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dc.contributor.authorAsker, Selvi
dc.contributor.authorTaşpınar, Mehmet
dc.contributor.authorKoyun, Hasan
dc.contributor.authorÖzbay, Bülent
dc.contributor.authorArısoy, Ahmet
dc.date.accessioned2020-11-20T14:55:18Z
dc.date.available2020-11-20T14:55:18Z
dc.date.issued2017
dc.identifier.issn1354-750X
dc.identifier.issn1366-5804
dc.identifier.urihttps://doi.org/10.1080/1354750X.2016.1204007
dc.identifier.urihttps://hdl.handle.net/20.500.12809/2224
dc.descriptionWOS: 000393903600011en_US
dc.descriptionPubMed ID: 27321703en_US
dc.description.abstractObjective: To investigate the associations of G14713A and T29107A polymorphic variants of Caveolin-1 with severe obstructive sleep apnea (OSA). Materials and methods: This study was performed on 86 severe OSA patients and 86 controls. Genotyping was performed to investigate the association of G14713A and T29107A polymorphisms of Caveolin-1 with severe OSA. Results: The distribution of genotypes of T29107A was significantly different between controls and OSA patients with a higher proportion of TT carriers in the OSA group. Conclusion: T29107A-specific genotype of Caveolin-1 may be linked with severe OSA pathogenesis.en_US
dc.item-language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.item-rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectG14713Aen_US
dc.subjectGenotypeen_US
dc.subjectPolymorphic Varianten_US
dc.subjectT29107Aen_US
dc.titleCaveolin-1 polymorphisms in patients with severe obstructive sleep apneaen_US
dc.item-typearticleen_US
dc.contributor.departmentMÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorÖzbay, Bülent
dc.identifier.doi10.1080/1354750X.2016.1204007
dc.identifier.volume22en_US
dc.identifier.issue1en_US
dc.identifier.startpage77en_US
dc.identifier.endpage80en_US
dc.relation.journalBiomarkersen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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