메뉴 건너뛰기




Volumn 79, Issue 1, 2005, Pages 9-13

Prevalence of the Factor V G1691A and the Factor II/prothrombin G20210A gene polymorphisms among Tamilians

Author keywords

Factor V G1691A; Single nucleotide polymorphisms; Tamilians

Indexed keywords

BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; PROTHROMBIN;

EID: 22144472522     PISSN: 00144800     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.yexmp.2005.03.003     Document Type: Article
Times cited : (23)

References (28)
  • 1
    • 0028106062 scopus 로고
    • High prevalence of a mutation in the factor V gene within the UK population: Relationship to activated protein C resistance and familial thrombosis
    • N.J. Beauchamp, M.E. Daly, K.K. Hampton, P.C. Cooper, and E. Preston High prevalence of a mutation in the factor V gene within the UK population: relationship to activated protein C resistance and familial thrombosis Hypertension 88 1994 219 222
    • (1994) Hypertension , vol.88 , pp. 219-222
    • Beauchamp, N.J.1    Daly, M.E.2    Hampton, K.K.3    Cooper, P.C.4    Preston, E.5
  • 3
    • 0026755597 scopus 로고
    • Structure of the gene for human coagulation factor V
    • L.D. Cripe, K.D. Moore, and W.H. Kane Structure of the gene for human coagulation factor V Biochemistry 31 1992 3777 3785
    • (1992) Biochemistry , vol.31 , pp. 3777-3785
    • Cripe, L.D.1    Moore, K.D.2    Kane, W.H.3
  • 4
    • 0023230641 scopus 로고
    • Nucleotide sequence of the gene for human prothrombin
    • S.J.F. Degen, and E.W. Davie Nucleotide sequence of the gene for human prothrombin Biochemistry 26 1987 6165
    • (1987) Biochemistry , vol.26 , pp. 6165
    • Degen, S.J.F.1    Davie, E.W.2
  • 6
    • 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
    • C.J. Doggen, V.M. Cats, R.M. Bertina, and F. Rosendaal Interaction of coagulation defects and cardiovascular risk factors increased risk of myocardial infarction associated with factor V leiden or prothrombin 20210A Circulation 97 1998 1037 1041
    • (1998) Circulation , vol.97 , pp. 1037-1041
    • Doggen, C.J.1    Cats, V.M.2    Bertina, R.M.3    Rosendaal, F.4
  • 7
    • 0027155952 scopus 로고
    • Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants
    • J. Flint, R.M. Harding, J.B. Clegg, and A.J. Boyce Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants Hum. Genet. 91 1993 91 117
    • (1993) Hum. Genet. , vol.91 , pp. 91-117
    • Flint, J.1    Harding, R.M.2    Clegg, J.B.3    Boyce, A.J.4
  • 8
    • 0031856405 scopus 로고    scopus 로고
    • Prevalence of the G20210A polymorphism in the 3′-untranslated region of the prothrombin gene in different human populations
    • R.F. Franco, S.E.B. Santos, J. Elion, M.H. Tavella, and M.A. Zago Prevalence of the G20210A polymorphism in the 3′-untranslated region of the prothrombin gene in different human populations Acta Haematol. 100 1998 9 12
    • (1998) Acta Haematol. , vol.100 , pp. 9-12
    • Franco, R.F.1    Santos, S.E.B.2    Elion, J.3    Tavella, M.H.4    Zago, M.A.5
  • 9
    • 0027428481 scopus 로고
    • Anticoagulant protein C pathway defective in majority of thrombophilic patients
    • J.H. Griffin, B. Evatt, C. Wideman, and J.A. Fernandez Anticoagulant protein C pathway defective in majority of thrombophilic patients Blood 82 1993 1989 1993
    • (1993) Blood , vol.82 , pp. 1989-1993
    • Griffin, J.H.1    Evatt, B.2    Wideman, C.3    Fernandez, J.A.4
  • 10
    • 0030742356 scopus 로고    scopus 로고
    • Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell disease
    • D. Helley, C. Besmond, R. Ducrocq, F. da Silva, M.C. Guillin, A. Bezeaud, and J. Elion Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell disease Hum. Genet. 100 1996 245 248
    • (1996) Hum. Genet. , vol.100 , pp. 245-248
    • Helley, D.1    Besmond, C.2    Ducrocq, R.3    Da Silva, F.4    Guillin, M.C.5    Bezeaud, A.6    Elion, J.7
  • 11
    • 32744456450 scopus 로고    scopus 로고
    • Genotype distribution of the mutations in the coagulation factor V gene in the Korean population: Absence of its association with coronary artery disease
    • S.H. Hong Genotype distribution of the mutations in the coagulation factor V gene in the Korean population: absence of its association with coronary artery disease Korean J. Biol. Sci. 7 2003 255 259
    • (2003) Korean J. Biol. Sci. , vol.7 , pp. 255-259
    • Hong, S.H.1
  • 12
    • 0032005263 scopus 로고    scopus 로고
    • The prothrombin gene 3′-untranslated region is frequently associated with factor V Leiden in thrombophilic patients and shows ethnic-specific variation in allele frequency
    • T.E. Howard, M. Marusa, and J. Boisza The prothrombin gene 3′-untranslated region is frequently associated with factor V Leiden in thrombophilic patients and shows ethnic-specific variation in allele frequency Blood 91 1998 1092
    • (1998) Blood , vol.91 , pp. 1092
    • Howard, T.E.1    Marusa, M.2    Boisza, J.3
  • 16
    • 0029116980 scopus 로고
    • Molecular detection of a common mutation in coagulation factor V causing thrombosis via hereditary resistance to activated protein C
    • X.Y. Liu, D. Nelson, C. Grant, V. Morthland, S.H. Goodnight, and R.D. Press Molecular detection of a common mutation in coagulation factor V causing thrombosis via hereditary resistance to activated protein C Diagn. Mol. Pathol. 4 1995 191 197
    • (1995) Diagn. Mol. Pathol. , vol.4 , pp. 191-197
    • Liu, X.Y.1    Nelson, D.2    Grant, C.3    Morthland, V.4    Goodnight, S.H.5    Press, R.D.6
  • 19
    • 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
    • S.R. Poort, F.R. Rosendaal, P.H. Reitsma, and R.M. Bertina 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    Bertina, R.M.4
  • 20
    • 0028810738 scopus 로고
    • World distribution of factor V Leiden
    • D.C. Rees, M. Cox, and J.B. Clegg World distribution of factor V Leiden Lancet 346 1995 1133 1134
    • (1995) Lancet , vol.346 , pp. 1133-1134
    • Rees, D.C.1    Cox, M.2    Clegg, J.B.3
  • 21
    • 0028931717 scopus 로고
    • High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance)
    • F.R. Rosendaal, T. Koster, J.P. Vandenbroucke, and P.H. Reitsma High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance) Blood 85 1995 1504 1508
    • (1995) Blood , vol.85 , pp. 1504-1508
    • Rosendaal, F.R.1    Koster, T.2    Vandenbroucke, J.P.3    Reitsma, P.H.4
  • 22
    • 0030921663 scopus 로고    scopus 로고
    • A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women
    • F.R. Rosendaal, D.S. Siscovick, S.M. Schwartz, B.M. Psaty, T.E. Raghunathan, and H.L. Vos A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women Blood 90 1997 1747 1750
    • (1997) Blood , vol.90 , pp. 1747-1750
    • Rosendaal, F.R.1    Siscovick, D.S.2    Schwartz, S.M.3    Psaty, B.M.4    Raghunathan, T.E.5    Vos, H.L.6
  • 25
    • 0035912152 scopus 로고    scopus 로고
    • Genetic susceptibility to venous thrombosis
    • U. Seligsohn, and A. Lubetsky Genetic susceptibility to venous thrombosis N. Engl. J. Med. 344 2001 1222 1231
    • (2001) N. Engl. J. Med. , vol.344 , pp. 1222-1231
    • Seligsohn, U.1    Lubetsky, A.2
  • 26
    • 85088671715 scopus 로고
    • APC-resistance and MnlI genotype (Gln 506) of coagulation factor V are rare in Japanese population [letter]
    • O. Takamiya, F. Ishida, and H. Kodaira APC-resistance and MnlI genotype (Gln 506) of coagulation factor V are rare in Japanese population [letter] Thromb. Haemostasis 74 1995 996
    • (1995) Thromb. Haemostasis , vol.74 , pp. 996
    • Takamiya, O.1    Ishida, F.2    Kodaira, H.3
  • 27
    • 2942603511 scopus 로고    scopus 로고
    • The contribution of factor V Leiden and prothrombin G20210A mutation to the risk of central venous catheter-related thrombosis
    • C.J. van Rooden, F.R. Rosendaal, A.E. Meinders, J.A. Van oostayen, F.J.M. vander Meer, and M.V. Huisman The contribution of factor V Leiden and prothrombin G20210A mutation to the risk of central venous catheter-related thrombosis Haematologica 89 2004 201 206 (B S T R A C T)
    • (2004) Haematologica , vol.89 , pp. 201-206
    • Van Rooden, C.J.1    Rosendaal, F.R.2    Meinders, A.E.3    Van Oostayen, J.A.4    Vander Meer, F.J.M.5    Huisman, M.V.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.