1 Ruan C, "frequency of P475S polymorphism in von Willebrand factor- cleaving protease in the Chinese population and its relevance to arterial thrombotic disorders" 91 : 1257-1258, 2004
2 Bianchi V, "Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders: a severely deficient activity is specific for thrombotic thrombocytopenic purpura" 100 : 710-713, 2002
3 Veyradier A, "Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome)" 2 : 424-429, 2004
4 Zheng X, "Structure of von Willebrand factor- cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura" 276 : 41059-41063, 2001
5 Fujikawa K, "Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family" 98 : 1662-1666, 2001
6 Gerritsen HE, "Partial amino acid sequence of purified von Willebrand factor-cleaving protease" 98 : 1654-1661, 2001
7 Levy GG, "Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura" 413 : 488-494, 2001
8 Kokame K, "Mutations and common polymorphisms in ADAMTS-13 gene responsible for von Willebrand factor-cleaving protease activity" 99 : 11902-11907, 2002
9 Ginsburg D, "Identifying novel genetic determinants of hemostatic balance" 3 : 1561-1568, 2005
10 Uchida T, "Identification of novel mutations in ADAMTS13 in an adult patient with congenital thrombotic thrombocytopenic purpura" 104 : 2081-2083, 2004
1 Ruan C, "frequency of P475S polymorphism in von Willebrand factor- cleaving protease in the Chinese population and its relevance to arterial thrombotic disorders" 91 : 1257-1258, 2004
2 Bianchi V, "Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders: a severely deficient activity is specific for thrombotic thrombocytopenic purpura" 100 : 710-713, 2002
3 Veyradier A, "Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome)" 2 : 424-429, 2004
4 Zheng X, "Structure of von Willebrand factor- cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura" 276 : 41059-41063, 2001
5 Fujikawa K, "Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family" 98 : 1662-1666, 2001
6 Gerritsen HE, "Partial amino acid sequence of purified von Willebrand factor-cleaving protease" 98 : 1654-1661, 2001
7 Levy GG, "Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura" 413 : 488-494, 2001
8 Kokame K, "Mutations and common polymorphisms in ADAMTS-13 gene responsible for von Willebrand factor-cleaving protease activity" 99 : 11902-11907, 2002
9 Ginsburg D, "Identifying novel genetic determinants of hemostatic balance" 3 : 1561-1568, 2005
10 Uchida T, "Identification of novel mutations in ADAMTS13 in an adult patient with congenital thrombotic thrombocytopenic purpura" 104 : 2081-2083, 2004
11 Kokame K, "FRETS-VWF73, a first fluorogenic substrate for ADAMTS13 assay" 129 : 93-100, 2005
12 Tsai HM, "Antibody inhibitors to von Willebrand factor metalloproteinase and increased binding of von Willebrand factor to platelets in ticlopidine-associated thrombotic thrombocytopenic purpura" 132 : 794-799, 2000
13 Tsai HM, "Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura" 339 : 1585-1594, 1998
14 Bongers TN, "Absence of Pro475Ser polymorphism in ADAMTS-13 in Caucasians" 3 : 805-, 2005
15 Dong JF, "ADAMTS-13 metalloprotease interacts with the endothelial cell-derived ultra-large von Willebrand factor" 278 : 29633-29639, 2003
16 Soejima K, "A novel human metalloprotease synthesized in the liver and secreted into the blood: possibly, the von Willebrand factor- cleaving protease?" 130 : 475-480, 2001