-
1
-
-
0021750055
-
Characterization of the human factor VIII gene
-
Gitschier J., Wood W.I., Goralka T.M., Wion K.L., Chen E.Y., Eaton D.H., et al. Characterization of the human factor VIII gene. Nature. 312:1984;326-330
-
(1984)
Nature
, vol.312
, pp. 326-330
-
-
Gitschier, J.1
Wood, W.I.2
Goralka, T.M.3
Wion, K.L.4
Chen, E.Y.5
Eaton, D.H.6
-
2
-
-
0021715168
-
Expression of active human factor VIII from recombinant DNA clones
-
Wood W.I., Capon D.J., Simonsen C.C., Eaton D.L., Gitschier J., Keyt B., et al. Expression of active human factor VIII from recombinant DNA clones. Nature. 312:1984;330-337
-
(1984)
Nature
, vol.312
, pp. 330-337
-
-
Wood, W.I.1
Capon, D.J.2
Simonsen, C.C.3
Eaton, D.L.4
Gitschier, J.5
Keyt, B.6
-
3
-
-
0021715169
-
Molecular cloning of a cDNA encoding human antihaemophilic factor
-
Toole J.J., Knopf J.L., Wozney J.M., Sultzman L.A., Buecker J.L., Pittman D.D., et al. Molecular cloning of a cDNA encoding human antihaemophilic factor. Nature. 312:1984;342-347
-
(1984)
Nature
, vol.312
, pp. 342-347
-
-
Toole, J.J.1
Knopf, J.L.2
Wozney, J.M.3
Sultzman, L.A.4
Buecker, J.L.5
Pittman, D.D.6
-
4
-
-
0031804517
-
The factor VIII structure and mutation resource site: HAMSTeRS version 4
-
Kemball-Cook G., Tuddenham E.G.D., Wacey A.I. The factor VIII structure and mutation resource site: HAMSTeRS version 4. Nucleic Acids Res. 26:1998;216-219
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 216-219
-
-
Kemball-Cook, G.1
Tuddenham, E.G.D.2
Wacey, A.I.3
-
5
-
-
0035964179
-
Metal ion-independent association of factor VIII subunits and the roles of calcium and copper ions for cofactor activity and inter-subunit affinity
-
Wakabayashi H., Koszelak M.E., Mastri M., Fay P.J. Metal ion-independent association of factor VIII subunits and the roles of calcium and copper ions for cofactor activity and inter-subunit affinity. Biochemistry. 40:2001;10293-10300
-
(2001)
Biochemistry
, vol.40
, pp. 10293-10300
-
-
Wakabayashi, H.1
Koszelak, M.E.2
Mastri, M.3
Fay, P.J.4
-
6
-
-
0023918416
-
Reconstitution of human factor VIII from isolated subunits
-
Fay P.J. Reconstitution of human factor VIII from isolated subunits. Arch. Biochem. Biophys. 262:1988;525-531
-
(1988)
Arch. Biochem. Biophys.
, vol.262
, pp. 525-531
-
-
Fay, P.J.1
-
7
-
-
0029841943
-
Exposed hydrophobic sites in factor VIII and isolated subunits
-
Sudhakar K., Fay P.J. Exposed hydrophobic sites in factor VIII and isolated subunits. J. Biol. Chem. 271:1996;23015-23021
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 23015-23021
-
-
Sudhakar, K.1
Fay, P.J.2
-
8
-
-
0028358217
-
Copper-atom identification in the active and inactive forms of plasma-derived FVIII and recombinant FVIII-ΔII
-
Bihoreau N., Pin S., Kersabiec A.M.D., Vodot F., Fontaine-Aupart M.P. Copper-atom identification in the active and inactive forms of plasma-derived FVIII and recombinant FVIII-ΔII. Eur. J. Biochem. 220:1994;41-48
-
(1994)
Eur. J. Biochem.
, vol.220
, pp. 41-48
-
-
Bihoreau, N.1
Pin, S.2
Kersabiec, A.M.D.3
Vodot, F.4
Fontaine-Aupart, M.P.5
-
9
-
-
0030783138
-
Identification and functional requirement of Cu(I) and its ligands within coagulation factor VIII
-
Tagliavacca L., Moon N., Dunham W.R., Kaufman R.J. Identification and functional requirement of Cu(I) and its ligands within coagulation factor VIII. J. Biol. Chem. 272:1997;27428-27434
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 27428-27434
-
-
Tagliavacca, L.1
Moon, N.2
Dunham, W.R.3
Kaufman, R.J.4
-
10
-
-
0021677942
-
Structure of human factor VIII
-
Vehar G.A., Keyt B., Eaton D., Rodriguez H., O'Brien D.P., Rotblat F., et al. Structure of human factor VIII. Nature. 312:1984;337-342
-
(1984)
Nature
, vol.312
, pp. 337-342
-
-
Vehar, G.A.1
Keyt, B.2
Eaton, D.3
Rodriguez, H.4
O'Brien, D.P.5
Rotblat, F.6
-
11
-
-
0030903424
-
A molecular model for the triplicated a domains of human factor VIII based on the crystal structure of human ceruloplasmin
-
Pemberton S., Lindley P., Zaitsev V., Card G., Tuddenham E.G., Kemball-Cook G. A molecular model for the triplicated A domains of human factor VIII based on the crystal structure of human ceruloplasmin. Blood. 89:1997;2413-2421
-
(1997)
Blood
, vol.89
, pp. 2413-2421
-
-
Pemberton, S.1
Lindley, P.2
Zaitsev, V.3
Card, G.4
Tuddenham, E.G.5
Kemball-Cook, G.6
-
12
-
-
9644282804
-
Copper binding site(s) in factor VIII involved in the regulation of cofactor specific activity
-
Wakabayashi H., Zhou Q., Fay P.J. Copper binding site(s) in factor VIII involved in the regulation of cofactor specific activity. J. Thromb. Haemost. (Suppl.):2003;OC112
-
(2003)
J. Thromb. Haemost. Suppl.
, pp. 112
-
-
Wakabayashi, H.1
Zhou, Q.2
Fay, P.J.3
-
13
-
-
0035827682
-
2+-dependent complex of fragments bound to phospholipid
-
2+-dependent complex of fragments bound to phospholipid. J. Biol. Chem. 276:2001;19929-19936
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 19929-19936
-
-
Zeibdawi, A.R.1
Pryzdial, E.L.2
-
14
-
-
0024509988
-
The reassociation of factor Va from its isolated subunits
-
Krishnaswamy S., Russell G.D., Mann K.G. The reassociation of factor Va from its isolated subunits. J. Biol. Chem. 264:1989;3160-3168
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 3160-3168
-
-
Krishnaswamy, S.1
Russell, G.D.2
Mann, K.G.3
-
15
-
-
0037007964
-
Ca(2+) binding to both the heavy and light chains of factor VIII is required for cofactor activity
-
Wakabayashi H., Schmidt K.M., Fay P.J. Ca(2+) binding to both the heavy and light chains of factor VIII is required for cofactor activity. Biochemistry. 41:2002;8485-8492
-
(2002)
Biochemistry
, vol.41
, pp. 8485-8492
-
-
Wakabayashi, H.1
Schmidt, K.M.2
Fay, P.J.3
-
18
-
-
1042276751
-
Activation of factor VIII and mechanisms of cofactor action
-
Fay P.J. Activation of factor VIII and mechanisms of cofactor action. Blood Rev. 18:2004;1-15
-
(2004)
Blood Rev.
, vol.18
, pp. 1-15
-
-
Fay, P.J.1
-
19
-
-
0021726422
-
Comparisons of one-stage and two-stage assays of Factor VIII:C
-
Barrowcliffe T.W. Comparisons of one-stage and two-stage assays of Factor VIII:C. Scand. J. Haematol. 41(Suppl.):1984;39-54
-
(1984)
Scand. J. Haematol.
, vol.41
, Issue.SUPPL.
, pp. 39-54
-
-
Barrowcliffe, T.W.1
-
20
-
-
0028022060
-
Familial discrepancy between the one-stage and two-stage factor VIII methods in a subgroup of patients with haemophilia a
-
Duncan E.M., Duncan B.M., Tunbridge L.J., Lloyd J.V. Familial discrepancy between the one-stage and two-stage factor VIII methods in a subgroup of patients with haemophilia A. Br. J. Haematol. 87:1994;846-848
-
(1994)
Br. J. Haematol.
, vol.87
, pp. 846-848
-
-
Duncan, E.M.1
Duncan, B.M.2
Tunbridge, L.J.3
Lloyd, J.V.4
-
21
-
-
0029886287
-
Mutations in a subgroup of patients with mild haemophilia a and a familial discrepancy between the one-stage and two-stage factor VIII:C methods
-
Rudzki Z., Duncan E.M., Casey G.J., Neumann M., Favaloro E.J., Lloyd J.V. Mutations in a subgroup of patients with mild haemophilia A and a familial discrepancy between the one-stage and two-stage factor VIII:C methods. Br. J. Haematol. 94:1996;400-406
-
(1996)
Br. J. Haematol.
, vol.94
, pp. 400-406
-
-
Rudzki, Z.1
Duncan, E.M.2
Casey, G.J.3
Neumann, M.4
Favaloro, E.J.5
Lloyd, J.V.6
-
22
-
-
0032932325
-
Mild hemophilia a caused by increased rate of factor VIII A2 subunit dissociation. evidence for nonproteolytic inactivation of factor VIIIa in vivo
-
Pipe S.W., Eickhorst A.N., McKinley S.H., Saenko E.L., Kaufman R.J. Mild hemophilia A caused by increased rate of factor VIII A2 subunit dissociation. evidence for nonproteolytic inactivation of factor VIIIa in vivo. Blood. 93:1999;176-183
-
(1999)
Blood
, vol.93
, pp. 176-183
-
-
Pipe, S.W.1
Eickhorst, A.N.2
McKinley, S.H.3
Saenko, E.L.4
Kaufman, R.J.5
-
23
-
-
0035254221
-
Hemophilia a mutations associated with 1-stage/2-stage activity discrepancy disrupt protein-protein interactions within the triplicated a domains of thrombin-activated factor VIIIa
-
Pipe S.W., Saenko E.L., Eickhorst A.N., Kemball-Cook G., Kaufman R.J. Hemophilia A mutations associated with 1-stage/2-stage activity discrepancy disrupt protein-protein interactions within the triplicated A domains of thrombin-activated factor VIIIa. Blood. 97:2001;685-691
-
(2001)
Blood
, vol.97
, pp. 685-691
-
-
Pipe, S.W.1
Saenko, E.L.2
Eickhorst, A.N.3
Kemball-Cook, G.4
Kaufman, R.J.5
-
24
-
-
0036845615
-
Hemophilia a mutations within the factor VIII A2-A3 subunit interface destabilize factor VIIIa and cause one-stage/two-stage activity discrepancy
-
Hakeos W.H., Miao H., Sirachainan N., Kemball-Cook G., Saenko E.L., Kaufman R.J., et al. Hemophilia A mutations within the factor VIII A2-A3 subunit interface destabilize factor VIIIa and cause one-stage/two-stage activity discrepancy. Thromb. Haemost. 88:2002;781-787
-
(2002)
Thromb. Haemost.
, vol.88
, pp. 781-787
-
-
Hakeos, W.H.1
Miao, H.2
Sirachainan, N.3
Kemball-Cook, G.4
Saenko, E.L.5
Kaufman, R.J.6
-
25
-
-
0032402122
-
The life cycle of coagulation factor VIII in view of its structure and function
-
Lenting P.J., van Mourik J.A., Mertens K. The life cycle of coagulation factor VIII in view of its structure and function. Blood. 92:1998;3983-3996
-
(1998)
Blood
, vol.92
, pp. 3983-3996
-
-
Lenting, P.J.1
Van Mourik, J.A.2
Mertens, K.3
-
27
-
-
0024497345
-
The interaction between human blood-coagulation factor VIII and von Willebrand factor. Characterization of a high-affinity binding site on factor VIII
-
Leyte A., Verbeet M.P., Brodniewicz-Proba T., Van Mourik J.A., Mertens K. The interaction between human blood-coagulation factor VIII and von Willebrand factor. Characterization of a high-affinity binding site on factor VIII. Biochem. J. 257:1989;679-683
-
(1989)
Biochem. J.
, vol.257
, pp. 679-683
-
-
Leyte, A.1
Verbeet, M.P.2
Brodniewicz-Proba, T.3
Van Mourik, J.A.4
Mertens, K.5
-
28
-
-
0027457180
-
A factor VIII neutralizing monoclonal antibody and a human inhibitor alloantibody recognizing epitopes in the C2 domain inhibit factor VIII binding to von Willebrand factor and to phosphatidylserine
-
Shima M., Scandella D., Yoshioka A., Nakai H., Tanaka I., Kamisue S., et al. A factor VIII neutralizing monoclonal antibody and a human inhibitor alloantibody recognizing epitopes in the C2 domain inhibit factor VIII binding to von Willebrand factor and to phosphatidylserine. Thromb. Haemost. 69:1993;240-246
-
(1993)
Thromb. Haemost.
, vol.69
, pp. 240-246
-
-
Shima, M.1
Scandella, D.2
Yoshioka, A.3
Nakai, H.4
Tanaka, I.5
Kamisue, S.6
-
29
-
-
0030800963
-
The acidic region of the Factor VIII light chain and the C2 domain together form the high affinity binding site for von Willebrand factor
-
Saenko E.L., Scandella D. The acidic region of the Factor VIII light chain and the C2 domain together form the high affinity binding site for von Willebrand factor. J. Biol. Chem. 272:1997;18007-18014
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 18007-18014
-
-
Saenko, E.L.1
Scandella, D.2
-
30
-
-
0033962015
-
A human antibody directed to the factor VIII C1 domain inhibits factor VIII cofactor activity and binding to von Willebrand factor
-
Jacquemin M., Benhida A., Peerlinck K., Desqueper B., Vander Elst L., Lavend'homme R., et al. A human antibody directed to the factor VIII C1 domain inhibits factor VIII cofactor activity and binding to von Willebrand factor. Blood. 95:2000;156-163
-
(2000)
Blood
, vol.95
, pp. 156-163
-
-
Jacquemin, M.1
Benhida, A.2
Peerlinck, K.3
Desqueper, B.4
Vander Elst, L.5
Lavend'Homme, R.6
-
31
-
-
0025924755
-
Sulfation of Tyr1680 of human blood coagulation factor VIII is essential for the interaction of factor VIII with von Willebrand factor
-
Leyte A., van Schijndel H.B., Niehrs C., Huttner W.B., Verbeet M.P., Mertens K., et al. Sulfation of Tyr1680 of human blood coagulation factor VIII is essential for the interaction of factor VIII with von Willebrand factor. J. Biol. Chem. 266:1991;740-746
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 740-746
-
-
Leyte, A.1
Van Schijndel, H.B.2
Niehrs, C.3
Huttner, W.B.4
Verbeet, M.P.5
Mertens, K.6
-
32
-
-
0028887059
-
Characterization of mutations within the factor VIII gene of 73 unrelated mild and moderate haemophiliacs
-
Schwaab R., Oldenburg J., Schwaab U., Johnson D.J., Schmidt W., Olek K., et al. Characterization of mutations within the factor VIII gene of 73 unrelated mild and moderate haemophiliacs. Br. J. Haematol. 91:1995;458-464
-
(1995)
Br. J. Haematol.
, vol.91
, pp. 458-464
-
-
Schwaab, R.1
Oldenburg, J.2
Schwaab, U.3
Johnson, D.J.4
Schmidt, W.5
Olek, K.6
-
33
-
-
0033604501
-
Structure of the C2 domain of human factor VIII at 1.5 a resolution
-
Pratt K.P., Shen B.W., Takeshima K., Davie E.W., Fujikawa K., Stoddard B.L. Structure of the C2 domain of human factor VIII at 1.5 A resolution. Nature. 402:1999;439-442
-
(1999)
Nature
, vol.402
, pp. 439-442
-
-
Pratt, K.P.1
Shen, B.W.2
Takeshima, K.3
Davie, E.W.4
Fujikawa, K.5
Stoddard, B.L.6
-
34
-
-
0034254264
-
Hemophilic factor VIII C1- and C2-domain missense mutations and their modeling to the 1.5-angstrom human C2-domain crystal structure
-
Liu M.L., Shen B.W., Nakaya S., Pratt K.P., Fujikawa K., Davie E.W., et al. Hemophilic factor VIII C1- and C2-domain missense mutations and their modeling to the 1.5-angstrom human C2-domain crystal structure. Blood. 96:2000;979-987
-
(2000)
Blood
, vol.96
, pp. 979-987
-
-
Liu, M.L.1
Shen, B.W.2
Nakaya, S.3
Pratt, K.P.4
Fujikawa, K.5
Davie, E.W.6
-
35
-
-
0024361839
-
In situ-generated thrombin is the only enzyme that effectively activates factor VIII and factor V in thromboplastin-activated plasma
-
Pieters J., Lindhout T., Hemker H.C. In situ-generated thrombin is the only enzyme that effectively activates factor VIII and factor V in thromboplastin-activated plasma. Blood. 74:1989;1021-1024
-
(1989)
Blood
, vol.74
, pp. 1021-1024
-
-
Pieters, J.1
Lindhout, T.2
Hemker, H.C.3
-
36
-
-
0035853784
-
Cleavage of factor VIII heavy chain is required for the functional interaction of A2 subunit with factor IXa
-
Fay P.J., Mastri M., Koszelak M.E., Wakabayashi H. Cleavage of factor VIII heavy chain is required for the functional interaction of A2 subunit with factor IXa. J. Biol. Chem. 276:2001;12434-12439
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 12434-12439
-
-
Fay, P.J.1
Mastri, M.2
Koszelak, M.E.3
Wakabayashi, H.4
-
37
-
-
0023677854
-
Association of the factor VIII light chain with von Willebrand factor
-
Lollar P., Hill-Eubanks D.C., Parker C.G. Association of the factor VIII light chain with von Willebrand factor. J. Biol. Chem. 263:1988;10451-10455
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 10451-10455
-
-
Lollar, P.1
Hill-Eubanks, D.C.2
Parker, C.G.3
-
38
-
-
0028933042
-
Cleavage of factor VIII light chain is required for maximal generation of factor VIIIa activity
-
Regan L.M., Fay P.J. Cleavage of factor VIII light chain is required for maximal generation of factor VIIIa activity. J. Biol. Chem. 270:1995;8546-8552
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 8546-8552
-
-
Regan, L.M.1
Fay, P.J.2
-
39
-
-
0028919216
-
The role of cleavage of the light chain at positions Arg1689 or Arg1721 in subunit interaction and activation of human blood coagulation factor VIII
-
Donath M.S., Lenting P.J., van Mourik J.A., Mertens K. The role of cleavage of the light chain at positions Arg1689 or Arg1721 in subunit interaction and activation of human blood coagulation factor VIII. J. Biol. Chem. 270:1995;3648-3655
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 3648-3655
-
-
Donath, M.S.1
Lenting, P.J.2
Van Mourik, J.A.3
Mertens, K.4
-
40
-
-
2242455930
-
Extended interactions with prothrombinase enforce affinity and specificity for its macromolecular substrate
-
Orcutt S.J., Pietropaolo C., Krishnaswamy S. Extended interactions with prothrombinase enforce affinity and specificity for its macromolecular substrate. J. Biol. Chem. 277:2002;46191-46196
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 46191-46196
-
-
Orcutt, S.J.1
Pietropaolo, C.2
Krishnaswamy, S.3
-
41
-
-
0028052967
-
Inhibition by heparin of thrombin-catalyzed activation of the factor VIII-von Willebrand factor complex
-
Barrow R.T., Healey J.F., Lollar P. Inhibition by heparin of thrombin-catalyzed activation of the factor VIII-von Willebrand factor complex. J. Biol. Chem. 269:1994;593-598
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 593-598
-
-
Barrow, R.T.1
Healey, J.F.2
Lollar, P.3
-
42
-
-
0029935853
-
Involvement of thrombin anion-binding exosites 1 and 2 in the activation of factor V and factor VIII
-
Esmon C.T., Lollar P. Involvement of thrombin anion-binding exosites 1 and 2 in the activation of factor V and factor VIII. J. Biol. Chem. 271:1996;13882-13887
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 13882-13887
-
-
Esmon, C.T.1
Lollar, P.2
-
43
-
-
0037108447
-
Structural requirements for the activation of human factor VIII by thrombin
-
Myles T., Yun T.H., Leung L.L. Structural requirements for the activation of human factor VIII by thrombin. Blood. 100:2002;2820-2826
-
(2002)
Blood
, vol.100
, pp. 2820-2826
-
-
Myles, T.1
Yun, T.H.2
Leung, L.L.3
-
44
-
-
4243553807
-
Unusual discrepant factor VIII:C assays in heamoplilia a in patients with Tyr346Cys and Glu321Lys FVIII gene mutations
-
Goodeve A.C., Hinks J.L., Nesbitt I.M., Sampson B., Burgess C., Khair K., et al. Unusual discrepant factor VIII:C assays in heamoplilia A in patients with Tyr346Cys and Glu321Lys FVIII gene mutations. Thromb. Haemost. (Suppl.):2001;P1370
-
(2001)
Thromb. Haemost. Suppl.
, pp. 1370
-
-
Goodeve, A.C.1
Hinks, J.L.2
Nesbitt, I.M.3
Sampson, B.4
Burgess, C.5
Khair, K.6
-
45
-
-
0035982216
-
A Tyr346 → Cys substitution in the interdomain acidic region a1 of factor VIII in an individual with factor VIII:C assay discrepancy
-
Mumford A.D., Laffan M., O'Donnell J., McVey J.H., Johnson D.J., Manning R.A., et al. A Tyr346. → Cys substitution in the interdomain acidic region a1 of factor VIII in an individual with factor VIII:C assay discrepancy Br. J. Haematol. 118:2002;589-594
-
(2002)
Br. J. Haematol.
, vol.118
, pp. 589-594
-
-
Mumford, A.D.1
Laffan, M.2
O'Donnell, J.3
McVey, J.H.4
Johnson, D.J.5
Manning, R.A.6
-
46
-
-
4243543147
-
Altered sensitivity towards factor IXa explains assay discrepancies in plasma of haemophilia a patients with a Glu720 to Lys substitution in factor VIII
-
Roelse J.C., de Laaf R.T.M., Mertens K., van Mourik J.A., Oldenburg J.J.V. Altered sensitivity towards factor IXa explains assay discrepancies in plasma of haemophilia A patients with a Glu720 to Lys substitution in factor VIII. Thromb. Haemost. 82(Suppl.):1999;2
-
(1999)
Thromb. Haemost.
, vol.82
, Issue.SUPPL.
, pp. 2
-
-
Roelse, J.C.1
De Laaf, R.T.M.2
Mertens, K.3
Van Mourik, J.A.4
Oldenburg, J.J.V.5
-
47
-
-
0028058606
-
Identification of individual tyrosine sulfation sites within factor VIII required for optimal activity and efficient thrombin cleavage
-
Michnick D.A., Pittman D.D., Wise R.J., Kaufman R.J. Identification of individual tyrosine sulfation sites within factor VIII required for optimal activity and efficient thrombin cleavage. J. Biol. Chem. 269:1994;20095-20102
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 20095-20102
-
-
Michnick, D.A.1
Pittman, D.D.2
Wise, R.J.3
Kaufman, R.J.4
-
48
-
-
0037241152
-
Structure-function relationships in factor IX and factor IXa
-
Schmidt A.E., Bajaj S.P. Structure-function relationships in factor IX and factor IXa. Trends Cardiovasc. Med. 13:2003;39-45
-
(2003)
Trends Cardiovasc. Med.
, vol.13
, pp. 39-45
-
-
Schmidt, A.E.1
Bajaj, S.P.2
-
49
-
-
0028239173
-
Identification of a binding site for blood coagulation factor IXa on the light chain of human factor VIII
-
Lenting P.J., Donath M.J., van Mourik J.A., Mertens K. Identification of a binding site for blood coagulation factor IXa on the light chain of human factor VIII. J. Biol. Chem. 269:1994;7150-7155
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 7150-7155
-
-
Lenting, P.J.1
Donath, M.J.2
Van Mourik, J.A.3
Mertens, K.4
-
50
-
-
9644256994
-
Factor VIII-factor IX interactions probed by chimeric factor VIII/V variants: Complex assembly and cofactor function involve different residues within the A3 domain region 1803-1818
-
Van Stempvoort G., Fribourg C., Celie P.H.N., Lenting P.J., Mertens K. Factor VIII-factor IX interactions probed by chimeric factor VIII/V variants: complex assembly and cofactor function involve different residues within the A3 domain region 1803-1818. J. Thromb. Haemost. (Suppl.):2003;OC111
-
(2003)
J. Thromb. Haemost. Suppl.
, pp. 111
-
-
Van Stempvoort, G.1
Fribourg, C.2
Celie, P.H.N.3
Lenting, P.J.4
Mertens, K.5
-
51
-
-
0028235757
-
Factor IXa protects factor VIIIa from activated protein C. Factor IXa inhibits activated protein C-catalyzed cleavage of factor VIIIa at Arg562
-
Regan L.M., Lamphear B.J., Huggins C.F., Walker F.J., Fay P.J. Factor IXa protects factor VIIIa from activated protein C. Factor IXa inhibits activated protein C-catalyzed cleavage of factor VIIIa at Arg562. J. Biol. Chem. 269:1994;9445-9452
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 9445-9452
-
-
Regan, L.M.1
Lamphear, B.J.2
Huggins, C.F.3
Walker, F.J.4
Fay, P.J.5
-
52
-
-
0027938728
-
Factor VIIIa A2 subunit residues 558-565 represent a factor IXa interactive site
-
Fay P.J., Beattie T., Huggins C.F., Regan L.M. Factor VIIIa A2 subunit residues 558-565 represent a factor IXa interactive site. J. Biol. Chem. 269:1994;20522-20527
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 20522-20527
-
-
Fay, P.J.1
Beattie, T.2
Huggins, C.F.3
Regan, L.M.4
-
53
-
-
0026653380
-
Hemophilia a due to mutations that create new N-glycosylation sites
-
Aly A.M., Higuchi M., Kasper C.K., Kazazian H.H. Jr., Antonarakis S.E., Hoyer L.W. Hemophilia A due to mutations that create new N-glycosylation sites. Proc. Natl. Acad. Sci. USA. 89:1992;4933-4937
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 4933-4937
-
-
Aly, A.M.1
Higuchi, M.2
Kasper, C.K.3
Kazazian Jr., H.H.4
Antonarakis, S.E.5
Hoyer, L.W.6
-
54
-
-
0031972733
-
The molecular basis for cross-reacting material-positive hemophilia a due to missense mutations within the A2-domain of factor VIII
-
Amano K., Sarkar R., Pemberton S., Kemball-Cook G., Kazazian H.H. Jr., Kaufman R.J. The molecular basis for cross-reacting material-positive hemophilia A due to missense mutations within the A2-domain of factor VIII. Blood. 91:1998;538-548
-
(1998)
Blood
, vol.91
, pp. 538-548
-
-
Amano, K.1
Sarkar, R.2
Pemberton, S.3
Kemball-Cook, G.4
Kazazian Jr., H.H.5
Kaufman, R.J.6
-
55
-
-
0037100409
-
Mutations associated with hemophilia a in the 558-565 loop of the factor VIIIa A2 subunit alter the catalytic activity of the factor Xase complex
-
Jenkins P.V., Freas J., Schmidt K.M., Zhou Q., Fay P.J. Mutations associated with hemophilia A in the 558-565 loop of the factor VIIIa A2 subunit alter the catalytic activity of the factor Xase complex. Blood. 100:2002;501-508
-
(2002)
Blood
, vol.100
, pp. 501-508
-
-
Jenkins, P.V.1
Freas, J.2
Schmidt, K.M.3
Zhou, Q.4
Fay, P.J.5
-
56
-
-
0035844226
-
Factor IXa:factor VIIIa interaction. helix 330-338 of factor IXa interacts with residues 558-565 and spatially adjacent regions of the A2 subunit of factor VIIIa
-
Bajaj S.P., Schmidt A.E., Mathur A., Padmanabhan K., Zhong D., Mastri M., et al. Factor IXa:factor VIIIa interaction. helix 330-338 of factor IXa interacts with residues 558-565 and spatially adjacent regions of the A2 subunit of factor VIIIa. J. Biol. Chem. 276:2001;16302-16309
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 16302-16309
-
-
Bajaj, S.P.1
Schmidt, A.E.2
Mathur, A.3
Padmanabhan, K.4
Zhong, D.5
Mastri, M.6
-
57
-
-
0033603299
-
Protease and EGF1 domains of factor IXa play distinct roles in binding to factor VIIIa. Importance of helix 330 (helix 162 in chymotrypsin) of protease domain of factor IXa in its interaction with factor VIIIa
-
Mathur A., Bajaj S.P. Protease and EGF1 domains of factor IXa play distinct roles in binding to factor VIIIa. Importance of helix 330 (helix 162 in chymotrypsin) of protease domain of factor IXa in its interaction with factor VIIIa. J. Biol. Chem. 274:1999;18477-18486
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 18477-18486
-
-
Mathur, A.1
Bajaj, S.P.2
-
58
-
-
2142704289
-
Contribution of factor VIIIa A2 and A3-C1-C2 subunits to the affinity for factor IXa in factor Xase
-
[in press]
-
Jenkins PV, Dill J, Zhou Q, Fay PJ. Contribution of factor VIIIa A2 and A3-C1-C2 subunits to the affinity for factor IXa in factor Xase. Biochemistry, [in press]
-
Biochemistry
-
-
Jenkins, P.V.1
Dill, J.2
Zhou, Q.3
Fay, P.J.4
-
59
-
-
0022358562
-
The functional defect of factor VIII Leiden, a genetic variant of coagulation factor VIII
-
Mertens K., van Wijngaarden A., Bertina R.M., Veltkamp J.J. The functional defect of factor VIII Leiden, a genetic variant of coagulation factor VIII. Thromb. Haemost. 54:1985;650-653
-
(1985)
Thromb. Haemost.
, vol.54
, pp. 650-653
-
-
Mertens, K.1
Van Wijngaarden, A.2
Bertina, R.M.3
Veltkamp, J.J.4
-
60
-
-
0029030435
-
Residues 484-508 contain a major determinant of the inhibitory epitope in the A2 domain of human factor VIII
-
Healey J.F., Lubin I.M., Nakai H., Saenko E.L., Hoyer L.W., Scandella D., et al. Residues 484-508 contain a major determinant of the inhibitory epitope in the A2 domain of human factor VIII. J. Biol. Chem. 270:1995;14505-14509
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 14505-14509
-
-
Healey, J.F.1
Lubin, I.M.2
Nakai, H.3
Saenko, E.L.4
Hoyer, L.W.5
Scandella, D.6
-
61
-
-
2142835518
-
Clustered basic residues within segment 484-510 of the factor VIIIa A2 subunit contribute to the catalytic efficiency for factor Xa generation
-
[in press]
-
Jenkins PV, Dill JL, Zhou Q, Fay PJ. Clustered basic residues within segment 484-510 of the factor VIIIa A2 subunit contribute to the catalytic efficiency for factor Xa generation. J Thromb Haemost [in press]
-
J Thromb Haemost
-
-
Jenkins, P.V.1
Dill, J.L.2
Zhou, Q.3
Fay, P.J.4
-
62
-
-
0036263042
-
New insights into binding interfaces of coagulation factors V and VIII and their homologues lessons from high resolution crystal structures
-
Fuentes-Prior P., Fujikawa K., Pratt K.P. New insights into binding interfaces of coagulation factors V and VIII and their homologues lessons from high resolution crystal structures. Curr. Protein Peptide Sci. 3:2002;313-339
-
(2002)
Curr. Protein Peptide Sci.
, vol.3
, pp. 313-339
-
-
Fuentes-Prior, P.1
Fujikawa, K.2
Pratt, K.P.3
-
63
-
-
0037155149
-
Four hydrophobic amino acids of the factor VIII C2 domain are constituents of both the membrane-binding and von Willebrand factor-binding motifs
-
Gilbert G.E., Kaufman R.J., Arena A.A., Miao H., Pipe S.W. Four hydrophobic amino acids of the factor VIII C2 domain are constituents of both the membrane-binding and von Willebrand factor-binding motifs. J. Biol. Chem. 277:2002;6374-6481
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 6374-6481
-
-
Gilbert, G.E.1
Kaufman, R.J.2
Arena, A.A.3
Miao, H.4
Pipe, S.W.5
-
64
-
-
0033588163
-
The light chain of factor VIII comprises a binding site for low density lipoprotein receptor-related protein
-
Lenting P.J., Neels J.G., van den Berg B.M., Clijsters P.P., Meijerman D.W., Pannekoek H., et al. The light chain of factor VIII comprises a binding site for low density lipoprotein receptor-related protein. J. Biol. Chem. 274:1999;23734-23739
-
(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
-
65
-
-
0033621486
-
Role of the low density lipoprotein-related protein receptor in mediation of factor VIII catabolism
-
Saenko E.L., Yakhyaev A.V., Mikhailenko I., Strickland D.K., Sarafanov A.G. Role of the low density lipoprotein-related protein receptor in mediation of factor VIII catabolism. J. Biol. Chem. 274:1999;37685-37692
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 37685-37692
-
-
Saenko, E.L.1
Yakhyaev, A.V.2
Mikhailenko, I.3
Strickland, D.K.4
Sarafanov, A.G.5
-
66
-
-
0034210883
-
In vivo inhibition of low density lipoprotein receptor-related protein improves survival of factor VIII in the absence of von Willebrand factor
-
Turecek P.L., Schwarz H.P., Binder B.R. In vivo inhibition of low density lipoprotein receptor-related protein improves survival of factor VIII in the absence of von Willebrand factor. Blood. 95:2000;3637-3638
-
(2000)
Blood
, vol.95
, pp. 3637-3638
-
-
Turecek, P.L.1
Schwarz, H.P.2
Binder, B.R.3
-
67
-
-
0037646492
-
Low density lipoprotein receptor-related protein and factor IXa share structural requirements for binding to the A3 domain of coagulation factor VIII
-
Bovenschen N., Boertjes R.C., van Stempvoort G., Voorberg J., Lenting P.J., Meijer A.B., et al. Low density lipoprotein receptor-related protein and factor IXa share structural requirements for binding to the A3 domain of coagulation factor VIII. J. Biol. Chem. 278:2003;9370-9377
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 9370-9377
-
-
Bovenschen, N.1
Boertjes, R.C.2
Van Stempvoort, G.3
Voorberg, J.4
Lenting, P.J.5
Meijer, A.B.6
-
68
-
-
0035853843
-
Cell surface heparan sulfate proteoglycans participate in factor VIII catabolism mediated by low density lipoprotein receptor-related protein
-
Sarafanov A.G., Ananyeva N.M., Shima M., Saenko E.L. Cell surface heparan sulfate proteoglycans participate in factor VIII catabolism mediated by low density lipoprotein receptor-related protein. J. Biol. Chem. 276:2001;11970-11979
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 11970-11979
-
-
Sarafanov, A.G.1
Ananyeva, N.M.2
Shima, M.3
Saenko, E.L.4
-
69
-
-
0032882449
-
Epitope specificity and inactivation mechanisms of factor VIII inhibitor antibodies
-
Scandella D. Epitope specificity and inactivation mechanisms of factor VIII inhibitor antibodies. Vox Sanguinis. 77:1999;17-20
-
(1999)
Vox Sanguinis
, vol.77
, pp. 17-20
-
-
Scandella, D.1
-
71
-
-
0036207024
-
Haemophilia A: Effects of inhibitory antibodies on factor VIII functional interactions and approaches to prevent their action
-
Saenko E.L., Ananyeva N.M., Kouiavskaia D.V., Khrenov A.V., Anderson J.A., Shima M., et al. Haemophilia A: effects of inhibitory antibodies on factor VIII functional interactions and approaches to prevent their action. Haemophilia. 8:2002;1-11
-
(2002)
Haemophilia
, vol.8
, pp. 1-11
-
-
Saenko, E.L.1
Ananyeva, N.M.2
Kouiavskaia, D.V.3
Khrenov, A.V.4
Anderson, J.A.5
Shima, M.6
-
72
-
-
0344776562
-
Epitope mapping of human factor VIII inhibitor antibodies by deletion analysis of factor VIII fragments expressed in Escherichia coli
-
[published erratum appears in Proc Natl Acad Sci USA 1989 Feb;86(4):1387]
-
Scandella D., DeGraaf Mahoney S., Mattingly M., Roeder D., Timmons L., Fulcher C.A. Epitope mapping of human factor VIII inhibitor antibodies by deletion analysis of factor VIII fragments expressed in Escherichia coli. [published erratum appears in Proc Natl Acad Sci USA 1989 Feb;86(4):1387] Proc. Natl. Acad. Sci. USA. 85:1988;6152-6156
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 6152-6156
-
-
Scandella, D.1
Degraaf Mahoney, S.2
Mattingly, M.3
Roeder, D.4
Timmons, L.5
Fulcher, C.A.6
-
73
-
-
0028307616
-
Elimination of a major inhibitor epitope in factor VIII
-
Lubin I.M., Healey J.F., Scandella D., Runge M.S., Lollar P. Elimination of a major inhibitor epitope in factor VIII. J. Biol. Chem. 269:1994;8639-8641
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 8639-8641
-
-
Lubin, I.M.1
Healey, J.F.2
Scandella, D.3
Runge, M.S.4
Lollar, P.5
-
74
-
-
0033570089
-
Human inhibitor antibodies specific for the factor VIII A2 domain disrupt the interaction between the subunit and factor IXa
-
Fay P.J., Scandella D. Human inhibitor antibodies specific for the factor VIII A2 domain disrupt the interaction between the subunit and factor IXa. J. Biol. Chem. 274:1999;29826-29830
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 29826-29830
-
-
Fay, P.J.1
Scandella, D.2
-
75
-
-
0028263884
-
Inhibition of human factor VIIIa by anti-A2 subunit antibodies
-
Lollar P., Parker E.T., Curtis J.E., Helgerson S.L., Hoyer L.W., Scott M.E., et al. Inhibition of human factor VIIIa by anti-A2 subunit antibodies. J. Clin. Invest. 93:1994;2497-2504
-
(1994)
J. Clin. Invest.
, vol.93
, pp. 2497-2504
-
-
Lollar, P.1
Parker, E.T.2
Curtis, J.E.3
Helgerson, S.L.4
Hoyer, L.W.5
Scott, M.E.6
-
76
-
-
0030807719
-
Analysis of the human factor VIII A2 inhibitor epitope by alanine scanning mutagenesis
-
Lubin I.M., Healey J.F., Barrow R.T., Scandella D., Lollar P. Analysis of the human factor VIII A2 inhibitor epitope by alanine scanning mutagenesis. J. Biol. Chem. 272:1997;30191-30195
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 30191-30195
-
-
Lubin, I.M.1
Healey, J.F.2
Barrow, R.T.3
Scandella, D.4
Lollar, P.5
-
77
-
-
0032533220
-
Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIII
-
Healey J.F., Barrow R.T., Tamim H.M., Lubin I.M., Shima M., Scandella D., et al. Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIII. Blood. 92:1998;3701-3709
-
(1998)
Blood
, vol.92
, pp. 3701-3709
-
-
Healey, J.F.1
Barrow, R.T.2
Tamim, H.M.3
Lubin, I.M.4
Shima, M.5
Scandella, D.6
-
78
-
-
0035169521
-
Antigenicity of putative phospholipid membrane-binding residues in factor VIII
-
Barrow R.T., Healey J.F., Jacquemin M.G., Saint-Remy J.M., Lollar P. Antigenicity of putative phospholipid membrane-binding residues in factor VIII. Blood. 97:2001;169-174
-
(2001)
Blood
, vol.97
, pp. 169-174
-
-
Barrow, R.T.1
Healey, J.F.2
Jacquemin, M.G.3
Saint-Remy, J.M.4
Lollar, P.5
-
79
-
-
0035412387
-
Structure of a factor VIII C2 domain-immunoglobulin G4kappa Fab complex: Identification of an inhibitory antibody epitope on the surface of factor VIII
-
Spiegel P.C. Jr., Jacquemin M., Saint-Remy J.M., Stoddard B.L., Pratt K.P. Structure of a factor VIII C2 domain-immunoglobulin G4kappa Fab complex: identification of an inhibitory antibody epitope on the surface of factor VIII. Blood. 98:2001;13-19
-
(2001)
Blood
, vol.98
, pp. 13-19
-
-
Spiegel Jr., P.C.1
Jacquemin, M.2
Saint-Remy, J.M.3
Stoddard, B.L.4
Pratt, K.P.5
-
80
-
-
0031876273
-
Can we improve on nature? "super molecules" of factor VIII
-
Kaufman R.J., Pipe S.W. Can we improve on nature? "Super molecules" of factor VIII. Haemophilia. 4:1998;370-379
-
(1998)
Haemophilia
, vol.4
, pp. 370-379
-
-
Kaufman, R.J.1
Pipe, S.W.2
-
81
-
-
0038170070
-
Development of improved factor VIII molecules and new gene transfer approaches for hemophilia a
-
Saenko E.L., Ananyeva N.M., Moayeri M., Ramezani A., Hawley R.G. Development of improved factor VIII molecules and new gene transfer approaches for hemophilia A. Curr. Gene Therapy. 3:2003;27-41
-
(2003)
Curr. Gene Therapy
, vol.3
, pp. 27-41
-
-
Saenko, E.L.1
Ananyeva, N.M.2
Moayeri, M.3
Ramezani, A.4
Hawley, R.G.5
-
82
-
-
2542543315
-
The future of recombinant coagulation factors
-
Saenko E.L., Ananyeva N.M., Shima M., Hauser C.A.E., Pipe S.W. The future of recombinant coagulation factors. J. Thromb. Haemost. 1:2003;922-930
-
(2003)
J. Thromb. Haemost.
, vol.1
, pp. 922-930
-
-
Saenko, E.L.1
Ananyeva, N.M.2
Shima, M.3
Hauser, C.A.E.4
Pipe, S.W.5
-
83
-
-
0029670912
-
The sequence Glu1811-Lys1818 of human blood coagulation factor VIII comprises a binding site for activated factor IX
-
Lenting P.J., van de Loo J.W., Donath M.J., van Mourik J.A., Mertens K. The sequence Glu1811-Lys1818 of human blood coagulation factor VIII comprises a binding site for activated factor IX. J. Biol. Chem. 271:1996;1935-1940
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 1935-1940
-
-
Lenting, P.J.1
Van De Loo, J.W.2
Donath, M.J.3
Van Mourik, J.A.4
Mertens, K.5
-
84
-
-
0030664471
-
Characterization of a genetically engineered inactivation-resistant coagulation factor VIIIa
-
Pipe S.W., Kaufman R.J. Characterization of a genetically engineered inactivation-resistant coagulation factor VIIIa. Proc. Natl. Acad. Sci. USA. 94:1997;11851-11856
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 11851-11856
-
-
Pipe, S.W.1
Kaufman, R.J.2
-
85
-
-
2342666603
-
An engineered interdomain disulfide bond stabilizes human blood coagulation factor VIIIa
-
Gale A.J., Pellequer J.-L. An engineered interdomain disulfide bond stabilizes human blood coagulation factor VIIIa. J. Thromb. Haemost. 1:2003;1966-1971
-
(2003)
J. Thromb. Haemost.
, vol.1
, pp. 1966-1971
-
-
Gale, A.J.1
Pellequer, J.-L.2
-
86
-
-
0034651022
-
Reduction of the antigenicity of factor VIII toward complex inhibitory antibody plasmas using multiply-substituted hybrid human/porcine factor VIII molecules
-
Barrow R.T., Healey J.F., Gailani D., Scandella D., Lollar P. Reduction of the antigenicity of factor VIII toward complex inhibitory antibody plasmas using multiply-substituted hybrid human/porcine factor VIII molecules. Blood. 95:2000;564-568
-
(2000)
Blood
, vol.95
, pp. 564-568
-
-
Barrow, R.T.1
Healey, J.F.2
Gailani, D.3
Scandella, D.4
Lollar, P.5
-
87
-
-
0037082464
-
3-Dimensional structure of membrane-bound coagulation factor VIII: Modeling of the factor VIII heterodimer within a 3-dimensional density map derived by electron crystallography
-
Stoilova-McPhie S., Villoutreix B.O., Mertens K., Kemball-Cook G., Holzenburg A. 3-Dimensional structure of membrane-bound coagulation factor VIII: modeling of the factor VIII heterodimer within a 3-dimensional density map derived by electron crystallography. Blood. 99:2002;1215-1223
-
(2002)
Blood
, vol.99
, pp. 1215-1223
-
-
Stoilova-Mcphie, S.1
Villoutreix, B.O.2
Mertens, K.3
Kemball-Cook, G.4
Holzenburg, A.5
-
88
-
-
0028801352
-
X-ray structure of clotting factor IXa: Active site and module structure related to Xase activity and hemophilia B
-
Brandstetter H., Bauer M., Huber R., Lollar P., Bode W. X-ray structure of clotting factor IXa: active site and module structure related to Xase activity and hemophilia B. Proc. Natl. Acad. Sci. USA. 92:1995;9796-9800
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 9796-9800
-
-
Brandstetter, H.1
Bauer, M.2
Huber, R.3
Lollar, P.4
Bode, W.5
|