ADAMTS13 (a disintegrin-like metalloprotease domain with thrombospondin type 1 motif, member 13) is a protease of crucial importance in the regulation of the size of von Willebrand factor multimers. Very low ADAMTS13 activity levels result in thrombotic thrombocytopenic purpura, a rare and life-threatening disease. The mechanisms involved can either be acquired (immune-mediated thrombotic thrombocytopenic purpura [iTTP]) or congenital (cTTP, Upshaw-Schulman syndrome) caused by the autosomal recessive inheritance of disease-causing variants (DCVs) located along the ADAMTS13 gene, which is located in chromosome 9q34. Apart from its role in TTP, and as a regulator of microthrombosis, ADAMTS13 has begun to be identified as a prognostic and/or d...
ADAMTS13 is the metalloprotease responsible for the proteolytic degradation of von Willebrand factor...
ongenital thrombotic thrombocytopenic purpura (TTP) is a rare form of thrombotic microangiopathy, in...
The inherited deficiency of the von Willebrand factor-cleaving protease ADAMTS13 is associated with ...
The regulation of VWF multimer size is essential in preventing spontaneous microvascular platelet cl...
ADAMTS13 (a disintegrin and metalloprotease with a thrombospondin type-1 motif, member 13) and von W...
ADAMTS13 is a 190 kDa zinc protease encoded by a gene located on chromosome 9q34. This protease spec...
13), a plasma metalloprotease, cleaves von Willebrand factor (VWF) [1,2]. This cleavage is crucial f...
A deficiency in ADAMTS13 (A Disintegrin And Metalloprotease with ThromboSpondin type-1 repeats, memb...
Thrombotic thrombocytopenic purpura is a rare, life-threatening disease which is portrayed by profou...
ADAMTS-13, the thirteenth member of the ADAMTS (A Disintegrin And Metalloprotease with Thrombo-Spond...
The metalloprotease ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif...
Thrombotic thrombocytopenic purpura (TTP) is a rare and life-threatening disease, which is caused by...
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease characterized by acute...
The last 10 years witnessed the publication of many studies on the pathophysiology of thrombotic thr...
Thrombotic thrombocytopenic purpura (TTP) is a life-threatening systemic illness of abrupt onset and...
ADAMTS13 is the metalloprotease responsible for the proteolytic degradation of von Willebrand factor...
ongenital thrombotic thrombocytopenic purpura (TTP) is a rare form of thrombotic microangiopathy, in...
The inherited deficiency of the von Willebrand factor-cleaving protease ADAMTS13 is associated with ...
The regulation of VWF multimer size is essential in preventing spontaneous microvascular platelet cl...
ADAMTS13 (a disintegrin and metalloprotease with a thrombospondin type-1 motif, member 13) and von W...
ADAMTS13 is a 190 kDa zinc protease encoded by a gene located on chromosome 9q34. This protease spec...
13), a plasma metalloprotease, cleaves von Willebrand factor (VWF) [1,2]. This cleavage is crucial f...
A deficiency in ADAMTS13 (A Disintegrin And Metalloprotease with ThromboSpondin type-1 repeats, memb...
Thrombotic thrombocytopenic purpura is a rare, life-threatening disease which is portrayed by profou...
ADAMTS-13, the thirteenth member of the ADAMTS (A Disintegrin And Metalloprotease with Thrombo-Spond...
The metalloprotease ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif...
Thrombotic thrombocytopenic purpura (TTP) is a rare and life-threatening disease, which is caused by...
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease characterized by acute...
The last 10 years witnessed the publication of many studies on the pathophysiology of thrombotic thr...
Thrombotic thrombocytopenic purpura (TTP) is a life-threatening systemic illness of abrupt onset and...
ADAMTS13 is the metalloprotease responsible for the proteolytic degradation of von Willebrand factor...
ongenital thrombotic thrombocytopenic purpura (TTP) is a rare form of thrombotic microangiopathy, in...
The inherited deficiency of the von Willebrand factor-cleaving protease ADAMTS13 is associated with ...