Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/5845
Full metadata record
DC FieldValueLanguage
dc.contributor.authorDodurga, Yavuz-
dc.contributor.authorAvci, C.B.-
dc.contributor.authorYilmaz, S.-
dc.contributor.authorDogan, Z.O.-
dc.contributor.authorKesen, Z.-
dc.contributor.authorTataroglu, C.-
dc.contributor.authorSatiroglu-Tufan, N.L.-
dc.date.accessioned2019-08-16T12:02:49Z-
dc.date.available2019-08-16T12:02:49Z-
dc.date.issued2011-
dc.identifier.issn1354-750X-
dc.identifier.urihttps://hdl.handle.net/11499/5845-
dc.identifier.urihttps://doi.org/10.3109/1354750X.2011.620627-
dc.description.abstractThis study was undertaken to evaluate the expression of DMBT1 in bladder cancer and its correlation with clinico-pathological parameters analyzed in bladder carcinoma patients. We investigated DMBT1 in 56 paraffin embedded specimens of transitional cell carcinoma of the urinary bladder. We assessed DMBT1 gene expression at mRNA level by RT-PCR. Our results show 100% expression of DMBT1 in bladder carcinoma samples. Due to this preliminary results; gene expression was compared to tumor grade, and a significant difference was detected between grade 1 and 3 (p=0.028). The down-regulation of DMBT1 gene expression in carcinomas suggests the possible role in bladder cancer. © 2011 Informa UK, Ltd.en_US
dc.language.isoenen_US
dc.relation.ispartofBiomarkersen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBladder canceren_US
dc.subjectDMBT1 geneen_US
dc.subjectgene expressionen_US
dc.subjectreal-time online RT-PCRen_US
dc.subjectmessenger RNAen_US
dc.subjectadulten_US
dc.subjectageden_US
dc.subjectarticleen_US
dc.subjectbladder carcinomaen_US
dc.subjectcancer gradingen_US
dc.subjectcancer patienten_US
dc.subjectDBMT1 geneen_US
dc.subjectdown regulationen_US
dc.subjectevaluationen_US
dc.subjectfemaleen_US
dc.subjectgene expression regulationen_US
dc.subjecthistopathologyen_US
dc.subjecthumanen_US
dc.subjecthuman tissueen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectoncogeneen_US
dc.subjectreverse transcription polymerase chain reactionen_US
dc.subjecttransitional cell carcinomaen_US
dc.subjectAdulten_US
dc.subjectAgeden_US
dc.subjectAged, 80 and overen_US
dc.subjectCarcinoma, Transitional Cellen_US
dc.subjectDown-Regulationen_US
dc.subjectFemaleen_US
dc.subjectGene Expression Regulation, Neoplasticen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectMiddle Ageden_US
dc.subjectNeoplasm Gradingen_US
dc.subjectReceptors, Cell Surfaceen_US
dc.subjectReverse Transcriptase Polymerase Chain Reactionen_US
dc.subjectRNA, Messengeren_US
dc.subjectUrinary Bladder Neoplasmsen_US
dc.titleEvaluation of deleted in malignant brain tumors 1 (DMBT1) gene expression in bladder carcinoma cases: Preliminary studyen_US
dc.typeArticleen_US
dc.identifier.volume16en_US
dc.identifier.issue7en_US
dc.identifier.startpage610-
dc.identifier.startpage610en_US
dc.identifier.endpage615en_US
dc.authorid0000-0002-4936-5954-
dc.identifier.doi10.3109/1354750X.2011.620627-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid21999583en_US
dc.identifier.scopus2-s2.0-80054954113en_US
dc.identifier.wosWOS:000296232100009en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.languageiso639-1en-
item.fulltextNo Fulltext-
crisitem.author.dept14.03. Basic Medical Sciences-
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
Show simple item record



CORE Recommender

SCOPUSTM   
Citations

5
checked on Nov 23, 2024

WEB OF SCIENCETM
Citations

5
checked on Nov 22, 2024

Page view(s)

34
checked on Aug 24, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.