Related references
Note: Only part of the references are listed.A von Willebrand factor fragment containing the D′D3 domains is sufficient to stabilize coagulation factor VIII in mice
Andrew Yee et al.
BLOOD (2014)
Allosteric activation of ADAMTS13 by von Willebrand factor
Joshua Muia et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Mechanisms by which von Willebrand Disease Mutations Destabilize the A2 Domain
Amy J. Xu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Light Chain of Factor VIII Is Sufficient for Accelerating Cleavage of von Willebrand Factor by ADAMTS13 Metalloprotease
Wenjing Cao et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Use of a mouse model to elucidate the phenotypic effects of the von Willebrand factor cleavage mutants, Y1605A/M1606A and R1597W
C. M. Pruss et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2012)
Unraveling the scissile bond: how ADAMTS13 recognizes and cleaves von Willebrand factor
James T. B. Crawley et al.
BLOOD (2011)
Mechanism of von Willebrand factor scissile bond cleavage by a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13)
Yaozu Xiang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Production, crystallization and preliminary crystallographic analysis of an exosite-containing fragment of human von Willebrand factor-cleaving proteinase ADAMTS13
Masashi Akiyama et al.
ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS (2009)
Crystal structures of the noncatalytic domains of ADAMTS13 reveal multiple discontinuous exosites for von Willebrand factor
Masashi Akiyama et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Mechanoenzymatic Cleavage of the Ultralarge Vascular Protein von Willebrand Factor
Xiaohui Zhang et al.
SCIENCE (2009)
Extensive contacts between ADAMTS13 exosites and von Willebrand factor domain A2 contribute to substrate specificity
Weiqiang Gao et al.
BLOOD (2008)
N-linked glycosylation of VWF modulates its interaction with ADAMTS13
Thomas A. J. McKinnon et al.
BLOOD (2008)
Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura
J. Evan Sadler
BLOOD (2008)
Factor VIII accelerates proteolytic cleavage of von Willebrand factor by ADAMTS13
Wenjing Cao et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Modifying murine von Willebrand factor A1 domain for in vivo assessment of human platelet therapies
Jianchun Chen et al.
NATURE BIOTECHNOLOGY (2008)
An IAP retrotransposon in the mouse ADAMTS13 gene creates ADAMTS 13 variant proteins that are less effective in cleaving von Willebrand factor multimers
Wenhua Zhou et al.
BLOOD (2007)
Exosite interactions contribute to tension-induced cleavage of von Willebrand factor by the antithrombotic ADAMTS13 metalloprotease
Weiqiang Gao et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Localization of ADAMTS 13 to the stellate cells of human liver
M Uemura et al.
BLOOD (2005)
ADAMTS13 is expressed in hepatic stellate cells
WH Zhou et al.
LABORATORY INVESTIGATION (2005)
VWF73, a region from D1596 to R1668 of von Willebrand factor, provides a minimal substrate for ADAMTS-13
K Kokame et al.
BLOOD (2004)
Binding of platelet glycoprotein Ibα to von Willebrand factor domain A1 stimulates the cleavage of the adjacent domain A2 by ADAMTS13
K Nishio et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Identification of strain-specific variants of mouse Adamts13 gene encoding von Willebrand factor-cleaving protease
F Banno et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura
XL Zheng et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
GG Levy et al.
NATURE (2001)
Share Paper
