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dc.creatorŽivković, Maja
dc.creatorĐurić, Tamara
dc.creatorDinčić, Evica
dc.creatorRaičević, Ranko
dc.creatorAlavantić, Dragan
dc.creatorStanković, Aleksandra
dc.date.accessioned2018-03-01T20:13:03Z
dc.date.available2018-03-01T20:13:03Z
dc.date.issued2007
dc.identifier.issn0165-5728
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/3299
dc.description.abstractMatrix metalloproteinase-9 (MMP-9) is suggested to play a role in MS by mediating T cell migration across subendothelial basement membrane and by contribution to myelin breakdown. We studied the association of MMP-9 -1562 C/T gene polymorphisms with MS susceptibility and severity in 187 patients from Serbia. The significant decrease in T allele carriership (p=0.01), was found in female NIS patients, In addition, a trend toward lower MSSS in T allele carriers was noticed (CC, mean 5.7 +/- 2.5 vs. CT+TT, mean 4.9 +/- 2.5). Further studies in different populations are needed to resolve the potential influence of MMP-9 gene polymorphism on MS. (C) 2007 Elsevier B.V. All rights reserved.en
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/145023/RS//
dc.rightsrestrictedAccessen
dc.sourceJournal of Neuroimmunologyen
dc.subjectMMP-9en
dc.subjectgeneen
dc.subjectpolymorphismen
dc.subjectmultiple sclerosisen
dc.titleMatrix metalloproteinase-9-1562 C/T gene polymorphism in Serbian patients with multiple sclerosisen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractДинциц, Евица; Раицевиц, Ранко; Живковић Маја; Ђурић Тамара; Aлавантић Драган; Станковић Aлександра;
dc.citation.volume189
dc.citation.issue1-2
dc.citation.spage147
dc.citation.epage150
dc.identifier.wos000250068800019
dc.identifier.doi10.1016/j.jneuroim.2007.06.022
dc.citation.rankM22
dc.identifier.pmid17655938
dc.type.versionpublishedVersion
dc.identifier.scopus2-s2.0-34548542224


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