-
1
-
-
84880639677
-
Clearance of von Willebrand factor
-
Casari C, Lenting PJ, Wohner N, Christophe OD, Denis CV. Clearance of von Willebrand factor. J Thromb Haemost 2013; 11 (Suppl. 1): 202-11.
-
(2013)
J Thromb Haemost
, vol.11
, pp. 202-211
-
-
Casari, C.1
Lenting, P.J.2
Wohner, N.3
Christophe, O.D.4
Denis, C.V.5
-
2
-
-
28444499005
-
Cysteine-mutations in von Willebrand factor associated with increased clearance
-
van Schooten CJ, Tjernberg P, Westein E, Terraube V, Castaman G, Mourik JA, Hollestelle MJ, Vos HL, Bertina RM, Berg HM, Eikenboom JC, Lenting PJ, Denis CV. Cysteine-mutations in von Willebrand factor associated with increased clearance. J Thromb Haemost 2005; 3: 2228-37.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 2228-2237
-
-
van Schooten, C.J.1
Tjernberg, P.2
Westein, E.3
Terraube, V.4
Castaman, G.5
Mourik, J.A.6
Hollestelle, M.J.7
Vos, H.L.8
Bertina, R.M.9
Berg, H.M.10
Eikenboom, J.C.11
Lenting, P.J.12
Denis, C.V.13
-
3
-
-
33751013939
-
Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival
-
Haberichter SL, Balistreri M, Christopherson P, Morateck P, Gavazova S, Bellissimo DB, Manco-Johnson MJ, Gill JC, Montgomery RR. Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival. Blood 2006; 108: 3344-51.
-
(2006)
Blood
, vol.108
, pp. 3344-3351
-
-
Haberichter, S.L.1
Balistreri, M.2
Christopherson, P.3
Morateck, P.4
Gavazova, S.5
Bellissimo, D.B.6
Manco-Johnson, M.J.7
Gill, J.C.8
Montgomery, R.R.9
-
4
-
-
51249123703
-
von Willebrand factor propeptide makes it easy to identify the shorter von Willebrand factor survival in patients with type 1 and type Vicenza von Willebrand disease
-
Sztukowska M, Gallinaro L, Cattini MG, Pontara E, Sartorello F, Daidone V, Padrini R, Pagnan A, Casonato A. von Willebrand factor propeptide makes it easy to identify the shorter von Willebrand factor survival in patients with type 1 and type Vicenza von Willebrand disease. Br J Haematol 2008; 143: 107-14.
-
(2008)
Br J Haematol
, vol.143
, pp. 107-114
-
-
Sztukowska, M.1
Gallinaro, L.2
Cattini, M.G.3
Pontara, E.4
Sartorello, F.5
Daidone, V.6
Padrini, R.7
Pagnan, A.8
Casonato, A.9
-
5
-
-
84877929463
-
VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease
-
Eikenboom J, Federici AB, Dirven RJ, Castaman G, Rodeghiero F, Budde U, Schneppenheim R, Batlle J, Canciani MT, Goudemand J, Peake I, Goodeve A. VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease. Blood 2013; 121: 2336-9.
-
(2013)
Blood
, vol.121
, pp. 2336-2339
-
-
Eikenboom, J.1
Federici, A.B.2
Dirven, R.J.3
Castaman, G.4
Rodeghiero, F.5
Budde, U.6
Schneppenheim, R.7
Batlle, J.8
Canciani, M.T.9
Goudemand, J.10
Peake, I.11
Goodeve, A.12
-
6
-
-
79955969561
-
Pathologic mechanisms of type 1 VWD mutations R1205H and Y1584C through in vitro and in vivo mouse models
-
Pruss CM, Golder M, Bryant A, Hegadorn CA, Burnett E, Laverty K, Sponagle K, Dhala A, Notley C, Haberichter S, Lillicrap D. Pathologic mechanisms of type 1 VWD mutations R1205H and Y1584C through in vitro and in vivo mouse models. Blood 2011; 117: 4358-66.
-
(2011)
Blood
, vol.117
, pp. 4358-4366
-
-
Pruss, C.M.1
Golder, M.2
Bryant, A.3
Hegadorn, C.A.4
Burnett, E.5
Laverty, K.6
Sponagle, K.7
Dhala, A.8
Notley, C.9
Haberichter, S.10
Lillicrap, D.11
-
7
-
-
60249092963
-
Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients
-
Federici AB, Mannucci PM, Castaman G, Baronciani L, Bucciarelli P, Canciani MT, Pecci A, Lenting PJ, De Groot PG. Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients. Blood 2009; 113: 526-34.
-
(2009)
Blood
, vol.113
, pp. 526-534
-
-
Federici, A.B.1
Mannucci, P.M.2
Castaman, G.3
Baronciani, L.4
Bucciarelli, P.5
Canciani, M.T.6
Pecci, A.7
Lenting, P.J.8
De Groot, P.G.9
-
8
-
-
33846445722
-
Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS-13
-
Rayes J, Hommais A, Legendre P, Tout H, Veyradier A, Obert B, Ribba AS, Girma JP. Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS-13. J Thromb Haemost 2007; 5: 321-8.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 321-328
-
-
Rayes, J.1
Hommais, A.2
Legendre, P.3
Tout, H.4
Veyradier, A.5
Obert, B.6
Ribba, A.S.7
Girma, J.P.8
-
9
-
-
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, Marx I, de Groot PG, Christophe OD, Lenting PJ, Denis CV. Mutation and ADAMTS13-dependent modulation of disease severity in a mouse model for von Willebrand disease type 2B. Blood 2010; 115: 4870-7.
-
(2010)
Blood
, vol.115
, pp. 4870-4877
-
-
Rayes, J.1
Hollestelle, M.J.2
Legendre, P.3
Marx, I.4
de Groot, P.G.5
Christophe, O.D.6
Lenting, P.J.7
Denis, C.V.8
-
10
-
-
51349154185
-
Platelet glycoprotein Ibalpha forms catch bonds with human WT vWF but not with type 2B von Willebrand disease vWF
-
Yago T, Lou J, Wu T, Yang J, Miner JJ, Coburn L, Lopez JA, Cruz MA, Dong JF, McIntire LV, McEver RP, Zhu C. Platelet glycoprotein Ibalpha forms catch bonds with human WT vWF but not with type 2B von Willebrand disease vWF. J Clin Invest 2008; 118: 3195-207.
-
(2008)
J Clin Invest
, vol.118
, pp. 3195-3207
-
-
Yago, T.1
Lou, J.2
Wu, T.3
Yang, J.4
Miner, J.J.5
Coburn, L.6
Lopez, J.A.7
Cruz, M.A.8
Dong, J.F.9
McIntire, L.V.10
McEver, R.P.11
Zhu, C.12
-
11
-
-
33750623252
-
Impaired megakaryocytopoiesis in type 2B von Willebrand disease with severe thrombocytopenia
-
Nurden P, Debili N, Vainchenker W, Bobe R, Bredoux R, Corvazier E, Combrie R, Fressinaud E, Meyer D, Nurden AT, Enouf J. Impaired megakaryocytopoiesis in type 2B von Willebrand disease with severe thrombocytopenia. Blood 2006; 108: 2587-95.
-
(2006)
Blood
, vol.108
, pp. 2587-2595
-
-
Nurden, P.1
Debili, N.2
Vainchenker, W.3
Bobe, R.4
Bredoux, R.5
Corvazier, E.6
Combrie, R.7
Fressinaud, E.8
Meyer, D.9
Nurden, A.T.10
Enouf, J.11
-
12
-
-
84890087195
-
von Willebrand factor mutation promotes thrombocytopathy by inhibiting integrin alphaIIbbeta3
-
Casari C, Berrou E, Lebret M, Adam F, Kauskot A, Bobe R, Desconclois C, Fressinaud E, Christophe OD, Lenting PJ, Rosa JP, Denis CV, Bryckaert M. von Willebrand factor mutation promotes thrombocytopathy by inhibiting integrin alphaIIbbeta3. J Clin Invest 2013; 123: 5071-81.
-
(2013)
J Clin Invest
, vol.123
, pp. 5071-5081
-
-
Casari, C.1
Berrou, E.2
Lebret, M.3
Adam, F.4
Kauskot, A.5
Bobe, R.6
Desconclois, C.7
Fressinaud, E.8
Christophe, O.D.9
Lenting, P.J.10
Rosa, J.P.11
Denis, C.V.12
Bryckaert, M.13
-
13
-
-
0033588163
-
The light chain of factor VIII comprises a binding site for low density lipoprotein receptor-related protein
-
Lenting PJ, Neels JG, van den Berg BM, Clijsters PP, Meijerman DW, Pannekoek H, van Mourik JA, Mertens K, van Zonneveld AJ. The light chain of factor VIII comprises a binding site for low density lipoprotein receptor-related protein. J Biol Chem 1999; 274: 23734-9.
-
(1999)
J Biol Chem
, vol.274
, pp. 23734-23739
-
-
Lenting, P.J.1
Neels, J.G.2
van den Berg, B.M.3
Clijsters, P.P.4
Meijerman, D.W.5
Pannekoek, H.6
van Mourik, J.A.7
Mertens, K.8
van Zonneveld, A.J.9
-
14
-
-
52649093281
-
Macrophages contribute to the cellular uptake of von Willebrand factor and factor VIII in vivo
-
van Schooten CJ, Shahbazi S, Groot E, Oortwijn BD, van den Berg HM, Denis CV, Lenting PJ. Macrophages contribute to the cellular uptake of von Willebrand factor and factor VIII in vivo. Blood 2008; 112: 1704-12.
-
(2008)
Blood
, vol.112
, pp. 1704-1712
-
-
van Schooten, C.J.1
Shahbazi, S.2
Groot, E.3
Oortwijn, B.D.4
van den Berg, H.M.5
Denis, C.V.6
Lenting, P.J.7
-
15
-
-
84857720357
-
Macrophage LRP1 contributes to the clearance of von Willebrand factor
-
Rastegarlari G, Pegon JN, Casari C, Odouard S, Navarrete AM, Saint-Lu N, van Vlijmen BJ, Legendre P, Christophe OD, Denis CV, Lenting PJ. Macrophage LRP1 contributes to the clearance of von Willebrand factor. Blood 2012; 119: 2126-34.
-
(2012)
Blood
, vol.119
, pp. 2126-2134
-
-
Rastegarlari, G.1
Pegon, J.N.2
Casari, C.3
Odouard, S.4
Navarrete, A.M.5
Saint-Lu, N.6
van Vlijmen, B.J.7
Legendre, P.8
Christophe, O.D.9
Denis, C.V.10
Lenting, P.J.11
-
16
-
-
84865740130
-
Shear stress is required for the endocytic uptake of the factor VIII-von Willebrand factor complex by macrophages
-
Castro-Nunez L, Dienava-Verdoold I, Herczenik E, Mertens K, Meijer AB. Shear stress is required for the endocytic uptake of the factor VIII-von Willebrand factor complex by macrophages. J Thromb Haemost 2012; 10: 1929-37.
-
(2012)
J Thromb Haemost
, vol.10
, pp. 1929-1937
-
-
Castro-Nunez, L.1
Dienava-Verdoold, I.2
Herczenik, E.3
Mertens, K.4
Meijer, A.B.5
-
17
-
-
33751194412
-
Macrophage low-density lipoprotein receptor-related protein deficiency enhances atherosclerosis in ApoE/LDLR double knockout mice
-
Hu L, Boesten LS, May P, Herz J, Bovenschen N, Huisman MV, Berbee JF, Havekes LM, van Vlijmen BJ, Tamsma JT. Macrophage low-density lipoprotein receptor-related protein deficiency enhances atherosclerosis in ApoE/LDLR double knockout mice. Arterioscler Thromb Vasc Biol 2006; 26: 2710-5.
-
(2006)
Arterioscler Thromb Vasc Biol
, vol.26
, pp. 2710-2715
-
-
Hu, L.1
Boesten, L.S.2
May, P.3
Herz, J.4
Bovenschen, N.5
Huisman, M.V.6
Berbee, J.F.7
Havekes, L.M.8
van Vlijmen, B.J.9
Tamsma, J.T.10
-
18
-
-
77950888338
-
Macrophage LRP-1 controls plaque cellularity by regulating efferocytosis and Akt activation
-
Yancey PG, Blakemore J, Ding L, Fan D, Overton CD, Zhang Y, Linton MF, Fazio S. Macrophage LRP-1 controls plaque cellularity by regulating efferocytosis and Akt activation. Arterioscler Thromb Vasc Biol 2010; 30: 787-95.
-
(2010)
Arterioscler Thromb Vasc Biol
, vol.30
, pp. 787-795
-
-
Yancey, P.G.1
Blakemore, J.2
Ding, L.3
Fan, D.4
Overton, C.D.5
Zhang, Y.6
Linton, M.F.7
Fazio, S.8
-
19
-
-
0032004972
-
Inducible inactivation of hepatic LRP gene by cre-mediated recombination confirms role of LRP in clearance of chylomicron remnants
-
Rohlmann A, Gotthardt M, Hammer RE, Herz J. Inducible inactivation of hepatic LRP gene by cre-mediated recombination confirms role of LRP in clearance of chylomicron remnants. J Clin Invest 1998; 101: 689-95.
-
(1998)
J Clin Invest
, vol.101
, pp. 689-695
-
-
Rohlmann, A.1
Gotthardt, M.2
Hammer, R.E.3
Herz, J.4
-
20
-
-
1842530336
-
An experimental model to study the in vivo survival of von Willebrand factor. Basic aspects and application to the R1205H mutation
-
Lenting PJ, Westein E, Terraube V, Ribba AS, Huizinga EG, Meyer D, de Groot PG, Denis CV. 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: 12102-9.
-
(2004)
J Biol Chem
, vol.279
, 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
-
21
-
-
84888239369
-
Accelerated uptake of VWF/platelet complexes in macrophages contributes to VWD type 2B-associated thrombocytopenia
-
Casari C, Du V, Wu YP, Kauskot A, de Groot PG, Christophe OD, Denis CV, de Laat B, Lenting PJ. Accelerated uptake of VWF/platelet complexes in macrophages contributes to VWD type 2B-associated thrombocytopenia. Blood 2013; 122: 2893-902.
-
(2013)
Blood
, vol.122
, pp. 2893-2902
-
-
Casari, C.1
Du, V.2
Wu, Y.P.3
Kauskot, A.4
de Groot, P.G.5
Christophe, O.D.6
Denis, C.V.7
de Laat, B.8
Lenting, P.J.9
-
22
-
-
0033615548
-
The second and fourth cluster of class A cysteine-rich repeats of the low density lipoprotein receptor-related protein share ligand-binding properties
-
Neels JG, van den Berg BM, Lookene A, Olivecrona G, Pannekoek H, van Zonneveld AJ. The second and fourth cluster of class A cysteine-rich repeats of the low density lipoprotein receptor-related protein share ligand-binding properties. J Biol Chem 1999; 274: 31305-11.
-
(1999)
J Biol Chem
, vol.274
, pp. 31305-31311
-
-
Neels, J.G.1
van den Berg, B.M.2
Lookene, A.3
Olivecrona, G.4
Pannekoek, H.5
van Zonneveld, A.J.6
-
23
-
-
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, Rupin A, Vallez MO, Verbeuren TJ, Denis CV. Altered thrombus formation in von Willebrand factor-deficient mice expressing von Willebrand factor variants with defective binding to collagen or GPIIbIIIa. Blood 2008; 112: 603-9.
-
(2008)
Blood
, vol.112
, pp. 603-609
-
-
Marx, I.1
Christophe, O.D.2
Lenting, P.J.3
Rupin, A.4
Vallez, M.O.5
Verbeuren, T.J.6
Denis, C.V.7
-
24
-
-
0032533592
-
Shear-dependent rolling on von Willebrand factor of mammalian cells expressing the platelet glycoprotein Ib-IX-V complex
-
Fredrickson BJ, Dong JF, McIntire LV, Lopez JA. Shear-dependent rolling on von Willebrand factor of mammalian cells expressing the platelet glycoprotein Ib-IX-V complex. Blood 1998; 92: 3684-93.
-
(1998)
Blood
, vol.92
, pp. 3684-3693
-
-
Fredrickson, B.J.1
Dong, J.F.2
McIntire, L.V.3
Lopez, J.A.4
-
25
-
-
29144487085
-
Identification of amino acid residues essential for heparin binding by the A1 domain of human von Willebrand factor
-
Adachi T, Matsushita T, Dong Z, Katsumi A, Nakayama T, Kojima T, Saito H, Sadler JE, Naoe T. Identification of amino acid residues essential for heparin binding by the A1 domain of human von Willebrand factor. Biochem Biophys Res Commun 2006; 339: 1178-83.
-
(2006)
Biochem Biophys Res Commun
, vol.339
, pp. 1178-1183
-
-
Adachi, T.1
Matsushita, T.2
Dong, Z.3
Katsumi, A.4
Nakayama, T.5
Kojima, T.6
Saito, H.7
Sadler, J.E.8
Naoe, T.9
-
26
-
-
40749119352
-
Correction of bleeding symptoms in von Willebrand factor-deficient mice by liver-expressed von Willebrand factor mutants
-
Marx I, Lenting PJ, Adler T, Pendu R, Christophe OD, Denis CV. Correction of bleeding symptoms in von Willebrand factor-deficient mice by liver-expressed von Willebrand factor mutants. Arterioscler Thromb Vasc Biol 2008; 28: 419-24.
-
(2008)
Arterioscler Thromb Vasc Biol
, vol.28
, pp. 419-424
-
-
Marx, I.1
Lenting, P.J.2
Adler, T.3
Pendu, R.4
Christophe, O.D.5
Denis, C.V.6
-
27
-
-
77956633476
-
A randomised pilot trial of the anti-von Willebrand factor aptamer ARC1779 in patients with type 2b von Willebrand disease
-
Jilma B, Paulinska P, Jilma-Stohlawetz P, Gilbert JC, Hutabarat R, Knobl P. A randomised pilot trial of the anti-von Willebrand factor aptamer ARC1779 in patients with type 2b von Willebrand disease. Thromb Haemost 2010; 104: 563-70.
-
(2010)
Thromb Haemost
, vol.104
, pp. 563-570
-
-
Jilma, B.1
Paulinska, P.2
Jilma-Stohlawetz, P.3
Gilbert, J.C.4
Hutabarat, R.5
Knobl, P.6
-
28
-
-
77956021805
-
Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia
-
Casonato A, Gallinaro L, Cattini MG, Pontara E, Padrini R, Bertomoro A, Daidone V, Pagnan A. Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia. Haematologica 2010; 95: 1366-72.
-
(2010)
Haematologica
, vol.95
, pp. 1366-1372
-
-
Casonato, A.1
Gallinaro, L.2
Cattini, M.G.3
Pontara, E.4
Padrini, R.5
Bertomoro, A.6
Daidone, V.7
Pagnan, A.8
-
29
-
-
12744273139
-
Biological and genetic factors influencing plasma factor VIII levels in a healthy family population: results from the Stanislas cohort
-
Morange PE, Tregouet DA, Frere C, Saut N, Pellegrina L, Alessi MC, Visvikis S, Tiret L, Juhan-Vague I. Biological and genetic factors influencing plasma factor VIII levels in a healthy family population: results from the Stanislas cohort. Br J Haematol 2005; 128: 91-9.
-
(2005)
Br J Haematol
, vol.128
, pp. 91-99
-
-
Morange, P.E.1
Tregouet, D.A.2
Frere, C.3
Saut, N.4
Pellegrina, L.5
Alessi, M.C.6
Visvikis, S.7
Tiret, L.8
Juhan-Vague, I.9
-
30
-
-
39749163475
-
Low density lipoprotein receptor-related protein polymorphisms are not risk factors for venous thromboembolism
-
Mello TB, Siqueira LH, Montavao SA, Ozello MC, Annichino-Bizzacchi JM. Low density lipoprotein receptor-related protein polymorphisms are not risk factors for venous thromboembolism. Thromb Res 2008; 121: 625-9.
-
(2008)
Thromb Res
, vol.121
, pp. 625-629
-
-
Mello, T.B.1
Siqueira, L.H.2
Montavao, S.A.3
Ozello, M.C.4
Annichino-Bizzacchi, J.M.5
|