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Volumn 44, Issue 11, 1998, Pages 2360-2362

Genotyping method for methylenetetrahydrofolate reductase (C677T thermolabile variant) using heteroduplex technology

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); FOLIC ACID;

EID: 0031757073     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (31)

References (11)
  • 1
    • 0029066299 scopus 로고
    • A quantitative assessment of plasma homocysteine as a risk factor for vascular disease-probable benefits of increasing folic acid intake
    • Boushey CJ, Beresford SAA, Omenn GS, Motulsky AG. A quantitative assessment of plasma homocysteine as a risk factor for vascular disease-probable benefits of increasing folic acid intake. JAMA 1995;274:1049-57.
    • (1995) JAMA , vol.274 , pp. 1049-1057
    • Boushey, C.J.1    Beresford, S.A.A.2    Omenn, G.S.3    Motulsky, A.G.4
  • 2
    • 0030611076 scopus 로고    scopus 로고
    • MTHFR 677C→T mutation, folate intake, neurl tube defect, and risk of cardiovascular disease
    • Wilcken DE. MTHFR 677C→T mutation, folate intake, neurl tube defect, and risk of cardiovascular disease. Lancet 1997;388:603-4.
    • (1997) Lancet , vol.388 , pp. 603-604
    • Wilcken, D.E.1
  • 4
    • 0027421353 scopus 로고
    • Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease
    • Kang SS, Passen EL, Ruggie N, Wong APWK, Sora H. Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease. Circulation 1993;88:1463-9.
    • (1993) Circulation , vol.88 , pp. 1463-1469
    • Kang, S.S.1    Passen, E.L.2    Ruggie, N.3    Wong, A.P.W.K.4    Sora, H.5
  • 5
    • 0030027668 scopus 로고    scopus 로고
    • Relation between folate status, a common mutation in methylene tetrahydrofolate reductase, and plasma homocysteine concentrations
    • Jacques PF, Bostom AG, William RR, Ellison RC, Eckfeldt JH, Rosenberg IH, et al. Relation between folate status, a common mutation in methylene tetrahydrofolate reductase, and plasma homocysteine concentrations. Circulation 1996;93:7-9.
    • (1996) Circulation , vol.93 , pp. 7-9
    • Jacques, P.F.1    Bostom, A.G.2    William, R.R.3    Ellison, R.C.4    Eckfeldt, J.H.5    Rosenberg, I.H.6
  • 6
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: A common mutation in methylene tetrahydrofolate reductase
    • Frosst P, Blom HL, Milos R, Goyette P, Sheppard CA, Matthews TH, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylene tetrahydrofolate reductase. Nat Genet 1995;10:111-3.
    • (1995) Nat Genet , vol.10 , pp. 111-113
    • Frosst, P.1    Blom, H.L.2    Milos, R.3    Goyette, P.4    Sheppard, C.A.5    Matthews, T.H.6
  • 7
    • 0030068698 scopus 로고    scopus 로고
    • Genetic screening and testing by induced heteroduplex formation
    • Wood N, Bidwell J. Genetic screening and testing by induced heteroduplex formation. Electrophoresis 1996;17:247-54.
    • (1996) Electrophoresis , vol.17 , pp. 247-254
    • Wood, N.1    Bidwell, J.2
  • 9
    • 7844220423 scopus 로고    scopus 로고
    • The 677C→T mutation in the methylene tetrahydrofolate reduc tase gene is not related to hyperhomocysteinaemia in thrombotic disease
    • Ankri A, Bonnefont JP, Chadefauz-Vekemans B, Mostefa AK, Aupetit J, Couty MC, et al. The 677C→T mutation in the methylene tetrahydrofolate reduc tase gene is not related to hyperhomocysteinaemia in thrombotic disease [Abstract]. Thromb Haemost Suppl 1997:P2160.
    • (1997) Thromb Haemost Suppl
    • Ankri, A.1    Bonnefont, J.P.2    Chadefauz-Vekemans, B.3    Mostefa, A.K.4    Aupetit, J.5    Couty, M.C.6
  • 10
    • 0029738540 scopus 로고    scopus 로고
    • The common thermolabile variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia
    • Harmon DL, Woodside JV, Yarnell JWG, McMaster D, Young IS, McCrum EE, et al. The common thermolabile variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia. Q J Med 1996;89:571-7.
    • (1996) Q J Med , vol.89 , pp. 571-577
    • Harmon, D.L.1    Woodside, J.V.2    Yarnell, J.W.G.3    McMaster, D.4    Young, I.S.5    McCrum, E.E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.