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Deciphering the role of DNA methylation in multiple sclerosis: emerging issues

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Autor
Sokratous M., Dardiotis E., Tsouris Z., Bellou E., Michalopoulou A., Siokas V., Arseniou S., Stamati T., Tsivgoulis G., Bogdanos D., Hadjigeorgiou G.M.
Fecha
2016
Language
en
DOI
10.1007/s13317-016-0084-z
Materia
DNA methyltransferase
DNA methyltransferase 1
DNA methyltransferase 3A
DNA methyltransferase 3B
HLA DRB1 antigen
HLA DRB5 antigen
Article
binocular convergence
DNA methylation
DNA replication
environmental factor
epigenetics
gene expression
genetic susceptibility
human
multiple sclerosis
nonhuman
priority journal
receptor down regulation
rheumatoid arthritis
systemic lupus erythematosus
Springer-Verlag Italia s.r.l.
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Resumen
Multiple sclerosis (MS) is an autoimmune inflammatory and neurodegenerative disease of the central nervous system that involves several not yet fully elucidated pathophysiologic mechanisms. There is increasing evidence that epigenetic modifications at level of DNA bases, histones, and micro-RNAs may confer risk for MS. DNA methylation seems to have a prominent role in the epigenetics of MS, as aberrant methylation in the promoter regions across genome may underlie several processes involved in the initiation and development of MS. In the present review, we discuss current understanding regarding the role of DNA methylation in MS, possible therapeutic implications and future emerging issues. © 2016, The Author(s).
URI
http://hdl.handle.net/11615/79171
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