-
1
-
-
0029850530
-
A common genetic variation in the 3′-untranslated 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′-untranslated 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
-
2
-
-
0034840147
-
Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism: Pooled analysis of 8 case-control studies including 2310 cases and 3204 controls: Study Group for Pooled-Analysis in Venous Thromboembolism
-
Emmerich J, Rosendaal FR, Cattaneo M, et al. Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism: pooled analysis of 8 case-control studies including 2310 cases and 3204 controls: Study Group for Pooled-Analysis in Venous Thromboembolism. Thromb Haemost. 2001;86:809-816.
-
(2001)
Thromb Haemost
, vol.86
, pp. 809-816
-
-
Emmerich, J.1
Rosendaal, F.R.2
Cattaneo, M.3
-
3
-
-
0034939628
-
Increased efficiency of mRNA 3′ end formation: A new genetic mechanism contributing to hereditary thrombophilia
-
Gehring NH, Frede U, Neu-Yilik G, et al. Increased efficiency of mRNA 3′ end formation: a new genetic mechanism contributing 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
-
4
-
-
3142552164
-
G20210A is a functional mutation in the prothrombin gene: Effect on protein levels and 3′-end formation
-
Ceelie H, Spaargaren-van Riel CC, Bertina RM, Vos HL. G20210A is a functional mutation in the prothrombin gene: effect on protein levels and 3′-end formation. J Thromb Haemost. 2004;2:119-127.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 119-127
-
-
Ceelie, H.1
Spaargaren-van Riel, C.C.2
Bertina, R.M.3
Vos, H.L.4
-
5
-
-
0032921209
-
Born to clot: The European burden
-
Rees DC, Chapman NH, Webster MT, Guerreiro JF, Rochette J, Clegg JB. Born to clot: the European burden. Br J Haematol. 1999;105:564-566.
-
(1999)
Br J Haematol
, vol.105
, pp. 564-566
-
-
Rees, D.C.1
Chapman, N.H.2
Webster, M.T.3
Guerreiro, J.F.4
Rochette, J.5
Clegg, J.B.6
-
6
-
-
0032529506
-
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene
-
Zivelin A, Rosenberg N, Faier S, et al. A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene. Blood. 1998;92:1119-1124.
-
(1998)
Blood
, vol.92
, pp. 1119-1124
-
-
Zivelin, A.1
Rosenberg, N.2
Faier, S.3
-
7
-
-
84874664749
-
-
National Center for Biotechnology Information. NCBI SNP database. http://www.ncbi.nlm.nih. gov. Accessed April 14, 2006.
-
NCBI SNP Database
-
-
-
8
-
-
0034973984
-
High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequence
-
Rannala B, Reeve JP. High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequence. Am J Hum Genet. 2001;69:159-178.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 159-178
-
-
Rannala, B.1
Reeve, J.P.2
-
9
-
-
0036300177
-
DMLE+: Bayesian linkage disequilibrium gene mapping
-
Reeve JP, Rannala B. DMLE+: Bayesian linkage disequilibrium gene mapping. Bioinformatics. 2002;18:894-895.
-
(2002)
Bioinformatics
, vol.18
, pp. 894-895
-
-
Reeve, J.P.1
Rannala, B.2
-
12
-
-
0031981017
-
Geographic distribution of the 20210 G to A prothrombin variant
-
Rosendaal FR, Doggen CJ, Zivelin A, et al. Geographic distribution of the 20210 G 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.2
Zivelin, A.3
-
13
-
-
0031023757
-
A single genetic origin for a common Caucasian risk factor for venous thrombosis
-
Zivelin A, Griffin JH, Xu X, et al. A single genetic origin for a common Caucasian risk factor for venous thrombosis. Blood. 1997;89:397-402.
-
(1997)
Blood
, vol.89
, pp. 397-402
-
-
Zivelin, A.1
Griffin, J.H.2
Xu, X.3
-
14
-
-
0030746618
-
Thrombophilia as a multigenic disorder
-
Seligsohn U, Zivelin A. Thrombophilia as a multigenic disorder. Thromb Haemost. 1997;78:297-301.
-
(1997)
Thromb Haemost
, vol.78
, pp. 297-301
-
-
Seligsohn, U.1
Zivelin, A.2
-
15
-
-
0033843870
-
The prevalence of factor V R506Q mutation-Leiden among apparently healthy Lebanese
-
Irani-Hakime N, Tamim H, Kreidy R, Almawi WY. 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.Y.4
-
16
-
-
0031594157
-
Factor V Q506 mutation (activated protein C resistance) associated with reduced intrapartum blood loss: A possible evolutionary selection mechanism
-
Lindqvist PG, Svensson PJ, Dahlback B, Marsal K. Factor V Q506 mutation (activated protein C resistance) associated with reduced intrapartum blood loss: a possible evolutionary selection mechanism. Thromb Haemost. 1998;79:69-73.
-
(1998)
Thromb Haemost
, vol.79
, pp. 69-73
-
-
Lindqvist, P.G.1
Svensson, P.J.2
Dahlback, B.3
Marsal, K.4
-
17
-
-
0035487920
-
Improved hemoglobin status and reduced menstrual blood loss among female carriers of factor V Leiden: An evolutionary advantage?
-
Lindqvist PG, Zoller B, Dahlback B. Improved hemoglobin status and reduced menstrual blood loss among female carriers of factor V Leiden: an evolutionary advantage? Thromb Haemost. 2001;86:1122-1123.
-
(2001)
Thromb Haemost
, vol.86
, pp. 1122-1123
-
-
Lindqvist, P.G.1
Zoller, B.2
Dahlback, B.3
-
18
-
-
0142245617
-
Survival advantage associated with heterozygous factor V Leiden mutation in patients with severe sepsis and in mouse endotoxemia
-
Kerlin BA, Yan SB, Isermann BH, et al. Survival advantage associated with heterozygous factor V Leiden mutation in patients with severe sepsis and in mouse endotoxemia. Blood. 2003;102:3085-3092.
-
(2003)
Blood
, vol.102
, pp. 3085-3092
-
-
Kerlin, B.A.1
Yan, S.B.2
Isermann, B.H.3
-
19
-
-
2942703851
-
Effect of factor V Leiden polymorphism in severe sepsis and on treatment with recombinant human activated protein C
-
Yan SB, Nelson DR. Effect of factor V Leiden polymorphism in severe sepsis and on treatment with recombinant human activated protein C. Crit Care Med. 2004;32:S239-S246.
-
(2004)
Crit Care Med
, vol.32
-
-
Yan, S.B.1
Nelson, D.R.2
-
20
-
-
27744590529
-
Influence of the factor V leiden mutation on infectious disease susceptibility and outcome: A population-based study
-
Benfield TL, Dahl M, Nordestgaard BG, Tybjaerg-Hansen A. Influence of the factor V leiden mutation on infectious disease susceptibility and outcome: a population-based study. J Infect Dis. 2005;192:1851-1857.
-
(2005)
J Infect Dis
, vol.192
, pp. 1851-1857
-
-
Benfield, T.L.1
Dahl, M.2
Nordestgaard, B.G.3
Tybjaerg-Hansen, A.4
|