Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7176
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dc.contributor.authorSahin, N.-
dc.contributor.authorAksu, K.-
dc.contributor.authorKamali, S.-
dc.contributor.authorBicakcigil, M.-
dc.contributor.authorÖzbalkan, Z.-
dc.contributor.authorFresko, I.-
dc.contributor.authorÖzer, H.-
dc.date.accessioned2019-08-16T12:17:09Z
dc.date.available2019-08-16T12:17:09Z
dc.date.issued2008-
dc.identifier.issn1462-0324-
dc.identifier.urihttps://hdl.handle.net/11499/7176-
dc.identifier.urihttps://doi.org/10.1093/rheumatology/ken106-
dc.description.abstractObjective. Takayasu's arteritis (TA) is a chronic, rare granulomatous panarteritis of unknown aetiology involving mainly the aorta and its major branches. In this study, genetic susceptibility to TA has been investigated by screening the functional single nucleotide polymorphism (SNP) of PTPN22 gene encoding the lymphoid-specific protein tyrosine phosphatase. Methods. Totally, 181 patients with TA and 177 healthy controls are genotyped by PCR-RFLP method for the SNP rs2476601 (A/G) of PTPN22 gene. Polymorphic region was amplified by PCR and digested with Xcm I enzyme. Results. Detected frequencies of heterozygous genotype (AG) were 5.1% (9/177) in control group and 3.8% (7/181) in TA group (P = 0.61, odds ratio: 0.75, 95% CI: 0.3, 2.0). No association with angiographic type, vascular involvement or prognosis of TA was observed either. Conclusion. The distribution of PTPN22 polymorphism did not reveal any association with TA in Turkey. © The Author 2008. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.en_US
dc.language.isoenen_US
dc.relation.ispartofRheumatologyen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPTPN22en_US
dc.subjectSingle nucleotide polymorphismen_US
dc.subjectTakayasu's arteritisen_US
dc.subjectadenineen_US
dc.subjectguanineen_US
dc.subjectprotein tyrosine phosphataseen_US
dc.subjectadulten_US
dc.subjectamino acid substitutionen_US
dc.subjectangiographyen_US
dc.subjectaorta arch syndromeen_US
dc.subjectarticleen_US
dc.subjectautoimmunityen_US
dc.subjectcase control studyen_US
dc.subjectcontrolled studyen_US
dc.subjectenzyme degradationen_US
dc.subjectfemaleen_US
dc.subjectgene amplificationen_US
dc.subjectgene frequencyen_US
dc.subjectgenetic associationen_US
dc.subjectgenetic polymorphismen_US
dc.subjectgenetic screeningen_US
dc.subjectgenetic susceptibilityen_US
dc.subjectgenotypeen_US
dc.subjectheterozygosityen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectpolymerase chain reactionen_US
dc.subjectpopulation geneticsen_US
dc.subjectpriority journalen_US
dc.subjectprognosisen_US
dc.subjectrestriction fragment length polymorphismen_US
dc.subjectsingle nucleotide polymorphismen_US
dc.subjectTurkey (republic)en_US
dc.subjectAdulten_US
dc.subjectCase-Control Studiesen_US
dc.subjectFemaleen_US
dc.subjectGene Frequencyen_US
dc.subjectGenetic Predisposition to Diseaseen_US
dc.subjectHeterozygoteen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectMiddle Ageden_US
dc.subjectPolymorphism, Restriction Fragment Lengthen_US
dc.subjectPolymorphism, Single Nucleotideen_US
dc.subjectProtein Tyrosine Phosphatase, Non-Receptor Type 22en_US
dc.subjectTakayasu Arteritisen_US
dc.subjectTurkeyen_US
dc.titlePTPN22 gene polymorphism in Takayasu's arteritisen_US
dc.typeArticleen_US
dc.identifier.volume47en_US
dc.identifier.issue5en_US
dc.identifier.startpage634
dc.identifier.startpage634en_US
dc.identifier.endpage635en_US
dc.identifier.doi10.1093/rheumatology/ken106-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid18375974en_US
dc.identifier.scopus2-s2.0-42949115825en_US
dc.identifier.wosWOS:000255315700015en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.grantfulltextopen-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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