-
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: 3698-703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
2
-
-
0023230641
-
Nucleotide sequence of the gene for human prothrombin
-
Degen SJ, Davie EW. Nucleotide sequence of the gene for human prothrombin. Biochemistry 1987; 26: 6165-77.
-
(1987)
Biochemistry
, vol.26
, pp. 6165-6177
-
-
Degen, S.J.1
Davie, E.W.2
-
3
-
-
0030921663
-
A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women
-
Rosendaal FR, Siscovick DS, Schwartz SM, Psaty BM, Raghunathan TE, Vos HL. A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women. Blood 1997; 90: 1747-50.
-
(1997)
Blood
, vol.90
, pp. 1747-1750
-
-
Rosendaal, F.R.1
Siscovick, D.S.2
Schwartz, S.M.3
Psaty, B.M.4
Raghunathan, T.E.5
Vos, H.L.6
-
4
-
-
0032562254
-
Interaction of coagulation defects and cardiovascular risk factors: Increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A
-
in press
-
Doggen CJM, Manger Cats V, Bertina RM, Rosendaal FR. Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A. Circulation 1998 (in press).
-
(1998)
Circulation
-
-
Doggen, C.J.M.1
Manger Cats, V.2
Bertina, R.M.3
Rosendaal, F.R.4
-
5
-
-
0001696183
-
The prevalence of the 20210 G>A mutation in the 3′-untranslated region of the prothrombin gene in patients with premature coronary artery disease
-
Franco RF, Trip MD, ten Cate H, Prins MH, Kastelein JJP, Reitsma PH:. The prevalence of the 20210 G>A mutation in the 3′-untranslated region of the prothrombin gene in patients with premature coronary artery disease (abstract). Thromb Haemost 1997; Suppl: 769-70.
-
(1997)
Thromb Haemost
, Issue.SUPPL.
, pp. 769-770
-
-
Franco, R.F.1
Trip, M.D.2
Ten Cate, H.3
Prins, M.H.4
Kastelein, J.J.P.5
Reitsma, P.H.6
-
6
-
-
0030744832
-
The 20210A allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic families
-
Alhenc-Gelas M, Le Cam-Duchez V, Emmerich J, Frebourg T, Fiessinger JN, Borg JY, Aiach M. The 20210A allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic families. Blood 1997; 90: 1711
-
(1997)
Blood
, vol.90
, pp. 1711
-
-
Alhenc-Gelas, M.1
Le Cam-Duchez, V.2
Emmerich, J.3
Frebourg, T.4
Fiessinger, J.N.5
Borg, J.Y.6
Aiach, M.7
-
7
-
-
0030845360
-
The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis
-
Hillarp A, Zöller B, Svensson PJ, Dahlbäck B. The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis. Thromb Haemost 1997; 78: 990-2.
-
(1997)
Thromb Haemost
, vol.78
, pp. 990-992
-
-
Hillarp, A.1
Zöller, B.2
Svensson, P.J.3
Dahlbäck, B.4
-
8
-
-
0343035591
-
Increased prevalence of a polymorphism in the gene coding for human prothrombin in patients with coronary heart disease
-
Watzke HH, Schüttrumpf J, Graf S, Huber K, Panzer S. Increased prevalence of a polymorphism in the gene coding for human prothrombin in patients with coronary heart disease. Thromb Res 1997; 87: 521-6.
-
(1997)
Thromb Res
, vol.87
, pp. 521-526
-
-
Watzke, H.H.1
Schüttrumpf, J.2
Graf, S.3
Huber, K.4
Panzer, S.5
-
9
-
-
0031442537
-
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilia and is not increased in frequency in arterial disease
-
in press
-
Ferraresi P, Marchetti G, Legnani C, Cavallari E, Castoldi E, Mascoli F, Ardissino D, Palareti G, Bernardi F: The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilia and is not increased in frequency in arterial disease. Arterioscler Thromb Vase Biol 1997 (in press).
-
(1997)
Arterioscler Thromb Vase Biol
-
-
Ferraresi, P.1
Marchetti, G.2
Legnani, C.3
Cavallari, E.4
Castoldi, E.5
Mascoli, F.6
Ardissino, D.7
Palareti, G.8
Bernardi, F.9
-
10
-
-
0030792668
-
The prothrombin gene G20210a variant: Prevalence in a U.K. anticoagulant clinic population
-
Cumming AM, Keeney S, Salden A, Bhavnani M, Shwe KH, Hay CRM. The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population. Br J Haematol 1997;98:353-5.
-
(1997)
Br J Haematol
, vol.98
, pp. 353-355
-
-
Cumming, A.M.1
Keeney, S.2
Salden, A.3
Bhavnani, M.4
Shwe, K.H.5
Hay, C.R.M.6
-
11
-
-
2642709543
-
Co-inheritance of the 20210A allele of the prothrombin gene increases the thrombotic risk in subjects with familial dirombophilia
-
Makris M, Preston FE, Beauchamp NJ, Hampton KK, Daly ME, Cooper P, Bayliss P, Peake IR. Co-inheritance of the 20210A allele of the prothrombin gene increases the thrombotic risk in subjects with familial dirombophilia (abstract). Thromb Haemost 1997; Suppl: 165.
-
(1997)
Thromb Haemost
, Issue.SUPPL.
, pp. 165
-
-
Makris, M.1
Preston, F.E.2
Beauchamp, N.J.3
Hampton, K.K.4
Daly, M.E.5
Cooper, P.6
Bayliss, P.7
Peake, I.R.8
-
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
-
-
0028810738
-
World distribution of factor V Leiden
-
Rees DC, Cox M, Clegg JB. World distribution of factor V Leiden. Lancet 1995; 346: 1133-4.
-
(1995)
Lancet
, vol.346
, pp. 1133-1134
-
-
Rees, D.C.1
Cox, M.2
Clegg, J.B.3
-
16
-
-
0031023757
-
A single genetic origin for a common Caucasian risk factor for venous thrombosis
-
Zivelin A, Griffin JH, Xu X, Pabinger I, Samama M, Conard J, Brenner B, Eldor A, Seligsohn U. A single genetic origin for a common Caucasian risk factor for venous thrombosis. Blood 1997; 2: 397-402.
-
(1997)
Blood
, vol.2
, 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
-
17
-
-
2642613990
-
A low frequency of two genetic risk factors for thrombosis in Yemenite-Jews who manifest a decreased incidence of coronary artery disease
-
Zivelin A, Rosenberg N, Dardik R, Amit Y, Kenet G, Kornbrot N, Fridman A, Seligsohn U. A low frequency of two genetic risk factors for thrombosis in Yemenite-Jews who manifest a decreased incidence of coronary artery disease (abstract). Thromb Haemost 1997; Suppl: 222-3.
-
(1997)
Thromb Haemost
, Issue.SUPPL.
, pp. 222-223
-
-
Zivelin, A.1
Rosenberg, N.2
Dardik, R.3
Amit, Y.4
Kenet, G.5
Kornbrot, N.6
Fridman, A.7
Seligsohn, U.8
-
18
-
-
0030610090
-
The mutation Ala677>Val in the methylene tetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosis
-
Arruda VR, Von Zuben PM, Chiaparini LC, Annichino-Bizacchi JM, Costa FF. The mutation Ala677>Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis. Thromb Haemost 1997;77:818-21.
-
(1997)
Thromb Haemost
, vol.77
, pp. 818-821
-
-
Arruda, V.R.1
Von Zuben, P.M.2
Chiaparini, L.C.3
Annichino-Bizacchi, J.M.4
Costa, F.F.5
|