Article
Open Access
Modulation of DNA Methyltransferase 1 Profile by γ-lrradiation Followed by Methyl Donor Starvation
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Vipen Batra
Published/Copyright:
August 10, 2013
Published Online: 2013-08-10
Published in Print: 2005-11
© 2013 by Walter de Gruyter GmbH & Co.
Articles in the same Issue
- Modulation of DNA Methyltransferase 1 Profile by γ-lrradiation Followed by Methyl Donor Starvation
- Neopterin as a Stimulator of Vascular Endothelial Growth Factor and Erythropoietin Gene Expression in an Ovarian Carcinoma Cell Line
- Urinary Neopterin and Microalbuminuria in Patients Treated by Low-density Lipoprotein Apheresis
- Pteridines, CXVI. (1) Synthesis and Reactivity of 6-Substituted l,3-Dimethyl-7-hydroxylumazines and 7-Substituted l,3-Dimethyl-(5H)-lumazin-6-ones
- Inflammation, Homocysteine, Pyridoxal-5-phosphate and Lipids in Patients with Coronary Artery Disease before and Six Months after Coronary Angioplasty Followed by Stent Implantation
- A Herbal Multicomponent Mixture Effective in Suppressing Biochemical Pathways in Mitogen-stimulated Human Peripheral Blood Mononuclear Cells
Keywords for this article
DNA methyltransferase;
γ-radiation;
DNA methylation. One-carbon transfer;
Methyl donors;
dnmt 1. Folate;
Choline;
Methionine
Creative Commons
BY-NC-ND 3.0
Articles in the same Issue
- Modulation of DNA Methyltransferase 1 Profile by γ-lrradiation Followed by Methyl Donor Starvation
- Neopterin as a Stimulator of Vascular Endothelial Growth Factor and Erythropoietin Gene Expression in an Ovarian Carcinoma Cell Line
- Urinary Neopterin and Microalbuminuria in Patients Treated by Low-density Lipoprotein Apheresis
- Pteridines, CXVI. (1) Synthesis and Reactivity of 6-Substituted l,3-Dimethyl-7-hydroxylumazines and 7-Substituted l,3-Dimethyl-(5H)-lumazin-6-ones
- Inflammation, Homocysteine, Pyridoxal-5-phosphate and Lipids in Patients with Coronary Artery Disease before and Six Months after Coronary Angioplasty Followed by Stent Implantation
- A Herbal Multicomponent Mixture Effective in Suppressing Biochemical Pathways in Mitogen-stimulated Human Peripheral Blood Mononuclear Cells
