-
2
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koster, T.3
Rosendaal, F.R.4
Dirven, R.J.5
De Ronde, H.6
Van der Velden, P.A.7
Reitsma, P.H.8
-
6
-
-
0007864268
-
Arg 506 Gln factor V mutation is uncommon in eastern Asian populations
-
(1995)
Blood
, vol.86
-
-
Kodaira, H.1
Ishida, F.2
Ito, T.3
Ichikawa, N.4
Shimodaira, S.5
Takamiva, O.6
Furihata, K.7
Kiyosawa, K.8
Kitano, K.9
-
11
-
-
0031023757
-
A single genetic origin for a common Caucasian risk factor for venous thrombosis
-
(1997)
Blood
, vol.89
, pp. 397-402
-
-
Zivelin, A.1
Griffin, J.H.2
Xu, X.3
Pabinger, I.4
Samama, M.5
Conard, J.6
Brenner, B.7
Eldor, A.8
Seligsohn, U.9
-
19
-
-
0033230321
-
Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden)
-
(1999)
Blood
, vol.94
, pp. 3062-3066
-
-
Faioni, E.M.1
Franchi, F.2
Bucciarelli, P.3
Margaglione, M.4
De Stefano, V.5
Castaman, G.6
Finazzi, G.7
Mannucci, P.M.8
-
20
-
-
0033059973
-
The factor V gene A4070G mutation and the risk of venous thrombosis
-
(1999)
Thromb Haemost
, vol.81
, pp. 193-197
-
-
Alhenc-Gelas, M.1
Nicaud, V.2
Gandrille, S.3
Van Dreden, P.4
Amiral, J.5
Aubry, M.L.6
Fiessinger, J.N.7
Emmerich, J.8
Aiach, M.9
-
22
-
-
0022485106
-
Haemostatic function and ischaemic heart disease: Principal results of the Northwick Park Heart Study
-
(1986)
Lancet
, vol.2
, pp. 533-537
-
-
Meade, T.W.1
Mellows, S.2
Brozovic, M.3
Miller, G.J.4
Chakrabarti, R.R.5
North, W.R.6
Haines, A.P.7
Stirling, Y.8
Imeson, J.D.9
Thompson, S.G.10
-
24
-
-
0034161456
-
Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease
-
(2000)
Blood
, vol.95
, pp. 1517-1532
-
-
Lane, D.A.1
Grant, P.J.2
-
27
-
-
0000413088
-
The physiology and biochemistry of factor XIII
-
Haemostasis and Thrombosis, 3rd ed.(Bloom AL, Forbes CD, Thomas DP, Tuddenham EGD, Eds.). Edinburgh: Churchill Livingstone
-
(1995)
, pp. 531
-
-
Ichinose, A.1
-
31
-
-
0032910569
-
Factor XIII Val34Leu is a genetic factor involved in the etiology of venous thrombosis
-
(1999)
Thromb Haemost
, vol.81
, pp. 676-679
-
-
Franco, R.F.1
Reitsma, P.H.2
Lourenco, D.3
Maffei, F.H.4
Morelli, V.5
Tavella, M.H.6
Araujo, A.G.7
Piccinato, C.E.8
Zago, M.A.9
-
32
-
-
0032532598
-
The Val34Leu polymorphism in the A subunit of coagulation factor XIII contributes to the large normal range in activity and demonstrates that the activation peptide plays a role in catalytic activity
-
(1998)
Blood
, vol.92
, pp. 2766-2770
-
-
Kangsadalampai, S.1
Board, P.G.2
-
35
-
-
0031981017
-
Geographic distribution of the 20210 G to A prothrombin variant
-
(1998)
Thromb Haemost
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Doggen, C.J.2
Zivelin, A.3
Arruda, V.R.4
Aiach, M.5
Siscovick, D.S.6
Hillarp, A.7
Watzke, H.H.8
Bernardi, F.9
Cumming, A.M.10
Preston, F.E.11
Reitsma, P.H.12
-
36
-
-
0032529506
-
A single genetic origin for the common prothrombotic G 20210A polymorphism in the prothrombin gene
-
(1998)
Blood
, vol.92
, pp. 1119-1124
-
-
Zivelin, A.1
Rosenberg, N.2
Faier, S.3
Kornbrot, N.4
Peretz, H.5
Mannhalter, C.6
Horellou, M.H.7
Seligsohn, U.8
-
41
-
-
0034016298
-
Polymorphisms in the 5' regulatory region of the tissue factor gene and the risk of myocardial infarction and venous thromboembolism: The ECTIM and PATHROS studies. Etude Cas-Temoins de l'Infarctus du Myocarde. Paris thrombosis case-control study
-
(2000)
Arterioscler Thromb Vasc Biol
, vol.20
, pp. 892-898
-
-
Arnaud, E.1
Barbalat, V.2
Nicaud, V.3
Cambien, F.4
Evans, A.5
Morrison, C.6
Arveiler, D.7
Luc, G.8
Ruidavets, J.B.9
Emmerich, J.10
Fiessinger, J.N.11
Aiach, M.12
-
53
-
-
0028083284
-
Homozygous antithrombin deficiency: Report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis
-
(1994)
Thromb Haemostas
, vol.72
, pp. 198-202
-
-
Chowdhury, V.1
Lane, D.A.2
Mille, B.3
Auberger, K.4
Gandenberger-Bachem, S.5
Pabinger, I.6
Olds, R.J.7
Thein, S.L.8
-
55
-
-
0031042986
-
Antithrombin mutation database: 2nd (1997) update. For the plasma coagulation inhibitors subcommittee of the scientific and standardization committee of the international society on thrombosis and haemostasis
-
(1997)
Thromb Haemostas
, vol.77
, pp. 197-211
-
-
Lane, D.A.1
Bayston, T.2
Olds, R.J.3
Fitches, A.C.4
Cooper, D.N.5
Millar, D.S.6
Jochmans, K.7
Perry, D.J.8
Okajima, K.9
Thein, S.L.10
Emmerich, J.11
-
57
-
-
0033566326
-
Structural and functional implications of the intron/exon organization of the human endothelial cell protein C/activated protein C receptor (EPCR) gene: Comparison with the structure of CD1/major histocompatibility complex alpha1 and alpha2 domains
-
(1999)
Blood
, vol.94
, pp. 632-641
-
-
Simmonds, R.E.1
Lane, D.A.2
-
58
-
-
0000020081
-
A 23bp insertion in the endothelial protein C receptor (EPCR) gene in patients with myocardial infarction and deep vein thrombosis
-
(1999)
Thromb Haemost
, vol.82
, pp. 507
-
-
Merati, G.B.1
Biguzzi, F.2
Oganesyan, N.3
Fetiveau, D.4
Qu, P.5
Bucciarelli, D.J.6
Stearns-Kurosawa, P.M.7
Mannucci, P.M.8
Esmon, C.T.9
Faioni, E.M.10
-
61
-
-
0029806282
-
A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects
-
(1996)
Thromb Haemostas
, vol.76
, pp. 505-509
-
-
Bernardi, F.1
Legnani, C.2
Micheletti, F.3
Lunghi, B.4
Ferraresi, P.5
Palareti, G.6
Biagi, R.7
Marchetti, G.8
-
63
-
-
0018672331
-
Human plasma protein C: Isolation, characterization, and mechanism of activation by a-thrombin
-
(1979)
J Clin Invest
, vol.64
, pp. 761-769
-
-
Kisiel, W.1
-
64
-
-
0025833619
-
Protein S and C4b-binding protein: Components involved in the regulation of the protein C anticoagulant system
-
(1991)
Thromb Haemost
, vol.66
, pp. 49-61
-
-
Dahlback, B.1
-
70
-
-
0029043736
-
Protein C deficiency: A database of mutations, 1995 update. On behalf of the subcommittee on plasma coagulation inhibitors of the scientific and standardization committee of the ISTH
-
(1995)
Thromb Haemostas
, vol.73
, pp. 876-889
-
-
Reitsma, P.H.1
Bernardi, F.2
Doig, R.G.3
Gandrille, S.4
Greengard, J.S.5
Ireland, H.6
Krawczak, M.7
Lind, B.8
Long, G.L.9
Poort, S.R.10
-
77
-
-
0030759695
-
Protein S deficiency: A database of mutations. For the plasma coagulation inhibitors subcommittee of the scientific and standardization committee of the international society on thrombosis and haemostasis
-
(1997)
Thromb Haemostas
, vol.77
, pp. 1201-1214
-
-
Gandrille, S.1
Borgel, D.2
Ireland, H.3
Lane, D.A.4
Simmonds, R.5
Reitsma, P.H.6
Mannhalter, C.7
Pabinger, I.8
Saito, H.9
Suzuki, K.10
Formstone, C.11
Cooper, D.N.12
Espinosa, Y.13
Sala, N.14
Bernardi, F.15
Aiach, M.16
-
79
-
-
0025151012
-
Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460
-
(1990)
Blood
, vol.76
, pp. 538-548
-
-
Bertina, R.M.1
Ploos Van Amstel, H.K.2
Van Wijngaarden, A.3
Coenen, J.4
Leemhuis, M.P.5
Deutz Terlouw, P.P.6
Van der Linden, I.K.7
Reitsma, P.H.8
-
80
-
-
0030970790
-
Absence of linkage between type III protein S deficiency and the PROS1 and C4BP genes in families carrying the protein S Heerlen allele
-
(1997)
Blood
, vol.89
, pp. 2799-2806
-
-
Espinosa-Parrilla, Y.1
Morell, M.2
Souto, J.C.3
Borrell, M.4
Heine-Suner, D.5
Tirado, I.6
Volpini, V.7
Estivill, X.8
Sala, N.9
-
81
-
-
0028850076
-
The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency
-
(1995)
Blood
, vol.86
, pp. 3436-3443
-
-
Duchemin, J.1
Gandrille, S.2
Borgel, D.3
Feurgard, P.4
Alhenc-Gelas, M.5
Matheron, C.6
Dreyfus, M.7
Dupuy, E.8
Juhan-Vague, I.9
Aiach, M.10
-
85
-
-
0032871414
-
Thrombomodulin with the Asp468Tyr mutation is expressed on the cell surface with normal cofactor activity for protein C activation
-
(1999)
Br J Haematol
, vol.106
, pp. 416-420
-
-
Nakazawa, F.1
Koyama, T.2
Saito, T.3
Shibakura, M.4
Yoshinaga, H.5
Chung, D.H.6
Kamiyama, R.7
Hirosawa, S.8
-
92
-
-
0032892214
-
Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects: Impact of the V264M substitution on plasma levels of TFPI
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.19
, pp. 862-869
-
-
Moatti, D.1
Seknadji, P.2
Galand, C.3
Poirier, O.4
Fumeron, F.5
Desprez, S.6
Garbarz, M.7
Dhermy, D.8
Arveiler, D.9
Evans, A.10
Luc, G.11
Ruidavets, J.B.12
Ollivier, V.13
Hakim, J.14
Aumont, M.C.15
De Prost, D.16
-
94
-
-
0032588298
-
The 536C → T transition in the human tissue factor pathway inhibitor (TFPI) gene is statistically associated with a higher risk for venous thrombosis
-
(1999)
Thromb Haemost
, vol.82
, pp. 1-5
-
-
Kleesiek, K.1
Schmidt, M.2
Gotting, C.3
Schwenz, B.4
Lange, S.5
Muller-Berghaus, G.6
Brinkmann, T.7
Prohaska, W.8
|