-
1
-
-
0022296676
-
Purified human factor VIII procoagulant protein: comparative hemostatic response after infusions into hemophilic and von Willebrand disease dogs
-
Brinkhous KM, Sandberg H, Garris JB, Mattsson C, Palm M, Griggs T, Read MS. Purified human factor VIII procoagulant protein: comparative hemostatic response after infusions into hemophilic and von Willebrand disease dogs. Proc Natl Acad Sci USA 1985; 82: 8752-6.
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 8752-8756
-
-
Brinkhous, K.M.1
Sandberg, H.2
Garris, J.B.3
Mattsson, C.4
Palm, M.5
Griggs, T.6
Read, M.S.7
-
2
-
-
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: 185-90.
-
(1986)
Cell
, vol.46
, pp. 185-190
-
-
Sporn, L.A.1
Marder, V.J.2
Wagner, D.D.3
-
3
-
-
45549087119
-
Basal secretion of von Willebrand factor from human endothelial cells
-
Giblin JP, Hewlett LJ, Hannah MJ. Basal secretion of von Willebrand factor from human endothelial cells. Blood 2008; 112: 957-64.
-
(2008)
Blood
, vol.112
, pp. 957-964
-
-
Giblin, J.P.1
Hewlett, L.J.2
Hannah, M.J.3
-
5
-
-
0023463127
-
Constitutive and regulated secretion of proteins
-
Burgess TL, Kelly RB. Constitutive and regulated secretion of proteins. Annu Rev Cell Biol 1987; 3: 243-93.
-
(1987)
Annu Rev Cell Biol
, vol.3
, pp. 243-293
-
-
Burgess, T.L.1
Kelly, R.B.2
-
6
-
-
41649119245
-
von Willebrand factor in cardiovascular disease: focus on acute coronary syndromes
-
Spiel AO, Gilbert JC, Jilma B. von Willebrand factor in cardiovascular disease: focus on acute coronary syndromes. Circulation 2008; 117: 1449-59.
-
(2008)
Circulation
, vol.117
, pp. 1449-1459
-
-
Spiel, A.O.1
Gilbert, J.C.2
Jilma, B.3
-
7
-
-
0025243601
-
Cell biology of von Willebrand factor
-
Wagner DD. Cell biology of von Willebrand factor. Annu Rev Cell Biol 1990; 6: 217-46.
-
(1990)
Annu Rev Cell Biol
, vol.6
, pp. 217-246
-
-
Wagner, D.D.1
-
8
-
-
0035852473
-
The genetics of haemostasis: a twin study
-
de Lange M, Snieder H, Ariens RA, Spector TD, Grant PJ. The genetics of haemostasis: a twin study. Lancet 2001; 357: 101-5.
-
(2001)
Lancet
, vol.357
, pp. 101-105
-
-
de Lange, M.1
Snieder, H.2
Ariens, R.A.3
Spector, T.D.4
Grant, P.J.5
-
9
-
-
33646061356
-
Genetic influence on thrombotic risk markers in the elderly - a Danish twin study
-
Bladbjerg EM, de Maat MP, Christensen K, Bathum L, Jespersen J, Hjelmborg J. Genetic influence on thrombotic risk markers in the elderly - a Danish twin study. J Thromb Haemost 2006; 4: 599-607.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 599-607
-
-
Bladbjerg, E.M.1
de Maat, M.P.2
Christensen, K.3
Bathum, L.4
Jespersen, J.5
Hjelmborg, J.6
-
10
-
-
29144451378
-
Impact of the Thr789Ala variant of the von Willebrand factor levels, on ristocetin co-factor and collagen binding capacity and its association with coronary heart disease in patients with diabetes mellitus type 2
-
Klemm T, Mehnert AK, Siegemund A, Wiesner TD, Gelbrich G, Bluher M, Paschke R. Impact of the Thr789Ala variant of the von Willebrand factor levels, on ristocetin co-factor and collagen binding capacity and its association with coronary heart disease in patients with diabetes mellitus type 2. Exp Clin Endocrinol Diabetes 2005; 113: 568-72.
-
(2005)
Exp Clin Endocrinol Diabetes
, vol.113
, pp. 568-572
-
-
Klemm, T.1
Mehnert, A.K.2
Siegemund, A.3
Wiesner, T.D.4
Gelbrich, G.5
Bluher, M.6
Paschke, R.7
-
11
-
-
0034029009
-
Association between high von willebrand factor levels and the Thr789Ala vWF gene polymorphism but not with nephropathy in type I diabetes. The GENEDIAB Study Group and the DESIR Study Group
-
Lacquemant C, Gaucher C, Delorme C, Chatellier G, Gallois Y, Rodier M, Passa P, Balkau B, Mazurier C, Marre M, Froguel P. Association between high von willebrand factor levels and the Thr789Ala vWF gene polymorphism but not with nephropathy in type I diabetes. The GENEDIAB Study Group and the DESIR Study Group. Kidney Int 2000; 57: 1437-43.
-
(2000)
Kidney Int
, vol.57
, pp. 1437-1443
-
-
Lacquemant, C.1
Gaucher, C.2
Delorme, C.3
Chatellier, G.4
Gallois, Y.5
Rodier, M.6
Passa, P.7
Balkau, B.8
Mazurier, C.9
Marre, M.10
Froguel, P.11
-
12
-
-
0036847634
-
von Willebrand factor and coronary heart disease: prospective study and meta-analysis
-
Whincup PH, Danesh J, Walker M, Lennon L, Thomson A, Appleby P, Rumley A, Lowe GD. von Willebrand factor and coronary heart disease: prospective study and meta-analysis. Eur Heart J 2002; 23: 1764-70.
-
(2002)
Eur Heart J
, vol.23
, pp. 1764-1770
-
-
Whincup, P.H.1
Danesh, J.2
Walker, M.3
Lennon, L.4
Thomson, A.5
Appleby, P.6
Rumley, A.7
Lowe, G.D.8
-
13
-
-
1842587885
-
C-reactive protein and other circulating markers of inflammation in the prediction of coronary heart disease
-
Danesh J, Wheeler JG, Hirschfield GM, Eda S, Eiriksdottir G, Rumley A, Lowe GD, Pepys MB, Gudnason V. C-reactive protein and other circulating markers of inflammation in the prediction of coronary heart disease. N Engl J Med 2004; 350: 1387-97.
-
(2004)
N Engl J Med
, vol.350
, pp. 1387-1397
-
-
Danesh, J.1
Wheeler, J.G.2
Hirschfield, G.M.3
Eda, S.4
Eiriksdottir, G.5
Rumley, A.6
Lowe, G.D.7
Pepys, M.B.8
Gudnason, V.9
-
14
-
-
0033578475
-
Prospective study of markers of hemostatic function with risk of ischemic stroke. The Atherosclerosis Risk in Communities (ARIC) Study Investigators
-
Folsom AR, Rosamond WD, Shahar E, Cooper LS, Aleksic N, Nieto FJ, Rasmussen ML, Wu KK. Prospective study of markers of hemostatic function with risk of ischemic stroke. The Atherosclerosis Risk in Communities (ARIC) Study Investigators. Circulation 1999; 100: 736-42.
-
(1999)
Circulation
, vol.100
, pp. 736-742
-
-
Folsom, A.R.1
Rosamond, W.D.2
Shahar, E.3
Cooper, L.S.4
Aleksic, N.5
Nieto, F.J.6
Rasmussen, M.L.7
Wu, K.K.8
-
15
-
-
8944243469
-
Experiments in plant hybridization
-
Mendel G. Experiments in plant hybridization. J R Hortic Soc 1901; 26: 1-32.
-
(1901)
J R Hortic Soc
, vol.26
, pp. 1-32
-
-
Mendel, G.1
-
16
-
-
1942436221
-
Mendelian randomization: prospects, potentials, and limitations
-
Smith GD, Ebrahim S. Mendelian randomization: prospects, potentials, and limitations. Int J Epidemiol 2004; 33: 30-42.
-
(2004)
Int J Epidemiol
, vol.33
, pp. 30-42
-
-
Smith, G.D.1
Ebrahim, S.2
-
17
-
-
31544475409
-
Thrombospondin-1 controls vascular platelet recruitment and thrombus adherence in mice by protecting (sub)endothelial VWF from cleavage by ADAMTS13
-
Bonnefoy A, Daenens K, Feys HB, De Vos R, Vandervoort P, Vermylen J, Lawler J, Hoylaerts MF. Thrombospondin-1 controls vascular platelet recruitment and thrombus adherence in mice by protecting (sub)endothelial VWF from cleavage by ADAMTS13. Blood 2006; 107: 955-64.
-
(2006)
Blood
, vol.107
, pp. 955-964
-
-
Bonnefoy, A.1
Daenens, K.2
Feys, H.B.3
De Vos, R.4
Vandervoort, P.5
Vermylen, J.6
Lawler, J.7
Hoylaerts, M.F.8
-
18
-
-
0035798582
-
Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura
-
Zheng X, Chung D, Takayama TK, Majerus EM, Sadler JE, Fujikawa K. Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura. J Biol Chem 2001; 276: 41059-63.
-
(2001)
J Biol Chem
, vol.276
, pp. 41059-41063
-
-
Zheng, X.1
Chung, D.2
Takayama, T.K.3
Majerus, E.M.4
Sadler, J.E.5
Fujikawa, K.6
-
19
-
-
34548158023
-
Thrombospondins, their polymorphisms, and cardiovascular disease
-
Stenina OI, Topol EJ, Plow EF. Thrombospondins, their polymorphisms, and cardiovascular disease. Arterioscler Thromb Vasc Biol 2007; 27: 1886-94.
-
(2007)
Arterioscler Thromb Vasc Biol
, vol.27
, pp. 1886-1894
-
-
Stenina, O.I.1
Topol, E.J.2
Plow, E.F.3
-
20
-
-
41949087721
-
Polymorphisms in thrombospondin genes and myocardial infarction: a case-control study and a meta-analysis of available evidence
-
Koch W, Hoppmann P, de Waha A, Schomig A, Kastrati A. Polymorphisms in thrombospondin genes and myocardial infarction: a case-control study and a meta-analysis of available evidence. Hum Mol Genet 2008; 17: 1120-6.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 1120-1126
-
-
Koch, W.1
Hoppmann, P.2
de Waha, A.3
Schomig, A.4
Kastrati, A.5
-
21
-
-
76449114159
-
Association between ADAMTS13 polymorphisms and risk of cardiovascular events in chronic coronary disease
-
Schettert IT, Pereira AC, Lopes NH, Hueb WA, Krieger JE. Association between ADAMTS13 polymorphisms and risk of cardiovascular events in chronic coronary disease. Thromb Res 2010; 125: 61-6.
-
(2010)
Thromb Res
, vol.125
, pp. 61-66
-
-
Schettert, I.T.1
Pereira, A.C.2
Lopes, N.H.3
Hueb, W.A.4
Krieger, J.E.5
-
22
-
-
12144286348
-
Endothelial cell markers and the risk of coronary heart disease: the Prospective Epidemiological Study of Myocardial Infarction (PRIME) study
-
Morange PE, Simon C, Alessi MC, Luc G, Arveiler D, Ferrieres J, Amouyel P, Evans A, Ducimetiere P, Juhan-Vague I. Endothelial cell markers and the risk of coronary heart disease: the Prospective Epidemiological Study of Myocardial Infarction (PRIME) study. Circulation 2004; 109: 1343-8.
-
(2004)
Circulation
, vol.109
, pp. 1343-1348
-
-
Morange, P.E.1
Simon, C.2
Alessi, M.C.3
Luc, G.4
Arveiler, D.5
Ferrieres, J.6
Amouyel, P.7
Evans, A.8
Ducimetiere, P.9
Juhan-Vague, I.10
-
23
-
-
58149378854
-
Von Willebrand factor, type 2 diabetes mellitus, and risk of cardiovascular disease: the framingham offspring study
-
Frankel DS, Meigs JB, Massaro JM, Wilson PW, O'Donnell CJ, D'Agostino RB, Tofler GH. Von Willebrand factor, type 2 diabetes mellitus, and risk of cardiovascular disease: the framingham offspring study. Circulation 2008; 118: 2533-9.
-
(2008)
Circulation
, vol.118
, pp. 2533-2539
-
-
Frankel, D.S.1
Meigs, J.B.2
Massaro, J.M.3
Wilson, P.W.4
O'Donnell, C.J.5
D'Agostino, R.B.6
Tofler, G.H.7
-
24
-
-
33750949797
-
High von Willebrand factor levels increase the risk of first ischemic stroke: influence of ADAMTS13, inflammation, and genetic variability
-
Bongers TN, de Maat MP, van Goor ML, Bhagwanbali V, van Vliet HH, Gomez Garcia EB, Dippel DW, Leebeek FW. High von Willebrand factor levels increase the risk of first ischemic stroke: influence of ADAMTS13, inflammation, and genetic variability. Stroke 2006; 37: 2672-7.
-
(2006)
Stroke
, vol.37
, pp. 2672-2677
-
-
Bongers, T.N.1
de Maat, M.P.2
van Goor, M.L.3
Bhagwanbali, V.4
van Vliet, H.H.5
Gomez Garcia, E.B.6
Dippel, D.W.7
Leebeek, F.W.8
-
25
-
-
0031467885
-
Von Willebrand factor and risk of ischemic stroke
-
Qizilbash N, Duffy S, Prentice CR, Boothby M, Warlow C. Von Willebrand factor and risk of ischemic stroke. Neurology 1997; 49: 1552-6.
-
(1997)
Neurology
, vol.49
, pp. 1552-1556
-
-
Qizilbash, N.1
Duffy, S.2
Prentice, C.R.3
Boothby, M.4
Warlow, C.5
-
26
-
-
0019957645
-
A study of hemostasis in ischemic cerebrovascular disease. I. Abnormalities in factor VIII and antithrombin
-
Mettinger KL. A study of hemostasis in ischemic cerebrovascular disease. I. Abnormalities in factor VIII and antithrombin. Thromb Res 1982; 26: 183-92.
-
(1982)
Thromb Res
, vol.26
, pp. 183-192
-
-
Mettinger, K.L.1
-
27
-
-
0030794115
-
von Willebrand factor and factor VIII: C in acute cerebrovascular disease. Relationship to stroke subtype and mortality
-
Catto AJ, Carter AM, Barrett JH, Bamford J, Rice PJ, Grant PJ. von Willebrand factor and factor VIII: C in acute cerebrovascular disease. Relationship to stroke subtype and mortality. Thromb Haemost 1997; 77: 1104-8.
-
(1997)
Thromb Haemost
, vol.77
, pp. 1104-1108
-
-
Catto, A.J.1
Carter, A.M.2
Barrett, J.H.3
Bamford, J.4
Rice, P.J.5
Grant, P.J.6
-
28
-
-
70350566703
-
Lower levels of ADAMTS13 are associated with cardiovascular disease in young patients
-
Bongers TN, de Bruijne EL, Dippel DW, de Jong AJ, Deckers JW, Poldermans D, de Maat MP, Leebeek FW. Lower levels of ADAMTS13 are associated with cardiovascular disease in young patients. Atherosclerosis 2009; 207: 250-4.
-
(2009)
Atherosclerosis
, vol.207
, pp. 250-254
-
-
Bongers, T.N.1
de Bruijne, E.L.2
Dippel, D.W.3
de Jong, A.J.4
Deckers, J.W.5
Poldermans, D.6
de Maat, M.P.7
Leebeek, F.W.8
-
29
-
-
77958021914
-
High von Willebrand factor levels increase the risk of stroke. The Rotterdam Study
-
Wieberdink RG, van Schie MC, Koudstaal PJ, Hofman A, Witteman JC, de Maat MP, Leebeek FW, Breteler MM. High von Willebrand factor levels increase the risk of stroke. The Rotterdam Study. Stroke 2010; 41: 2151-6.
-
(2010)
Stroke
, vol.41
, pp. 2151-2156
-
-
Wieberdink, R.G.1
van Schie, M.C.2
Koudstaal, P.J.3
Hofman, A.4
Witteman, J.C.5
de Maat, M.P.6
Leebeek, F.W.7
Breteler, M.M.8
-
30
-
-
33644558735
-
Oligosaccharide structures of von Willebrand factor and their potential role in von Willebrand disease
-
Millar CM, Brown SA. Oligosaccharide structures of von Willebrand factor and their potential role in von Willebrand disease. Blood Rev 2006; 20: 83-92.
-
(2006)
Blood Rev
, vol.20
, pp. 83-92
-
-
Millar, C.M.1
Brown, S.A.2
-
31
-
-
43549116884
-
A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor
-
Gallinaro L, Cattini MG, Sztukowska M, Padrini R, Sartorello F, Pontara E, Bertomoro A, Daidone V, Pagnan A, Casonato A. A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor. Blood 2008; 111: 3540-5.
-
(2008)
Blood
, vol.111
, pp. 3540-3545
-
-
Gallinaro, L.1
Cattini, M.G.2
Sztukowska, M.3
Padrini, R.4
Sartorello, F.5
Pontara, E.6
Bertomoro, A.7
Daidone, V.8
Pagnan, A.9
Casonato, A.10
-
32
-
-
33748926468
-
ABO blood group determines plasma von Willebrand factor levels: a biologic function after all?
-
Jenkins PV, O'Donnell JS. ABO blood group determines plasma von Willebrand factor levels: a biologic function after all? Transfusion 2006; 46: 1836-44.
-
(2006)
Transfusion
, vol.46
, pp. 1836-1844
-
-
Jenkins, P.V.1
O'Donnell, J.S.2
-
33
-
-
0025292376
-
ABO blood group and ischaemic heart disease in British men
-
Whincup PH, Cook DG, Phillips AN, Shaper AG. ABO blood group and ischaemic heart disease in British men. BMJ 1990; 300: 1679-82.
-
(1990)
BMJ
, vol.300
, pp. 1679-1682
-
-
Whincup, P.H.1
Cook, D.G.2
Phillips, A.N.3
Shaper, A.G.4
-
34
-
-
37549068918
-
ABO(H) blood groups and vascular disease: a systematic review and meta-analysis
-
Wu O, Bayoumi N, Vickers MA, Clark P. ABO(H) blood groups and vascular disease: a systematic review and meta-analysis. J Thromb Haemost 2008; 6: 62-9.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 62-69
-
-
Wu, O.1
Bayoumi, N.2
Vickers, M.A.3
Clark, P.4
-
35
-
-
0028909230
-
Hemostatic factors and the risk of myocardial infarction or sudden death in patients with angina pectoris. European Concerted Action on Thrombosis and Disabilities Angina Pectoris Study Group
-
Thompson SG, Kienast J, Pyke SD, Haverkate F, van de Loo JC. Hemostatic factors and the risk of myocardial infarction or sudden death in patients with angina pectoris. European Concerted Action on Thrombosis and Disabilities Angina Pectoris Study Group. N Engl J Med 1995; 332: 635-41.
-
(1995)
N Engl J Med
, vol.332
, pp. 635-641
-
-
Thompson, S.G.1
Kienast, J.2
Pyke, S.D.3
Haverkate, F.4
van de Loo, J.C.5
-
36
-
-
13244252462
-
High pulse pressure and nondipping circadian blood pressure in patients with coronary artery disease: relationship to thrombogenesis and endothelial damage/dysfunction
-
Lee KW, Blann AD, Lip GY. High pulse pressure and nondipping circadian blood pressure in patients with coronary artery disease: relationship to thrombogenesis and endothelial damage/dysfunction. Am J Hypertens 2005; 18: 104-15.
-
(2005)
Am J Hypertens
, vol.18
, pp. 104-115
-
-
Lee, K.W.1
Blann, A.D.2
Lip, G.Y.3
-
37
-
-
0041624428
-
A comparison of flow-mediated dilatation and von Willebrand factor as markers of endothelial cell function in health and in hypertension: relationship to cardiovascular risk and effects of treatment: a substudy of the Anglo-Scandinavian Cardiac Outcomes Trial
-
Felmeden DC, Blann AD, Spencer CG, Beevers DG, Lip GY. A comparison of flow-mediated dilatation and von Willebrand factor as markers of endothelial cell function in health and in hypertension: relationship to cardiovascular risk and effects of treatment: a substudy of the Anglo-Scandinavian Cardiac Outcomes Trial. Blood Coagul Fibrinolysis 2003; 14: 425-31.
-
(2003)
Blood Coagul Fibrinolysis
, vol.14
, pp. 425-431
-
-
Felmeden, D.C.1
Blann, A.D.2
Spencer, C.G.3
Beevers, D.G.4
Lip, G.Y.5
-
38
-
-
0028862870
-
Altered levels of soluble adhesion molecules in rheumatoid arthritis, vasculitis and systemic sclerosis
-
Blann AD, Herrick A, Jayson MI. Altered levels of soluble adhesion molecules in rheumatoid arthritis, vasculitis and systemic sclerosis. Br J Rheumatol 1995; 34: 814-9.
-
(1995)
Br J Rheumatol
, vol.34
, pp. 814-819
-
-
Blann, A.D.1
Herrick, A.2
Jayson, M.I.3
-
39
-
-
33646771330
-
von Willebrand factor, endothelial dysfunction, and cardiovascular disease
-
Vischer UM. von Willebrand factor, endothelial dysfunction, and cardiovascular disease. J Thromb Haemost 2006; 4: 1186-93.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 1186-1193
-
-
Vischer, U.M.1
-
40
-
-
0027256179
-
von Willebrand factor and endothelial damage in essential hypertension
-
Blann AD, Naqvi T, Waite M, McCollum CN. von Willebrand factor and endothelial damage in essential hypertension. J Hum Hypertens 1993; 7: 107-11.
-
(1993)
J Hum Hypertens
, vol.7
, pp. 107-111
-
-
Blann, A.D.1
Naqvi, T.2
Waite, M.3
McCollum, C.N.4
-
41
-
-
0030054995
-
von Willebrand factor and soluble E-selectin in hypertension: influence of treatment and value in predicting the progression of atherosclerosis
-
Blann AD, Waite MA. von Willebrand factor and soluble E-selectin in hypertension: influence of treatment and value in predicting the progression of atherosclerosis. Coron Artery Dis 1996; 7: 143-7.
-
(1996)
Coron Artery Dis
, vol.7
, pp. 143-147
-
-
Blann, A.D.1
Waite, M.A.2
-
42
-
-
34547492326
-
Fluvastatin inhibits regulated secretion of endothelial cell von Willebrand factor in response to diverse secretagogues
-
Fish RJ, Yang H, Viglino C, Schorer R, Dunoyer-Geindre S, Kruithof EK. Fluvastatin inhibits regulated secretion of endothelial cell von Willebrand factor in response to diverse secretagogues. Biochem J 2007; 405: 597-604.
-
(2007)
Biochem J
, vol.405
, pp. 597-604
-
-
Fish, R.J.1
Yang, H.2
Viglino, C.3
Schorer, R.4
Dunoyer-Geindre, S.5
Kruithof, E.K.6
-
43
-
-
47749119560
-
Early effects of low versus high dose atorvastatin treatment on coagulation and inflammation parameters in patients with acute coronary syndromes
-
Ordulu E, Erdogan O. Early effects of low versus high dose atorvastatin treatment on coagulation and inflammation parameters in patients with acute coronary syndromes. Int J Cardiol 2008; 128: 282-4.
-
(2008)
Int J Cardiol
, vol.128
, pp. 282-284
-
-
Ordulu, E.1
Erdogan, O.2
-
44
-
-
0021844825
-
Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization
-
Ginsburg D, Handin RI, Bonthron DT, Donlon TA, Bruns GA, Latt SA, Orkin SH. Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization. Science 1985; 228: 1401-6.
-
(1985)
Science
, vol.228
, pp. 1401-1406
-
-
Ginsburg, D.1
Handin, R.I.2
Bonthron, D.T.3
Donlon, T.A.4
Bruns, G.A.5
Latt, S.A.6
Orkin, S.H.7
-
45
-
-
0021879269
-
Molecular cloning of cDNA for human von Willebrand factor: authentication by a new method
-
Lynch DC, Zimmerman TS, Collins CJ, Brown M, Morin MJ, Ling EH, Livingston DM. Molecular cloning of cDNA for human von Willebrand factor: authentication by a new method. Cell 1985; 41: 49-56.
-
(1985)
Cell
, vol.41
, pp. 49-56
-
-
Lynch, D.C.1
Zimmerman, T.S.2
Collins, C.J.3
Brown, M.4
Morin, M.J.5
Ling, E.H.6
Livingston, D.M.7
-
46
-
-
0033564853
-
Variation at the von Willebrand factor (vWF) gene locus is associated with plasma vWF:Ag levels: identification of three novel single nucleotide polymorphisms in the vWF gene promoter
-
Keightley AM, Lam YM, Brady JN, Cameron CL, Lillicrap D. Variation at the von Willebrand factor (vWF) gene locus is associated with plasma vWF:Ag levels: identification of three novel single nucleotide polymorphisms in the vWF gene promoter. Blood 1999; 93: 4277-83.
-
(1999)
Blood
, vol.93
, pp. 4277-4283
-
-
Keightley, A.M.1
Lam, Y.M.2
Brady, J.N.3
Cameron, C.L.4
Lillicrap, D.5
-
47
-
-
0034078215
-
A single nucleotide polymorphism at nucleotide -1793 in the von Willebrand factor (VWF) regulatory region is associated with plasma VWF:Ag levels
-
Harvey PJ, Keightley AM, Lam YM, Cameron C, Lillicrap D. A single nucleotide polymorphism at nucleotide -1793 in the von Willebrand factor (VWF) regulatory region is associated with plasma VWF:Ag levels. Br J Haematol 2000; 109: 349-53.
-
(2000)
Br J Haematol
, vol.109
, pp. 349-353
-
-
Harvey, P.J.1
Keightley, A.M.2
Lam, Y.M.3
Cameron, C.4
Lillicrap, D.5
-
48
-
-
62449136753
-
Microsatellite (GT)(n) repeats and SNPs in the von Willebrand factor gene promoter do not influence circulating von Willebrand factor levels under normal conditions
-
Daidone V, Cattini MG, Pontara E, Sartorello F, Gallinaro L, Marotti A, Scaroni C, Pagnan A, Casonato A. Microsatellite (GT)(n) repeats and SNPs in the von Willebrand factor gene promoter do not influence circulating von Willebrand factor levels under normal conditions. Thromb Haemost 2009; 101: 298-304.
-
(2009)
Thromb Haemost
, vol.101
, pp. 298-304
-
-
Daidone, V.1
Cattini, M.G.2
Pontara, E.3
Sartorello, F.4
Gallinaro, L.5
Marotti, A.6
Scaroni, C.7
Pagnan, A.8
Casonato, A.9
-
49
-
-
0035675680
-
The -1185 A/G and -1051G/A dimorphisms in the von Willebrand factor gene promoter and risk of myocardial infarction
-
Di Bitondo R, Cameron CL, Daly ME, Croft SA, Steeds RP, Channer KS, Samani NJ, Lillicrap D, Winship PR. The -1185 A/G and -1051G/A dimorphisms in the von Willebrand factor gene promoter and risk of myocardial infarction. Br J Haematol 2001; 115: 701-6.
-
(2001)
Br J Haematol
, vol.115
, pp. 701-706
-
-
Di Bitondo, R.1
Cameron, C.L.2
Daly, M.E.3
Croft, S.A.4
Steeds, R.P.5
Channer, K.S.6
Samani, N.J.7
Lillicrap, D.8
Winship, P.R.9
-
50
-
-
0037085703
-
Analysis of the -1185A/G von Willebrand factor (VWF) gene polymorphism in two Brazilian ethnic groups and its effect on the plasma VWF levels
-
Simon D, Palatnik M, Roisenberg I. Analysis of the -1185A/G von Willebrand factor (VWF) gene polymorphism in two Brazilian ethnic groups and its effect on the plasma VWF levels. Thromb Res 2002; 105: 519-22.
-
(2002)
Thromb Res
, vol.105
, pp. 519-522
-
-
Simon, D.1
Palatnik, M.2
Roisenberg, I.3
-
51
-
-
0842308833
-
Genetic variability of von Willebrand factor and risk of coronary heart disease: the Rotterdam Study
-
van der Meer IM, Brouwers GJ, Bulk S, Leebeek FW, van der Kuip DA, Hofman A, Witteman JC, Gomez Garcia EB. Genetic variability of von Willebrand factor and risk of coronary heart disease: the Rotterdam Study. Br J Haematol 2004; 124: 343-7.
-
(2004)
Br J Haematol
, vol.124
, pp. 343-347
-
-
van der Meer, I.M.1
Brouwers, G.J.2
Bulk, S.3
Leebeek, F.W.4
van der Kuip, D.A.5
Hofman, A.6
Witteman, J.C.7
Gomez Garcia, E.B.8
-
52
-
-
0001273624
-
Two novel polymorphisms of the von Willebrand factor gene promoter and association with ischemic heart disease (Abstract)
-
June Suppl: 375.
-
Heywood DMH, Ossei-Gerning N, Grant PJ. Two novel polymorphisms of the von Willebrand factor gene promoter and association with ischemic heart disease (Abstract). Haemost Thromb 1997; June Suppl: 375.
-
(1997)
Haemost Thromb
-
-
Heywood, D.M.H.1
Ossei-Gerning, N.2
Grant, P.J.3
-
53
-
-
0038784548
-
Association studies between -1185A/G von Willebrand factor gene polymorphism and coronary artery disease
-
Simon D, Paludo CA, Ghisleni GC, Manfroi WC, Roisenberg I. Association studies between -1185A/G von Willebrand factor gene polymorphism and coronary artery disease. Braz J Med Biol Res 2003; 36: 709-14.
-
(2003)
Braz J Med Biol Res
, vol.36
, pp. 709-714
-
-
Simon, D.1
Paludo, C.A.2
Ghisleni, G.C.3
Manfroi, W.C.4
Roisenberg, I.5
-
54
-
-
0028321794
-
Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin
-
Zhang ZP, Blomback M, Egberg N, Falk G, Anvret M. Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin. Genomics 1994; 21: 188-93.
-
(1994)
Genomics
, vol.21
, pp. 188-193
-
-
Zhang, Z.P.1
Blomback, M.2
Egberg, N.3
Falk, G.4
Anvret, M.5
-
55
-
-
0023357159
-
(dC-dA)n.(dG-dT)n sequences have evolutionarily conserved chromosomal locations in Drosophila with implications for roles in chromosome structure and function
-
Pardue ML, Lowenhaupt K, Rich A, Nordheim A. (dC-dA)n.(dG-dT)n sequences have evolutionarily conserved chromosomal locations in Drosophila with implications for roles in chromosome structure and function. EMBO J 1987; 6: 1781-9.
-
(1987)
EMBO J
, vol.6
, pp. 1781-1789
-
-
Pardue, M.L.1
Lowenhaupt, K.2
Rich, A.3
Nordheim, A.4
-
56
-
-
0037803571
-
Timeline: Z-DNA: the long road to biological function
-
Rich A, Zhang S. Timeline: Z-DNA: the long road to biological function. Nat Rev Genet 2003; 4: 566-72.
-
(2003)
Nat Rev Genet
, vol.4
, pp. 566-572
-
-
Rich, A.1
Zhang, S.2
-
57
-
-
45549109475
-
Influence of a GT repeat element on shear stress responsiveness of the VWF gene promoter
-
Hough C, Cameron CL, Notley CR, Brown C, O'Brien L, Keightley AM, Berber E, Lillicrap D. Influence of a GT repeat element on shear stress responsiveness of the VWF gene promoter. J Thromb Haemost 2008; 6: 1183-90.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 1183-1190
-
-
Hough, C.1
Cameron, C.L.2
Notley, C.R.3
Brown, C.4
O'Brien, L.5
Keightley, A.M.6
Berber, E.7
Lillicrap, D.8
-
58
-
-
38949136359
-
Frequency of the von Willebrand factor Tyr1584Cys polymorphism in arterial thrombosis
-
Bongers T, de Maat M, Deckers J, Dippel D, Leebeek F. Frequency of the von Willebrand factor Tyr1584Cys polymorphism in arterial thrombosis. Br J Haematol 2008; 140: 578-9.
-
(2008)
Br J Haematol
, vol.140
, pp. 578-579
-
-
Bongers, T.1
de Maat, M.2
Deckers, J.3
Dippel, D.4
Leebeek, F.5
-
59
-
-
1642581706
-
An amino acid polymorphism in von Willebrand factor correlates with increased susceptibility to proteolysis by ADAMTS13
-
Bowen DJ, Collins PW. An amino acid polymorphism in von Willebrand factor correlates with increased susceptibility to proteolysis by ADAMTS13. Blood 2004; 103: 941-7.
-
(2004)
Blood
, vol.103
, pp. 941-947
-
-
Bowen, D.J.1
Collins, P.W.2
-
60
-
-
67649649805
-
C1584: effect on von Willebrand factor proteolysis and von Willebrand factor antigen levels
-
Davies JA, Collins PW, Hathaway LS, Bowen DJ. C1584: effect on von Willebrand factor proteolysis and von Willebrand factor antigen levels. Acta Haematol 2009; 121: 98-101.
-
(2009)
Acta Haematol
, vol.121
, pp. 98-101
-
-
Davies, J.A.1
Collins, P.W.2
Hathaway, L.S.3
Bowen, D.J.4
-
61
-
-
33947583665
-
Effect of von Willebrand factor Y/C1584 on in vivo protein level and function and interaction with ABO blood group
-
Davies JA, Collins PW, Hathaway LS, Bowen DJ. Effect of von Willebrand factor Y/C1584 on in vivo protein level and function and interaction with ABO blood group. Blood 2007; 109: 2840-6.
-
(2007)
Blood
, vol.109
, pp. 2840-2846
-
-
Davies, J.A.1
Collins, P.W.2
Hathaway, L.S.3
Bowen, D.J.4
-
62
-
-
79251545488
-
Variation in the von Willebrand factor gene is associated with von Willebrand factor levels and with the risk for cardiovascular disease
-
van Schie MC, de Maat MP, Isaacs A, van Duijn CM, Deckers JW, Dippel DW, Leebeek FW. Variation in the von Willebrand factor gene is associated with von Willebrand factor levels and with the risk for cardiovascular disease. Blood 2011; 117: 1393-9.
-
(2011)
Blood
, vol.117
, pp. 1393-1399
-
-
van Schie, M.C.1
de Maat, M.P.2
Isaacs, A.3
van Duijn, C.M.4
Deckers, J.W.5
Dippel, D.W.6
Leebeek, F.W.7
-
63
-
-
77950217693
-
Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium
-
Smith NL, Chen MH, Dehghan A, Strachan DP, Basu S, Soranzo N, Hayward C, Rudan I, Sabater-Lleal M, Bis JC, de Maat MP, Rumley A, Kong X, Yang Q, Williams FM, Vitart V, Campbell H, Malarstig A, Wiggins KL, Van Duijn CM, et al. Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. Circulation 2010; 121: 1382-92.
-
(2010)
Circulation
, vol.121
, pp. 1382-1392
-
-
Smith, N.L.1
Chen, M.H.2
Dehghan, A.3
Strachan, D.P.4
Basu, S.5
Soranzo, N.6
Hayward, C.7
Rudan, I.8
Sabater-Lleal, M.9
Bis, J.C.10
de Maat, M.P.11
Rumley, A.12
Kong, X.13
Yang, Q.14
Williams, F.M.15
Vitart, V.16
Campbell, H.17
Malarstig, A.18
Wiggins, K.L.19
Van Duijn, C.M.20
more..
-
64
-
-
59049084330
-
ABO genotype and risk of thrombotic events and hemorrhagic stroke
-
Wiggins KL, Smith NL, Glazer NL, Rosendaal FR, Heckbert SR, Psaty BM, Rice KM, Lumley T. ABO genotype and risk of thrombotic events and hemorrhagic stroke. J Thromb Haemost 2009; 7: 263-9.
-
(2009)
J Thromb Haemost
, vol.7
, pp. 263-269
-
-
Wiggins, K.L.1
Smith, N.L.2
Glazer, N.L.3
Rosendaal, F.R.4
Heckbert, S.R.5
Psaty, B.M.6
Rice, K.M.7
Lumley, T.8
-
65
-
-
35748980883
-
Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study
-
Yang Q, Kathiresan S, Lin JP, Tofler GH, O'Donnell CJ. Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. BMC Med Genet 2007; 8(Suppl. 1): S12.
-
(2007)
BMC Med Genet
, vol.8
, Issue.SUPPL. 1
-
-
Yang, Q.1
Kathiresan, S.2
Lin, J.P.3
Tofler, G.H.4
O'Donnell, C.J.5
-
66
-
-
35748943204
-
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports
-
Cupples LA, Arruda HT, Benjamin EJ, D'Agostino RB Sr, Demissie S, DeStefano AL, Dupuis J, Falls KM, Fox CS, Gottlieb DJ, Govindaraju DR, Guo CY, Heard-Costa NL, Hwang SJ, Kathiresan S, Kiel DP, Laramie JM, Larson MG, Levy D, Liu CY, et al. The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports. BMC Med Genet 2007; 8(Suppl. 1): S1.
-
(2007)
BMC Med Genet
, vol.8
, Issue.SUPPL. 1
-
-
Cupples, L.A.1
Arruda, H.T.2
Benjamin, E.J.3
D'Agostino Sr, R.B.4
Demissie, S.5
DeStefano, A.L.6
Dupuis, J.7
Falls, K.M.8
Fox, C.S.9
Gottlieb, D.J.10
Govindaraju, D.R.11
Guo, C.Y.12
Heard-Costa, N.L.13
Hwang, S.J.14
Kathiresan, S.15
Kiel, D.P.16
Laramie, J.M.17
Larson, M.G.18
Levy, D.19
Liu, C.Y.20
more..
-
67
-
-
70749096913
-
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
-
Myocardial Infarction Genetics C
-
Myocardial Infarction Genetics C, Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, Anand S, Engert JC, Samani NJ, Schunkert H, Erdmann J, Reilly MP, Rader DJ, Morgan T, Spertus JA, Stoll M, Girelli D, McKeown PP, Patterson CC, et al. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet 2009; 41: 334-41.
-
(2009)
Nat Genet
, vol.41
, pp. 334-341
-
-
Kathiresan, S.1
Voight, B.F.2
Purcell, S.3
Musunuru, K.4
Ardissino, D.5
Mannucci, P.M.6
Anand, S.7
Engert, J.C.8
Samani, N.J.9
Schunkert, H.10
Erdmann, J.11
Reilly, M.P.12
Rader, D.J.13
Morgan, T.14
Spertus, J.A.15
Stoll, M.16
Girelli, D.17
McKeown, P.P.18
Patterson, C.C.19
-
68
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Wellcome Trust Case Control C.
-
Wellcome Trust Case Control C. Genome-wide association study of 14, 000 cases of seven common diseases and 3, 000 shared controls. Nature 2007; 447: 661-78.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
69
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, Barrett JH, Konig IR, Stevens SE, Szymczak S, Tregouet DA, Iles MM, Pahlke F, Pollard H, Lieb W, Cambien F, et al. Genomewide association analysis of coronary artery disease. N Engl J Med 2007; 357: 443-53.
-
(2007)
N Engl J Med
, vol.357
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
Hengstenberg, C.4
Mangino, M.5
Mayer, B.6
Dixon, R.J.7
Meitinger, T.8
Braund, P.9
Wichmann, H.E.10
Barrett, J.H.11
Konig, I.R.12
Stevens, S.E.13
Szymczak, S.14
Tregouet, D.A.15
Iles, M.M.16
Pahlke, F.17
Pollard, H.18
Lieb, W.19
Cambien, F.20
more..
-
70
-
-
35748960247
-
Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes
-
Larson MG, Atwood LD, Benjamin EJ, Cupples LA, D'Agostino RB Sr, Fox CS, Govindaraju DR, Guo CY, Heard-Costa NL, Hwang SJ, Murabito JM, Newton-Cheh C, O'Donnell CJ, Seshadri S, Vasan RS, Wang TJ, Wolf PA, Levy D. Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. BMC Med Genet 2007; 8(Suppl. 1): S5.
-
(2007)
BMC Med Genet
, vol.8
, Issue.SUPPL. 1
-
-
Larson, M.G.1
Atwood, L.D.2
Benjamin, E.J.3
Cupples, L.A.4
D'Agostino Sr, R.B.5
Fox, C.S.6
Govindaraju, D.R.7
Guo, C.Y.8
Heard-Costa, N.L.9
Hwang, S.J.10
Murabito, J.M.11
Newton-Cheh, C.12
O'Donnell, C.J.13
Seshadri, S.14
Vasan, R.S.15
Wang, T.J.16
Wolf, P.A.17
Levy, D.18
-
71
-
-
65949090748
-
Genomewide association studies of stroke
-
Ikram MA, Seshadri S, Bis JC, Fornage M, DeStefano AL, Aulchenko YS, Debette S, Lumley T, Folsom AR, van den Herik EG, Bos MJ, Beiser A, Cushman M, Launer LJ, Shahar E, Struchalin M, Du Y, Glazer NL, Rosamond WD, Rivadeneira F, et al. Genomewide association studies of stroke. N Engl J Med 2009; 360: 1718-28.
-
(2009)
N Engl J Med
, vol.360
, pp. 1718-1728
-
-
Ikram, M.A.1
Seshadri, S.2
Bis, J.C.3
Fornage, M.4
DeStefano, A.L.5
Aulchenko, Y.S.6
Debette, S.7
Lumley, T.8
Folsom, A.R.9
van den Herik, E.G.10
Bos, M.J.11
Beiser, A.12
Cushman, M.13
Launer, L.J.14
Shahar, E.15
Struchalin, M.16
Du, Y.17
Glazer, N.L.18
Rosamond, W.D.19
Rivadeneira, F.20
more..
-
73
-
-
79952813198
-
Effect of genetic variations in syntaxin-binding protein-5 and syntaxin-2 on von Willebrand factor concentration and cardiovascular risk
-
van Loon JE, Leebeek FW, Deckers JW, Dippel DW, Poldermans D, Strachan DP, Tang W, O'Donnell CJ, Smith NL, de Maat MP. Effect of genetic variations in syntaxin-binding protein-5 and syntaxin-2 on von Willebrand factor concentration and cardiovascular risk. Circ Cardiovasc Genet 2010; 3: 507-12.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 507-512
-
-
van Loon, J.E.1
Leebeek, F.W.2
Deckers, J.W.3
Dippel, D.W.4
Poldermans, D.5
Strachan, D.P.6
Tang, W.7
O'Donnell, C.J.8
Smith, N.L.9
de Maat, M.P.10
-
74
-
-
0035807348
-
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
-
Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD Jr, Ginsburg D, Tsai HM. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 2001; 413: 488-94.
-
(2001)
Nature
, vol.413
, 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
-
75
-
-
0036460780
-
Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura
-
Tsai HM. Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura. J Mol Med 2002; 80: 639-47.
-
(2002)
J Mol Med
, vol.80
, pp. 639-647
-
-
Tsai, H.M.1
-
76
-
-
1242272379
-
Deficiency of ADAMTS13 and thrombotic thrombocytopenic purpura
-
author reply 40-2.
-
Tsai HM. Deficiency of ADAMTS13 and thrombotic thrombocytopenic purpura. Blood 2002; 100: 3839-40; author reply 40-2.
-
(2002)
Blood
, vol.100
, pp. 3839-3840
-
-
Tsai, H.M.1
-
77
-
-
33847380326
-
ADAMTS13 and von Willebrand factor and the risk of myocardial infarction in men
-
Chion CK, Doggen CJ, Crawley JT, Lane DA, Rosendaal FR. ADAMTS13 and von Willebrand factor and the risk of myocardial infarction in men. Blood 2007; 109: 1998-2000.
-
(2007)
Blood
, vol.109
, pp. 1998-2000
-
-
Chion, C.K.1
Doggen, C.J.2
Crawley, J.T.3
Lane, D.A.4
Rosendaal, F.R.5
-
78
-
-
41049088840
-
Evidence that high von Willebrand factor and low ADAMTS-13 levels independently increase the risk of a non-fatal heart attack
-
Crawley JT, Lane DA, Woodward M, Rumley A, Lowe GD. Evidence that high von Willebrand factor and low ADAMTS-13 levels independently increase the risk of a non-fatal heart attack. J Thromb Haemost 2008; 6: 583-8.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 583-588
-
-
Crawley, J.T.1
Lane, D.A.2
Woodward, M.3
Rumley, A.4
Lowe, G.D.5
-
79
-
-
33750058829
-
Reduced von Willebrand factor-cleaving protease (ADAMTS13) activity in acute myocardial infarction
-
Kaikita K, Soejima K, Matsukawa M, Nakagaki T, Ogawa H. Reduced von Willebrand factor-cleaving protease (ADAMTS13) activity in acute myocardial infarction. J Thromb Haemost 2006; 4: 2490-3.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 2490-2493
-
-
Kaikita, K.1
Soejima, K.2
Matsukawa, M.3
Nakagaki, T.4
Ogawa, H.5
-
80
-
-
0037015057
-
Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity
-
Kokame K, Matsumoto M, Soejima K, Yagi H, Ishizashi H, Funato M, Tamai H, Konno M, Kamide K, Kawano Y, Miyata T, Fujimura Y. Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity. Proc Natl Acad Sci USA 2002; 99: 11902-7.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 11902-11907
-
-
Kokame, K.1
Matsumoto, M.2
Soejima, K.3
Yagi, H.4
Ishizashi, H.5
Funato, M.6
Tamai, H.7
Konno, M.8
Kamide, K.9
Kawano, Y.10
Miyata, T.11
Fujimura, Y.12
-
81
-
-
3042538950
-
The frequency of P475S polymorphism in von Willebrand factor-cleaving protease in the Chinese population and its relevance to arterial thrombotic disorders
-
Ruan C, Dai L, Su J, Wang Z, Ruan C. The frequency of P475S polymorphism in von Willebrand factor-cleaving protease in the Chinese population and its relevance to arterial thrombotic disorders. Thromb Haemost 2004; 91: 1257-8.
-
(2004)
Thromb Haemost
, vol.91
, pp. 1257-1258
-
-
Ruan, C.1
Dai, L.2
Su, J.3
Wang, Z.4
Ruan, C.5
-
82
-
-
23644454623
-
Absence of Pro475Ser polymorphism in ADAMTS-13 in Caucasians
-
Bongers TN, De Maat MP, Dippel DW, Uitterlinden AG, Leebeek FW. Absence of Pro475Ser polymorphism in ADAMTS-13 in Caucasians. J Thromb Haemost 2005; 3: 805.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 805
-
-
Bongers, T.N.1
De Maat, M.P.2
Dippel, D.W.3
Uitterlinden, A.G.4
Leebeek, F.W.5
-
83
-
-
79955644139
-
Modulation of von Willebrand Factor Cleaving Protease (ADAMTS-13) activity by polymorphisms in the ADAMTS-13 gene
-
Peyvandi F, Lavoretano S, Canciani M, Manucci P. Modulation of von Willebrand Factor Cleaving Protease (ADAMTS-13) activity by polymorphisms in the ADAMTS-13 gene. Blood; 102: 801A (2967).
-
Blood
, vol.102
, Issue.2967
-
-
Peyvandi, F.1
Lavoretano, S.2
Canciani, M.3
Manucci, P.4
-
84
-
-
77449138720
-
Association between genetic variation at the ADAMTS13 locus and ischemic stroke
-
Hanson E, Jood K, Nilsson S, Blomstrand C, Jern C. Association between genetic variation at the ADAMTS13 locus and ischemic stroke. J Thromb Haemost 2009; 7: 2147-8.
-
(2009)
J Thromb Haemost
, vol.7
, pp. 2147-2148
-
-
Hanson, E.1
Jood, K.2
Nilsson, S.3
Blomstrand, C.4
Jern, C.5
-
85
-
-
0343951615
-
Cultured human fibroblasts synthesize and secrete thrombospondin and incorporate it into extracellular matrix
-
Jaffe EA, Ruggiero JT, Leung LK, Doyle MJ, McKeown-Longo PJ, Mosher DF. Cultured human fibroblasts synthesize and secrete thrombospondin and incorporate it into extracellular matrix. Proc Natl Acad Sci USA 1983; 80: 998-1002.
-
(1983)
Proc Natl Acad Sci USA
, vol.80
, pp. 998-1002
-
-
Jaffe, E.A.1
Ruggiero, J.T.2
Leung, L.K.3
Doyle, M.J.4
McKeown-Longo, P.J.5
Mosher, D.F.6
-
86
-
-
0020313151
-
Synthesis and secretion of thrombospondin by cultured human endothelial cells
-
Mosher DF, Doyle MJ, Jaffe EA. Synthesis and secretion of thrombospondin by cultured human endothelial cells. J Cell Biol 1982; 93: 343-8.
-
(1982)
J Cell Biol
, vol.93
, pp. 343-348
-
-
Mosher, D.F.1
Doyle, M.J.2
Jaffe, E.A.3
-
87
-
-
0031911316
-
Immunolocalization of thrombospondin-1 in human atherosclerotic and restenotic arteries
-
Riessen R, Kearney M, Lawler J, Isner JM. Immunolocalization of thrombospondin-1 in human atherosclerotic and restenotic arteries. Am Heart J 1998; 135: 357-64.
-
(1998)
Am Heart J
, vol.135
, pp. 357-364
-
-
Riessen, R.1
Kearney, M.2
Lawler, J.3
Isner, J.M.4
-
88
-
-
0041703023
-
Thrombospondin-1 mediates platelet adhesion at high shear via glycoprotein Ib (GPIb): an alternative/backup mechanism to von Willebrand factor
-
Jurk K, Clemetson KJ, de Groot PG, Brodde MF, Steiner M, Savion N, Varon D, Sixma JJ, van Aken H, Kehrel BE. Thrombospondin-1 mediates platelet adhesion at high shear via glycoprotein Ib (GPIb): an alternative/backup mechanism to von Willebrand factor. FASEB J 2003; 17: 1490-2.
-
(2003)
FASEB J
, vol.17
, pp. 1490-1492
-
-
Jurk, K.1
Clemetson, K.J.2
de Groot, P.G.3
Brodde, M.F.4
Steiner, M.5
Savion, N.6
Varon, D.7
Sixma, J.J.8
van Aken, H.9
Kehrel, B.E.10
-
89
-
-
79251545488
-
Variation in the von Willebrand Factor gene is associated with VWF levels and with the risk of cardiovascular disease
-
van Schie MC, de Maat MP, Isaacs A, van Duijn CM, Deckers JW, Dippel DW, Leebeek FW. Variation in the von Willebrand Factor gene is associated with VWF levels and with the risk of cardiovascular disease. Blood 2011; 117: 1393-9.
-
(2011)
Blood
, vol.117
, pp. 1393-1399
-
-
van Schie, M.C.1
de Maat, M.P.2
Isaacs, A.3
van Duijn, C.M.4
Deckers, J.W.5
Dippel, D.W.6
Leebeek, F.W.7
-
90
-
-
65849124141
-
Thrombospondin-1 in von Willebrand factor function
-
Bonnefoy A, Hoylaerts MF. Thrombospondin-1 in von Willebrand factor function. Curr Drug Targets 2008; 9: 822-32.
-
(2008)
Curr Drug Targets
, vol.9
, pp. 822-832
-
-
Bonnefoy, A.1
Hoylaerts, M.F.2
-
91
-
-
0035960593
-
Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction
-
Topol EJ, McCarthy J, Gabriel S, Moliterno DJ, Rogers WJ, Newby LK, Freedman M, Metivier J, Cannata R, O'Donnell CJ, Kottke-Marchant K, Murugesan G, Plow EF, Stenina O, Daley GQ. Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction. Circulation 2001; 104: 2641-4.
-
(2001)
Circulation
, vol.104
, pp. 2641-2644
-
-
Topol, E.J.1
McCarthy, J.2
Gabriel, S.3
Moliterno, D.J.4
Rogers, W.J.5
Newby, L.K.6
Freedman, M.7
Metivier, J.8
Cannata, R.9
O'Donnell, C.J.10
Kottke-Marchant, K.11
Murugesan, G.12
Plow, E.F.13
Stenina, O.14
Daley, G.Q.15
-
92
-
-
33747179855
-
The thrombospondin-1 N700S polymorphism is associated with early myocardial infarction without altering von Willebrand factor multimer size
-
Zwicker JI, Peyvandi F, Palla R, Lombardi R, Canciani MT, Cairo A, Ardissino D, Bernardinelli L, Bauer KA, Lawler J, Mannucci P. The thrombospondin-1 N700S polymorphism is associated with early myocardial infarction without altering von Willebrand factor multimer size. Blood 2006; 108: 1280-3.
-
(2006)
Blood
, vol.108
, pp. 1280-1283
-
-
Zwicker, J.I.1
Peyvandi, F.2
Palla, R.3
Lombardi, R.4
Canciani, M.T.5
Cairo, A.6
Ardissino, D.7
Bernardinelli, L.8
Bauer, K.A.9
Lawler, J.10
Mannucci, P.11
-
93
-
-
34247144499
-
Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study
-
Morgan TM, Krumholz HM, Lifton RP, Spertus JA. Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study. JAMA 2007; 297: 1551-61.
-
(2007)
JAMA
, vol.297
, pp. 1551-1561
-
-
Morgan, T.M.1
Krumholz, H.M.2
Lifton, R.P.3
Spertus, J.A.4
-
94
-
-
65349125946
-
Deficiency of von Willebrand factor protects mice from ischemic stroke
-
Kleinschnitz C, De Meyer SF, Schwarz T, Austinat M, Vanhoorelbeke K, Nieswandt B, Deckmyn H, Stoll G. Deficiency of von Willebrand factor protects mice from ischemic stroke. Blood 2009; 113: 3600-3.
-
(2009)
Blood
, vol.113
, pp. 3600-3603
-
-
Kleinschnitz, C.1
De Meyer, S.F.2
Schwarz, T.3
Austinat, M.4
Vanhoorelbeke, K.5
Nieswandt, B.6
Deckmyn, H.7
Stoll, G.8
-
95
-
-
77949905138
-
ADAMTS13 gene deletion aggravates ischemic brain damage: a possible neuroprotective role of ADAMTS13 by ameliorating postischemic hypoperfusion
-
Fujioka M, Hayakawa K, Mishima K, Kunizawa A, Irie K, Higuchi S, Nakano T, Muroi C, Fukushima H, Sugimoto M, Banno F, Kokame K, Miyata T, Fujiwara M, Okuchi K, Nishio K. ADAMTS13 gene deletion aggravates ischemic brain damage: a possible neuroprotective role of ADAMTS13 by ameliorating postischemic hypoperfusion. Blood 2010; 115: 1650-3.
-
(2010)
Blood
, vol.115
, pp. 1650-1653
-
-
Fujioka, M.1
Hayakawa, K.2
Mishima, K.3
Kunizawa, A.4
Irie, K.5
Higuchi, S.6
Nakano, T.7
Muroi, C.8
Fukushima, H.9
Sugimoto, M.10
Banno, F.11
Kokame, K.12
Miyata, T.13
Fujiwara, M.14
Okuchi, K.15
Nishio, K.16
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