-
1
-
-
0029925856
-
Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis
-
Furlan M, Robles R, Lämmle B. Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis. Blood. 1996;87(10):4223-4234. (Pubitemid 26152266)
-
(1996)
Blood
, vol.87
, Issue.10
, pp. 4223-4234
-
-
Furlan, M.1
Robles, R.2
Lammle, B.3
-
2
-
-
0035807348
-
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
-
DOI 10.1038/35097008
-
Levy GG, Nichols WC, Lian EC, et al. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 2001;413(6855):488-494. (Pubitemid 32938741)
-
(2001)
Nature
, vol.413
, Issue.6855
, pp. 488-494
-
-
Levy, G.G.1
Nichols, W.C.2
Lian, E.C.3
Foroud, T.4
McClintick, J.N.5
McGee, B.M.6
Yang, A.Y.7
Siemieniak, D.R.8
Stark, K.R.9
Gruppo, R.10
Sarode, R.11
Shurin, S.B.12
Chandrasekaran, V.13
Stabler, S.P.14
Sabio, H.15
Bouhassira, E.E.16
Upshaw Jr., J.D.17
Ginsburg, D.18
Tsai, H.-M.19
-
3
-
-
0022504431
-
Inducible secretion of large, biologically potent von Willebrand factor multimers
-
Sporn LA, Marder VJ, Wagner DD. Inducible secretion of large, biologically potent von Willebrand factor multimers. Cell. 1986;46(2):185-190. (Pubitemid 16031685)
-
(1986)
Cell
, vol.46
, Issue.2
, pp. 185-190
-
-
Sporn, L.A.1
Marder, V.J.2
Wagner, D.D.3
-
4
-
-
0020428664
-
Unusually large plasma factor VIII: Von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura
-
Moake JL, Rudy CK, Troll JH, et al. Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura. N Engl J Med. 1982;307(23):1432-1435. (Pubitemid 13234018)
-
(1982)
New England Journal of Medicine
, vol.307
, Issue.23
, pp. 1432-1435
-
-
Moake, J.L.1
Rudy, C.K.2
Troll, J.H.3
-
5
-
-
0037158606
-
Thrombotic microangiopathies
-
Moake JL. Thrombotic microangiopathies. N Engl J Med. 2002;347(8):589-600.
-
(2002)
N Engl J Med
, vol.347
, Issue.8
, pp. 589-600
-
-
Moake, J.L.1
-
6
-
-
84880585209
-
Animal models for thrombotic thrombocytopenic purpura
-
Vanhoorelbeke K, De Meyer SF. Animal models for thrombotic thrombocytopenic purpura. J Thromb Haemost. 2013;11(Suppl 1):2-10.
-
(2013)
J Thromb Haemost
, vol.11
, Issue.SUPPL. 1
, pp. 2-10
-
-
Vanhoorelbeke, K.1
De Meyer, S.F.2
-
7
-
-
33645728657
-
Complete deficiency in ADAMTS13 is prothrombotic, but it alone is not sufficient to cause thrombotic thrombocytopenic purpura
-
Banno F, Kokame K, Okuda T, et al. Complete deficiency in ADAMTS13 is prothrombotic, but it alone is not sufficient to cause thrombotic thrombocytopenic purpura. Blood. 2006;107(8):3161-3166.
-
(2006)
Blood
, vol.107
, Issue.8
, pp. 3161-3166
-
-
Banno, F.1
Kokame, K.2
Okuda, T.3
-
8
-
-
26444551183
-
Shigatoxin triggers thrombic thrombocytopenic purpura in genetically susceptible ADAMTS13-deficient mice
-
DOI 10.1172/JCI26007
-
Motto DG, Chauhan AK, Zhu G, et al. Shigatoxin triggers thrombotic thrombocytopenic purpura in genetically susceptible ADAMTS13-deficient mice. J Clin Invest. 2005;115(10):2752-2761. (Pubitemid 41434402)
-
(2005)
Journal of Clinical Investigation
, vol.115
, Issue.10
, pp. 2752-2761
-
-
Motto, D.G.1
Chauhan, A.K.2
Zhu, G.3
Homeister, J.4
Lamb, C.B.5
Desch, K.C.6
Zhang, W.7
Tsai, H.-M.8
Wagner, D.D.9
Ginsburg, D.10
-
9
-
-
66749099068
-
Mechanoenzymatic cleavage of the ultralarge vascular protein von Willebrand factor
-
Zhang X, Halvorsen K, Zhang CZ, Wong WP, Springer TA. Mechanoenzymatic cleavage of the ultralarge vascular protein von Willebrand factor. Science. 2009;324(5932):1330-1334.
-
(2009)
Science
, vol.324
, Issue.5932
, pp. 1330-1334
-
-
Zhang, X.1
Halvorsen, K.2
Zhang, C.Z.3
Wong, W.P.4
Springer, T.A.5
-
10
-
-
75649138819
-
Force-induced cleavage of single VWFA1A2A3 tridomains by ADAMTS-13
-
Wu T, Lin J, Cruz MA, Dong JF, Zhu C. Force-induced cleavage of single VWFA1A2A3 tridomains by ADAMTS-13. Blood. 2010;115(2):370-378.
-
(2010)
Blood
, vol.115
, Issue.2
, pp. 370-378
-
-
Wu, T.1
Lin, J.2
Cruz, M.A.3
Dong, J.F.4
Zhu, C.5
-
11
-
-
1842530336
-
An experimental model to study the in vivo survival of von Willebrand factor: Basic aspects and application to the R1205H mutation
-
DOI 10.1074/jbc.M310436200
-
Lenting PJ, Westein E, Terraube V, et al. An experimental model to study the in vivo survival of von Willebrand factor. Basic aspects and application to the R1205H mutation. J Biol Chem. 2004;279(13):12102-12109. (Pubitemid 38445774)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.13
, pp. 12102-12109
-
-
Lenting, P.J.1
Westein, E.2
Terraube, V.3
Ribba, A.-S.4
Huizinga, E.G.5
Meyer, D.6
De Groot, P.G.7
Denis, C.V.8
-
12
-
-
27144461083
-
A novel nanobody that detects the gain-of-function phenotype of von Willebrand factor in ADAMTS13 deficiency and von Willebrand disease type 2B
-
DOI 10.1182/blood-2005-03-1153
-
Hulstein JJ, de Groot PG, Silence K, Veyradier A, Fijnheer R, Lenting PJ. A novel nanobody that detects the gain-of-function phenotype of von Willebrand factor in ADAMTS13 deficiency and von Willebrand disease type 2B. Blood. 2005;106(9):3035-3042. (Pubitemid 41565896)
-
(2005)
Blood
, vol.106
, Issue.9
, pp. 3035-3042
-
-
Hulstein, J.J.J.1
De Groot, P.G.2
Silence, K.3
Veyradier, A.4
Fijnheer, R.5
Lenting, P.J.6
-
13
-
-
3242676770
-
Binding of platelet glycoprotein Ibalpha to von Willebrand factor domain A1 stimulates the cleavage of the adjacent domain A2 by ADAMTS13
-
DOI 10.1073/pnas.0402041101
-
Nishio K, Anderson PJ, Zheng XL, Sadler JE. Binding of platelet glycoprotein Ibalpha to von Willebrand factor domain A1 stimulates the cleavage of the adjacent domain A2 by ADAMTS13. Proc Natl Acad Sci U S A. 2004;101(29):10578-10583. (Pubitemid 38955784)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.29
, pp. 10578-10583
-
-
Nishio, K.1
Anderson, P.J.2
Zheng, X.L.3
Sadler, J.E.4
-
15
-
-
50949116621
-
Altered thrombus formation in von Willebrand factor-deficient mice expressing von Willebrand factor variants with defective binding to collagen or GPIIbIIIa
-
Marx I, Christophe OD, Lenting PJ, et al. Altered thrombus formation in von Willebrand factor-deficient mice expressing von Willebrand factor variants with defective binding to collagen or GPIIbIIIa. Blood. 2008;112(3):603-609.
-
(2008)
Blood
, vol.112
, Issue.3
, pp. 603-609
-
-
Marx, I.1
Christophe, O.D.2
Lenting, P.J.3
-
16
-
-
0032483024
-
A mouse model of severe von Willebrand disease: Defects in hemostasis and thrombosis
-
DOI 10.1073/pnas.95.16.9524
-
Denis C, Methia N, Frenette PS, et al. A mouse model of severe von Willebrand disease: defects in hemostasis and thrombosis. Proc Natl Acad Sci USA. 1998;95(16):9524-9529. (Pubitemid 28506264)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.16
, pp. 9524-9529
-
-
Denis, C.1
Methia, N.2
Frenette, P.S.3
Rayburn, H.4
Ullman-Cullere, M.5
Hynes, R.O.6
Wagner, D.D.7
-
17
-
-
77956574499
-
Multigranular exocytosis of Weibel-Palade bodies in vascular endothelial cells
-
Valentijn KM, van Driel LF, Mourik MJ, et al. Multigranular exocytosis of Weibel-Palade bodies in vascular endothelial cells. Blood. 2010;116(10): 1807-1816.
-
(2010)
Blood
, vol.116
, Issue.10
, pp. 1807-1816
-
-
Valentijn, K.M.1
Van Driel, L.F.2
Mourik, M.J.3
-
18
-
-
67249086879
-
Structural specializations of A2, a force-sensing domain in the ultralarge vascular protein von Willebrand factor
-
Zhang Q, Zhou YF, Zhang CZ, Zhang X, Lu C, Springer TA. Structural specializations of A2, a force-sensing domain in the ultralarge vascular protein von Willebrand factor. Proc Natl Acad Sci USA. 2009;106(23):9226-9231.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, Issue.23
, pp. 9226-9231
-
-
Zhang, Q.1
Zhou, Y.F.2
Zhang, C.Z.3
Zhang, X.4
Lu, C.5
Springer, T.A.6
-
19
-
-
77954750391
-
Mutation and ADAMTS13-dependent modulation of disease severity in a mouse model for von Willebrand disease type 2B
-
Rayes J, Hollestelle MJ, Legendre P, et al. Mutation and ADAMTS13-dependent modulation of disease severity in a mouse model for von Willebrand disease type 2B. Blood. 2010;115(23):4870-4877.
-
(2010)
Blood
, vol.115
, Issue.23
, pp. 4870-4877
-
-
Rayes, J.1
Hollestelle, M.J.2
Legendre, P.3
-
20
-
-
84888239369
-
Accelerated uptake of VWF/platelet complexes in macrophages contributes to VWD type 2B-associated thrombocytopenia
-
Casari C, Du V, Wu YP, et al. Accelerated uptake of VWF/platelet complexes in macrophages contributes to VWD type 2B-associated thrombocytopenia. Blood. 2013;122(16):2893-2902.
-
(2013)
Blood
, vol.122
, Issue.16
, pp. 2893-2902
-
-
Casari, C.1
Du, V.2
Wu, Y.P.3
-
21
-
-
84866851266
-
Formation of platelet-binding von Willebrand factor strings on non-endothelial cells
-
Wang JW, Valentijn JA, Valentijn KM, et al. Formation of platelet-binding von Willebrand factor strings on non-endothelial cells. J Thromb Haemost. 2012;10(10):2168-2178.
-
(2012)
J Thromb Haemost
, vol.10
, Issue.10
, pp. 2168-2178
-
-
Wang, J.W.1
Valentijn, J.A.2
Valentijn, K.M.3
-
22
-
-
70349569566
-
Leukocyte proteases cleave von Willebrand factor at or near the ADAMTS13 cleavage site
-
Raife TJ, Cao W, Atkinson BS, et al. Leukocyte proteases cleave von Willebrand factor at or near the ADAMTS13 cleavage site. Blood. 2009;114(8):1666-1674.
-
(2009)
Blood
, vol.114
, Issue.8
, pp. 1666-1674
-
-
Raife, T.J.1
Cao, W.2
Atkinson, B.S.3
-
23
-
-
80053146780
-
Unraveling the scissile bond: How ADAMTS13 recognizes and cleaves von Willebrand factor
-
Crawley JT, de Groot R, Xiang Y, Luken BM, Lane DA. Unraveling the scissile bond: how ADAMTS13 recognizes and cleaves von Willebrand factor. Blood. 2011;118(12):3212-3221.
-
(2011)
Blood
, vol.118
, Issue.12
, pp. 3212-3221
-
-
Crawley, J.T.1
De Groot, R.2
Xiang, Y.3
Luken, B.M.4
Lane, D.A.5
-
24
-
-
79960991896
-
Mechanism of von Willebrand factor scissile bond cleavage by a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13)
-
Xiang Y, de Groot R, Crawley JT, Lane DA. Mechanism of von Willebrand factor scissile bond cleavage by a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13). Proc Natl Acad Sci USA. 2011;108(28):11602-11607.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, Issue.28
, pp. 11602-11607
-
-
Xiang, Y.1
De Groot, R.2
Crawley, J.T.3
Lane, D.A.4
-
25
-
-
79955977529
-
A novel calcium-binding site of von Willebrand factor A2 domain regulates its cleavage by ADAMTS13
-
Zhou M, Dong X, Baldauf C, et al. A novel calcium-binding site of von Willebrand factor A2 domain regulates its cleavage by ADAMTS13. Blood. 2011;117(17):4623-4631.
-
(2011)
Blood
, vol.117
, Issue.17
, pp. 4623-4631
-
-
Zhou, M.1
Dong, X.2
Baldauf, C.3
-
26
-
-
82755189074
-
In vivo von Willebrand factor size heterogeneity in spite of the clinical deficiency of ADAMTS-13
-
De Meyer SF, Budde U, Deckmyn H, Vanhoorelbeke K. In vivo von Willebrand factor size heterogeneity in spite of the clinical deficiency of ADAMTS-13. J Thromb Haemost. 2011;9(12):2506-2508.
-
(2011)
J Thromb Haemost
, vol.9
, Issue.12
, pp. 2506-2508
-
-
De Meyer, S.F.1
Budde, U.2
Deckmyn, H.3
Vanhoorelbeke, K.4
-
27
-
-
80052342947
-
Cleavage of von Willebrand factor by granzyme M destroys its factor VIII binding capacity
-
Hollestelle MJ, Lai KW, van Deuren M, et al. Cleavage of von Willebrand factor by granzyme M destroys its factor VIII binding capacity. PLoS ONE. 2011;6(9):e24216.
-
(2011)
PLoS ONE
, vol.6
, Issue.9
-
-
Hollestelle, M.J.1
Lai, K.W.2
Van Deuren, M.3
-
28
-
-
84872334022
-
Unwinding the von Willebrand factor strings puzzle
-
De Ceunynck K, De Meyer SF, Vanhoorelbeke K. Unwinding the von Willebrand factor strings puzzle. Blood. 2013;121(2):270-277.
-
(2013)
Blood
, vol.121
, Issue.2
, pp. 270-277
-
-
De Ceunynck, K.1
De Meyer, S.F.2
Vanhoorelbeke, K.3
-
29
-
-
0023116024
-
Epitope mapping of the von Willebrand factor subunit distinguishes fragments present in normal and type IIA von Willebrand disease from those generated by plasmin
-
Berkowitz SD, Dent J, Roberts J, et al. Epitope mapping of the von Willebrand factor subunit distinguishes fragments present in normal and type IIA von Willebrand disease from those generated by plasmin. J Clin Invest. 1987;79(2):524-531. (Pubitemid 17009689)
-
(1987)
Journal of Clinical Investigation
, vol.79
, Issue.2
, pp. 524-531
-
-
Berkowitz, S.D.1
Dent, J.2
Roberts, J.3
-
30
-
-
84897114562
-
Plasmin Cleavage of von Willebrand Factor as an Emergency Bypass for ADAMTS13 Deficiency in Thrombotic Microangiopathy
-
Tersteeg C, de Maat S, De Meyer SF, et al. Plasmin Cleavage of von Willebrand Factor as an Emergency Bypass for ADAMTS13 Deficiency in Thrombotic Microangiopathy. Circulation. 2014;129(12):1320-1331.
-
(2014)
Circulation
, vol.129
, Issue.12
, pp. 1320-1331
-
-
Tersteeg, C.1
De Maat, S.2
De Meyer, S.F.3
-
31
-
-
80052396255
-
Platelet reactive conformation and multimeric pattern of von Willebrand factor in acquired thrombotic thrombocytopenic purpura during acute disease and remission
-
Lotta LA, Lombardi R, Mariani M, et al. Platelet reactive conformation and multimeric pattern of von Willebrand factor in acquired thrombotic thrombocytopenic purpura during acute disease and remission. J Thromb Haemost. 2011;9(9):1744-1751.
-
(2011)
J Thromb Haemost
, vol.9
, Issue.9
, pp. 1744-1751
-
-
Lotta, L.A.1
Lombardi, R.2
Mariani, M.3
-
32
-
-
34250692515
-
Purified A2 domain of von Willebrand factor binds to the active conformation of von Willebrand factor and blocks the interaction with platelet glycoprotein Ibalpha
-
DOI 10.1111/j.1538-7836.2007.02536.x
-
Martin C, Morales LD, Cruz MA. Purified A2 domain of von Willebrand factor binds to the active conformation of von Willebrand factor and blocks the interaction with platelet glycoprotein Ibalpha. J Thromb Haemost. 2007;5(7):1363-1370. (Pubitemid 46965360)
-
(2007)
Journal of Thrombosis and Haemostasis
, vol.5
, Issue.7
, pp. 1363-1370
-
-
Martin, C.1
Morales, L.D.2
Cruz, M.A.3
-
33
-
-
84876542457
-
Hierarchical organization in the hemostatic response and its relationship to the platelet-signaling network
-
Stalker TJ, Traxler EA, Wu J, et al. Hierarchical organization in the hemostatic response and its relationship to the platelet-signaling network. Blood. 2013;121(10):1875-1885.
-
(2013)
Blood
, vol.121
, Issue.10
, pp. 1875-1885
-
-
Stalker, T.J.1
Traxler, E.A.2
Wu, J.3
-
34
-
-
0036799775
-
Real-time in vivo imaging of platelets, tissue factor and fibrin during arterial thrombus formation in the mouse
-
Falati S, Gross P, Merrill-Skoloff G, Furie BC, Furie B. Real-time in vivo imaging of platelets, tissue factor and fibrin during arterial thrombus formation in the mouse. Nat Med. 2002;8(10):1175-1181.
-
(2002)
Nat Med
, vol.8
, Issue.10
, pp. 1175-1181
-
-
Falati, S.1
Gross, P.2
Merrill-Skoloff, G.3
Furie, B.C.4
Furie, B.5
|