메뉴 건너뛰기




Volumn 4, Issue 5, 1997, Pages 347-352

Genetic markers: Genes involved in thrombosis

Author keywords

Acute myocardial infarction; Antithrombin III; Factor V Leiden; Factor VII; Fibrinogen; Plasminogen activator inhibitor 1; Protein C; Protein S; Venous thrombosis

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ANTITHROMBIN III; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; FIBRINOGEN; GLYCOPROTEIN IIIA; HOMOCYSTEINE; LEUCINE; PLASMINOGEN ACTIVATOR INHIBITOR 1; PROLINE; PROTEIN C; PROTEIN S;

EID: 0031417169     PISSN: 13506277     EISSN: None     Source Type: Journal    
DOI: 10.1097/00043798-199710000-00005     Document Type: Article
Times cited : (9)

References (44)
  • 1
    • 0027446268 scopus 로고
    • Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C
    • Dahlback B, Carlsson M, Svensson PJ: Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C. Proc Natl Acad Sci USA 1993, 90:1004-1008.
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 1004-1008
    • Dahlback, B.1    Carlsson, M.2    Svensson, P.J.3
  • 2
    • 0028098218 scopus 로고
    • Inherited resistance to activated protein C is corrected by anticoagulant cofactor activity found to be a property of factor V
    • Dahlback B, Hildebrand B: Inherited resistance to activated protein C is corrected by anticoagulant cofactor activity found to be a property of factor V. Proc Natl Acad Sci USA 1994, 91:1396-1400.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 1396-1400
    • Dahlback, B.1    Hildebrand, B.2
  • 4
    • 0028959158 scopus 로고
    • Inherited thrombophilia: Resistance to activated protein C as a pathogenic factor of venous thromboembolism
    • Dahlback B: Inherited thrombophilia: resistance to activated protein C as a pathogenic factor of venous thromboembolism. Blood 1995, 85:607-614.
    • (1995) Blood , vol.85 , pp. 607-614
    • Dahlback, B.1
  • 6
    • 0023855237 scopus 로고
    • Genes for vitamin Independent plasma protein C and S are located on chromosome 2 and 3, respectively
    • Long GL, Marshall A, Gardner JC, Naylor SL: Genes for vitamin Independent plasma protein C and S are located on chromosome 2 and 3, respectively. Somat Cell Mol Genet 1988, 14:93-97.
    • (1988) Somat Cell Mol Genet , vol.14 , pp. 93-97
    • Long, G.L.1    Marshall, A.2    Gardner, J.C.3    Naylor, S.L.4
  • 9
    • 0023233223 scopus 로고
    • Absence of thrombosis in subjects with heterozygous protein C deficiency
    • Miletich JP, Sherman L, Broze GJ Jr: Absence of thrombosis in subjects with heterozygous protein C deficiency. N Engl J Med 1987, 317:991-994.
    • (1987) N Engl J Med , vol.317 , pp. 991-994
    • Miletich, J.P.1    Sherman, L.2    Broze, G.J.3
  • 10
    • 0001877945 scopus 로고
    • Approach to thrombophilia patients
    • Third Edition. Edited by Colman RW, Hirsh J, Marder VJ, Salzman EW. Philadelphia: J.B. Lippincott Co.
    • Hirsh J, Prins MH, Samama M: Approach to thrombophilia patients. In Hemostasis and Thrombosis, Third Edition. Edited by Colman RW, Hirsh J, Marder VJ, Salzman EW. Philadelphia: J.B. Lippincott Co.; 1994:1543-1561.
    • (1994) Hemostasis and Thrombosis , pp. 1543-1561
    • Hirsh, J.1    Prins, M.H.2    Samama, M.3
  • 11
    • 0025003450 scopus 로고
    • Intron-exon organization of the active human protein S gene PS alpha and its pseudogene PS β: Duplication and silencing during primate evolution
    • Ploos van Amstel HK, Reitsma PH, van der Logt CPE, Bertina RM: Intron-exon organization of the active human protein S gene PS alpha and its pseudogene PS β: duplication and silencing during primate evolution. Biochem 1990, 29:7853-7861.
    • (1990) Biochem , vol.29 , pp. 7853-7861
    • Ploos van Amstel, H.K.1    Reitsma, P.H.2    van der Logt, C.P.E.3    Bertina, R.M.4
  • 12
    • 0020042262 scopus 로고
    • Genetic mapping of the structural gene for antithrombin III and Duffy Blood group and assignment of AT-III to 1 q22-q25
    • Winter JH, Bennett B, Watt JL, Brown T, San Román C, Schinzel A, et al.: Genetic mapping of the structural gene for antithrombin III and Duffy Blood group and assignment of AT-III to 1 q22-q25. Ann Hum Genet 1982, 46:29-34.
    • (1982) Ann Hum Genet , vol.46 , pp. 29-34
    • Winter, J.H.1    Bennett, B.2    Watt, J.L.3    Brown, T.4    San Román, C.5    Schinzel, A.6
  • 13
    • 0022408486 scopus 로고
    • Intron structure of the human AT-III gene differs from that of other members of the serine protease inhibitor superfamily
    • Prochowni KEV, Bock SC, Orkin SH: Intron structure of the human AT-III gene differs from that of other members of the serine protease inhibitor superfamily. J Biol Chem 1985, 260:9608-9612.
    • (1985) J Biol Chem , vol.260 , pp. 9608-9612
    • Prochowni, K.E.V.1    Bock, S.C.2    Orkin, S.H.3
  • 14
    • 0001627642 scopus 로고
    • Inherited antithrombin deficiency causing thrombophilia
    • Egeberg O: Inherited antithrombin deficiency causing thrombophilia. Thromb Diath Haemorrh 1965, 13:516.
    • (1965) Thromb Diath Haemorrh , vol.13 , pp. 516
    • Egeberg, O.1
  • 17
    • 0029743426 scopus 로고    scopus 로고
    • Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficiency newborn with massive thrombosis
    • Brenner B, Zivelin A, Lanir H, Greengard JS, Griffin JH, Seligsohn U: Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficiency newborn with massive thrombosis. Blood 1996, 88:877-880.
    • (1996) Blood , vol.88 , pp. 877-880
    • Brenner, B.1    Zivelin, A.2    Lanir, H.3    Greengard, J.S.4    Griffin, J.H.5    Seligsohn, U.6
  • 18
    • 0025598202 scopus 로고
    • Platelet hyperaggregability and prognosis in survivors of myocardial infarction
    • Trip MD, Cats VM, van Capelle FJ, Vreeken J: Platelet hyperaggregability and prognosis in survivors of myocardial infarction. N Engl J Med 1990, 323:1549-1554.
    • (1990) N Engl J Med , vol.323 , pp. 1549-1554
    • Trip, M.D.1    Cats, V.M.2    van Capelle, F.J.3    Vreeken, J.4
  • 19
    • 0030069693 scopus 로고    scopus 로고
    • Platelet activation mechanisms and markers in arterial thrombosis
    • Wu KK: Platelet activation mechanisms and markers in arterial thrombosis. J Intern Med 1996, 239:17-34.
    • (1996) J Intern Med , vol.239 , pp. 17-34
    • Wu, K.K.1
  • 20
    • 0022485106 scopus 로고
    • Haemostatic function and ischemic heart disease: Principal results of the Northwick Park Heart Study
    • Meade TW, Mellows S, Brtozovic M, Miller GJ, Chakrabarti RR, North WR, et al.: Haemostatic function and ischemic heart disease: Principal results of the Northwick Park Heart Study. Lancet 1986, ii:533-537.
    • (1986) Lancet , vol.2 , pp. 533-537
    • Meade, T.W.1    Mellows, S.2    Brtozovic, M.3    Miller, G.J.4    Chakrabarti, R.R.5    North, W.R.6
  • 22
    • 0023644095 scopus 로고
    • Fibrinogen and risk of cardiovascular disease: The Framingham Study
    • Kannel WB, Wolf PA, Castelli WP, D’Agostino RB: Fibrinogen and risk of cardiovascular disease: The Framingham Study. JAMA 1987, 258:1183-1186.
    • (1987) JAMA , vol.258 , pp. 1183-1186
    • Kannel, W.B.1    Wolf, P.A.2    Castelli, W.P.3    D’Agostino, R.B.4
  • 23
    • 0028127942 scopus 로고
    • Fibrinogen and factor VII in the prediction of coronary risk: Results from the PROCAM study in healthy men
    • Heinrich J, Balleisen L, Schulte H, Assmann G, van de Loo J: Fibrinogen and factor VII in the prediction of coronary risk: results from the PROCAM study in healthy men. Arterioscler Thromb 1994, 14:54-59.
    • (1994) Arterioscler Thromb , vol.14 , pp. 54-59
    • Heinrich, J.1    Balleisen, L.2    Schulte, H.3    Assmann, G.4    van de Loo, J.5
  • 24
    • 0027485501 scopus 로고
    • Association of hemostatic variables with prevalent cardiovascular disease and asymptomatic carotid artery atherosclerosis
    • Folsom AR, Wu KK, Shahar E, Davis CE: Association of hemostatic variables with prevalent cardiovascular disease and asymptomatic carotid artery atherosclerosis. Arterioscler Thromb 1993, 13:1829-1836.
    • (1993) Arterioscler Thromb , vol.13 , pp. 1829-1836
    • Folsom, A.R.1    Wu, K.K.2    Shahar, E.3    Davis, C.E.4
  • 26
    • 0029160815 scopus 로고
    • Human platelet alloantigens: Recent findings, new perspectives
    • Newman PJ, Valentin N: Human platelet alloantigens: recent findings, new perspectives. Thromb Haemost 1995, 74:234-239.
    • (1995) Thromb Haemost , vol.74 , pp. 234-239
    • Newman, P.J.1    Valentin, N.2
  • 28
    • 0019955397 scopus 로고
    • Fibrinogen γ chain locus on chromosome 4 in man
    • Olarsen B, Teisberg P, Gedde-Dahl T Jr: Fibrinogen γ chain locus on chromosome 4 in man. Hum Genet 1982, 61:24-26.
    • (1982) Hum Genet , vol.61 , pp. 24-26
    • Olarsen, B.1    Teisberg, P.2    Gedde-Dahl, T.3
  • 29
    • 0000751868 scopus 로고
    • Evolution and organization of the fibrinogen locus on chromosome 4: Gene duplication accompanied by transposition and inversion
    • Kant JA, Fornace AJ Jr, Saxe D, Simon Ml, McBride OW, Crabtree GR: Evolution and organization of the fibrinogen locus on chromosome 4: Gene duplication accompanied by transposition and inversion. Proc Natl Acad Sci USA 1985, 82:2344-2348.
    • (1985) Proc Natl Acad Sci USA , vol.82 , pp. 2344-2348
    • Kant, J.A.1    Fornace, A.J.2    Saxe, D.3    Ml, S.4    McBride, O.W.5    Crabtree, G.R.6
  • 30
    • 0028010815 scopus 로고
    • Overexpression of any fibrinogen chain by Hep G2 cells specifically elevates the expression of the other two chains
    • Roy S, Overton O, Redman C: Overexpression of any fibrinogen chain by Hep G2 cells specifically elevates the expression of the other two chains. J Biol Chem 1994, 269:691-695.
    • (1994) J Biol Chem , vol.269 , pp. 691-695
    • Roy, S.1    Overton, O.2    Redman, C.3
  • 31
    • 0027428484 scopus 로고
    • Human fibrinogen polymorphic site analysis by restriction endonuclease digestion and allele-specific polymerase chain reaction amplification: Identification of polymorphisms at positions Aa312 and Bβ448
    • Baumann RE, Henschen AH: Human fibrinogen polymorphic site analysis by restriction endonuclease digestion and allele-specific polymerase chain reaction amplification: identification of polymorphisms at positions Aa312 and Bβ448. Blood 1993, 82:2117-2124.
    • (1993) Blood , vol.82 , pp. 2117-2124
    • Baumann, R.E.1    Henschen, A.H.2
  • 32
    • 0023255622 scopus 로고
    • Role of genetic variation at the fibrinogen locus in determination of plasma fibrinogen concentrations
    • Humphries SE, Cook M, Dubowitz M, Stirling Y, Meade TW: Role of genetic variation at the fibrinogen locus in determination of plasma fibrinogen concentrations. Lancet 1987, i:1452-1455.
    • (1987) Lancet , vol.1 , pp. 1452-1455
    • Humphries, S.E.1    Cook, M.2    Dubowitz, M.3    Stirling, Y.4    Meade, T.W.5
  • 33
    • 0025754041 scopus 로고
    • Variation in the promoter region of the β-fibrinogen gene is associated with plasma fibrinogen levels in smokers and non-smokers
    • Thomas AE, Green FR, Kelleher CH, Wilkes PJ, Meade TW, Humphries SE: Variation in the promoter region of the β-fibrinogen gene is associated with plasma fibrinogen levels in smokers and non-smokers. Thromb Haemost 1991, 65:487-490.
    • (1991) Thromb Haemost , vol.65 , pp. 487-490
    • Thomas, A.E.1    Green, F.R.2    Kelleher, C.H.3    Wilkes, P.J.4    Meade, T.W.5    Humphries, S.E.6
  • 34
    • 9044240867 scopus 로고    scopus 로고
    • β-Fibrinogen gene polymorphisms are associated with plasma fibrinogen and coronary artery disease in patients with myocardial infarction. The ECTIM Study
    • Behague I, Poirier O, Nicaud V, Evans A, Arveiler D, Luc G, et al.: β-Fibrinogen gene polymorphisms are associated with plasma fibrinogen and coronary artery disease in patients with myocardial infarction. The ECTIM Study. Circulation 1996, 93:440-449.
    • (1996) Circulation , vol.93 , pp. 440-449
    • Behague, I.1    Poirier, O.2    Nicaud, V.3    Evans, A.4    Arveiler, D.5    Luc, G.6
  • 35
    • 0004330552 scopus 로고
    • Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation
    • O’Hara PJ, Grant FJ, Haldeman BA: Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation. Proc Natl Acad Sci USA 1987, 84:5158-5162.
    • (1987) Proc Natl Acad Sci USA , vol.84 , pp. 5158-5162
    • O’Hara, P.J.1    Grant, F.J.2    Haldeman, B.A.3
  • 36
    • 0025860324 scopus 로고
    • A common genetic polymorphism associated with lower coagulation factor VII levels in healthy individuals
    • Green F, Kelleher C, Wilkes H, Temple A, Meade T, Humphries S: A common genetic polymorphism associated with lower coagulation factor VII levels in healthy individuals. Arterioscler Thromb 1991, 11:540-546.
    • (1991) Arterioscler Thromb , vol.11 , pp. 540-546
    • Green, F.1    Kelleher, C.2    Wilkes, H.3    Temple, A.4    Meade, T.5    Humphries, S.6
  • 38
    • 0027947548 scopus 로고
    • Elevated levels of factor VII activity in the postprandial state: Effect of factor V arg-gln polymorphism
    • Silveira A, Green F, Karpe F, Blombäck MM, Humphries S, Hamsten A: Elevated levels of factor VII activity in the postprandial state: effect of factor V arg-gln polymorphism. Thromb Haemost 1994, 72:734-739.
    • (1994) Thromb Haemost , vol.72 , pp. 734-739
    • Silveira, A.1    Green, F.2    Karpe, F.3    Blombäck, M.M.4    Humphries, S.5    Hamsten, A.6
  • 40
    • 0022354051 scopus 로고
    • Increased plasma levels of a repaid inhibitor of PAI-1 in young survivors of myocardial infarction
    • Hamsten A, Wiman B, de Faire U, Blombsck M: Increased plasma levels of a repaid inhibitor of PAI-1 in young survivors of myocardial infarction. N Engl J Med 1985, 313:1557-1563.
    • (1985) N Engl J Med , vol.313 , pp. 1557-1563
    • Hamsten, A.1    Wiman, B.2    de Faire, U.3    Blombsck, M.4
  • 41
    • 0026016865 scopus 로고
    • Genetic variation at the plasminogen activator inhibitor-1 locus is associated with altered levels of PAI-1 activity
    • Dawson S, Hamsten A, Wiman B, Henny A, Humphries SE: Genetic variation at the plasminogen activator inhibitor-1 locus is associated with altered levels of PAI-1 activity. Atheroscler Thromb 1991, 11:183-190.
    • (1991) Atheroscler Thromb , vol.11 , pp. 183-190
    • Dawson, S.1    Hamsten, A.2    Wiman, B.3    Henny, A.4    Humphries, S.E.5
  • 42
    • 0028901713 scopus 로고
    • Allele specific increase in basal transcription of the PAI-1 gene is associated with myocardial infarction
    • Eriksson P, Kallin B, Van’t Hooft FM, Blivenholm P, Hamsten A: Allele specific increase in basal transcription of the PAI-1 gene is associated with myocardial infarction. Proc Natl Acad Sci USA 1995, 92:1851-1855.
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 1851-1855
    • Eriksson, P.1    Kallin, B.2    Van’t Hooft, F.M.3    Blivenholm, P.4    Hamsten, A.5
  • 43
    • 0029124975 scopus 로고
    • The 4G/5G genetic polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene is associated with differences in plasma PAI-1 activity but not with risk of myocardial infarction in the ECTIM Study
    • Ye S, Green FR, Scarabin PY, Nicaud V, Bara L, Dawson SJ, et al.: The 4G/5G genetic polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene is associated with differences in plasma PAI-1 activity but not with risk of myocardial infarction in the ECTIM Study. Thromb Haemost 1995, 74:837-841.
    • (1995) Thromb Haemost , vol.74 , pp. 837-841
    • Ye, S.1    Green, F.R.2    Scarabin, P.Y.3    Nicaud, V.4    Bara, L.5    Dawson, S.J.6
  • 44
    • 0025336443 scopus 로고
    • Hyperhomocyst(e)inemia. A common and easily reversible risk factor for occlusive atherosclerosis
    • Malinow MR: Hyperhomocyst(e)inemia. A common and easily reversible risk factor for occlusive atherosclerosis. Circulation 1990, 81:2004-2006.
    • (1990) Circulation , vol.81 , pp. 2004-2006
    • Malinow, M.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.