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Volumn 3, Issue 7, 2005, Pages 1467-1471

HR2 haplotype in Arab population and patients with venous thrombosis in Kuwait

Author keywords

Arab patients; HR2 haplotype; Polymerase chain reaction; Restriction fragment length polymorphism; Venous thrombosis

Indexed keywords

BLOOD CLOTTING FACTOR 5;

EID: 25144466083     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2005.01326.x     Document Type: Article
Times cited : (16)

References (31)
  • 1
    • 0028959158 scopus 로고
    • Inherited thrombophilia: Resistance to activated protein C as a pathogenetic factor in venous thromboembolism
    • Dahlbäck B. Inherited thrombophilia: resistance to activated protein C as a pathogenetic factor in venous thromboembolism. Blood 1995; 85: 607-14.
    • (1995) Blood , vol.85 , pp. 607-614
    • Dahlbäck, B.1
  • 2
    • 0030905597 scopus 로고    scopus 로고
    • Resistance to activated protein C and factor V Leiden
    • Perry DJ, Pasi KJ. Resistance to activated protein C and factor V Leiden. Q J Med 1997; 90: 379-85.
    • (1997) Q J Med , vol.90 , pp. 379-385
    • Perry, D.J.1    Pasi, K.J.2
  • 3
    • 0031012256 scopus 로고    scopus 로고
    • Inherited thrombotic disorders: An update
    • Florell SR, Rodgers GM. Inherited thrombotic disorders: an update. Am J Hematol 1997; 54: 53-60.
    • (1997) Am J Hematol , vol.54 , pp. 53-60
    • Florell, S.R.1    Rodgers, G.M.2
  • 6
    • 0029850530 scopus 로고    scopus 로고
    • A common genetic variation in the 3′-untranslated region of the pro thrombin 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 pro thrombin 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
  • 7
    • 0030798660 scopus 로고    scopus 로고
    • A laboratory approach to the evaluation of hereditary hypercoagulability
    • Adcock DM, Fink L, Marlar RA. A laboratory approach to the evaluation of hereditary hypercoagulability. Am J Clin Pathol 1997; 108: 434-49.
    • (1997) Am J Clin Pathol , vol.108 , pp. 434-449
    • Adcock, D.M.1    Fink, L.2    Marlar, R.A.3
  • 9
    • 0030860494 scopus 로고    scopus 로고
    • A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype
    • Bernardi F, Faioni EM, Castoldi E, Lunghi B, Castaman G, Sacchi E, Mannucci PM. A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype. Blood 1997; 90: 1552-7.
    • (1997) Blood , vol.90 , pp. 1552-1557
    • Bernardi, F.1    Faioni, E.M.2    Castoldi, E.3    Lunghi, B.4    Castaman, G.5    Sacchi, E.6    Mannucci, P.M.7
  • 12
    • 0242362217 scopus 로고    scopus 로고
    • The factor V HR2 haplotype and the risk of venous thrombosis: A meta-analysis
    • Castaman G, Faioni EM, Tosetto A, Bernardi F. The factor V HR2 haplotype and the risk of venous thrombosis: a meta-analysis. Haematologica 2003; 88: 1182-9.
    • (2003) Haematologica , vol.88 , pp. 1182-1189
    • Castaman, G.1    Faioni, E.M.2    Tosetto, A.3    Bernardi, F.4
  • 14
    • 0034995296 scopus 로고    scopus 로고
    • The factor V HR2 haplotype: Prevalence and association of the A4070G and A6755G polymorphisms
    • Pecheniuk NM, Morris CP, Walsh TP, Marsh NA. The factor V HR2 haplotype: prevalence and association of the A4070G and A6755G polymorphisms. Blood Coagul Fibrinolysis 2001; 12: 201-6.
    • (2001) Blood Coagul Fibrinolysis , vol.12 , pp. 201-206
    • Pecheniuk, N.M.1    Morris, C.P.2    Walsh, T.P.3    Marsh, N.A.4
  • 16
    • 0030698229 scopus 로고    scopus 로고
    • Phenotypic homozygous activated protein C resistance associated with compound heterozygosity for Arg506Gln (factor V Leiden) and His1299Arg substitutions in factor V
    • Castaman G, Lunghi B, Missiaglia E, Bernardi F, Rodeghiero F. Phenotypic homozygous activated protein C resistance associated with compound heterozygosity for Arg506Gln (factor V Leiden) and His1299Arg substitutions in factor V. Br J Haematol 1997; 99: 257-61.
    • (1997) Br J Haematol , vol.99 , pp. 257-261
    • Castaman, G.1    Lunghi, B.2    Missiaglia, E.3    Bernardi, F.4    Rodeghiero, F.5
  • 17
    • 0033230321 scopus 로고    scopus 로고
    • Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden)
    • Faioni EM, Franchi F, Bucciarelli P, Margaglione M, De Stefano V, Castaman G, Finazzi G, Mannucci PM. Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden). Blood 1999; 94: 3062-6.
    • (1999) Blood , vol.94 , pp. 3062-3066
    • Faioni, E.M.1    Franchi, F.2    Bucciarelli, P.3    Margaglione, M.4    De Stefano, V.5    Castaman, G.6    Finazzi, G.7    Mannucci, P.M.8
  • 18
    • 0033972844 scopus 로고    scopus 로고
    • The factor V R2 allele: Risk of venous thromboembolism, factor V levels and resistance to activated protein C
    • Luddington R, Jackson A, Pannerselvam S, Brown K, Baglin T. The factor V R2 allele: risk of venous thromboembolism, factor V levels and resistance to activated protein C. Thromb Haemost 2000; 83: 204-8.
    • (2000) Thromb Haemost , vol.83 , pp. 204-208
    • Luddington, R.1    Jackson, A.2    Pannerselvam, S.3    Brown, K.4    Baglin, T.5
  • 19
    • 0034127421 scopus 로고    scopus 로고
    • The HR2 haplotype of factor V: Effects on factor V levels, normalized activated protein C sensitivity ratios and the risk of venous thrombosis
    • de Visser MC, Guasch JF, Kamphuisen PW, Vos HL, Rosendaal FR, Bertina RM. The HR2 haplotype of factor V: effects on factor V levels, normalized activated protein C sensitivity ratios and the risk of venous thrombosis. Thromb Haemost 2000; 83: 577-82.
    • (2000) Thromb Haemost , vol.83 , pp. 577-582
    • De Visser, M.C.1    Guasch, J.F.2    Kamphuisen, P.W.3    Vos, H.L.4    Rosendaal, F.R.5    Bertina, R.M.6
  • 21
    • 0034059522 scopus 로고    scopus 로고
    • Factor V HR2: An ancient haplotype out of Africa - Reasons for being interested
    • Faioni EM. Factor V HR2: an ancient haplotype out of Africa - reasons for being interested. Thromb Haemost 2000; 83: 358-9.
    • (2000) Thromb Haemost , vol.83 , pp. 358-359
    • Faioni, E.M.1
  • 22
    • 0032569021 scopus 로고    scopus 로고
    • The C-terminal region of the factor V B-domain is crucial for the anticoagulant activity of factor V
    • Thorelli E, Kaufmean RJ, Dahkbäck B. The C-terminal region of the factor V B-domain is crucial for the anticoagulant activity of factor V. J Biol Chem 1998; 273: 16140-5.
    • (1998) J Biol Chem , vol.273 , pp. 16140-16145
    • Thorelli, E.1    Kaufmean, R.J.2    Dahkbäck, B.3
  • 24
    • 0037946750 scopus 로고    scopus 로고
    • Evaluation of the factor V HR2 haplotype as a risk factor for ischemic cerebrovascular disease
    • Lecumberri R, Ceberio I, Montes R, Lopez ML, Alberca I, Rocha E. Evaluation of the factor V HR2 haplotype as a risk factor for ischemic cerebrovascular disease. Haematologica 2003; 88: 236-7.
    • (2003) Haematologica , vol.88 , pp. 236-237
    • Lecumberri, R.1    Ceberio, I.2    Montes, R.3    Lopez, M.L.4    Alberca, I.5    Rocha, E.6
  • 31
    • 0036145792 scopus 로고    scopus 로고
    • Is homozygosity for the HR2 haplotype a risk factor for venous thromboembolism?
    • Aras O, Hanson NQ, Tsai MY, Key NS. Is homozygosity for the HR2 haplotype a risk factor for venous thromboembolism? Thromb Haemost 2002; 87: 173-4.
    • (2002) Thromb Haemost , vol.87 , pp. 173-174
    • Aras, O.1    Hanson, N.Q.2    Tsai, M.Y.3    Key, N.S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.