-
1
-
-
0034653497
-
Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor
-
Allen S, Abuzenadah AM, Blagg JL et al. Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor. Blood 2000; 95: 2000-2007. (Pubitemid 30151638)
-
(2000)
Blood
, vol.95
, Issue.6
, pp. 2000-2007
-
-
Allen, S.1
Abuzenadah, A.M.2
Blagg, J.L.3
Hinks, J.4
Nesbitt, I.M.5
Goodeve, A.C.6
Gursel, T.7
Ingerslev, J.8
Peake, I.R.9
Daly, M.E.10
-
2
-
-
0034661897
-
A novel Von Willebrand disease-causing mutation (Arg273Trp) in the Von Willebrand factor propeptide that results in defective multimerization and secretion
-
Allen S, Abuzenadah AM, Hinks J et al. A novel von Willebrand disease-causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretion. Blood 2000; 96: 560-568. (Pubitemid 30463376)
-
(2000)
Blood
, vol.96
, Issue.2
, pp. 560-568
-
-
Allen, S.1
Abuzenadah, A.M.2
Hinks, J.3
Blagg, J.L.4
Gursel, T.5
Ingerslev, J.6
Goodeve, A.C.7
Peake, I.R.8
Daly, M.E.9
-
3
-
-
0034810825
-
Endoplasmic reticulum retention and prolonged association of a von Willebrand's disease-causing von Willebrand factor variant with ERp57 and calnexin
-
DOI 10.1006/bbrc.2000.4139
-
Allen S, Goodeve AC, Peake IR et al. Endoplasmic reticulum retention and prolonged association of a von Willebrand's disease-causing von Willebrand factor variant with ERp57 and calnexin. Biochem Biophys Res Commun 2001; 280: 448-453. (Pubitemid 32912810)
-
(2001)
Biochemical and Biophysical Research Communications
, vol.280
, Issue.2
, pp. 448-453
-
-
Allen, S.1
Goodeve, A.C.2
Peake, I.R.3
Daly, M.E.4
-
4
-
-
70350035716
-
An assessment of the pathogenic significance of the R924Q von Willebrand factor substitution
-
Berber E, James PD, Hough C et al. An assessment of the pathogenic significance of the R924Q von Willebrand factor substitution. J Thromb Haemost 2009; 7: 1672-1679.
-
(2009)
J Thromb Haemost
, vol.7
, pp. 1672-1679
-
-
Berber, E.1
James, P.D.2
Hough, C.3
-
5
-
-
0019424266
-
Characterization and properties of cultured human von Willebrand umbilical vein endothelial cells
-
Booyse FM, Quarfoot AJ, Chediak J et al. Characterization and properties of cultured human von Willebrand umbilical vein endothelial cells. Blood 1981; 58: 788-796. (Pubitemid 11015837)
-
(1981)
Blood
, vol.58
, Issue.4
, pp. 788-796
-
-
Booyse, F.M.1
Quarfoot, A.J.2
Chediak, J.3
-
6
-
-
9644280969
-
A new L1446P mutation is responsible for impaired von Willebrand factor synthesis, structure, and function
-
Casonato A, Cattini MG, Soldera C et al. A new L1446P mutation is responsible for impaired von Willebrand factor synthesis, structure, and function. J Lab Clin Med 2004; 144: 254-259.
-
(2004)
J Lab Clin Med
, vol.144
, pp. 254-259
-
-
Casonato, A.1
Cattini, M.G.2
Soldera, C.3
-
7
-
-
0037222943
-
An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant
-
DOI 10.1182/blood-2002-04-1046
-
Casonato A, Sartorello F, Cattini MG et al. An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant. Blood 2003; 101: 151-156. (Pubitemid 36025901)
-
(2003)
Blood
, vol.101
, Issue.1
, pp. 151-156
-
-
Casonato, A.1
Sartorello, F.2
Cattini, M.G.3
Pontara, E.4
Soldera, C.5
Bertomoro, A.6
Girolami, A.7
-
8
-
-
36949030473
-
A novel von Willebrand factor mutation (I1372S) associated with type 2B-like von Willebrand disease: An elusive phenotype and a difficult diagnosis
-
DOI 10.1160/TH07-05-0347
-
Casonato A, Sartorello F, Pontara E et al. A novel von Willebrand factor mutation (I1372S) associated with type 2B-like von Willebrand disease: an elusive phenotype and a difficult diagnosis. Thromb Haemost 2007; 98: 1182-1187. (Pubitemid 350239088)
-
(2007)
Thrombosis and Haemostasis
, vol.98
, Issue.6
, pp. 1182-1187
-
-
Casonato, A.1
Sartorello, F.2
Pontara, E.3
Gallinaro, L.4
Bertomoro, A.5
Cattini, M.G.6
Daidone, V.7
Szukowska, M.8
Pagnan, A.9
-
9
-
-
0021962882
-
Eccentric localization of von Willebrand factor in an internal structure of platelet alpha-granule resembling that of Weibel-Palade bodies
-
Cramer EM, Meyer D, le Menn R et al. Eccentric localization of von Willebrand factor in an internal structure of platelet alpha-granule resembling that of Weibel-Palade bodies. Blood 1985; 66: 710-713. (Pubitemid 15230782)
-
(1985)
Blood
, vol.66
, Issue.3
, pp. 710-713
-
-
Cramer, E.M.1
Meyer, D.2
Le Menn, R.3
Breton-Gorius, J.4
-
10
-
-
33751219230
-
An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type I von Willebrand disease
-
DOI 10.1160/TH06-07-0383
-
Cumming A, Grundy P, Keeney S et al. An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease. Thromb Haemost 2006; 96: 630-641. (Pubitemid 44782544)
-
(2006)
Thrombosis and Haemostasis
, vol.96
, Issue.5
, pp. 630-641
-
-
Cumming, A.1
Grundy, P.2
Keeney, S.3
Lester, W.4
Enayat, S.5
Guilliatt, A.6
Bowen, D.7
Pasi, J.8
Keeling, D.9
Hill, F.10
Bolton-Maggs, P.H.B.11
Hay, C.12
Collins, P.13
-
11
-
-
0343086006
-
Von Willebrand factor synthesized by endothelial cells from a patient with type IIB von Willebrand disease supports platelet adhesion normally but has an increased affinity for platelets
-
de Groot PG, Federici AB, de Boer HC et al. von Willebrand factor synthesized by endothelial cells from a patient with type IIB von Willebrand disease supports platelet adhesion normally but has an increased affinity for platelets. Proc Natl Acad Sci USA 1989; 86: 3793-3797.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 3793-3797
-
-
De Groot, P.G.1
Federici, A.B.2
De Boer, H.C.3
-
13
-
-
0036893186
-
ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions
-
DOI 10.1182/blood-2002-05-1401
-
Dong JF, Moake JL, Nolasco L et al. ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions. Blood 2002; 100: 4033-4039. (Pubitemid 35396870)
-
(2002)
Blood
, vol.100
, Issue.12
, pp. 4033-4039
-
-
Dong, J.-F.1
Moake, J.L.2
Nolasco, L.3
Bernardo, A.4
Arceneaux, W.5
Shrimpton, C.N.6
Schade, A.J.7
McIntire, L.V.8
Fujikawa, K.9
Lopez, J.A.10
-
14
-
-
67949124719
-
Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study
-
Eikenboom J, Hilbert L, Ribba AS et al. Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study. J Thromb Haemost 2009; 7: 1304-1312.
-
(2009)
J Thromb Haemost
, vol.7
, pp. 1304-1312
-
-
Eikenboom, J.1
Hilbert, L.2
Ribba, A.S.3
-
15
-
-
0034912198
-
Congenital von Willebrand disease type 3: Clinical manifestations, pathophysiology and molecular biology
-
DOI 10.1053/beha.2001.0139
-
Eikenboom JC. Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biology. Best Pract Res Clin Haematol 2001; 14: 365-379. (Pubitemid 32677085)
-
(2001)
Best Practice and Research in Clinical Haematology
, vol.14
, Issue.2
, pp. 365-379
-
-
Eikenboom, J.C.J.1
-
16
-
-
0029817840
-
Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor
-
Eikenboom JC, Matsushita T, Reitsma PH et al. Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor. Blood 1996; 88: 2433-2441. (Pubitemid 26327491)
-
(1996)
Blood
, vol.88
, Issue.7
, pp. 2433-2441
-
-
Eikenboom, J.C.J.1
Matsushita, T.2
Reitsma, P.H.3
Tuley, E.A.4
Castaman, G.5
Briet, E.6
Sadler, J.E.7
-
17
-
-
0025261767
-
Molecular studies of von Willebrand disease: Reduced von Willebrand factor biosynthesis, storage, and release in endothelial cells derived from patients with type I von Willebrand disease
-
Ewenstein BM, Inbal A, Pober JS et al. Molecular studies of von Willebrand disease: reduced von Willebrand factor biosynthesis, storage, and release in endothelial cells derived from patients with type I von Willebrand disease. Blood 1990; 75: 1466-1472.
-
(1990)
Blood
, vol.75
, pp. 1466-1472
-
-
Ewenstein, B.M.1
Inbal, A.2
Pober, J.S.3
-
18
-
-
0027465930
-
Type I von Willebrand disease, subtype 'platelet low': Decreased platelet adhesion can be explained by low synthesis of von Willebrand factor in endothelial cells
-
Federici AB, de Groot PG, Moia M et al. Type I von Willebrand disease, subtype 'platelet low': decreased platelet adhesion can be explained by low synthesis of von Willebrand factor in endothelial cells. Br J Haematol 1993; 83: 88-93.
-
(1993)
Br J Haematol
, vol.83
, pp. 88-93
-
-
Federici, A.B.1
De Groot, P.G.2
Moia, M.3
-
19
-
-
0026350727
-
Heterogeneous distribution of Weibel-Palade bodies and von Willebrand factor along the porcine vascular tree
-
Gebrane-Younes J, Drouet L, Caen JP et al. Heterogeneous distribution of Weibel-Palade bodies and von Willebrand factor along the porcine vascular tree. Am J Pathol 1991; 139: 1471-1484.
-
(1991)
Am J Pathol
, vol.139
, pp. 1471-1484
-
-
Gebrane-Younes, J.1
Drouet, L.2
Caen, J.P.3
-
20
-
-
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: 957-964.
-
(2008)
Blood
, vol.112
, pp. 957-964
-
-
Giblin, J.P.1
Hewlett, L.J.2
Hannah, M.J.3
-
21
-
-
0023257218
-
The effect of ABO blood group on the diagnosis of von Willebrand disease
-
Gill JC, Endres-Brooks J, Bauer PJ et al. The effect of ABO blood group on the diagnosis of von Willebrand disease. Blood 1987; 69: 1691-1695. (Pubitemid 17091627)
-
(1987)
Blood
, vol.69
, Issue.6
, pp. 1691-1695
-
-
Gill, J.C.1
Endres-Brooks, J.2
Bauer, P.J.3
-
22
-
-
33845967766
-
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
-
Goodeve A, Eikenboom J, Castaman G et al. Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD). Blood 2007; 109: 112-121.
-
(2007)
Blood
, vol.109
, pp. 112-121
-
-
Goodeve, A.1
Eikenboom, J.2
Castaman, G.3
-
23
-
-
63049092852
-
Genetic alteration of the D2 domain abolishes von Willebrand factor multimerization and trafficking into storage
-
Haberichter SL, Allmann AM, Jozwiak MA et al. Genetic alteration of the D2 domain abolishes von Willebrand factor multimerization and trafficking into storage. J Thromb Haemost 2009; 7: 641-650.
-
(2009)
J Thromb Haemost
, vol.7
, pp. 641-650
-
-
Haberichter, S.L.1
Allmann, A.M.2
Jozwiak, M.A.3
-
24
-
-
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 et al. Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival. Blood 2006; 108: 3344-3351.
-
(2006)
Blood
, vol.108
, pp. 3344-3351
-
-
Haberichter, S.L.1
Balistreri, M.2
Christopherson, P.3
-
25
-
-
46749133213
-
Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: Molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD)
-
Haberichter SL, Castaman G, Budde U et al. Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD). Blood 2008; 111: 4979-4985.
-
(2008)
Blood
, vol.111
, pp. 4979-4985
-
-
Haberichter, S.L.1
Castaman, G.2
Budde, U.3
-
26
-
-
11144247649
-
Re-establishment of VWF-dependent Weibel-Palade bodies in VWD endothelial cells
-
Haberichter SL, Merricks EP, Fahs SA et al. Re-establishment of VWF-dependent Weibel-Palade bodies in VWD endothelial cells. Blood 2005; 105: 145-152.
-
(2005)
Blood
, vol.105
, pp. 145-152
-
-
Haberichter, S.L.1
Merricks, E.P.2
Fahs, S.A.3
-
27
-
-
0036702298
-
ER-associated degradation in protein quality control and cellular regulation
-
Hampton RY. ER-associated degradation in protein quality control and cellular regulation. Curr Opin Cell Biol 2002; 14: 476-482.
-
(2002)
Curr Opin Cell Biol
, vol.14
, pp. 476-482
-
-
Hampton, R.Y.1
-
28
-
-
33644872573
-
Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion
-
Hommais A, Stepanian A, Fressinaud E et al. Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion. J Thromb Haemost 2006; 4: 148-157.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 148-157
-
-
Hommais, A.1
Stepanian, A.2
Fressinaud, E.3
-
29
-
-
0033927564
-
Assembly of multimeric von Willebrand factor directs sorting of P- Selectin
-
Hop C, Guilliatt A, Daly M et al. Assembly of multimeric von Willebrand factor directs sorting of P-selectin. Arterioscler Thromb Vasc Biol 2000; 20: 1763-1768. (Pubitemid 30470591)
-
(2000)
Arteriosclerosis, Thrombosis, and Vascular Biology
, vol.20
, Issue.7
, pp. 1763-1768
-
-
Hop, C.1
Guilliatt, A.2
Daly, M.3
De Leeuw, H.P.4
Brinkman, H.-J.M.5
Peake, I.R.6
Van Mourik, J.A.7
Pannekoek, H.8
-
30
-
-
38649115965
-
Assembly of Weibel-Palade body-like tubules from N-terminal domains of von Willebrand factor
-
DOI 10.1073/pnas.0710079105
-
Huang RH, Wang Y, Roth R et al. Assembly of Weibel-Palade body-like tubules from N-terminal domains of von Willebrand factor. Proc Natl Acad Sci USA 2008; 105: 482-487. (Pubitemid 351171734)
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.2
, pp. 482-487
-
-
Huang, R.-H.1
Wang, Y.2
Roth, R.3
Yu, X.4
Purvis, A.R.5
Heuser, J.E.6
Egelman, E.H.7
Sadler, J.E.8
-
31
-
-
33846026307
-
The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study
-
DOI 10.1182/blood-2006-05-021105.
-
James PD, Notley C, Hegadorn C et al. The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study. Blood 2007; 109: 145-154. (Pubitemid 46053055)
-
(2007)
Blood
, vol.109
, Issue.1
, pp. 145-154
-
-
James, P.D.1
Notley, C.2
Hegadorn, C.3
Leggo, J.4
Tuttle, A.5
Tinlin, S.6
Brown, C.7
Andrews, C.8
Labelle, A.9
Chirinian, Y.10
O'Brien, L.11
Othman, M.12
Rivard, G.13
Rapson, D.14
Hough, C.15
Lillicrap, D.16
-
32
-
-
0021670840
-
Use of monoclonal and colloidal gold in E.M. localization of Von Willebrand factor in megakaryocytes and platelets
-
DOI 10.1016/0309-1651(84)90067-5
-
Jeanneau C, Avner P, Sultan Y. Use of monoclonal antibody and colloidal gold in E.M. localization of von Willebrand factor in megakaryocytes and platelets. Cell Biol Int Rep 1984; 8: 841-848. (Pubitemid 15108409)
-
(1984)
Cell Biology International Reports
, vol.8
, Issue.10
, pp. 841-848
-
-
Jeanneau, C.1
Avner, P.2
Sultan, Y.3
-
33
-
-
0027456818
-
Von Willebrand factor storage requires intact prosequence cleavage site
-
Journet AM, Saffaripour S, Cramer EM et al. Von Willebrand factor storage requires intact prosequence cleavage site. Eur J Cell Biol 1993; 60: 31-41. (Pubitemid 23092660)
-
(1993)
European Journal of Cell Biology
, vol.60
, Issue.1
, pp. 31-41
-
-
Journet, A.M.1
Saffaripour, S.2
Cramer, E.M.3
Tenza, D.4
Wagner, D.D.5
-
34
-
-
0030040896
-
The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor
-
Kroner PA, Foster PA, Fahs SA et al. The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor. Blood 1996; 87: 1013-1021.
-
(1996)
Blood
, vol.87
, pp. 1013-1021
-
-
Kroner, P.A.1
Foster, P.A.2
Fahs, S.A.3
-
35
-
-
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: 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
-
36
-
-
0023483277
-
Expression of abnormal von Willebrand factor by endothelial cells from a patient with type IIA von Willebrand disease
-
DOI 10.1073/pnas.84.18.6550
-
Levene RB, Booyse FM, Chediak J et al. Expression of abnormal von Willebrand factor by endothelial cells from a patient with type IIA von Willebrand disease. Proc Natl Acad Sci USA 1987; 84: 6550-6554. (Pubitemid 18002818)
-
(1987)
Proceedings of the National Academy of Sciences of the United States of America
, vol.84
, Issue.18
, pp. 6550-6554
-
-
Levene, R.B.1
Booyse, F.M.2
Chediak, J.3
Zimmerman, T.S.4
Livingston, D.M.5
Lynch, D.C.6
-
38
-
-
0026630044
-
Impaired intracellular transport produced by a subset of type IIA von Willebrand disease mutations
-
Lyons SE, Bruck ME, Bowie EJ et al. Impaired intracellular transport produced by a subset of type IIA von Willebrand disease mutations. J Biol Chem 1992; 267: 4424-4430.
-
(1992)
J Biol Chem
, vol.267
, pp. 4424-4430
-
-
Lyons, S.E.1
Bruck, M.E.2
Bowie, E.J.3
-
40
-
-
31744437770
-
The physiological function of von Willebrand's factor depends on its tubular storage in endothelial Weibel-Palade bodies
-
DOI 10.1016/j.devcel.2005.12.012, PII S1534580706000049
-
Michaux G, Abbitt KB, Collinson LM et al. The physiological function of von Willebrand's factor depends on its tubular storage in endothelial Weibel-Palade bodies. Dev Cell 2006; 10: 223-232. (Pubitemid 43174955)
-
(2006)
Developmental Cell
, vol.10
, Issue.2
, pp. 223-232
-
-
Michaux, G.1
Abbitt, K.B.2
Collinson, L.M.3
Haberichter, S.L.4
Norman, K.E.5
Cutler, D.F.6
-
41
-
-
0141705326
-
Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factor
-
DOI 10.1182/blood-2003-02-0599
-
Michaux G, Hewlett LJ, Messenger SL et al. Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factor. Blood 2003; 102: 2452-2458. (Pubitemid 37193582)
-
(2003)
Blood
, vol.102
, Issue.7
, pp. 2452-2458
-
-
Michaux, G.1
Hewlett, L.J.2
Messenger, S.L.3
Goodeve, A.C.4
Peake, I.R.5
Daly, M.E.6
Cutler, D.F.7
-
42
-
-
34247155835
-
ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with a and B antigens
-
DOI 10.1160/TH06-09-0549
-
Morelli VM, de Visser MC, van Tilburg NH et al. ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with A and B antigens. Thromb Haemost 2007; 97: 534-541. (Pubitemid 46592929)
-
(2007)
Thrombosis and Haemostasis
, vol.97
, Issue.4
, pp. 534-541
-
-
Morelli, V.M.1
De Visser, M.C.H.2
Van Tilburg, N.H.3
Vos, H.L.4
Eikenboom, J.C.J.5
Rosendaal, F.R.6
Bertina, R.M.7
-
43
-
-
0004491249
-
Von Willebrand's disease and its correction with human plasma fraction 1-0
-
Nilsson IM, Blomback M, Jorpes E et al. Von Willebrand's disease and its correction with human plasma fraction 1-0. Acta Med Scand 1957; 159: 179-188.
-
(1957)
Acta Med Scand
, vol.159
, pp. 179-188
-
-
Nilsson, I.M.1
Blomback, M.2
Jorpes, E.3
-
44
-
-
0023164845
-
Epidemiological investigations of the prevalence of von Willebrand's disease
-
Rodeghiero F, Castaman G, Dini E. Epidemiological investigation of the prevalence of von Willebrand's disease. Blood 1987; 69: 454-459. (Pubitemid 17022013)
-
(1987)
Blood
, vol.69
, Issue.2
, pp. 454-459
-
-
Rodeghiero, F.1
Castaman, G.2
Dini, E.3
-
45
-
-
33646455345
-
Dynamics and plasticity of Weibel-Palade bodies in endothelial cells
-
DOI 10.1161/01.ATV.0000209501.56852.6c, PII 0004360520060500000010
-
Rondaij MG, Bierings R, Kragt A et al. Dynamics and plasticity of Weibel-Palade bodies in endothelial cells. Arterioscler Thromb Vasc Biol 2006; 26: 1002-1007. (Pubitemid 43732104)
-
(2006)
Arteriosclerosis, Thrombosis, and Vascular Biology
, vol.26
, Issue.5
, pp. 1002-1007
-
-
Rondaij, M.G.1
Bierings, R.2
Kragt, A.3
Van Mourik, J.A.4
Voorberg, J.5
-
46
-
-
0032007271
-
Intracellular trafficking of factor VIII to von Willebrand factor storage granules
-
Rosenberg JB, Foster PA, Kaufman RJ et al. Intracellular trafficking of factor VIII to von Willebrand factor storage granules. J Clin Invest 1998; 101: 613-624. (Pubitemid 28084245)
-
(1998)
Journal of Clinical Investigation
, vol.101
, Issue.3
, pp. 613-624
-
-
Rosenberg, J.B.1
Foster, P.A.2
Kaufman, R.J.3
Vokac, E.A.4
Moussalli, M.5
Kroner, P.A.6
Montgomery, R.R.7
-
47
-
-
0036721163
-
The role of the D1 domain of the von Willebrand factor propeptide in multimerization of VWF
-
DOI 10.1182/blood-2002-03-0789
-
Rosenberg JB, Haberichter SL, Jozwiak MA et al. The role of the D1 domain of the von Willebrand factor propeptide in multimerization of VWF. Blood 2002; 100: 1699-1706. (Pubitemid 34925147)
-
(2002)
Blood
, vol.100
, Issue.5
, pp. 1699-1706
-
-
Rosenberg, J.B.1
Haberichter, S.L.2
Jozwiak, M.A.3
Vokac, E.A.4
Kroner, P.A.5
Fahs, S.A.6
Kawai, Y.7
Montgomery, R.R.8
-
48
-
-
0037369605
-
Differential intracellular trafficking of von Willebrand factor (vWF) and vWF propeptide in porcine endothelial cells lacking Weibel-Palade bodies and in human endothelial cells
-
DOI 10.1016/S0021-9150(02)00393-3, PII S0021915002003933
-
Royo T, Martinez-Gonzalez J, Vilahur G et al. Differential intracellular trafficking of von Willebrand factor (VWF) and VWF propeptide in porcine endothelial cells lacking Weibel-Palade bodies and in human endothelial cells. Atherosclerosis 2003; 167: 55-63. (Pubitemid 36255635)
-
(2003)
Atherosclerosis
, vol.167
, Issue.1
, pp. 55-63
-
-
Royo, T.1
Martinez-Gonzalez, J.2
Vilahur, G.3
Badimon, L.4
-
49
-
-
0031686041
-
Biochemistry and genetics of von Willebrand factor
-
DOI 10.1146/annurev.biochem.67.1.395
-
Sadler JE. Biochemistry and genetics of von Willebrand factor. Ann Rev Biochem 1998; 67: 395-424. (Pubitemid 28411134)
-
(1998)
Annual Review of Biochemistry
, vol.67
, pp. 395-424
-
-
Sadler, J.E.1
-
50
-
-
33748802581
-
Update on the pathophysiology and classification of von Willebrand disease: A report of the Subcommittee on von Willebrand factor
-
DOI 10.1111/j.1538-7836.2006.02146.x
-
Sadler JE, Budde U, Eikenboom JC et al. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor. J Thromb Haemost 2006; 4: 2103-2114. (Pubitemid 44403432)
-
(2006)
Journal of Thrombosis and Haemostasis
, vol.4
, Issue.10
, pp. 2103-2114
-
-
Sadler, J.E.1
Budde, U.2
Eikenboom, J.C.J.3
Favaloro, E.J.4
Hill, F.G.H.5
Holmberg, L.6
Ingerslev, J.7
Lee, C.A.8
Lillicrap, D.9
Mannucci, P.M.10
Mazurier, C.11
Meyer, D.12
Nichols, W.L.13
Nishino, M.14
Peake, I.R.15
Rodeghiero, F.16
Schneppenheim, R.17
Ruggeri, Z.M.18
Srivastava, A.19
Montgomery, R.R.20
Federici, A.B.21
more..
-
51
-
-
0029916821
-
Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease
-
Schneppenheim R, Brassard J, Krey S et al. Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease. Proc Natl Acad Sci USA 1996; 93: 3581-3586.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 3581-3586
-
-
Schneppenheim, R.1
Brassard, J.2
Krey, S.3
-
52
-
-
28444499005
-
Cysteine-mutations in von willebrand factor associated with increased clearance
-
DOI 10.1111/j.1538-7836.2005.01571.x
-
Schooten CJ, Tjernberg P, Westein E et al. Cysteine-mutations in von Willebrand factor associated with increased clearance. J Thromb Haemost 2005; 3: 2228-2237. (Pubitemid 41727201)
-
(2005)
Journal of Thrombosis and Haemostasis
, vol.3
, Issue.10
, pp. 2228-2237
-
-
Van Schooten, C.J.1
Tjernberg, P.2
Westein, E.3
Terraube, V.4
Castaman, G.5
Van Mourik, J.A.6
Hollestelle, M.J.7
Vos, H.L.8
Bertina, R.M.9
Van Den Berg, H.M.10
Eikenboom, J.C.J.11
Denis, C.V.12
Lenting, P.J.13
-
53
-
-
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: 185-190.
-
(1986)
Cell
, vol.46
, pp. 185-190
-
-
Sporn, L.A.1
Marder, V.J.2
Wagner, D.D.3
-
54
-
-
0023193482
-
Von Willebrand factor released from Weibel-Palade bodies binds more avidly to extracellular matrix than that secreted constitutively
-
Sporn LA, Marder VJ, Wagner DD. von Willebrand factor released from Weibel-Palade bodies binds more avidly to extracellular matrix than that secreted constitutively. Blood 1987; 69: 1531-1534.
-
(1987)
Blood
, vol.69
, pp. 1531-1534
-
-
Sporn, L.A.1
Marder, V.J.2
Wagner, D.D.3
-
55
-
-
33645837652
-
Homozygous C2362F von Willebrand factor induces intracellular retention of mutant von Willebrand factor resulting in autosomal recessive severe von Willebrand disease
-
Tjernberg P, Castaman G, Vos HL et al. Homo - zygous C2362F von Willebrand factor induces intracellular retention of mutant von Willebrand factor resulting in autosomal recessive severe von Willebrand disease. Br J Haematol 2006; 133: 409-418.
-
(2006)
Br J Haematol
, vol.133
, pp. 409-418
-
-
Tjernberg, P.1
Castaman, G.2
Vos, H.L.3
-
56
-
-
4644240711
-
Dimerization and multimerization defects of von Willebrand factor due to mutated cysteine residues
-
DOI 10.1111/j.1538-7836.2003.00435.x
-
Tjernberg P, Vos HL, Castaman G et al. Dimerization and multimerization defects of von Willebrand factor due to mutated cysteine residues. J Thromb Haemost 2004; 2: 257-265. (Pubitemid 40186039)
-
(2004)
Journal of Thrombosis and Haemostasis
, vol.2
, Issue.2
, pp. 257-265
-
-
Tjernberg, P.1
Vos, H.L.2
Castaman, G.3
Bertina, R.M.4
Eikenboom, J.C.J.5
-
57
-
-
33845369823
-
Differential effects of the loss of intrachain- Versus interchain-disulfide bonds in the cystine-knot domain of von Willebrand factor on the clinical phenotype of von Willebrand disease
-
DOI 10.1160/TH06-08-0460
-
Tjernberg P, Vos HL, Spaargaren-van Riel CC et al. Differential effects of the loss of intrachain- versus interchain-disulfide bonds in the cystine-knot domain of von Willebrand factor on the clinical phenotype of von Willebrand disease. Thromb Haemost 2006; 96: 717-724. (Pubitemid 44883810)
-
(2006)
Thrombosis and Haemostasis
, vol.96
, Issue.6
, pp. 717-724
-
-
Tjernberg, P.1
Vos, H.L.2
Spaargaren-van Riel, C.C.3
Luken, B.M.4
Voorberg, J.5
Bertina, R.M.6
Eikenboom, J.C.J.7
-
58
-
-
57749177100
-
ADAMTS-13 cleaves long von Willebrand factor multimeric strings anchored to endothelial cells in the absence of flow, platelets or conformation-altering chemicals
-
Turner N, Nolasco L, Dong JF et al. ADAMTS-13 cleaves long von Willebrand factor multimeric strings anchored to endothelial cells in the absence of flow, platelets or conformation-altering chemicals. J Thromb Haemost 2009; 7: 229-232.
-
(2009)
J Thromb Haemost
, vol.7
, pp. 229-232
-
-
Turner, N.1
Nolasco, L.2
Dong, J.F.3
-
59
-
-
40649126584
-
A new look at Weibel-Palade body structure in endothelial cells using electron tomography
-
Valentijn KM, Valentijn JA, Jansen KA et al. A new look at Weibel-Palade body structure in endothelial cells using electron tomography. J Struct Biol 2008; 161: 447-458.
-
(2008)
J Struct Biol
, vol.161
, pp. 447-458
-
-
Valentijn, K.M.1
Valentijn, J.A.2
Jansen, K.A.3
-
60
-
-
66049139957
-
Storage and regulated secretion of factor VIII in blood outgrowth endothelial cells
-
Van den Biggelaar M, Bouwens EA, Kootstra NA et al. Storage and regulated secretion of factor VIII in blood outgrowth endothelial cells. Haematologica 2009; 94: 670-678.
-
(2009)
Haematologica
, vol.94
, pp. 670-678
-
-
Van Den Biggelaar, M.1
Bouwens, E.A.2
Kootstra, N.A.3
-
61
-
-
63849281084
-
Intracellular cotrafficking of factor VIII and von Willebrand factor type 2N variants to storage organelles
-
Van den Biggelaar M, Meijer AB, Voorberg J et al. Intracellular cotrafficking of factor VIII and von Willebrand factor type 2N variants to storage organelles. Blood 2009; 113: 3102-3109.
-
(2009)
Blood
, vol.113
, pp. 3102-3109
-
-
Van Den Biggelaar, M.1
Meijer, A.B.2
Voorberg, J.3
-
62
-
-
0028242239
-
Von Willebrand factor proteolytic processing and multimerization precede the formation of Weibel-Palade bodies
-
Vischer UM, Wagner DD. Von Willebrand factor proteolytic processing and multimerization precede the formation of Weibel-Palade bodies. Blood 1994; 83: 3536-3544.
-
(1994)
Blood
, vol.83
, pp. 3536-3544
-
-
Vischer, U.M.1
Wagner, D.D.2
-
63
-
-
0027395949
-
Biogenesis of von Willebrand factor-containing organelles in heterologous transfected CV-1 cells
-
Voorberg J, Fontijn R, Calafat J et al. Biogenesis of von Willebrand factor-containing organelles in heterologous transfected CV-1 cells. EMBO J 1993; 12: 749-758. (Pubitemid 23073723)
-
(1993)
EMBO Journal
, vol.12
, Issue.2
, pp. 749-758
-
-
Voorberg, J.1
Fontijn, R.2
Calafat, J.3
Janssen, H.4
Van Mourik, J.A.5
Pannekoek, H.6
-
64
-
-
0025243601
-
Cell biology of von Willebrand factor
-
Wagner DD. Cell biology of von Willebrand factor. Annu Rev Cell Biol 1990; 6: 217-246.
-
(1990)
Annu Rev Cell Biol
, vol.6
, pp. 217-246
-
-
Wagner, D.D.1
-
65
-
-
0021874448
-
Inhibition of disulfide bonding of von Willebrand protein by monensin results in small, functionally defective multimers
-
DOI 10.1083/jcb.101.1.112
-
Wagner DD, Mayadas T, Urban-Pickering M et al. Inhibition of disulfide bonding of von Willebrand protein by monensin results in small, functionally defective multimers. J Cell Biol 1985; 101: 112-120. (Pubitemid 15061260)
-
(1985)
Journal of Cell Biology
, vol.101
, Issue.1
, pp. 112-120
-
-
Wagner, D.D.1
Mayadas, T.2
Urban-Pickering, M.3
-
66
-
-
0020355947
-
Immunolocalization of von Willebrand protein in Weibel-Palade bodies of human endothelial cells
-
Wagner DD, Olmsted JB, Marder VJ. Immunolocalization of von Willebrand protein in Weibel-Palade bodies of human endothelial cells. J Cell Biol 1982; 95: 355-360.
-
(1982)
J Cell Biol
, vol.95
, pp. 355-360
-
-
Wagner, D.D.1
Olmsted, J.B.2
Marder, V.J.3
-
67
-
-
0026020865
-
Induction of specific storage organelles by von willebrand factor propolypeptide
-
Wagner DD, Saffaripour S, Bonfanti R et al. Induction of specific storage organelles by von Willebrand factor propolypeptide. Cell 1991; 64: 403-413. (Pubitemid 121001264)
-
(1991)
Cell
, vol.64
, Issue.2
, pp. 403-413
-
-
Wagner, D.D.1
Saffaripour, S.2
Bonfanti, R.3
Sadler, J.E.4
Cramer, E.M.5
Chapman, B.6
Mayadas, T.N.7
-
68
-
-
0000534956
-
New cytoplasmic components in arterial endothelia
-
Weibel ER, Palade GE. New cytoplasmic components in arterial endothelia. J Cell Biol 1964; 23: 101-112.
-
(1964)
J Cell Biol
, vol.23
, pp. 101-112
-
-
Weibel, E.R.1
Palade, G.E.2
|