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Volumn 54, Issue 5, 2005, Pages 733-734

Genotypes 677TT and 677CT+ 1298AC of methylenetetrahydrofolate reductase are associated with the severity of ulcerative colitis in central China [10]

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);

EID: 17644380328     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.2004.062539     Document Type: Letter
Times cited : (18)

References (10)
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    • Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with inflammatory bowel disease, and its clinical implications
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    • (1999) Gut , vol.45 , pp. 389-394
    • Mahmud, N.1    Molloy, A.2    McPartlin, J.3
  • 2
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    • Review article: Inherited thrombophilia in inflammatory bowel disease
    • Papa A, Danese S, Grillo A, et al. Review article: inherited thrombophilia in inflammatory bowel disease. Am J Gastroenterol 2003;98:1247-51.
    • (2003) Am J Gastroenterol , vol.98 , pp. 1247-1251
    • Papa, A.1    Danese, S.2    Grillo, A.3
  • 4
    • 0033856051 scopus 로고    scopus 로고
    • Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with IBD
    • Nielsen JN, Larsen TB, Fredholm L, et al. Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with IBD. Gut 2000;47:456-7.
    • (2000) Gut , vol.47 , pp. 456-457
    • Nielsen, J.N.1    Larsen, T.B.2    Fredholm, L.3
  • 5
    • 0033869354 scopus 로고    scopus 로고
    • Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis
    • Vecchi M, Sacchi E, Saibeni S, et al. Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis. Dig Dis Sci 2000;45:1465-9.
    • (2000) Dig Dis Sci , vol.45 , pp. 1465-1469
    • Vecchi, M.1    Sacchi, E.2    Saibeni, S.3
  • 6
    • 0034827834 scopus 로고    scopus 로고
    • Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease
    • Papa A, De Stefano V, Danese S, et al. Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease: Am J Gastroenterol 2001;96:2677-82.
    • (2001) Am J Gastroenterol , vol.96 , pp. 2677-2682
    • Papa, A.1    De Stefano, V.2    Danese, S.3
  • 7
    • 0343807499 scopus 로고    scopus 로고
    • Prothrombotic inherited abnormalities other than factor V Leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease
    • Guedon C, Le Cam-Duchez, Lalaude O, et al. Prothrombotic inherited abnormalities other than factor V Leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease. Am J Gatroenterol 2001;96:1448-54.
    • (2001) Am J Gatroenterol , vol.96 , pp. 1448-1454
    • Guedon, C.1    Le Cam-Duchez2    Lalaude, O.3
  • 8
    • 0035865701 scopus 로고    scopus 로고
    • Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: Relation to transcobolamin and homocysteine concentration in blood
    • Namour F, Olivier JL, Abdelmouttaleb I, et al. Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobolamin and homocysteine concentration in blood. Blood 2001;97:1092-8.
    • (2001) Blood , vol.97 , pp. 1092-1098
    • Namour, F.1    Olivier, J.L.2    Abdelmouttaleb, I.3
  • 9
    • 2142819381 scopus 로고    scopus 로고
    • High prevalence of hyperhomocysteinemia related to folate deficiency and mutated 677 C→MTHFR, in the coast of West Africa
    • Amouzou E, Chabi N, Adjalla C, et al. High prevalence of hyperhomocysteinemia related to folate deficiency and mutated 677 C→MTHFR, in the coast of West Africa. Am J Clin Nutr 2004;79:619-24.
    • (2004) Am J Clin Nutr , vol.79 , pp. 619-624
    • Amouzou, E.1    Chabi, N.2    Adjalla, C.3
  • 10
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    • Genetic determinants of folates and vitamin B12 metabolisms: A common pathway in neural tube defect and Down syndrome
    • Guéant JL, Rodriguez-Guéant RM, Anello G, et al. Genetic determinants of folates and vitamin B12 metabolisms: a common pathway in neural tube defect and Down syndrome. Clin Chem Lab Med 2003;41:1473-7.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.