ADAMTS13 wt Allele

Known as: ADAMTS-13, DKFZp434C2322, A Disintegrin-Like and Metalloprotease With Thrombospondin Type 1 Motif, 13 Gene 
Human ADAMTS13 wild-type allele is located in the vicinity of 9q34 and is approximately 45 kb in length. This allele, which encodes a disintegrin and… (More)
National Institutes of Health

Papers overview

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2009
2009
Vascular occlusion, thromboembolism and strokes are hallmark events in sickle cell disease (SCD). The von Willebrand factor (VWF… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND A disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS-13) may influence von… (More)
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2008
2008
BACKGROUND Over the last 4 years ADAMTS-13 measurement underwent dramatic progress with newer and simpler methods. AIMS Blind… (More)
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2008
2008
BACKGROUND Thrombotic thrombocytopenic purpura (TTP) is most commonly associated with deficiency or inhibition of von Willebrand… (More)
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2007
Highly Cited
2007
Thrombotic thrombocytopenic purpura (TTP) is a life-threatening disorder and plasma exchange (PEX) remains the primary treatment… (More)
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2007
Highly Cited
2007
OBJECTIVE The inability to regulate the inflammatory response initiated upon infection leads to severe sepsis, characterized by… (More)
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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
The therapeutic efficacy of plasma exchange (PE) in thrombotic thrombocytopenic purpura (TTP) is attributed to the restoration in… (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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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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