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dc.contributor.authorTahmasebivand , Mahsa
dc.date.accessioned2020-11-11T06:35:37Z
dc.date.available2020-11-11T06:35:37Z
dc.date.issued2020en_US
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/63003
dc.description.abstractMultiple sclerosis is immune-mediated disease of the central nervous system characterized by demyelination in axons. IFN-β is first-line treatment of MS. Biomarkers are needed for early prediction of responders and non responders to therapy in the first month of treatment to avoid further disabilities. Methods: In this study, we analyzed the expression level of miR-504 and miR-711 in 52 IFN-β responder patients in comparison to 53 non-responders. In the next step, the in-silico analysis was used to enrich related signaling pathways Results: The expression level of miR-504 was significantly higher in patients who respond to IFN-β therapy, compared with non-responders and we obtain related statistically significant KEGG molecular signalingen_US
dc.language.isofaen_US
dc.publisherTabriz University of Medical Sciences, Faculty of Medicineen_US
dc.relation.isversionofhttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/63002
dc.subjectMultiple sclerosisen_US
dc.subjectInterferon-betaen_US
dc.subjectmiRNAen_US
dc.subjectBiomarkeren_US
dc.titleEvaluation of miR-504-3p and miR-711 expression levels as diagnostic biomarkers in peripheral blood of responders and non responders to interferon-Beta in people with multiple sclerosisen_US
dc.typeThesisen_US
dc.contributor.supervisorEmamalizadeh, Babak
dc.identifier.docno609688en_US
dc.identifier.callno9688en_US
dc.description.disciplineMedical Geneticsen_US
dc.description.degreeM. Sc degreeen_US


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