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Volumn 9, Issue 10, 2003, Pages

Haemostatic gene polymorphisms in young Indian Asian subjects with acute myocardial infarction

Author keywords

FactorV; Indian asian; Myocardial infarction; Polymorphism; Prothrombin; Thrombomodulin

Indexed keywords

BLOOD CLOTTING FACTOR 5 LEIDEN; PROTHROMBIN; THROMBOMODULIN;

EID: 0142184231     PISSN: 12341010     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (15)

References (30)
  • 1
    • 0028314865 scopus 로고
    • Mutation in blood coagulation factor V associated with resistance to activated protein C
    • Bertina RM, Koeleman BP, Koster T et al: Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature, 1994; 369: 64-7
    • (1994) Nature , vol.369 , pp. 64-67
    • Bertina, R.M.1    Koeleman, B.P.2    Koster, T.3
  • 2
    • 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
  • 3
    • 0028910906 scopus 로고
    • Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men
    • Ridker PM, Hennekens CH, Lindpaintner K et al: Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men. New Engl J Med, 1995; 332: 912-7
    • (1995) New Engl J Med , vol.332 , pp. 912-917
    • Ridker, P.M.1    Hennekens, C.H.2    Lindpaintner, K.3
  • 4
    • 0031593917 scopus 로고    scopus 로고
    • No association between the 20210 G/A prothrombin gene mutation and premature coronary artery disease
    • Eikelboom JW, Baker RI, Parsons R et al: No association between the 20210 G/A prothrombin gene mutation and premature coronary artery disease. Thromb Haemost, 1998; 80: 878-80
    • (1998) Thromb Haemost , vol.80 , pp. 878-880
    • Eikelboom, J.W.1    Baker, R.I.2    Parsons, R.3
  • 5
    • 0032946813 scopus 로고    scopus 로고
    • The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease
    • Vargas M, Soto I, Pinto CR et al: The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease. Blood Coagul Fibrinolysis, 1999; 10: 39-41
    • (1999) Blood Coagul Fibrinolysis , vol.10 , pp. 39-41
    • Vargas, M.1    Soto, I.2    Pinto, C.R.3
  • 6
    • 0035933001 scopus 로고    scopus 로고
    • G20210A prothrombin gene polymorphism and prothrombin activity in subjects with or without angiographically documented coronary artery disease
    • Russo C, Girelli D, Olivieri O et al: G20210A prothrombin gene polymorphism and prothrombin activity in subjects with or without angiographically documented coronary artery disease. Circulation, 2001; 103: 2436-40
    • (2001) Circulation , vol.103 , pp. 2436-2440
    • Russo, C.1    Girelli, D.2    Olivieri, O.3
  • 7
    • 0036770450 scopus 로고    scopus 로고
    • Prevalence of the 20210 G→A prothrombin variant and its association with coronary artery disease in a Middle Eastern Arab population
    • Abu-Amero KK, Wyngaard CA, Kambouris M, Dzimiri N: Prevalence of the 20210 G→A prothrombin variant and its association with coronary artery disease in a Middle Eastern Arab population. Arch Pathol Lab Med, 2002; 126: 1087-90
    • (2002) Arch Pathol Lab Med , vol.126 , pp. 1087-1090
    • Abu-Amero, K.K.1    Wyngaard, C.A.2    Kambouris, M.3    Dzimiri, N.4
  • 8
    • 0036660164 scopus 로고    scopus 로고
    • Factor V Leiden: The Copenhagen City Heart Study and 2 meta-analyses
    • Juul K, Tybjaerg-Hansen A et al: Factor V Leiden: The Copenhagen City Heart Study and 2 meta-analyses. Blood, 2002; 100: 3-10
    • (2002) Blood , vol.100 , pp. 3-10
    • Juul, K.1    Tybjaerg-Hansen, A.2
  • 9
    • 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
    • Doggen CJ, Cats VM, 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; 97: 1037-41
    • (1998) Circulation , vol.97 , pp. 1037-1041
    • Doggen, C.J.1    Cats, V.M.2    Bertina, R.M.3    Rosendaal, F.R.4
  • 10
    • 0033037741 scopus 로고    scopus 로고
    • The factor II G202101A and factor V G1691A gene transitions and coronary heart disease
    • Gardemann A, Arsic T, Katz N et al: The factor II G202101A and factor V G1691A gene transitions and coronary heart disease. Thromb Haemost, 1999; 81: 208-13
    • (1999) Thromb Haemost , vol.81 , pp. 208-213
    • Gardemann, A.1    Arsic, T.2    Katz, N.3
  • 11
    • 0033669567 scopus 로고    scopus 로고
    • Thrombophilia, polymorphisms and vascular disease
    • Sykes TC, Fegan C, Mosquera D: Thrombophilia, polymorphisms and vascular disease. Mol Pathol, 2000; 53: 300-6
    • (2000) Mol Pathol , vol.53 , pp. 300-306
    • Sykes, T.C.1    Fegan, C.2    Mosquera, D.3
  • 12
    • 0035672995 scopus 로고    scopus 로고
    • Gene polymorphisms of the haemostatic system and the risk of arterial thrombotic disease
    • Franco RF, Reitsma PH. Gene polymorphisms of the haemostatic system and the risk of arterial thrombotic disease. Br J Haemat, 2001; 115: 491-506
    • (2001) Br J Haemat , vol.115 , pp. 491-506
    • Franco, R.F.1    Reitsma, P.H.2
  • 13
    • 0031056791 scopus 로고    scopus 로고
    • A common thrombomodulin amino acid dimorphism is associated with myocardial infarction
    • Norlund L, Holm J, Zoller B, Ohlin AK. A common thrombomodulin amino acid dimorphism is associated with myocardial infarction. Thromb Haemost, 1997; 77: 248-251
    • (1997) Thromb Haemost , vol.77 , pp. 248-251
    • Norlund, L.1    Holm, J.2    Zoller, B.3    Ohlin, A.K.4
  • 14
    • 0025801573 scopus 로고
    • A frequent thrombomodulin amino acid dimorphism is not associated with thrombophilia
    • Van der Velden PA, Krommenhock-Van Es T, Alaart CF et al: A frequent thrombomodulin amino acid dimorphism is not associated with thrombophilia. Thromb. Haemost, 1991; 65: 511-3
    • (1991) Thromb Haemost , vol.65 , pp. 511-513
    • Van der Velden, P.A.1    Krommenhock-Van Es, T.2    Alaart, C.F.3
  • 15
    • 0027771362 scopus 로고
    • Coronary heart disease in South African Indians: Role of insulin resistance and hypertension
    • Seedat YK, Mayet FGH: Coronary heart disease in South African Indians: role of insulin resistance and hypertension. J Hum Hyperten, 1993; 7: 525-7
    • (1993) J Hum Hyperten , vol.7 , pp. 525-527
    • Seedat, Y.K.1    Mayet, F.G.H.2
  • 16
    • 0034922928 scopus 로고    scopus 로고
    • Factor V R506Q mutation-Leiden: An independent risk factor for venous thrombosis but not coronary artery disease
    • Irani-Hakime N, Tamin H, Elias G et al: Factor V R506Q mutation-Leiden: an independent risk factor for venous thrombosis but not coronary artery disease. J Thromb Thrombolysis, 2001; 11: 111-6
    • (2001) J Thromb Thrombolysis , vol.11 , pp. 111-116
    • Irani-Hakime, N.1    Tamin, H.2    Elias, G.3
  • 17
    • 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
  • 18
    • 0034050916 scopus 로고    scopus 로고
    • Prevalence of factor V Leiden in patients with myocardial infarction and normal coronary angiography
    • Mansourati J, Da Costa A, Munier S et al: Prevalence of factor V Leiden in patients with myocardial infarction and normal coronary angiography. Thromb Haemost, 2000, 83: 822-5
    • (2000) Thromb Haemost , vol.83 , pp. 822-825
    • Mansourati, J.1    Da Costa, A.2    Munier, S.3
  • 19
    • 0031775509 scopus 로고
    • A mutation in the thrombomodulin gene 127 G to A coding for Ala25 Thr and the risk of myocardial infarction in men
    • Doggen CJ, Kunz G, Rosendall FR et al: A mutation in the thrombomodulin gene 127 G to A coding for Ala25 Thr and the risk of myocardial infarction in men. Thromb Haemost, 1988; 80: 743-8
    • (1988) Thromb Haemost , vol.80 , pp. 743-748
    • Doggen, C.J.1    Kunz, G.2    Rosendall, F.R.3
  • 20
    • 0032725352 scopus 로고    scopus 로고
    • Molecular risk factors for thrombosis
    • Bertina RM: Molecular risk factors for thrombosis. Thromb Haemost, 1999; 82 601-9
    • (1999) Thromb Haemost , vol.82 , pp. 601-609
    • Bertina, R.M.1
  • 21
    • 0034161456 scopus 로고    scopus 로고
    • Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease
    • Lane DA, Grant PJ: Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease. Blood, 2000; 95: 1517-32
    • (2000) Blood , vol.95 , pp. 1517-1532
    • Lane, D.A.1    Grant, P.J.2
  • 22
    • 0035349825 scopus 로고    scopus 로고
    • The gentics of venous and arterial thromboembolism
    • Lillicrap D: The gentics of venous and arterial thromboembolism. Curr Atheroscler Rep, 2002; 3: 209-15
    • (2002) Curr Atheroscler Rep , vol.3 , pp. 209-215
    • Lillicrap, D.1
  • 23
    • 0036189958 scopus 로고    scopus 로고
    • Genetic polymorphisms in cardiovascular disease
    • Kottke-Marchant: Genetic polymorphisms in cardiovascular disease. Arch Pathol Lab Med, 2002; 126: 295-304
    • (2002) Arch Pathol Lab Med , vol.126 , pp. 295-304
    • Kottke-Marchant1
  • 24
    • 0031856405 scopus 로고    scopus 로고
    • The prevalence of the G20210A polymorphism in the 3′-untranslated region of the prothrombin gene in difference human populations
    • Franco RF, Santos SE, Elion J et al: The prevalence of the G20210A polymorphism in the 3′-untranslated region of the prothrombin gene in difference human populations. Acta Haematologica, 1998; 100: 9-12
    • (1998) Acta Haematologica , vol.100 , pp. 9-12
    • Franco, R.F.1    Santos, S.E.2    Elion, J.3
  • 25
    • 0031975409 scopus 로고    scopus 로고
    • A new factor V gene polymorphism (His1254Arg) present in subjects of African origin mimics the R2 polymorphism (His1299Arg)]
    • Lunghi B, Castoldi E, Mingozzi F, Bernardi F: A new factor V gene polymorphism (His1254Arg) present in subjects of African origin mimics the R2 polymorphism (His1299Arg)]. Blood, 1998; 91: 364-5
    • (1998) Blood , vol.91 , pp. 364-365
    • Lunghi, B.1    Castoldi, E.2    Mingozzi, F.3    Bernardi, F.4
  • 26
    • 0032520034 scopus 로고    scopus 로고
    • A novel mutation of Arg306 of factor V gene in Hong Kong Chinese
    • Chan WP, Lee CK, Kwong YL et al: A novel mutation of Arg306 of factor V gene in Hong Kong Chinese. Blood, 1998; 91: 1135-9
    • (1998) Blood , vol.91 , pp. 1135-1139
    • Chan, W.P.1    Lee, C.K.2    Kwong, Y.L.3
  • 27
    • 0034053358 scopus 로고    scopus 로고
    • Association of the R485K polymorphism of the factor V gene with poor response to activated protein C and increased risk of coronary artery disease in the Chinese population
    • Le W, Yu JD, Lu L et al: Association of the R485K polymorphism of the factor V gene with poor response to activated protein C and increased risk of coronary artery disease in the Chinese population. Clin Genet, 2000; 57: 296-303
    • (2000) Clin Genet , vol.57 , pp. 296-303
    • Le, W.1    Yu, J.D.2    Lu, L.3
  • 28
    • 0030855091 scopus 로고    scopus 로고
    • Thrombomodulin gene mutations associated with myocardial infarction
    • Ireland H, Kunz G, Kyriakoulis K et al: Thrombomodulin gene mutations associated with myocardial infarction. Circulation, 1997; 96: 15-8
    • (1997) Circulation , vol.96 , pp. 15-18
    • Ireland, H.1    Kunz, G.2    Kyriakoulis, K.3
  • 29
    • 0037093228 scopus 로고    scopus 로고
    • Naturally occurring mutations in the thrombomodulin gene leading to impaired expression and function
    • Kunz G, Ohlin AK, Adam A et al: Naturally occurring mutations in the thrombomodulin gene leading to impaired expression and function. Blood, 2002; 99: 3646-53
    • (2002) Blood , vol.99 , pp. 3646-3653
    • Kunz, G.1    Ohlin, A.K.2    Adam, A.3
  • 30
    • 0036145726 scopus 로고    scopus 로고
    • Synegistic effect of thrombomodulin promoter -33G/A polymorphism and smoking on the onset of acute myocardial infarction
    • Li YH, Chen JH, Tsai WC et al: Synegistic effect of thrombomodulin promoter -33G/A polymorphism and smoking on the onset of acute myocardial infarction. Thromb Haemost, 2002; 87: 86-91
    • (2002) Thromb Haemost , vol.87 , pp. 86-91
    • Li, Y.H.1    Chen, J.H.2    Tsai, W.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.