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Volumn 14, Issue 7, 2007, Pages 635-638

The prothrombin gene G20210A variant and puerperal cerebral venous and sinus thrombosis in South Indian women

Author keywords

Prothrombin G20210A polymorphism; Puerperal cerebral veno sinus thrombosis

Indexed keywords

G20210A PROTEIN; GENE PRODUCT; PROTHROMBIN; UNCLASSIFIED DRUG;

EID: 34249045125     PISSN: 09675868     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jocn.2006.05.001     Document Type: Article
Times cited : (10)

References (29)
  • 1
    • 0034628404 scopus 로고    scopus 로고
    • The challenge of thrombophilia in maternal-fetal medicine
    • Greer I.A. The challenge of thrombophilia in maternal-fetal medicine. N Engl J Med 342 (2000) 424-425
    • (2000) N Engl J Med , vol.342 , pp. 424-425
    • Greer, I.A.1
  • 2
    • 0021079081 scopus 로고
    • Cerebral venous and arterial thrombosis in pregnancy and puerperium. A study of 135 patients
    • Srinivasan K. Cerebral venous and arterial thrombosis in pregnancy and puerperium. A study of 135 patients. Angiology 34 (1983) 731-746
    • (1983) Angiology , vol.34 , pp. 731-746
    • Srinivasan, K.1
  • 3
    • 0345062283 scopus 로고    scopus 로고
    • The prothrombin gene variant 20210A in venous and arterial thromboembolism
    • Vicente V., Gonzalez-Conejero R., Rivera J., et al. The prothrombin gene variant 20210A in venous and arterial thromboembolism. Haematologica 84 (1999) 356-362
    • (1999) Haematologica , vol.84 , pp. 356-362
    • Vicente, V.1    Gonzalez-Conejero, R.2    Rivera, J.3
  • 4
    • 0031981017 scopus 로고    scopus 로고
    • Geographic distribution of the 20210 G to A prothrombin variant
    • Rosendaal F.R., Doggen C.J., and Zivelin A. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 79 (1998) 706-708
    • (1998) Thromb Haemost , vol.79 , pp. 706-708
    • Rosendaal, F.R.1    Doggen, C.J.2    Zivelin, A.3
  • 5
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller S.A., Dykes D.D., and Polesky H.F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucl Acids Res 16 (1988) 1215
    • (1988) Nucl Acids Res , vol.16 , pp. 1215
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 6
    • 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 S.R., Rosendaal F.R., Reitsma P.H., et al. 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 88 (1996) 3698-3703
    • (1996) Blood , vol.88 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3
  • 7
    • 0036339190 scopus 로고    scopus 로고
    • Treatment of cerebral sinus/venous thrombosis
    • Nagaraja D., and Sarma G.R. Treatment of cerebral sinus/venous thrombosis. Neurol India 50 (2002) 114-116
    • (2002) Neurol India , vol.50 , pp. 114-116
    • Nagaraja, D.1    Sarma, G.R.2
  • 8
    • 0023230641 scopus 로고
    • Nucleotide sequence of the gene for human prothrombin
    • Degan S.J.F., and Davie E.W. Nucleotide sequence of the gene for human prothrombin. Biochemistry 26 (1987) 6165
    • (1987) Biochemistry , vol.26 , pp. 6165
    • Degan, S.J.F.1    Davie, E.W.2
  • 9
    • 0034939628 scopus 로고    scopus 로고
    • Increased efficiency of mRNA 3′ end formation: a new genetic mechanism contributing to hereditary thrombophilia
    • Gehring N.H., Frede U., Neu-Yilik G., et al. Increased efficiency of mRNA 3′ end formation: a new genetic mechanism contributing to hereditary thrombophilia. Nat Genet 28 (2001) 389-392
    • (2001) Nat Genet , vol.28 , pp. 389-392
    • Gehring, N.H.1    Frede, U.2    Neu-Yilik, G.3
  • 10
    • 0034310731 scopus 로고    scopus 로고
    • Hyperprothrombinemia may result in acquired activated protein C resistance
    • Tripodi A., Chantarangkul V., Mannucci P.M., et al. Hyperprothrombinemia may result in acquired activated protein C resistance. Blood 96 (2000) 3295-3296
    • (2000) Blood , vol.96 , pp. 3295-3296
    • Tripodi, A.1    Chantarangkul, V.2    Mannucci, P.M.3
  • 11
    • 0030792668 scopus 로고    scopus 로고
    • The prothrombin gene G20210A variant: prevalence in a UK anticoagulant clinic population
    • Cumming A.M., Keeney S., Salden A., et al. The prothrombin gene G20210A variant: prevalence in a UK anticoagulant clinic population. Br J Haematol 98 (1997) 353-355
    • (1997) Br J Haematol , vol.98 , pp. 353-355
    • Cumming, A.M.1    Keeney, S.2    Salden, A.3
  • 12
    • 0032387846 scopus 로고    scopus 로고
    • Prevalence of the prothrombin 20210 G-to-A variant in blacks: infants, patients with venous thrombosis, patients with myocardial infarction, and control subjects
    • Dilley A., Austin H., Hooper W.C., et al. Prevalence of the prothrombin 20210 G-to-A variant in blacks: infants, patients with venous thrombosis, patients with myocardial infarction, and control subjects. J Lab Clin Med 132 (1998) 452-455
    • (1998) J Lab Clin Med , vol.132 , pp. 452-455
    • Dilley, A.1    Austin, H.2    Hooper, W.C.3
  • 13
    • 0031618374 scopus 로고    scopus 로고
    • Frequencies of prothrombin 20210 G → A mutation may be different among races-studies on Japanese populations with various forms of thrombotic disorders and healthy subjects
    • Isshiki I., Murata M., Watanabe R., et al. Frequencies of prothrombin 20210 G → A mutation may be different among races-studies on Japanese populations with various forms of thrombotic disorders and healthy subjects. Blood Coagul Fibrinolysis 9 (1998) 105-106
    • (1998) Blood Coagul Fibrinolysis , vol.9 , pp. 105-106
    • Isshiki, I.1    Murata, M.2    Watanabe, R.3
  • 14
    • 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., Zoller B., Svensson P.J., et al. The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis. Thromb Haemost 78 (1997) 990-992
    • (1997) Thromb Haemost , vol.78 , pp. 990-992
    • Hillarp, A.1    Zoller, B.2    Svensson, P.J.3
  • 15
    • 20044382874 scopus 로고    scopus 로고
    • Clinical manifestations of the prothrombin G20210A mutation in children: a pediatric coagulation consortium study
    • Young G., Manco-Johnson M., Gill J.C., et al. Clinical manifestations of the prothrombin G20210A mutation in children: a pediatric coagulation consortium study. J Thromb Haemost 1 (2003) 958-962
    • (2003) J Thromb Haemost , vol.1 , pp. 958-962
    • Young, G.1    Manco-Johnson, M.2    Gill, J.C.3
  • 16
    • 0031756655 scopus 로고    scopus 로고
    • Inherited prothrombotic risk factors and cerebral venous thrombosis
    • Hillier C.E., Collins P.W., Bowen D.J., et al. Inherited prothrombotic risk factors and cerebral venous thrombosis. QJM 91 (1998) 677-680
    • (1998) QJM , vol.91 , pp. 677-680
    • Hillier, C.E.1    Collins, P.W.2    Bowen, D.J.3
  • 17
    • 0033920794 scopus 로고    scopus 로고
    • G20210A PRTH gene mutation and other thrombophilic polymorphisms in cerebral venous thrombosis
    • Madonna P., de Stefano A., Coppola A., et al. G20210A PRTH gene mutation and other thrombophilic polymorphisms in cerebral venous thrombosis. Stroke 31 (2000) 1787-1788
    • (2000) Stroke , vol.31 , pp. 1787-1788
    • Madonna, P.1    de Stefano, A.2    Coppola, A.3
  • 18
    • 0032543748 scopus 로고    scopus 로고
    • High risk of cerebral-vein thrombosis in carriers of a prothrombin gene mutation and in users of oral contraceptives
    • Martinelli I., Sacchi E., Landi G., et al. High risk of cerebral-vein thrombosis in carriers of a prothrombin gene mutation and in users of oral contraceptives. N Engl J Med 338 (1998) 1793-1797
    • (1998) N Engl J Med , vol.338 , pp. 1793-1797
    • Martinelli, I.1    Sacchi, E.2    Landi, G.3
  • 19
    • 0031595694 scopus 로고    scopus 로고
    • Prothrombin gene G20210-A transition is a risk factor for cerebral venous thrombosis
    • Reuner K.H., Ruf A., Grau A., et al. Prothrombin gene G20210-A transition is a risk factor for cerebral venous thrombosis. Stroke 29 (1998) 1765-1769
    • (1998) Stroke , vol.29 , pp. 1765-1769
    • Reuner, K.H.1    Ruf, A.2    Grau, A.3
  • 20
    • 11444268843 scopus 로고    scopus 로고
    • Prothrombin G20210A mutation, and not factor V Leiden mutation, is a risk factor for cerebral venous thrombosis in Brazilian patients
    • Rodrigues C.A., Rocha L.K., Morelli V.M., et al. Prothrombin G20210A mutation, and not factor V Leiden mutation, is a risk factor for cerebral venous thrombosis in Brazilian patients. J Thromb Haemost 2 (2004) 1211-1212
    • (2004) J Thromb Haemost , vol.2 , pp. 1211-1212
    • Rodrigues, C.A.1    Rocha, L.K.2    Morelli, V.M.3
  • 21
    • 11444253333 scopus 로고    scopus 로고
    • Prothrombin 20210A and oral contraceptive use as risk factors for cerebral venous thrombosis
    • Gadelha T., Andre C., Juca A.A., et al. Prothrombin 20210A and oral contraceptive use as risk factors for cerebral venous thrombosis. Cerebrovasc Dis 19 (2005) 49-52
    • (2005) Cerebrovasc Dis , vol.19 , pp. 49-52
    • Gadelha, T.1    Andre, C.2    Juca, A.A.3
  • 22
    • 33644933673 scopus 로고    scopus 로고
    • Risk of cerebral venous thrombosis and novel gene polymorphisms of the coagulation and fibrinolytic systems
    • Lichy C., Dong-Si T., Reuner K., et al. Risk of cerebral venous thrombosis and novel gene polymorphisms of the coagulation and fibrinolytic systems. J Neurol 253 (2006) 16-20
    • (2006) J Neurol , vol.253 , pp. 16-20
    • Lichy, C.1    Dong-Si, T.2    Reuner, K.3
  • 23
    • 33645510408 scopus 로고    scopus 로고
    • Thrombophilic abnormalities, oral contraceptives and risk of cerebral vein thrombosis: a meta-analysis
    • Dentali F., Crowther M., and Dentali W.A. Thrombophilic abnormalities, oral contraceptives and risk of cerebral vein thrombosis: a meta-analysis. Blood 107 (2006) 2766-2773
    • (2006) Blood , vol.107 , pp. 2766-2773
    • Dentali, F.1    Crowther, M.2    Dentali, W.A.3
  • 24
    • 0031904536 scopus 로고    scopus 로고
    • Coincidence of factor V Leiden mutation and a mutation in the prothrombin gene at position 20210 in a patient with puerperal cerebral venous thrombosis
    • Weih M., Mehraein S., Valdueza J.M., et al. Coincidence of factor V Leiden mutation and a mutation in the prothrombin gene at position 20210 in a patient with puerperal cerebral venous thrombosis. Stroke 29 (1998) 1739-1740
    • (1998) Stroke , vol.29 , pp. 1739-1740
    • Weih, M.1    Mehraein, S.2    Valdueza, J.M.3
  • 25
    • 2442637355 scopus 로고    scopus 로고
    • Prothrombin 20210A is not prevalent in North India
    • Garewal G., Das R., Ahluwalia J., et al. Prothrombin 20210A is not prevalent in North India. J Thromb Haemost 1 (2003) 2253-2254
    • (2003) J Thromb Haemost , vol.1 , pp. 2253-2254
    • Garewal, G.1    Das, R.2    Ahluwalia, J.3
  • 26
    • 0035088186 scopus 로고    scopus 로고
    • Venous thromboembolism in young patients from western India: a study
    • Ghosh K., Shetty S., Madkaikar M., et al. Venous thromboembolism in young patients from western India: a study. Clin Appl Thromb Hemost 7 (2001) 158-165
    • (2001) Clin Appl Thromb Hemost , vol.7 , pp. 158-165
    • Ghosh, K.1    Shetty, S.2    Madkaikar, M.3
  • 27
    • 30644460368 scopus 로고    scopus 로고
    • Prothrombin G20210A gene variant is not associated with idiopathic portal vein thrombosis in an area endemic for portal vein thrombosis
    • Koshy A., and Jeyakumari M. Prothrombin G20210A gene variant is not associated with idiopathic portal vein thrombosis in an area endemic for portal vein thrombosis. Ann Hematol 85 (2006) 126-128
    • (2006) Ann Hematol , vol.85 , pp. 126-128
    • Koshy, A.1    Jeyakumari, M.2
  • 28
    • 22144472522 scopus 로고    scopus 로고
    • Prevalence of the Factor V G1691A and the Factor II/prothrombin G20210A gene polymorphisms among Tamilians
    • Angeline T., Bentley H.A., Hawk A.B., et al. Prevalence of the Factor V G1691A and the Factor II/prothrombin G20210A gene polymorphisms among Tamilians. Exp Mol Pathol 79 (2005) 9-13
    • (2005) Exp Mol Pathol , vol.79 , pp. 9-13
    • Angeline, T.1    Bentley, H.A.2    Hawk, A.B.3


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