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©The Author(s) 2015.
World J Gastroenterol. Jan 28, 2015; 21(4): 1081-1090
Published online Jan 28, 2015. doi: 10.3748/wjg.v21.i4.1081
Published online Jan 28, 2015. doi: 10.3748/wjg.v21.i4.1081
Figure 1 Metabolism of homocysteine[7].
dUMP: Desoxyuridine monophosphate; dTMP: Desoxytimidine monophosphste; THF: Tetrahydrofolate; DHF: Dihydrofolate; 5-MTHF: 5-methyltetrahydrofolate; 5,10-MTHF: 5,10-methyltetrahydrofolate; 5,10 MTHFR: 5,10- methyltetrahydrofolate reductase; MS: Metionin synthase; MSR: Metionin synthase reductase; B12: Vitamin B12; SAM: S-adenosylmethionine; SAH: S-adenosylhomocysteine; CBS: Cystathionine β-synthase; GCT: γ-cystathionase; B6: Vitamin B6.
- Citation: Keshteli AH, Baracos VE, Madsen KL. Hyperhomocysteinemia as a potential contributor of colorectal cancer development in inflammatory bowel diseases: A review. World J Gastroenterol 2015; 21(4): 1081-1090
- URL: https://www.wjgnet.com/1007-9327/full/v21/i4/1081.htm
- DOI: https://dx.doi.org/10.3748/wjg.v21.i4.1081