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Volumn 79, Issue 4, 1998, Pages 706-708

Geographic distribution of the 20210 G to A prothrombin variant

Author keywords

[No Author keywords available]

Indexed keywords

PROTHROMBIN;

EID: 0031981017     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1615049     Document Type: Article
Times cited : (666)

References (18)
  • 1
    • 0029850530 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 10
    • 0030792668 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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
  • 17
    • 2642613990 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.