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Volumn 21, Issue 5, 2010, Pages 385-388

Deep venous thrombosis and thrombophilic mutations in western Iran: Association with factor v Leiden

Author keywords

Deep venous thrombosis; factor V Leiden; methylenetetrahydrofolate reductase c.677C>T; prevalence; prothrombin g.20210G>A; western Iran

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BLOOD CLOTTING FACTOR 5 LEIDEN; PROTHROMBIN; RESTRICTION ENDONUCLEASE;

EID: 77954661369     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/MBC.0b013e328330e69a     Document Type: Article
Times cited : (29)

References (23)
  • 1
    • 33645296094 scopus 로고    scopus 로고
    • Prevalence of factor v Leiden and prothrombin G20210A mutations in Chinese patients with deep venous thrombosis and pulmonary embolism
    • Jun ZJ, Ping T, Lei Y, Li L, Ming SY, Jing W. Prevalence of factor V Leiden and prothrombin G20210A mutations in Chinese patients with deep venous thrombosis and pulmonary embolism. Clin Lab Haem 2006; 28:111-116.
    • (2006) Clin Lab Haem , vol.28 , pp. 111-116
    • Jun, Z.J.1    Ping, T.2    Lei, Y.3    Li, L.4    Ming, S.Y.5    Jing, W.6
  • 3
    • 35748974858 scopus 로고    scopus 로고
    • Molecular analysis of factor v Leiden, factor v Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients
    • Dölek B, Eraslan S, Eroglu S, Kesim BE, Ulutin T, Yalçiner A, et al. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients. Clin Appl Thromb Hemost 2007; 13:435-438.
    • (2007) Clin Appl Thromb Hemost , vol.13 , pp. 435-438
    • Dölek, B.1    Eraslan, S.2    Eroglu, S.3    Kesim, B.E.4    Ulutin, T.5    Yalçiner, A.6
  • 4
    • 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, Stampfer MJ, Eisenberg PR, Miletich JP. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men. N Engl J Med 1995; 332:912-917.
    • (1995) N Engl J Med , vol.332 , pp. 912-917
    • Ridker, P.M.1    Hennekens, C.H.2    Lindpaintner, K.3    Stampfer, M.J.4    Eisenberg, P.R.5    Miletich, J.P.6
  • 6
    • 0032897895 scopus 로고    scopus 로고
    • The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: Prevalence and association with factor v G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels
    • Cattaneo M, Chantarangkul V, Taioli E, Santos JH, Tagliabue L. The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels. Thromb Res 1999; 93:1-8.
    • (1999) Thromb Res , vol.93 , pp. 1-8
    • Cattaneo, M.1    Chantarangkul, V.2    Taioli, E.3    Santos, J.H.4    Tagliabue, L.5
  • 7
    • 0029850530 scopus 로고    scopus 로고
    • A common genetic variation in the 30-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 30-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
  • 8
    • 0002804385 scopus 로고
    • Gene analysis
    • Weatherall DJ, editor. London: Churchill Livingstone
    • Old JM, Higgs DR. Gene analysis. In: Weatherall DJ, editor. Methods in hematology. The thalassemias. Vol.6. London: Churchill Livingstone; 1983. pp. 74-101.
    • (1983) Methods in Hematology. The Thalassemias , vol.6 , pp. 74-101
    • Old, J.M.1    Higgs, D.R.2
  • 9
    • 0028314865 scopus 로고
    • Mutation in blood coagulation factor v associated with resistance to activated protein C
    • Bertina RM, Koeleman BPC, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369:64-67.
    • (1994) Nature , vol.369 , pp. 64-67
    • Bertina, R.M.1    Bpc, K.2    Koster, T.3    Rosendaal, F.R.4    Dirven, R.J.5    De Ronde, H.6
  • 10
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
    • Frosst P, Blom HJ, Milos R, Goyatte P, Sheppard CA, Mathews RG, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995; 10:111-113.
    • (1995) Nat Genet , vol.10 , pp. 111-113
    • Frosst, P.1    Blom, H.J.2    Milos, R.3    Goyatte, P.4    Sheppard, C.A.5    Mathews, R.G.6
  • 11
    • 44649129978 scopus 로고    scopus 로고
    • Prevalence of factor v Leiden (G1691A) and prothrombin (G20210A) among Kurdish population from Western Iran
    • Rahimi Z, Vaisi-Raygani A, Mozafari H, Kharrazi H, Rezaei M, Nagel RL. Prevalence of factor V Leiden (G1691A) and prothrombin (G20210A) among Kurdish population from Western Iran. J Thromb Thrombolysis 2008; 25:280-283.
    • (2008) J Thromb Thrombolysis , vol.25 , pp. 280-283
    • Rahimi, Z.1    Vaisi-Raygani, A.2    Mozafari, H.3    Kharrazi, H.4    Rezaei, M.5    Nagel, R.L.6
  • 12
    • 0028931717 scopus 로고
    • High risk of thrombosis in patients homozygous for factor v Leiden (activated protein C resistance)
    • Rosendaal FR, Koster T, Vandenbroucke JP, Reitsma PH. High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance). Blood 1995; 85:1504-1508.
    • (1995) Blood , vol.85 , pp. 1504-1508
    • Rosendaal, F.R.1    Koster, T.2    Vandenbroucke, J.P.3    Reitsma, P.H.4
  • 13
    • 23844551772 scopus 로고    scopus 로고
    • A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis
    • Almawi WY, Tamim H, Kreidy R, Timson G, Rahal E, NabulsiM, et al. A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis. J Thromb Thrombolysis 2005; 19:189-196.
    • (2005) J Thromb Thrombolysis , vol.19 , pp. 189-196
    • Almawi, W.Y.1    Tamim, H.2    Kreidy, R.3    Timson, G.4    Nabulsim, R.E.5
  • 14
  • 15
    • 40549119459 scopus 로고    scopus 로고
    • Hereditary thrombophilic risk factors and venous thromboembolism in Istanbul, Turkey: The role in different clinical manifestations of venous thromboembolism
    • Okumus G, Kiyan E, Arseven O, Tabak L, Diz-Kucukkaya R, Unlucerci Y, et al. Hereditary thrombophilic risk factors and venous thromboembolism in Istanbul, Turkey: the role in different clinical manifestations of venous thromboembolism. Clin Appl Thromb Hemost 2008; 14: 168-173.
    • (2008) Clin Appl Thromb Hemost , vol.14 , pp. 168-173
    • Okumus, G.1    Kiyan, E.2    Arseven, O.3    Tabak, L.4    Diz-Kucukkaya, R.5    Unlucerci, Y.6
  • 16
    • 33645729527 scopus 로고    scopus 로고
    • Risk of recurrent venous thromboembolism in patients with common thrombophilia
    • Ho WH, Hankey GJ, Quinlan DJ, Eikelboom JW. Risk of recurrent venous thromboembolism in patients with common thrombophilia. Arch Intern Med 2006; 166:729-736.
    • (2006) Arch Intern Med , vol.166 , pp. 729-736
    • Ho, W.H.1    Hankey, G.J.2    Quinlan, D.J.3    Eikelboom, J.W.4
  • 17
    • 51849149604 scopus 로고    scopus 로고
    • Factor v Leiden prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients
    • Altinisik J, Ates O, Ulutin T, Cengiz M, Buyru N. Factor V Leiden, prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients. Clin Appl Thromb Hemost 2008; 14:415-420.
    • (2008) Clin Appl Thromb Hemost , vol.14 , pp. 415-420
    • Altinisik, J.1    Ates, O.2    Ulutin, T.3    Cengiz, M.4    Buyru, N.5
  • 19
    • 0032969605 scopus 로고    scopus 로고
    • No evidence for an increased risk of venous thrombosis in patients with factor v Leiden by the homozygous 677C to T mutation in the methylene- tetrahydrofolate-reductase gene
    • Rintelen C, Mannhalter C, Lechner K, Eichinger S, Kyrle PA, Papagiannopoulos M, et al. No evidence for an increased risk of venous thrombosis in patients with factor V Leiden by the homozygous 677C to T mutation in the methylene-tetrahydrofolate-reductase gene. Blood Coagul Fibrinolysis 1999; 10:101-105.
    • (1999) Blood Coagul Fibrinolysis , vol.10 , pp. 101-105
    • Rintelen, C.1    Mannhalter, C.2    Lechner, K.3    Eichinger, S.4    Kyrle, P.A.5    Papagiannopoulos, M.6
  • 20
    • 0030760946 scopus 로고    scopus 로고
    • A common mutation in the methylenetetrahydrofolate reductase gene (C677T). increases the risk for deep-vein thrombosis in patients with mutant factor v (factor V:Q506)
    • Cattaneo M, Tsai MY, Bucciarelli P, Taioli E, Zighetti ML, Bignell M, Manaucci PM. A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506). Arterioscler Thromb Vasc Biol 1997; 17:1662-1666.
    • (1997) Arterioscler Thromb Vasc Biol , vol.17 , pp. 1662-1666
    • Cattaneo, M.1    Tsai, M.Y.2    Bucciarelli, P.3    Taioli, E.4    Zighetti, M.L.5    Bignell, M.6    Manaucci, P.M.7
  • 22
    • 33947251140 scopus 로고    scopus 로고
    • No association between the common MTHFR 677C!T polymorphism and venous thrombosis
    • Bezemer ID, Doggen CJM, Vos HL, Rosendaal FR. No association between the common MTHFR 677C!T polymorphism and venous thrombosis. Arch Intern Med 2007; 167:497-501.
    • (2007) Arch Intern Med , vol.167 , pp. 497-501
    • Bezemer, I.D.1    Cjm, D.2    Vos, H.L.3    Rosendaal, F.R.4
  • 23
    • 33846899709 scopus 로고    scopus 로고
    • Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South Indians
    • Naushad S, Jamal NJ, Angalena R, Prasad CK, Devi AR. Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South Indians. Blood Coagul Fibrinolysis 2007; 18:113-117.
    • (2007) Blood Coagul Fibrinolysis , vol.18 , pp. 113-117
    • Naushad, S.1    Jamal, N.J.2    Angalena, R.3    Prasad, C.K.4    Devi, A.R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.