-
1
-
-
0035885972
-
Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family
-
Fujikawa K., Suzuki H., McMullen B., and Chung D. Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family. Blood 98 6 (2001) 1662-1666
-
(2001)
Blood
, vol.98
, Issue.6
, pp. 1662-1666
-
-
Fujikawa, K.1
Suzuki, H.2
McMullen, B.3
Chung, D.4
-
2
-
-
0037111571
-
Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13)
-
Plaimauer B., Zimmermann K., Volkel D., Antoine G., Kerschbaumer R., Jenab P., et al. Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13). Blood 100 10 (2002) 3626-3632
-
(2002)
Blood
, vol.100
, Issue.10
, pp. 3626-3632
-
-
Plaimauer, B.1
Zimmermann, K.2
Volkel, D.3
Antoine, G.4
Kerschbaumer, R.5
Jenab, P.6
-
3
-
-
0029907370
-
Von Willebrand factor: molecular size and functional activity
-
Furlan M. Von Willebrand factor: molecular size and functional activity. Ann Hematol 72 (1996) 341-348
-
(1996)
Ann Hematol
, vol.72
, pp. 341-348
-
-
Furlan, M.1
-
4
-
-
0036624844
-
Ultra-large multimers of von Willebrand factor form spontaneous high-strength bonds with the platelet GP Ib-IX complex: studies using optical tweezers
-
Arya M., Anvari B., Romo G.M., Cruz M.A., Dong J.-F., McIntire L.V., et al. Ultra-large multimers of von Willebrand factor form spontaneous high-strength bonds with the platelet GP Ib-IX complex: studies using optical tweezers. Blood 99 (2002) 3971-3977
-
(2002)
Blood
, vol.99
, pp. 3971-3977
-
-
Arya, M.1
Anvari, B.2
Romo, G.M.3
Cruz, M.A.4
Dong, J.-F.5
McIntire, L.V.6
-
5
-
-
0036893186
-
ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions
-
Dong J.-F., Moake J.L., Nolasco L., Bernardo A., Arceneaux W., Shrimpton C.N., et al. ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions. Blood 100 (2002) 4033-4039
-
(2002)
Blood
, vol.100
, pp. 4033-4039
-
-
Dong, J.-F.1
Moake, J.L.2
Nolasco, L.3
Bernardo, A.4
Arceneaux, W.5
Shrimpton, C.N.6
-
6
-
-
12344296265
-
Interplay between ADAMTS13 and von Willebrand factor in inherited and acquired thrombotic microangiopathies
-
Soejima K., and Nakagaki T. Interplay between ADAMTS13 and von Willebrand factor in inherited and acquired thrombotic microangiopathies. Semin Hematol 42 1 (2005) 56-62
-
(2005)
Semin Hematol
, vol.42
, Issue.1
, pp. 56-62
-
-
Soejima, K.1
Nakagaki, T.2
-
7
-
-
0030973267
-
Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura
-
Furlan M., Robles R., Solenthaler M., Wassmer M., Sandoz P., Lämmle B., et al. Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. Blood 89 (1997) 3097-3103
-
(1997)
Blood
, vol.89
, pp. 3097-3103
-
-
Furlan, M.1
Robles, R.2
Solenthaler, M.3
Wassmer, M.4
Sandoz, P.5
Lämmle, B.6
-
8
-
-
0032569884
-
Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the haemolytic uremic syndrome
-
Furlan M., Robles R., Galbusera M., Remuzzi G., Kyrle P.A., Brenner B., et al. Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the haemolytic uremic syndrome. N Engl J Med 339 (1998) 1578-1584
-
(1998)
N Engl J Med
, vol.339
, pp. 1578-1584
-
-
Furlan, M.1
Robles, R.2
Galbusera, M.3
Remuzzi, G.4
Kyrle, P.A.5
Brenner, B.6
-
9
-
-
0032569840
-
Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura
-
Tsai H.M., and Lian E.C. Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med 339 (1998) 1585-1594
-
(1998)
N Engl J Med
, vol.339
, pp. 1585-1594
-
-
Tsai, H.M.1
Lian, E.C.2
-
10
-
-
0032522952
-
Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura
-
Furlan M., Robles R., Solenthaler M., and Lämmle B. Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura. Blood 91 (1998) 2839-2846
-
(1998)
Blood
, vol.91
, pp. 2839-2846
-
-
Furlan, M.1
Robles, R.2
Solenthaler, M.3
Lämmle, B.4
-
11
-
-
0026048114
-
Comparison of plasma exchange with plasma infusion in treatment of thrombotic thrombocytopenic purpura
-
Rock G.A., Shumak K.H., Buskard N.A., Blanchette V.S., Kelton J.C., Nair R.C., et al. Comparison of plasma exchange with plasma infusion in treatment of thrombotic thrombocytopenic purpura. N Engl J Med 325 (1991) 393-397
-
(1991)
N Engl J Med
, vol.325
, pp. 393-397
-
-
Rock, G.A.1
Shumak, K.H.2
Buskard, N.A.3
Blanchette, V.S.4
Kelton, J.C.5
Nair, R.C.6
-
12
-
-
0029925856
-
Partial purification and characterization of protease from human plasma cleaving von Willebrand factor to fragment produced by in vivo proteolysis
-
Furlan M., Robles R., and Lamie B. Partial purification and characterization of protease from human plasma cleaving von Willebrand factor to fragment produced by in vivo proteolysis. Blood 87 (1996) 4223-4234
-
(1996)
Blood
, vol.87
, pp. 4223-4234
-
-
Furlan, M.1
Robles, R.2
Lamie, B.3
-
13
-
-
0742305180
-
Clinical usefulness of a functional assay for the von Willebrand factor cleaving protease (ADAMTS-13) and its inhibitor in a patient with thrombotic thrombocytopenic purpura
-
Rick M.E., Austin H., Leitman S.F., Krizek D.M., and Aronson D.L. Clinical usefulness of a functional assay for the von Willebrand factor cleaving protease (ADAMTS-13) and its inhibitor in a patient with thrombotic thrombocytopenic purpura. Am J Hematol 75 2 (2004) 96-100
-
(2004)
Am J Hematol
, vol.75
, Issue.2
, pp. 96-100
-
-
Rick, M.E.1
Austin, H.2
Leitman, S.F.3
Krizek, D.M.4
Aronson, D.L.5
-
14
-
-
0141832540
-
Is severe deficiency of ADAMTS-13 specific for thrombotic thrombocytopenic purpura? Yes
-
Tsai H.M. Is severe deficiency of ADAMTS-13 specific for thrombotic thrombocytopenic purpura? Yes. J Thromb Haemost 1 4 (2003) 625-631
-
(2003)
J Thromb Haemost
, vol.1
, Issue.4
, pp. 625-631
-
-
Tsai, H.M.1
-
15
-
-
0017040282
-
Contributions to the optimal use of human blood FVIII. Stability of blood coagulation factor VIII during collection and storage of whole blood and plasma
-
Vermeer C., Soute B.A., Ates G., Hellings J.A., and Brummelhuis H.G. Contributions to the optimal use of human blood FVIII. Stability of blood coagulation factor VIII during collection and storage of whole blood and plasma. Vox Sang 31 (1976) 55-67
-
(1976)
Vox Sang
, vol.31
, pp. 55-67
-
-
Vermeer, C.1
Soute, B.A.2
Ates, G.3
Hellings, J.A.4
Brummelhuis, H.G.5
|