Publication: Toll-like receptor 9 polymorphism in patients with erythema multiforme, Stevens Johnson syndrome and Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome
dc.contributor.buuauthor | Turan, Hakan | |
dc.contributor.buuauthor | Başkan, Emel Bülbül | |
dc.contributor.buuauthor | Yakut, Tahsin | |
dc.contributor.buuauthor | Karkucak, Mutlu | |
dc.contributor.buuauthor | Tunali, Şükran | |
dc.contributor.buuauthor | Sarıcaoğlu, Hayriye | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Genetik Tıp Ana Bilim Dalı | |
dc.contributor.scopusid | 16835681500 | tr_TR |
dc.contributor.scopusid | 43760921800 | tr_TR |
dc.contributor.scopusid | 6602802424 | tr_TR |
dc.contributor.scopusid | 35388323500 | tr_TR |
dc.contributor.scopusid | 7004191748 | tr_TR |
dc.contributor.scopusid | 6603722836 | tr_TR |
dc.date.accessioned | 2022-03-18T07:30:12Z | |
dc.date.available | 2022-03-18T07:30:12Z | |
dc.date.issued | 2011 | |
dc.description.abstract | Background: "Toll like receptor" (TLR) 9 functions in stepping in of native immune system against different viral and bacterial pathogens and induction of adaptive immune response effectively. TLR 9 gene polymorphism makes host predisposed to microbial pathogens by affecting the functional capabilities of the receptor. Objective: We aimed to determine if TLR 9 gene polymorphism makes a predisposition to "erythema multiforme" (EM), "Stevens Johnson syndrome" (SJS) and "Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome" (SJS/TEN). Methods: Forty-two patients clinically and/or histopathologically diagnosed as EM, SJS, and SJS/TEN overlap syndrome and 50 healthy control subjects were enrolled in our study. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was applied for TLR 9 gene 1237 thymine/cytosine (T/C) polymorphism. Genotypes were determined according to bands occurring on agarose gel electrophoresis. Results: In patients group, the frequencies of IT and TC genotypes were 73.8 % and 26.2 % while CC genotype wasn't detected. In control group, the frequencies of TT, TC and CC genotypes were 74 %, 24 %, and 2 %. There wasn't a statistically significant difference for TT, TC and CC genotypes between patients and controls. The frequencies of T and C alleles were 84.5 % and 15.5 % in patients and 86 % and 14 % in controls, respectively. Conclusion: Our results showed that there isn't any association between TLR gene polymorphism and EM, SJS, SJS/TEN overlap syndrome (Tab. 1, Fig. 1, Ref. 30). | en_US |
dc.identifier.citation | Turan, H. vd.(2011). "Toll-like receptor 9 polymorphism in patients with erythema multiforme, Stevens Johnson syndrome and Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome". Bratislava Medical Journal-Bratislavske Lekarske Listy, 112(5), 260-263. | en_US |
dc.identifier.endpage | 263 | tr_TR |
dc.identifier.issn | 0006-9248 | |
dc.identifier.issue | 5 | tr_TR |
dc.identifier.pubmed | 21682079 | tr_TR |
dc.identifier.scopus | 2-s2.0-79957924998 | tr_TR |
dc.identifier.startpage | 260 | tr_TR |
dc.identifier.uri | http://hdl.handle.net/11452/25172 | |
dc.identifier.volume | 112 | tr_TR |
dc.identifier.wos | 000290424100006 | |
dc.indexed.pubmed | Pubmed | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.wos | SCIE | en_US |
dc.language.iso | en | en_US |
dc.publisher | Comenius Univ | en_US |
dc.relation.journal | Bratislava Medical Journal | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | General & internal medicine | en_US |
dc.subject | Erythema multiforme | en_US |
dc.subject | Stevens Johnson syndrome | en_US |
dc.subject | Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome | en_US |
dc.subject | Toll like receptor 9 | en_US |
dc.subject | Polymorphism | en_US |
dc.subject | Single-nucleotide polymorphisms | en_US |
dc.subject | Systemic-lupus-erythematosus | en_US |
dc.subject | Dermatological disease | en_US |
dc.subject | Gene polymorphism | en_US |
dc.subject | Japanese patients | en_US |
dc.subject | Drosophila toll | en_US |
dc.subject | Association | en_US |
dc.subject | Tlr9 | en_US |
dc.subject | Susceptibility | en_US |
dc.subject | Dna | en_US |
dc.subject.emtree | Toll like receptor 9 | en_US |
dc.subject.emtree | Adolescent | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Aged | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Child | en_US |
dc.subject.emtree | Erythema multiforme | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Genetic polymorphism | en_US |
dc.subject.emtree | Genetics | en_US |
dc.subject.emtree | Genotype | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Immunology | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Middle aged | en_US |
dc.subject.emtree | Reverse transcription polymerase chain reaction | en_US |
dc.subject.emtree | Stevens Johnson syndrome | en_US |
dc.subject.emtree | Toxic epidermal necrolysis | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Child | en_US |
dc.subject.mesh | Epidermal necrolysis, toxic | en_US |
dc.subject.mesh | Erythema multiforme | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Genotype | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Polymorphism, genetic | en_US |
dc.subject.mesh | Reverse transcriptase polymerase chain reaction | en_US |
dc.subject.mesh | Stevens-Johnson syndrome | en_US |
dc.subject.mesh | Toll-like receptor 9 | en_US |
dc.subject.mesh | Young adult | en_US |
dc.subject.scopus | Stevens-Johnson Syndrome; Erythema Multiforme; Acute Generalized Exanthematous Pustulosis | en_US |
dc.subject.wos | Medicine, general & internal | en_US |
dc.title | Toll-like receptor 9 polymorphism in patients with erythema multiforme, Stevens Johnson syndrome and Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome | en_US |
dc.type | Article | |
dc.wos.quartile | Q4 | en_US |
dspace.entity.type | Publication | |
local.contributor.department | Tıp Fakültesi/Genetik Tıp Ana Bilim Dalı | tr_TR |
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