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dc.contributor.authorYigit, Serbulent
dc.contributor.authorTural, Sengul
dc.contributor.authorRustemoglu, Aydin
dc.contributor.authorInanir, Ahmet
dc.contributor.authorGul, Ulker
dc.contributor.authorKalkan, Goknur
dc.contributor.authorAtes, Omer
dc.date.accessioned2020-06-21T14:16:55Z
dc.date.available2020-06-21T14:16:55Z
dc.date.issued2013
dc.identifier.issn0301-4851
dc.identifier.issn1573-4978
dc.identifier.urihttps://doi.org/10.1007/s11033-012-2069-y
dc.identifier.urihttps://hdl.handle.net/20.500.12712/16170
dc.descriptionRustemoglu, Aydin/0000-0002-1354-4598; Gul, Ulker/0000-0003-4203-7998; Yigit, Serbulent/0000-0002-1019-3964en_US
dc.descriptionWOS: 000312435500042en_US
dc.descriptionPubMed: 23065219en_US
dc.description.abstractBehcet's disease (BD) is a chronic, multi-systemic and inflammatory disorder. The local renin-angiotensin system (RAS) in the vessel wall plays a role in the endothelial control and contributes to inflammatory processes. Angiotensin-converting enzyme (ACE) is the regulatory component of the RAS. This study was conducted in Turkish patients with BD to determine the frequency of I/D polymorphism genotypes of ACE gene. Genomic DNA obtained from 566 persons (266 patients with BD and 300 healthy controls). ACE gene I/D polymorphism genotypes were determined using polymerase chain reaction using I and D allele-specific primers. There was statistically significant difference between the groups with respect to genotype distribution (p < 0.001). This study is the largest study in Turkish population that ACE gene I/D polymorphism investigated in BD. As a result of this study, ACE gene I/D polymorphism DD genotype could be a genetic marker in BD in Turkish study population.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.relation.isversionof10.1007/s11033-012-2069-yen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAngiotensin-converting enzymeen_US
dc.subjectBehcet's diseaseen_US
dc.subjectPolymorphismen_US
dc.titleDD genotype of ACE gene I/D polymorphism is associated with Behcet disease in a Turkish populationen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume40en_US
dc.identifier.issue1en_US
dc.identifier.startpage365en_US
dc.identifier.endpage368en_US
dc.relation.journalMolecular Biology Reportsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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