-
1
-
-
0026766155
-
The structure and function of von Willebrand Factor
-
Ruggeri ZM, Ware J. The structure and function of von Willebrand Factor. Thromb Haemost 1992; 67: 594-9.
-
(1992)
Thromb Haemost
, vol.67
, pp. 594-599
-
-
Ruggeri, Z.M.1
Ware, J.2
-
2
-
-
0027179089
-
Von Willebrand Factor - Structure and function
-
Meyer D, Girma JP. von Willebrand Factor - structure and function. Thromb Haemost 1993; 70: 99-104.
-
(1993)
Thromb Haemost
, vol.70
, pp. 99-104
-
-
Meyer, D.1
Girma, J.P.2
-
3
-
-
0022475523
-
Human von Willebrand Factor: A multivalent protein composed of identical subunits
-
Chopek MW, Girma JP, Fujikawa K, Davie EW, Titani K. Human von Willebrand Factor: a multivalent protein composed of identical subunits. Biochemistry 1986; 25: 3146-55.
-
(1986)
Biochemistry
, vol.25
, pp. 3146-3155
-
-
Chopek, M.W.1
Girma, J.P.2
Fujikawa, K.3
Davie, E.W.4
Titani, K.5
-
4
-
-
0022457087
-
Amino acid sequence of human von Willebrand Factor
-
Titani K, Kumar S, Ericsson LH, Wade RD, Ashida K, Walsh KA, Chopek MW, Sadler JE, Fujikawa K. Amino acid sequence of human von Willebrand Factor. Biochemistry 1986; 25: 3171-84.
-
(1986)
Biochemistry
, vol.25
, pp. 3171-3184
-
-
Titani, K.1
Kumar, S.2
Ericsson, L.H.3
Wade, R.D.4
Ashida, K.5
Walsh, K.A.6
Chopek, M.W.7
Sadler, J.E.8
Fujikawa, K.9
-
5
-
-
0024421750
-
Cross linking of a monomeric 39/34 kDa dispase fragment of von Willebrand Factor (Leu480/Val481-Gly718) to the N-terminal region of the α-chain of membrane glycoprotein Ib on the intact platelets with bis (sulfosuccinimidyl) suberate
-
Andrews RK, Gorman JJ, Booth WJ, Corino GL, Castaldi PA, Berndt MC. Cross linking of a monomeric 39/34 kDa dispase fragment of von Willebrand Factor (Leu480/Val481-Gly718) to the N-terminal region of the α-chain of membrane glycoprotein Ib on the intact platelets with bis (sulfosuccinimidyl) suberate. Biochemistry 1989; 28: 8326-36.
-
(1989)
Biochemistry
, vol.28
, pp. 8326-8336
-
-
Andrews, R.K.1
Gorman, J.J.2
Booth, W.J.3
Corino, G.L.4
Castaldi, P.A.5
Berndt, M.C.6
-
6
-
-
0023547917
-
Identification of disulfide-bridged substructures within human von Willebrand Factor
-
Marti T, Rösselet SJ, Titani K, Walsh KA. Identification of disulfide-bridged substructures within human von Willebrand Factor. Biochemistry 1987; 26: 8099-109.
-
(1987)
Biochemistry
, vol.26
, pp. 8099-8109
-
-
Marti, T.1
Rösselet, S.J.2
Titani, K.3
Walsh, K.A.4
-
7
-
-
0022517442
-
Subunit composition of plasma von Willebrand Factor. Cleavage is present in normal individuals, increased in type IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE)
-
Zimmerman TS, Dent JA, Ruggeri ZM, Nannini LH. Subunit composition of plasma von Willebrand Factor. Cleavage is present in normal individuals, increased in type IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE). J Clin Invest 1986; 77: 947-51.
-
(1986)
J Clin Invest
, vol.77
, pp. 947-951
-
-
Zimmerman, T.S.1
Dent, J.A.2
Ruggeri, Z.M.3
Nannini, L.H.4
-
8
-
-
0026069774
-
Heterogeneity of plasma von Willebrand Factor multimers resulting from proteolysis of the constituent subunit
-
Dent J A, Galbusera M, Ruggeri Z M. Heterogeneity of plasma von Willebrand Factor multimers resulting from proteolysis of the constituent subunit. J Clin Invest 1991; 88: 774-82.
-
(1991)
J Clin Invest
, vol.88
, pp. 774-782
-
-
Dent, J.A.1
Galbusera, M.2
Ruggeri, Z.M.3
-
9
-
-
0029925856
-
Partial purification and characterization of a protease from human plasma cleaving von Willebrand Factor to fragments produced by in vivo proteolysis
-
Furlan M, Robles R, Lammle B. Partial purification and characterization of a protease from human plasma cleaving von Willebrand Factor to fragments produced by in vivo proteolysis. Blood 1996; 87: 4223-34.
-
(1996)
Blood
, vol.87
, pp. 4223-4234
-
-
Furlan, M.1
Robles, R.2
Lammle, B.3
-
10
-
-
0029878123
-
Physiologic cleavage of von Willebrand Factor by a plasma protease is dependent on its conformation and requires calcium ion
-
Tsai HM. Physiologic cleavage of von Willebrand Factor by a plasma protease is dependent on its conformation and requires calcium ion. Blood 1996; 87: 4235-44.
-
(1996)
Blood
, vol.87
, pp. 4235-4244
-
-
Tsai, H.M.1
-
11
-
-
0023116024
-
Epitope mapping of the von Willebrand Factor sub-unit distinguishes fragments present in normal and type HA von Willebrand disease from those generated by plasmin
-
Berkowitz SD, Dent J, Roberts J, Fujimura Y, Plow EF, Titani K, Ruggeri ZM, Zimmerman TS. Epitope mapping of the von Willebrand Factor sub-unit distinguishes fragments present in normal and type HA von Willebrand disease from those generated by plasmin. J Clin Invest 1987; 79: 524-31.
-
(1987)
J Clin Invest
, vol.79
, pp. 524-531
-
-
Berkowitz, S.D.1
Dent, J.2
Roberts, J.3
Fujimura, Y.4
Plow, E.F.5
Titani, K.6
Ruggeri, Z.M.7
Zimmerman, T.S.8
-
12
-
-
0025044664
-
Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in type Ha von Willebrand Factor
-
Dent JA, Berkowitz SD, Ware J, Kasper CK, Ruggeri ZM. Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in type HA von Willebrand Factor. Proc Natl Acad Sci USA 1990; 87: 6306-10.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 6306-6310
-
-
Dent, J.A.1
Berkowitz, S.D.2
Ware, J.3
Kasper, C.K.4
Ruggeri, Z.M.5
-
13
-
-
0028201807
-
A revised classification of von Willebrand disease
-
Sadler JE. A revised classification of von Willebrand disease. Thromb Haemost 1994; 71: 520-5.
-
(1994)
Thromb Haemost
, vol.71
, pp. 520-525
-
-
Sadler, J.E.1
-
14
-
-
0026630044
-
Impaired intracellular transport produced by a subset of type-IIa von Willebrand disease mutations
-
Lyons SE, Brack ME, Bowie EJW, Ginsburg D. Impaired intracellular transport produced by a subset of type-IIA von Willebrand disease mutations. J Biol Chem 1992; 267: 4424-30.
-
(1992)
J Biol Chem
, vol.267
, pp. 4424-4430
-
-
Lyons, S.E.1
Brack, M.E.2
Bowie, E.J.W.3
Ginsburg, D.4
-
15
-
-
25344443362
-
A novel von Willebrand Factor, Arg611Cys or vWF Columbia, associated with a dominant von Willebrand disease variant
-
abstr
-
Hakami N, Shibuya H, Johnson GS, Stoy SJ, Huang THM, Montgomery RR. A novel von Willebrand Factor, Arg611Cys or vWF Columbia, associated with a dominant von Willebrand disease variant. Blood 1993; 82: 149a(abstr).
-
(1993)
Blood
, vol.82
-
-
Hakami, N.1
Shibuya, H.2
Johnson, G.S.3
Stoy, S.J.4
Huang, T.H.M.5
Montgomery, R.R.6
-
16
-
-
0028913947
-
A novel candidate mutation (Arg(611)→His) in type I 'platelet discordant' von Willebrand's disease with desmopressin-induced thrombocytopenia
-
Castaman G, Eikenboom JCJ, Rodeghiero F, Briët E, Reitsma PH. A novel candidate mutation (Arg(611)→His) in type I 'platelet discordant' von Willebrand's disease with desmopressin-induced thrombocytopenia. Br J Haematol 1995; 89: 656-8.
-
(1995)
Br J Haematol
, vol.89
, pp. 656-658
-
-
Castaman, G.1
Eikenboom, J.C.J.2
Rodeghiero, F.3
Briët, E.4
Reitsma, P.H.5
-
17
-
-
0029101406
-
Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand Factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF
-
Hubert L, Gaucher C, Mazurier C. Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand Factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF. Blood 1995; 86: 1010-8.
-
(1995)
Blood
, vol.86
, pp. 1010-1018
-
-
Hubert, L.1
Gaucher, C.2
Mazurier, C.3
-
18
-
-
0020699959
-
Heterogeneous abnormalities in the multimeric structure, antigenic properties, and plasma-platelet content of factor VIII/von Willebrand Factor in subtypes of classic (type I) and variant (type IIA) von Willebrand's disease
-
Weiss HJ, Pietu G, Rabinowitz R, Girma JP, Rogers J, Meyer D. Heterogeneous abnormalities in the multimeric structure, antigenic properties, and plasma-platelet content of factor VIII/von Willebrand Factor in subtypes of classic (type I) and variant (type IIA) von Willebrand's disease. J Lab Clin Med 1983; 101: 411-25.
-
(1983)
J Lab Clin Med
, vol.101
, pp. 411-425
-
-
Weiss, H.J.1
Pietu, G.2
Rabinowitz, R.3
Girma, J.P.4
Rogers, J.5
Meyer, D.6
-
19
-
-
0024425034
-
New variant of von Willebrand disease with defective binding to Factor VIII
-
Nishino M, Girma JP, Rothschild C, Fressinaud E, Meyer D. New variant of von Willebrand disease with defective binding to Factor VIII. Blood 1989; 5: 1591-9.
-
(1989)
Blood
, vol.5
, pp. 1591-1599
-
-
Nishino, M.1
Girma, J.P.2
Rothschild, C.3
Fressinaud, E.4
Meyer, D.5
-
20
-
-
0020068005
-
Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human Factor VIII/von Willebrand Factor and enhanced adsorption of its high-molecular-weight multimers
-
Weiss HJ, Meyer D, Rabinowitz R, Pietu G, Girma JP, Vicie WJ, Rogers J. Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human Factor VIII/von Willebrand Factor and enhanced adsorption of its high-molecular-weight multimers. N Engl J Med 1982; 306: 326-33.
-
(1982)
N Engl J Med
, vol.306
, pp. 326-333
-
-
Weiss, H.J.1
Meyer, D.2
Rabinowitz, R.3
Pietu, G.4
Girma, J.P.5
Vicie, W.J.6
Rogers, J.7
-
21
-
-
0016689054
-
Platelets fixed with paraformaldehyde: A new reagent for assay of von Willebrand Factor and platelet aggregating factor
-
Allain JP, Cooper HA, Wagner RH, Brinkhous KM. Platelets fixed with paraformaldehyde: a new reagent for assay of von Willebrand Factor and platelet aggregating factor. J Lab Clin Med 1975; 85: 318-28.
-
(1975)
J Lab Clin Med
, vol.85
, pp. 318-328
-
-
Allain, J.P.1
Cooper, H.A.2
Wagner, R.H.3
Brinkhous, K.M.4
-
22
-
-
0021184617
-
Hybridoma antibodies to human von Willebrand Factor. I. Characterization of seven clone
-
Meyer D, Zimmerman TS, Obert B, Edgington TS. Hybridoma antibodies to human von Willebrand Factor. I. Characterization of seven clone. Br J Haematol 1984; 57: 597-608.
-
(1984)
Br J Haematol
, vol.57
, pp. 597-608
-
-
Meyer, D.1
Zimmerman, T.S.2
Obert, B.3
Edgington, T.S.4
-
23
-
-
0028291511
-
Influence of mutations and size of multimers in type II von Willebrand disease upon the function of von Willebrand Factor
-
Christophe O, Ribba AS, Baruch D, Obert B, Rouault C, Niinomi K, Pietu G, Meyer D, Girma JP. Influence of mutations and size of multimers in type II von Willebrand disease upon the function of von Willebrand Factor. Blood 1994; 83: 3553-61.
-
(1994)
Blood
, vol.83
, pp. 3553-3561
-
-
Christophe, O.1
Ribba, A.S.2
Baruch, D.3
Obert, B.4
Rouault, C.5
Niinomi, K.6
Pietu, G.7
Meyer, D.8
Girma, J.P.9
-
24
-
-
0028242921
-
Epitope mapping of inhibitory monoclonal antibodies to human von Willebrand Factor by using recombinant cDNA libraries
-
Pietu G, Ribba A S, Cherel G, Siguret V, Obert B, Rouault C, Ginsburg D, Meyer D. Epitope mapping of inhibitory monoclonal antibodies to human von Willebrand Factor by using recombinant cDNA libraries. Thromb Haemost 1994; 71: 788-92.
-
(1994)
Thromb Haemost
, vol.71
, pp. 788-792
-
-
Pietu, G.1
Ribba, A.S.2
Cherel, G.3
Siguret, V.4
Obert, B.5
Rouault, C.6
Ginsburg, D.7
Meyer, D.8
-
25
-
-
0018099888
-
"Variants" of von Willebrand's disease. Demonstration of a decreased anti-genic reactivity by immunoradiometric assay
-
Ardaillou N, Girma JP, Meyer D, Lavergne JM, Shoa'i I, Larrieu MJ. "Variants" of von Willebrand's disease. Demonstration of a decreased anti-genic reactivity by immunoradiometric assay. Thromb Res 1978; 12: 817-30.
-
(1978)
Thromb Res
, vol.12
, pp. 817-830
-
-
Ardaillou, N.1
Girma, J.P.2
Meyer, D.3
Lavergne, J.M.4
ShoA'I, I.5
Larrieu, M.J.6
-
26
-
-
0022547632
-
Limited proteolysis of human von Willebrand Factor by staphylococcus aureus V-8 protease: Isolation and partial characterization of a platelet-binding domain
-
Girma JP, Chopek MW, Titani K, Davie EW. Limited proteolysis of human von Willebrand Factor by staphylococcus aureus V-8 protease: isolation and partial characterization of a platelet-binding domain. Biochemistry 1986; 25: 3156-63.
-
(1986)
Biochemistry
, vol.25
, pp. 3156-3163
-
-
Girma, J.P.1
Chopek, M.W.2
Titani, K.3
Davie, E.W.4
-
27
-
-
0026066834
-
The binding domain of von Willebrand Factor to sulfatides is distinct from those interacting with glycoprotein Ib, heparin, and collagen and resides between amino acid residues Leu512 and Lys673
-
Christophe O, Oben B, Meyer D, Girma JP. The binding domain of von Willebrand Factor to sulfatides is distinct from those interacting with glycoprotein Ib, heparin, and collagen and resides between amino acid residues Leu512 and Lys673. Blood 1991; 78: 2310-7.
-
(1991)
Blood
, vol.78
, pp. 2310-2317
-
-
Christophe, O.1
Oben, B.2
Meyer, D.3
Girma, J.P.4
-
28
-
-
0029076691
-
A monoclonal antibody (B724) to von Willebrand Factor recognizing an epitope within the A1 disulphide loop (Cys509-Cys695) discriminates between type 2A and type 2B von Willebrand disease
-
Christophe O, Rouault C, Obert B, Pietu G, Meyer D, Girma JP. A monoclonal antibody (B724) to von Willebrand Factor recognizing an epitope within the A1 disulphide loop (Cys509-Cys695) discriminates between type 2A and type 2B von Willebrand disease. Br J Haematol 1995; 90: 195-203.
-
(1995)
Br J Haematol
, vol.90
, pp. 195-203
-
-
Christophe, O.1
Rouault, C.2
Obert, B.3
Pietu, G.4
Meyer, D.5
Girma, J.P.6
-
29
-
-
0024268037
-
Abnormality of the N-terminal portion of von Willebrand Factor in type IIA and IIC von Willebrand disease
-
Takahashi Y, Kalafatis M, Girma JP, Meyer D. Abnormality of the N-terminal portion of von Willebrand Factor in type IIA and IIC von Willebrand disease. Thromb Haemost 1988; 60: 498-505.
-
(1988)
Thromb Haemost
, vol.60
, pp. 498-505
-
-
Takahashi, Y.1
Kalafatis, M.2
Girma, J.P.3
Meyer, D.4
-
30
-
-
0014949207
-
Cleavage of structural proteins during the assembly of the head of the bacteriophage T4
-
Laemmli UK. Cleavage of structural proteins during the assembly of the head of the bacteriophage T4. Nature 1970; 227: 680-5.
-
(1970)
Nature
, vol.227
, pp. 680-685
-
-
Laemmli, U.K.1
-
31
-
-
0016711037
-
High resolution two-dimensional electrophoresis of proteins
-
O'Parrel PH. High resolution two-dimensional electrophoresis of proteins. J Biol Chem 1975; 250: 4007-21.
-
(1975)
J Biol Chem
, vol.250
, pp. 4007-4021
-
-
O'Parrel, P.H.1
-
32
-
-
0009482260
-
Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications
-
Towbin H, Stachelin T, Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci USA 1979; 76: 4350-4.
-
(1979)
Proc Natl Acad Sci USA
, vol.76
, pp. 4350-4354
-
-
Towbin, H.1
Stachelin, T.2
Gordon, J.3
-
33
-
-
0021610573
-
Improved technique utilizing nonfat dry milk for analysis of proteins and nucleic acids transferred to nitrocellulose
-
Johnson DA, Gautsch JW, Sportman JR, Elder JH. Improved technique utilizing nonfat dry milk for analysis of proteins and nucleic acids transferred to nitrocellulose. Gene Anal Techn 1984; 1: 3-8.
-
(1984)
Gene Anal Techn
, vol.1
, pp. 3-8
-
-
Johnson, D.A.1
Gautsch, J.W.2
Sportman, J.R.3
Elder, J.H.4
-
34
-
-
0020637308
-
India ink staining of proteins on nitrocellulose paper
-
Hancock K, Tsang VCW. India ink staining of proteins on nitrocellulose paper. Anal Biochem 1983; 133: 157-62.
-
(1983)
Anal Biochem
, vol.133
, pp. 157-162
-
-
Hancock, K.1
Tsang, V.C.W.2
-
35
-
-
0019442145
-
The complex multimeric composition of Factor VIII/von Willebrand Factor
-
Ruggeri ZM, Zimmerman TS. The complex multimeric composition of Factor VIII/von Willebrand Factor. Blood 1981; 57: 1140-3.
-
(1981)
Blood
, vol.57
, pp. 1140-1143
-
-
Ruggeri, Z.M.1
Zimmerman, T.S.2
-
36
-
-
0017874586
-
Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a, 6a-diphenylglycoluril
-
Fraker PJ, Speck JC. Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a, 6a-diphenylglycoluril. Biochem Biophys Res Commun 1978; 80: 849-57.
-
(1978)
Biochem Biophys Res Commun
, vol.80
, pp. 849-857
-
-
Fraker, P.J.1
Speck, J.C.2
-
37
-
-
0025986662
-
Duplication of a methionine within the glycoprotein Ib binding domain of von Willebrand Factor detected by denaturing gradient gel electrophoresis in a patient with type-IIB von Willebrand disease
-
Ribba AS, Lavergne JM, Bahnak BR, Derlon A, Pietu G, Meyer D. Duplication of a methionine within the glycoprotein Ib binding domain of von Willebrand Factor detected by denaturing gradient gel electrophoresis in a patient with type-IIB von Willebrand disease. Blood 1991; 78: 1738-43.
-
(1991)
Blood
, vol.78
, pp. 1738-1743
-
-
Ribba, A.S.1
Lavergne, J.M.2
Bahnak, B.R.3
Derlon, A.4
Pietu, G.5
Meyer, D.6
-
38
-
-
0027422221
-
Functional analysis of the Arg91Gln substitution in the Factor-VIII binding domain of von Willebrand Factor demonstrates variable phenotypic expression
-
Lavergne JM, Piao Y, Ribba AS, Girma JP, Siguret V, Pietu G, Boyer-Neumann C, Schandelong A, Bahnak BR, Meyer D. Functional analysis of the Arg91Gln substitution in the Factor-VIII binding domain of von Willebrand Factor demonstrates variable phenotypic expression. Thromb Haemost 1993; 70: 691-6.
-
(1993)
Thromb Haemost
, vol.70
, pp. 691-696
-
-
Lavergne, J.M.1
Piao, Y.2
Ribba, A.S.3
Girma, J.P.4
Siguret, V.5
Pietu, G.6
Boyer-Neumann, C.7
Schandelong, A.8
Bahnak, B.R.9
Meyer, D.10
-
40
-
-
0028205622
-
Proteolytic processing of von Willebrand Factor subunit - Heterogeneity in Type-IIA von Willebrand disease
-
Batlle J, Lasierra J, Villamor AF, Navarro JL, Pardo A, Campos M, Justice B, Fernandez MFL. Proteolytic processing of von Willebrand Factor subunit - heterogeneity in Type-IIA von Willebrand disease. Ann Hematol 1994; 68: 111-5.
-
(1994)
Ann Hematol
, vol.68
, pp. 111-115
-
-
Batlle, J.1
Lasierra, J.2
Villamor, A.F.3
Navarro, J.L.4
Pardo, A.5
Campos, M.6
Justice, B.7
Fernandez, M.F.L.8
-
41
-
-
0023483277
-
Expression of abnormal von Willebrand Factor by endothelial cells from a patient with type IIa von Willebrand disease
-
Levene RB, Booyse FM, Chediak J, Zimmerman TS, Livingston DM, Lynch DC. 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: 6550-4.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, 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
-
42
-
-
0023217139
-
A major Factor VIII binding domain resides within the amino-terminal 272 amino acid residues of von Willebrand Factor
-
Foster PA, Fulcher CA, Marti T, Titani K, Zimmerman TS. A major Factor VIII binding domain resides within the amino-terminal 272 amino acid residues of von Willebrand Factor. J Biol Chem 1987; 262: 8443-6.
-
(1987)
J Biol Chem
, vol.262
, pp. 8443-8446
-
-
Foster, P.A.1
Fulcher, C.A.2
Marti, T.3
Titani, K.4
Zimmerman, T.S.5
|