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Volumn 11, Issue 3, 2005, Pages 343-345

Roles of methylenetetrahydrofolate reductase C677T polymorphism in repeated pregnancy loss

Author keywords

Methylenetetrahydrofolate reductase; Polymorphism; Repeated pregnancy loss

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);

EID: 22544443919     PISSN: 10760296     EISSN: None     Source Type: Journal    
DOI: 10.1177/107602960501100315     Document Type: Article
Times cited : (12)

References (12)
  • 1
    • 0035016873 scopus 로고    scopus 로고
    • Recurrent pregnancy loss: Etiology of thrombophilia
    • Yamada H, Kato EH, Kobashi G, et al. Recurrent pregnancy loss: Etiology of thrombophilia. Semin Thromb Hemost 2001;27:121.
    • (2001) Semin Thromb Hemost , vol.27 , pp. 121
    • Yamada, H.1    Kato, E.H.2    Kobashi, G.3
  • 2
    • 0035552975 scopus 로고    scopus 로고
    • Polymorphisms in the methylenetetrahydrofolate reductase gene: Clinical consequences
    • Schwahn B, Rozen R. Polymorphisms in the methylenetetrahydrofolate reductase gene: Clinical consequences. Am J Pharmacogenomics 2001;1:189.
    • (2001) Am J Pharmacogenomics , vol.1 , pp. 189
    • Schwahn, B.1    Rozen, R.2
  • 3
    • 2442540135 scopus 로고    scopus 로고
    • Correlation between C677T MTHFR gene polymorphism, plasma homocysteine levels and the incidence of CAD
    • Nakai K, Itoh C, Nakai K, et al. Correlation between C677T MTHFR gene polymorphism, plasma homocysteine levels and the incidence of CAD. Am J Cardiovasc Drugs 2001;1:353.
    • (2001) Am J Cardiovasc Drugs , vol.1 , pp. 353
    • Nakai, K.1    Itoh, C.2    Nakai, K.3
  • 4
    • 1442300286 scopus 로고    scopus 로고
    • Polymorphisms in genes involved in folate metabolism and colorectal neoplasia: A huge review
    • Sharp L, Little J. Polymorphisms in genes involved in folate metabolism and colorectal neoplasia: A Huge review. Am J Epidemiol 2004;159:423.
    • (2004) Am J Epidemiol , vol.159 , pp. 423
    • Sharp, L.1    Little, J.2
  • 5
    • 4644240521 scopus 로고    scopus 로고
    • C677T and A1298C mutation of the methylenetetrahydrofolate reductase gene in unexplained recurrent spontaneous abortion
    • Wang XP, Lin QD, Ma ZW, Zhao AM. C677T and A1298C mutation of the methylenetetrahydrofolate reductase gene in unexplained recurrent spontaneous abortion. Zhonghua Fu Chan Ke Za Zhi 2004;39:238.
    • (2004) Zhonghua Fu Chan Ke Za Zhi , vol.39 , pp. 238
    • Wang, X.P.1    Lin, Q.D.2    Ma, Z.W.3    Zhao, A.M.4
  • 6
    • 0141538396 scopus 로고    scopus 로고
    • Analyzes of three common thrombophilic gene mutations in German women with recurrent abortions
    • Pauer HU, Voigt-Tschirschwitz T, Hinney B, et al. Analyzes of three common thrombophilic gene mutations in German women with recurrent abortions. Acta Obstet Gynecol Scand 2003;82:942.
    • (2003) Acta Obstet Gynecol Scand , vol.82 , pp. 942
    • Pauer, H.U.1    Voigt-Tschirschwitz, T.2    Hinney, B.3
  • 7
    • 0037258565 scopus 로고    scopus 로고
    • Plasma homocysteine levels correlated to interactions between folate status and methylene tetrahydrofolate reductase gene mutation in women with unexplained recurrent pregnancy loss
    • Kumar KS, Govindaiah V, Naushad SE, et al. Plasma homocysteine levels correlated to interactions between folate status and methylene tetrahydrofolate reductase gene mutation in women with unexplained recurrent pregnancy loss. J Obstet Gynaecol 2003;23:55.
    • (2003) J Obstet Gynaecol , vol.23 , pp. 55
    • Kumar, K.S.1    Govindaiah, V.2    Naushad, S.E.3
  • 8
    • 0035989412 scopus 로고    scopus 로고
    • Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss
    • Carp H, Salomon O, Seidman D, et al. Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss. Hum Reprod 2002;17:1633.
    • (2002) Hum Reprod , vol.17 , pp. 1633
    • Carp, H.1    Salomon, O.2    Seidman, D.3
  • 9
    • 0036129677 scopus 로고    scopus 로고
    • The C677T polymorphism of the methylenetetrahydrofolate reductase gene and idiopathic recurrent miscarriage
    • Unfried G, Griesmacher A, Weismuller W, et al. The C677T polymorphism of the methylenetetrahydrofolate reductase gene and idiopathic recurrent miscarriage. Obstet Gynecol 2002;99:614.
    • (2002) Obstet Gynecol , vol.99 , pp. 614
    • Unfried, G.1    Griesmacher, A.2    Weismuller, W.3
  • 10
    • 0033955432 scopus 로고    scopus 로고
    • Factor V leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages
    • Foka ZJ, Lambropoulos AF, Saravelos H, et al. Factor V leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages. Hum Reprod 2000;15:458.
    • (2000) Hum Reprod , vol.15 , pp. 458
    • Foka, Z.J.1    Lambropoulos, A.F.2    Saravelos, H.3
  • 11
    • 0032767244 scopus 로고    scopus 로고
    • Thrombophilic polymorphisms are common in women with fetal loss without apparent cause
    • Brenner B, Sarig G, Weiner Z, et al. Thrombophilic polymorphisms are common in women with fetal loss without apparent cause. Thromb Haemost 1999;82:6.
    • (1999) Thromb Haemost , vol.82 , pp. 6
    • Brenner, B.1    Sarig, G.2    Weiner, Z.3
  • 12
    • 0032891393 scopus 로고    scopus 로고
    • The C677T MTHFR gene mutation is not predictive of risk for recurrent fetal loss
    • Holmes ZR, Regan L, Chilcott I, Cohen H. The C677T MTHFR gene mutation is not predictive of risk for recurrent fetal loss. Br J Haematol 1999;105:98.
    • (1999) Br J Haematol , vol.105 , pp. 98
    • Holmes, Z.R.1    Regan, L.2    Chilcott, I.3    Cohen, H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.