Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29535
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dc.date.accessioned2022-11-22T10:21:05Z-
dc.date.available2022-11-22T10:21:05Z-
dc.date.issued2016-07-31-
dc.identifier.citationBudak, F. vd. (2016). "Altered expressions of miR-1238-3p, miR-494, miR-6069, and miR-139-3p in the formation of chronic Brucellosis". Journal of Immunology Research, 2016, 1-11.en_US
dc.identifier.issn2314-8861-
dc.identifier.issn2314-7156-
dc.identifier.urihttps://doi.org/10.1155/2016/4591468-
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046029/-
dc.identifier.urihttp://hdl.handle.net/11452/29535-
dc.description.abstractBrucellosis is a zoonotic disease that is still endemic in developing countries. Despite early diagnosis and treatment of patients, chronic infections are seen in 10-30% of patients. In this study, we aimed to investigate the immunological factors that play roles in the transition of brucellosis from acute infection into chronic infection. Here, more than 2000 miRNAs were screened in peripheral blood mononuclear cells (PBMCs) of patients with acute or chronic brucellosis and healthy controls by using miRNA array, and the results of the miRNA array were validated through qRT-PCR. Findings were evaluated using GeneSpring GX (Agilent) 13.0 software and KEGG pathway analysis. Four miRNAs were expressed in the chronic group but were not expressed in acute and control groups. Among these miRNAs, the expression level of miR-1238-3p was increased while miR-494, miR-6069, and miR-1393p were decreased (p< 0.05, fold change > 2). These miRNAs have the potential to be markers for chronic cases. The differentially expressed miRNAs and their predicted target genes involved in endocytosis, regulation of actin cytoskeleton, MAPK signaling pathway, and cytokine-cytokine receptor interaction and its chemokine signaling pathway indicate their potential roles in chronic brucellosis and its progression. It is the first study of miRNA expression analysis of human PBMC to clarify the mechanism of inveteracy in brucellosis.en_US
dc.language.isoenen_US
dc.publisherHindawien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectImmunologyen_US
dc.subjectDendritic cell maturationen_US
dc.subjectB-virus infectionen_US
dc.subjectMicrorna expressionen_US
dc.subjectGene-expressionen_US
dc.subjectUp-regulationen_US
dc.subjectIntegrated analysisen_US
dc.subjectAbortus invasionen_US
dc.subjectDown-regulationen_US
dc.subjectCancer cellsen_US
dc.subjectTNF-alphaen_US
dc.subject.meshAcute diseaseen_US
dc.subject.meshBiomarkersen_US
dc.subject.meshBrucellosisen_US
dc.subject.meshChronic diseaseen_US
dc.subject.meshFemaleen_US
dc.subject.meshGene expression profilingen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMetabolic networks and pathwaysen_US
dc.subject.meshMicroRNAsen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshReal-time polymerase chain reactionen_US
dc.titleAltered expressions of miR-1238-3p, miR-494, miR-6069, and miR-139-3p in the formation of chronic Brucellosisen_US
dc.typeArticleen_US
dc.identifier.wos000385116100001tr_TR
dc.identifier.scopus2-s2.0-84990876577tr_TR
dc.relation.tubitakSBAG-111S183en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/İmmünoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Klinik Mikrobiyoloji ve Enfeksiyon Hastalıkları Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Mikrobiyoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0003-0463-6818tr_TR
dc.contributor.orcid0000-0002-5956-8755tr_TR
dc.identifier.startpage1tr_TR
dc.identifier.endpage11tr_TR
dc.identifier.volume2016tr_TR
dc.relation.journalJournal of Immunology Researchen_US
dc.contributor.buuauthorBudak, Ferah-
dc.contributor.buuauthorBal, Salih Haldun-
dc.contributor.buuauthorTezcan, Gülçin-
dc.contributor.buuauthorAkalın, Halis-
dc.contributor.buuauthorGöral, Güher-
dc.contributor.buuauthorOral, Haluk Barbaros-
dc.contributor.researcheridK-7285-2012tr_TR
dc.contributor.researcheridAAU-8952-2020tr_TR
dc.contributor.researcheridF-4657-2014tr_TR
dc.contributor.researcheridF-8554-2017tr_TR
dc.contributor.researcheridAAH-3843-2020tr_TR
dc.identifier.pubmed27722176tr_TR
dc.subject.wosImmunologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid6701913697tr_TR
dc.contributor.scopusid57191480128tr_TR
dc.contributor.scopusid25650627600tr_TR
dc.contributor.scopusid57207553671tr_TR
dc.contributor.scopusid6603453166tr_TR
dc.contributor.scopusid7004498001tr_TR
dc.subject.scopusAnimals; Zoonosis; Bovine Brucellosisen_US
dc.subject.emtreeCytokineen_US
dc.subject.emtreeDoxycyclineen_US
dc.subject.emtreeMicroRNAen_US
dc.subject.emtreeMicrorna 1238 3pen_US
dc.subject.emtreeMicrorna 139 3pen_US
dc.subject.emtreeMicrorna 1914 3pen_US
dc.subject.emtreeMicrorna 22 5pen_US
dc.subject.emtreeMicrorna 335 5pen_US
dc.subject.emtreeMicrorna 339 5pen_US
dc.subject.emtreeMicrorna 494en_US
dc.subject.emtreeMicrorna 575en_US
dc.subject.emtreeMicrorna 6069en_US
dc.subject.emtreeMitogen activated protein kinaseen_US
dc.subject.emtreeRifampicinen_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeBiological markeren_US
dc.subject.emtreeMIRN1238 microRNA, humanen_US
dc.subject.emtreeMIRN139 microRNA, humanen_US
dc.subject.emtreeMIRN494 microRNA, humanen_US
dc.subject.emtreeActin filamenten_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBrucellosisen_US
dc.subject.emtreeChronic brucellosisen_US
dc.subject.emtreeChronicityen_US
dc.subject.emtreeClinical articleen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDisease courseen_US
dc.subject.emtreeEndocytosisen_US
dc.subject.emtreeFatigueen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeGene expressionen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeImmune responseen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreePeripheral blood mononuclear cellen_US
dc.subject.emtreeProtein protein interactionen_US
dc.subject.emtreeReverse transcription polymerase chain reactionen_US
dc.subject.emtreeSignal transductionen_US
dc.subject.emtreeAcute diseaseen_US
dc.subject.emtreeBlooden_US
dc.subject.emtreeBrucellosisen_US
dc.subject.emtreeChronic diseaseen_US
dc.subject.emtreeGene expression profilingen_US
dc.subject.emtreeGeneticsen_US
dc.subject.emtreeImmunologyen_US
dc.subject.emtreeMetabolismen_US
dc.subject.emtreeMicrobiologyen_US
dc.subject.emtreeMiddle ageden_US
dc.subject.emtreeReal time polymerase chain reactionen_US
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