-
1
-
-
0028810738
-
World distribution of factor v Leiden
-
Rees DC, Cox M, Clegg JB. World distribution of factor V Leiden. Lancet 1995; 346:1133-1134.
-
(1995)
Lancet
, vol.346
, pp. 1133-1134
-
-
Rees, D.C.1
Cox, M.2
Clegg, J.B.3
-
2
-
-
0030476647
-
The population genetics of factor v Leiden (Arg506Gln)
-
Rees DC. The population genetics of factor V Leiden (Arg506Gln). Br J Haematol 1996; 95:579-586.
-
(1996)
Br J Haematol
, vol.95
, pp. 579-586
-
-
Rees, D.C.1
-
3
-
-
0031059758
-
Prevalence of Factor v Leiden mutation in non-European population
-
Pepe G, Rickards O, Vanegas OC, Brunelli T, Gori AM, Giusti B, et al. Prevalence of Factor V Leiden mutation in non-European population. Thromb Haemost 1997; 77:329-331.
-
(1997)
Thromb Haemost
, vol.77
, pp. 329-331
-
-
Pepe, G.1
Rickards, O.2
Vanegas, O.C.3
Brunelli, T.4
Gori, A.M.5
Giusti, B.6
-
4
-
-
0034965498
-
Population genetics of factor v Leiden in Europe
-
Lucotte G, Mercier G. Population genetics of factor V Leiden in Europe. Blood Cells Mol Dis 2001; 27:362-367.
-
(2001)
Blood Cells Mol Dis
, vol.27
, pp. 362-367
-
-
Lucotte, G.1
Mercier, G.2
-
5
-
-
33645296094
-
Prevalence of factor v Leiden and prothrombin G20210 mutations in Chinese patients with deep venous thrombosis and pulmonary embolism
-
Jun ZJ, Ping T, Lei Y, Li L, Ming SY, Jing W. Prevalence of factor V Leiden and prothrombin G20210 mutations in Chinese patients with deep venous thrombosis and pulmonary embolism. Clin Lab Haematol 2006; 28:111-116.
-
(2006)
Clin Lab Haematol
, vol.28
, pp. 111-116
-
-
Jun, Z.J.1
Ping, T.2
Lei, Y.3
Li, L.4
Ming, S.Y.5
Jing, W.6
-
6
-
-
0033832644
-
Prevalence of the G1691A mutation in the factor v gene (factor v Leiden) and the G20210A prothrombin gene mutation in the Thai population
-
Angchaisuksiri P, Pingsuthiwong S, Aryuchai K, Busabaratana M, Sura T, Atichartakan V, et al. Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population. Am J Hematol 2000; 65:119-122.
-
(2000)
Am J Hematol
, vol.65
, pp. 119-122
-
-
Angchaisuksiri, P.1
Pingsuthiwong, S.2
Aryuchai, K.3
Busabaratana, M.4
Sura, T.5
Atichartakan, V.6
-
7
-
-
0033843870
-
The prevalence of factor v R506Q mutation Leiden among apparently healthy Lebanese
-
Irani-Hakime N, Tamim H, Kreidy R, Almawi W. The prevalence of factor V R506Q mutation Leiden among apparently healthy Lebanese. Am J Hematol 2000; 65:45-49.
-
(2000)
Am J Hematol
, vol.65
, pp. 45-49
-
-
Irani-Hakime, N.1
Tamim, H.2
Kreidy, R.3
Almawi, W.4
-
8
-
-
33746025917
-
Distinct association of Factor V-Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisian and Lebanon
-
Bouaziz-Borgi L, Almavwi WY, Mtiraoui N, Nsiri B, Keleshian SH, Kreidy R, et al. Distinct association of Factor V-Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisian and Lebanon. Am J Hematol 2006; 81:641-643.
-
(2006)
Am J Hematol
, vol.81
, pp. 641-643
-
-
Bouaziz-Borgi, L.1
Almavwi, W.Y.2
Mtiraoui, N.3
Nsiri, B.4
Keleshian, S.H.5
Kreidy, R.6
-
9
-
-
27944450847
-
Varied prevalence of Factor v G1691A (Leiden) and Prothrombin G20210 single nucleotide polymorphism among Arabs
-
Almawi WY, Keleshian SH, Borgi L, Fawaz NA, Abboud N, Mtiraoui N, et al. Varied prevalence of Factor V G1691A (Leiden) and Prothrombin G20210 single nucleotide polymorphism among Arabs. J Thromb Thrombol 2005; 20:163-168.
-
(2005)
J Thromb Thrombol
, vol.20
, pp. 163-168
-
-
Almawi, W.Y.1
Keleshian, S.H.2
Borgi, L.3
Fawaz, N.A.4
Abboud, N.5
Mtiraoui, N.6
-
10
-
-
0031981017
-
Geographic distribution of the 20210G to A prothrombin variant
-
Rosendaal FR, Doggen CJM, Zivelin A, Arruda VR, Aiach M, Siscovic DS, et al. Geographic distribution of the 20210G to A prothrombin variant. Thromb Haemost 1998; 79:706-708.
-
(1998)
Thromb Haemost
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Doggen, C.J.M.2
Zivelin, A.3
Arruda, V.R.4
Aiach, M.5
Siscovic, D.S.6
-
11
-
-
0034827541
-
Age-dependent prevalence of vascular disease-associated polymorphisms among 2689 volunteer blood donors
-
Hessner MJ, Dinauer DM, Kwiatowski R, Neri B, Raife TJ. Age-dependent prevalence of vascular disease-associated polymorphisms among 2689 volunteer blood donors. Clin Chem 2001; 47:1879-1884.
-
(2001)
Clin Chem
, vol.47
, pp. 1879-1884
-
-
Hessner, M.J.1
Dinauer, D.M.2
Kwiatowski, R.3
Neri, B.4
Raife, T.J.5
-
12
-
-
0031786802
-
The risk of mortality and of Factor v Leiden in a population-based cohort
-
Heijmans BT, Westendorp RG, Knook DL, Kluft C, Slaboom PE. The risk of mortality and of Factor V Leiden in a population-based cohort. Thromb Haemost 1998; 80:607-609.
-
(1998)
Thromb Haemost
, vol.80
, pp. 607-609
-
-
Heijmans, B.T.1
Westendorp, R.G.2
Knook, D.L.3
Kluft, C.4
Slaboom, P.E.5
-
13
-
-
20444462017
-
ABO blood group genotypes and the risk of venous thrombosis effect of factor v Leiden
-
Morelli VM, De Visser MCH, Vos HL, Bertina RM, Rosendaal R. ABO blood group genotypes and the risk of venous thrombosis effect of factor V Leiden. J Thromb Haemost 2005; 3:183-185.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 183-185
-
-
Morelli, V.M.1
De Visser, M.C.H.2
Vos, H.L.3
Bertina, R.M.4
Rosendaal, R.5
-
14
-
-
33750570455
-
ABO blood group but not haemostasis genetic polymorphisms significantly influence thrombotic risk: A study of 180 homozygotes for factor v Leiden mutation
-
Procare-GEHT Group
-
Procare-GEHT Group. ABO blood group but not haemostasis genetic polymorphisms significantly influence thrombotic risk: a study of 180 homozygotes for factor V Leiden mutation. Br J Haematol 2006; 135:697-702.
-
(2006)
Br J Haematol
, vol.135
, pp. 697-702
-
-
-
15
-
-
0027446268
-
Familial thrombophilia due to a previous unrecognised mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C
-
Dahlback B, Carlsson M, Svensson PJ. Familial thrombophilia due to a previous unrecognised mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C. Proc Natl Acad Sci U S A 1993; 90:1004-1008.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 1004-1008
-
-
Dahlback, B.1
Carlsson, M.2
Svensson, P.J.3
-
16
-
-
0028314865
-
Mutation in blood coagulation factor v associated with resistance to activated protein C
-
Bertina RM, Koeleman BPC, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369:64-67.
-
(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
-
17
-
-
0029850530
-
A common genetic variation in the 3'-unrelated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3'-unrelated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88:3698-3703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
18
-
-
0034939628
-
Increased efficiency of mRNA 3'end formation: A new genetic mechanism contribution to hereditary thrombophilia
-
Gehring NH, Frede U, Neu-Yilik G, Hundsdoerfer P, Vetter B, Hentze MW, Kulozik AE. Increased efficiency of mRNA 3'end formation: a new genetic mechanism contribution to hereditary thrombophilia. Nat Genet 2001; 28:389-392.
-
(2001)
Nat Genet
, vol.28
, pp. 389-392
-
-
Gehring, N.H.1
Frede, U.2
Neu-Yilik, G.3
Hundsdoerfer, P.4
Vetter, B.5
Hentze, M.W.6
Kulozik, A.E.7
-
19
-
-
33645546424
-
Protein S levels modulate the activated protein C resistance phenotype induced by elevated prothrombin levels
-
Brugge JM, Tans G, Rosing J, Castoldi E. Protein S levels modulate the activated protein C resistance phenotype induced by elevated prothrombin levels. Thromb Haemost 2006; 95:236-242.
-
(2006)
Thromb Haemost
, vol.95
, pp. 236-242
-
-
Brugge, J.M.1
Tans, G.2
Rosing, J.3
Castoldi, E.4
-
20
-
-
0031205597
-
Multiplex PCR-mediated sitedirected mutagenesis for one-step determination of factor v Leiden and G20210A transition of the prothrombin gene
-
Ripoll L, Paulin D, Thomas S, Drouet LO. Multiplex PCR-mediated sitedirected mutagenesis for one-step determination of factor V Leiden and G20210A transition of the prothrombin gene. Thromb Haemost 1997; 78:960-961.
-
(1997)
Thromb Haemost
, vol.78
, pp. 960-961
-
-
Ripoll, L.1
Paulin, D.2
Thomas, S.3
Drouet, L.O.4
-
21
-
-
0024284028
-
A simple salting out procedure for extraction DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extraction DNA from human nucleated cells. Nucleic Acid Res 1988; 16:1215.
-
(1988)
Nucleic Acid Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
22
-
-
0025875932
-
Measurement of platelet mediated force development during plasma clot formation
-
Carr ME, Zeckert SL. Measurement of platelet mediated force development during plasma clot formation. Am J Med Sci 1991; 302:13-18.
-
(1991)
Am J Med Sci
, vol.302
, pp. 13-18
-
-
Carr, M.E.1
Zeckert, S.L.2
-
23
-
-
0027931362
-
Quantitative assessment of platelet function and clot structure in patients with severe coronary artery disease
-
Greilich PE, Carr ME, Zekert SL, Dent RM. Quantitative assessment of platelet function and clot structure in patients with severe coronary artery disease. Am J Med Sci 1994; 307:15-20.
-
(1994)
Am J Med Sci
, vol.307
, pp. 15-20
-
-
Greilich, P.E.1
Carr, M.E.2
Zekert, S.L.3
Dent, R.M.4
-
24
-
-
0000449738
-
Frequency of Factor v Leiden (Arg506Gln) in France
-
Lucotte G, Mercier G. Frequency of Factor V Leiden (Arg506Gln) in France. Br J Haematol 1997; 99:237-241.
-
(1997)
Br J Haematol
, vol.99
, pp. 237-241
-
-
Lucotte, G.1
Mercier, G.2
-
25
-
-
0037812800
-
Assessment of the 20210 G to A prothrombin variant in a sample of patients from the French Basque country with various thrombophilic conditions
-
Bauduer F, Ducout L, Freyburger G. Assessment of the 20210 G to A prothrombin variant in a sample of patients from the French Basque country with various thrombophilic conditions. Ann Hematol 2003; 82:353-356.
-
(2003)
Ann Hematol
, vol.82
, pp. 353-356
-
-
Bauduer, F.1
Ducout, L.2
Freyburger, G.3
-
26
-
-
4644227898
-
The prevalence of factor v G1691A but not of prothrombin G20210A and methylenetetrahydrofolate reductase C677T is remarkably low in French Basques
-
Bauduer F, Zivelin A, Ducout L, Shpringer E, Seligsohn U. The prevalence of factor V G1691A but not of prothrombin G20210A and methylenetetrahydrofolate reductase C677T is remarkably low in French Basques. J Thromb Haemost 2004; 2:361-362.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 361-362
-
-
Bauduer, F.1
Zivelin, A.2
Ducout, L.3
Shpringer, E.4
Seligsohn, U.5
-
27
-
-
0036630829
-
Comparative evaluation of five different methods for the measurement of plasma factor II levels in carriers of the 20210A prothrombin variant
-
Delahouse B, Gilbert M, Nicham F, Thirion C, Giraudeau B, Gruel Y. Comparative evaluation of five different methods for the measurement of plasma factor II levels in carriers of the 20210A prothrombin variant. Blood Coagul Fibrinolysis 2002; 13:465-470.
-
(2002)
Blood Coagul Fibrinolysis
, vol.13
, pp. 465-470
-
-
Delahouse, B.1
Gilbert, M.2
Nicham, F.3
Thirion, C.4
Giraudeau, B.5
Gruel, Y.6
-
28
-
-
0034666712
-
Prothrombin activity and concentration in healthy subjects with and without the prothrombin G20210A mutation
-
Von Ahsen N, Lewczuk P, Schutz E, Oellerich M, Ehrenreich H. Prothrombin activity and concentration in healthy subjects with and without the prothrombin G20210A mutation. Thromb Res 2000; 99:549-556.
-
(2000)
Thromb Res
, vol.99
, pp. 549-556
-
-
Von Ahsen, N.1
Lewczuk, P.2
Schutz, E.3
Oellerich, M.4
Ehrenreich, H.5
-
29
-
-
0034976841
-
Polymorphisms in the prothrombin gene and their association with plasma prothrombin levels
-
Ceelie H, Bertina RM, van Hylckama Vlieg A, Rosendaal FR, Vos HL. Polymorphisms in the prothrombin gene and their association with plasma prothrombin levels. Thromb Haemost 2001; 85:1066-1070.
-
(2001)
Thromb Haemost
, vol.85
, pp. 1066-1070
-
-
Ceelie, H.1
Bertina, R.M.2
Van Hylckama Vlieg, A.3
Rosendaal, F.R.4
Vos, H.L.5
-
30
-
-
0031893737
-
Plasma lipoproteins support prothrombinase and other procoagulant enzymatic complexes
-
Moyer MP, Tracy RP, Tracy PB, Van't Veer C, Sparks CE, Mann KG. Plasma lipoproteins support prothrombinase and other procoagulant enzymatic complexes. Arterioscler Thromb Vasc Biol 1998; 18:458-465.
-
(1998)
Arterioscler Thromb Vasc Biol
, vol.18
, pp. 458-465
-
-
Moyer, M.P.1
Tracy, R.P.2
Tracy, P.B.3
Van'T Veer, C.4
Sparks, C.E.5
Mann, K.G.6
-
31
-
-
0028091598
-
Correlation of vitamin K dependent clotting factors with cholesterol and triglycerides in healthy young adults
-
Hoffman CJ, Lawson WE, Miller RH, Hultin MB. Correlation of vitamin K dependent clotting factors with cholesterol and triglycerides in healthy young adults. Arterioscler Thromb 1994; 14:1737-1740.
-
(1994)
Arterioscler Thromb
, vol.14
, pp. 1737-1740
-
-
Hoffman, C.J.1
Lawson, W.E.2
Miller, R.H.3
Hultin, M.B.4
-
32
-
-
0026555847
-
Correlation of factor VII activity and antigen with cholesterol and triglycerides in healthy young adults
-
Hoffman CJ, Miller RH, Hultin MB. Correlation of factor VII activity and antigen with cholesterol and triglycerides in healthy young adults. Arterioscler Thromb 1992; 12:267-270.
-
(1992)
Arterioscler Thromb
, vol.12
, pp. 267-270
-
-
Hoffman, C.J.1
Miller, R.H.2
Hultin, M.B.3
-
33
-
-
0037534900
-
Elevated prothrombin results in clots with an altered fiber structure: A possible mechanism of the increased thrombotic risk
-
Wolberg AS, Monroe DM, Roberts HR, Hoffman M. Elevated prothrombin results in clots with an altered fiber structure: a possible mechanism of the increased thrombotic risk. Blood 2003; 101:3008-3013.
-
(2003)
Blood
, vol.101
, pp. 3008-3013
-
-
Wolberg, A.S.1
Monroe, D.M.2
Roberts, H.R.3
Hoffman, M.4
-
34
-
-
33745105401
-
Prothrombin 20210G>A is an ancestral prothromotic mutation that occurred in whites approximately 24000 years ago
-
Zivelin A, Mor-Cohen R, Kovalsky V, Kombrot N, Connard J, Peyvandi F, et al. Prothrombin 20210G>A is an ancestral prothromotic mutation that occurred in whites approximately 24000 years ago. Blood 2006; 107:4666-4668.
-
(2006)
Blood
, vol.107
, pp. 4666-4668
-
-
Zivelin, A.1
Mor-Cohen, R.2
Kovalsky, V.3
Kombrot, N.4
Connard, J.5
Peyvandi, F.6
-
35
-
-
0029927689
-
Mutant factor v (Arg506Gln) in healthy centenarians
-
Mari D, Mannucci PM, Duca F, Bertolini S, Franceschi C. Mutant factor V (Arg506Gln) in healthy centenarians. Lancet 1996; 347:1044.
-
(1996)
Lancet
, vol.347
, pp. 1044
-
-
Mari, D.1
Mannucci, P.M.2
Duca, F.3
Bertolini, S.4
Franceschi, C.5
|