

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22 September 2017

32

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Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome: the role of von Willebrand factor-cleaving protease

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Thrombotic thrombocytopenic purpura: the systemic clumping "plague".

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Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura. Canadian Apheresis Study Group

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

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

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

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Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family

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Partial amino acid sequence of purified von Willebrand factor-cleaving protease

21 January 2018

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ADAM-TS5, ADAM-TS6, and ADAM-TS7, novel members of a new family of zinc metalloproteases. General features and genomic distribution of the ADAM-TS family

21 January 2018

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Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura

21 January 2018

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A novel human metalloprotease synthesized in the liver and secreted into the blood: possibly, the von Willebrand factor-cleaving protease?

21 January 2018

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Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

21 January 2018

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Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains

21 January 2018

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A new name in thrombosis, ADAMTS13.

21 January 2018

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Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity

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von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP.

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Mucin-like domain of enteropeptidase directs apical targeting in Madin-Darby canine kidney cells

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Primary amyloidosis with familial vitreous opacities: an unusual case and family

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Multimeric analysis of von Willebrand factor by molecular sieving electrophoresis in sodium dodecyl sulphate agarose gel.

21 January 2018

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Apical sorting of bovine enteropeptidase does not involve detergent-resistant association with sphingolipid-cholesterol rafts.

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21 January 2018

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Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13).

21 January 2018

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Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in type IIA von Willebrand factor

21 January 2018

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ADAMTS-1 protein anchors at the extracellular matrix through the thrombospondin type I motifs and its spacing region

21 January 2018

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Characterization of METH-1/ADAMTS1 processing reveals two distinct active forms

21 January 2018

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ADAMTS1/METH1 Inhibits Endothelial Cell Proliferation by Direct Binding and Sequestration of VEGF165

21 January 2018

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The thrombospondin motif of aggrecanase-1 (ADAMTS-4) is critical for aggrecan substrate recognition and cleavage

21 January 2018

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Autocatalytic cleavage of ADAMTS-4 (Aggrecanase-1) reveals multiple glycosaminoglycan-binding sites

21 January 2018

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Identification, characterization, and intracellular processing of ADAM-TS12, a novel human disintegrin with a complex structural organization involving multiple thrombospondin-1 repeats

21 January 2018

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ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13.

21 January 2018

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Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene

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Procollagen II amino propeptide processing by ADAMTS-3. Insights on dermatosparaxis

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Identifiers

DOI

10.1074/JBC.M305331200

1 reference

22 September 2017

1 reference