mtDNA nt13708A variant increases the risk of multiple sclerosis.
<h4>Background</h4>Mitochondrial DNA (mtDNA) polymorphism is a possible factor contributing to the maternal parent-of-origin effect in multiple sclerosis (MS) susceptibility.<h4>Methods and findings</h4>In order to investigate the role of mtDNA variations in MS, we investigat...
Main Authors: | Xinhua Yu, Dirk Koczan, Anna-Maija Sulonen, Denis A Akkad, Antje Kroner, Manuel Comabella, Gianna Costa, Daniela Corongiu, Robert Goertsches, Montserrat Camina-Tato, Hans-Juergen Thiesen, Harald I Nyland, Sverre J Mørk, Xavier Montalban, Peter Rieckmann, Maria G Marrosu, Kjell-Morten Myhr, Joerg T Epplen, Janna Saarela, Saleh M Ibrahim |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2008-02-01
|
Series: | PLoS ONE |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18270557/pdf/?tool=EBI |
Similar Items
-
Dietary vitamin D3 supplements reduce demyelination in the cuprizone model.
by: Stig Wergeland, et al.
Published: (2011-01-01) -
Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms.
by: Manuel Comabella, et al.
Published: (2008-01-01) -
Integrative modeling of transcriptional regulation in response to antirheumatic therapy
by: Thiesen Hans-Juergen, et al.
Published: (2009-08-01) -
Reassessment of blood gene expression markers for the prognosis of relapsing-remitting multiple sclerosis.
by: Michael Hecker, et al.
Published: (2011-01-01) -
MtDNA deletions and aging
by: Charlotte Sprason, et al.
Published: (2024-02-01)