نمایش مختصر رکورد

dc.contributor.authorMehdizadeh, Farideen_US
dc.contributor.authorBonyadi, Mortazaen_US
dc.contributor.authorBonyadi, Mohammed Hussainen_US
dc.contributor.authorJavadzadeh, Alirezaen_US
dc.date.accessioned1399-07-08T21:55:35Zfa_IR
dc.date.accessioned2020-09-29T21:55:35Z
dc.date.available1399-07-08T21:55:35Zfa_IR
dc.date.available2020-09-29T21:55:35Z
dc.date.issued2016-09-01en_US
dc.date.issued1395-06-11fa_IR
dc.date.submitted2016-06-30en_US
dc.date.submitted1395-04-10fa_IR
dc.identifier.citationMehdizadeh, Faride, Bonyadi, Mortaza, Bonyadi, Mohammed Hussain, Javadzadeh, Alireza. (2016). The Association of SMUG1 Gene Polymorphism with Age-related Macular Degeneration in Northwestern Iran. Journal of Advanced Medical Sciences and Applied Technologies, 2(3), 257-261. doi: 10.18869/nrip.jamsat.2.3.257en_US
dc.identifier.issn2423-5903
dc.identifier.issn2538-4473
dc.identifier.urihttps://dx.doi.org/10.18869/nrip.jamsat.2.3.257
dc.identifier.urihttps://jamsat.sums.ac.ir/article_42476.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/121128
dc.description.abstractAge-related macular degeneration (AMD) is the most common cause of irreversible vision loss and debilitating disease in old age, which involves the central retina/macula among elderly patients. The genetic and environmental factors have important role in this multifactorial disease. Oxidative stress and DNA damages would have important impact on the onset and progression of AMD.  In this study, the possible association of c.-31A>G (rs3087404) polymorphism in the promoter region of SMUG1 gene with AMD disease was investigated. Fifty five AMD patients and 130 healthy age-, gender- and ethnicity-matched unrelated people as control group were genotyped by restriction fragment length polymorphism PCR (RFLP-PCR). Both groups were from Northwest of Iran (Tabriz).  Statistical analysis showed a significant association of AG genotype of this polymorphism with AMD. These results suggest a possible protective effect of this genotype for AMD disease (P=0.02, OR=0.574) among patients from Northwest of Iran. This genotype was observed more frequently in controls compared to the patients (59.23% v s 45.45%).en_US
dc.languageEnglish
dc.language.isoen_US
dc.publisherShiraz University of Medical Sciencesen_US
dc.relation.ispartofJournal of Advanced Medical Sciences and Applied Technologiesen_US
dc.relation.isversionofhttps://dx.doi.org/10.18869/nrip.jamsat.2.3.257
dc.subjectAMDen_US
dc.subjectPolymorphismen_US
dc.subjectSMUG1 geneen_US
dc.subjectOxidative stressen_US
dc.titleThe Association of SMUG1 Gene Polymorphism with Age-related Macular Degeneration in Northwestern Iranen_US
dc.typeTexten_US
dc.typeOriginal Articlesen_US
dc.citation.volume2
dc.citation.issue3
dc.citation.spage257
dc.citation.epage261


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