ADAMTS13 protein, human

Known as: ADAMTS-13, A Disintegrin and Metalloproteinase With Thrombospondin Motifs 13, VWFCP protein, human 
A disintegrin and metalloproteinase with thrombospondin motifs 13 (1427 aa, ~154 kDa) is encoded by the human ADAMTS13 gene. This protein plays a… (More)
National Institutes of Health

Papers overview

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Review
2012
Review
2012
Thrombotic microangiopathy (TMA) is a term used to describe a group of disorders characterized by hemolytic anemia (with… (More)
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2007
2007
BACKGROUND Ultra-large von Willebrand factor (ULVWF) and the receptor P-selectin are released from endothelial Weibel-Palade… (More)
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Highly Cited
2006
Highly Cited
2006
Hepatic stellate cells have been considered to be a primary source for human plasma ADAMTS-13, the von Willebrand factor (VWF… (More)
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2005
2005
BACKGROUND von Willebrand disease (VWD) is a bleeding disorder caused by the decrease of functional von Willebrand factor (VWF… (More)
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2004
2004
The congenital or acquired deficiency of the von Willebrand factor (VWF) cleaving protease, ADAMTS-13 has been specifically… (More)
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2004
2004
ADAMTS-13, the metalloprotease that disposes physiologically of the most thrombogenic multimers of von Willebrand factor (VWF… (More)
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Highly Cited
2003
Highly Cited
2003
Acquired thrombotic thrombocytopenic purpura (TTP) has been linked to severe deficiency of ADAMTS-13 activity caused by… (More)
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2003
2003
BACKGROUND AND OBJECTIVES Autoantibodies inactivating the von Willebrand factor (VWF) cleaving protease, ADAMTS-13, are among the… (More)
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Highly Cited
2003
Highly Cited
2003
Thrombotic thrombocytopenic purpura is caused by congenital or acquired deficiency of ADAMTS-13, a metalloprotease that cleaves… (More)
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Highly Cited
2002
Highly Cited
2002
Thrombotic thrombocytopenic purpura (TTP) is a devastating thrombotic disorder caused by widespread microvascular thrombi… (More)
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