Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/33495
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dc.contributor.authorAbban, Mete, Gulcin-
dc.contributor.authorDodurga, Yavuz-
dc.contributor.authorSatıroglu, Tufan Naciye Lale-
dc.date.accessioned2023-08-15T11:14:48Z-
dc.date.available2023-08-15T11:14:48Z-
dc.date.issued2017-03-
dc.identifier.citationGök, Y. D. vd. (2017). ''Differential expression and localization of Nanog, Oct 3/4 and C-kıt in mouse ovarian tissue according to age''. Kuwait Medical Journal, 49(1), 29-39.en_US
dc.identifier.issn0023-5776-
dc.identifier.urihttp://hdl.handle.net/11452/33495-
dc.description.abstractObjective: To investigate the expression of embryonic/pluripotent stem cell markers including Nanog, Octamer Binding Protein (3)/(4) (Oct 3/4) and c-Kit from the newborn to aging period in the ovary tissues of mouse. Design: Experimental study using mouse ovary tissues. The expression and localization of Nanog, Oct 3/4 and c-Kit expression were studied in newborn, pubertal, adult and aging ovary. Setting: Department of Histology and Embryology, Pamukkale University, School of Medicine, Turkey Subjects: Newborn (n = 6), pubertal (38-day-old) (n = 6), adult (12-week-old) (n = 6) and aged (24-week-old) female Balb/c mice were used in this study. Intervention : No intervention Main Outcome Measure: The expression of Nanog, Oct 3/4 and c-kit was evaluated by immunohistochemistry and reverse transcriptase chain reaction (PCR). Results: Nanog, Oct 3/4 and c-Kit expression were positive in oocytes of newborn, pubertal and adult ovary. But they were negative in granulosa cells in newborn groups. The expression of these markers in adult period was increased. In addition, positive reaction for Nanog, Oct 3/4 and c-Kit was observed in granulosa cells in secondary and tertiary follicles in pubertal and adult ovary. Ovarian surface epithelium were positive for all stem cells markers in adult and aged. In addition to that, only c-kit positive expression was found in theca cells. Conclusion: According to our findings, each of the three stem cell markers may play an important role in folliculogenesis and ovarian pathology. However, c-kit may be more effective than others because stromal cells were positive in adult and pubertal ovaries as well as in aged ovary.en_US
dc.description.sponsorshipPamukkale Üniversitesi Bilimsel Araştırma Projeleri Koordinasyon Birimi ve Bayındır Hastanesi Ankaratr_TR
dc.language.isoenen_US
dc.publisherKuwait Medicana Assocen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGeneral & internal medicineen_US
dc.subjectImmunohistochemistryen_US
dc.subjectOvaryen_US
dc.subjectStem cellsen_US
dc.subjectGerm-cellsen_US
dc.subjectStem-cellsen_US
dc.subjectIdentificationen_US
dc.subjectPluripotencyen_US
dc.subjectGenesen_US
dc.subjectRolesen_US
dc.subjectLineen_US
dc.subjectSOX2en_US
dc.titleDifferential expression and localization of Nanog, Oct 3/4 and C-kıt in mouse ovarian tissue according to ageen_US
dc.typeArticleen_US
dc.identifier.wos000398102100006tr_TR
dc.identifier.scopus2-s2.0-85014116115tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Histoloji ve Embriyoloji Anabilim Dalı.tr_TR
dc.identifier.startpage29tr_TR
dc.identifier.endpage39tr_TR
dc.identifier.volume49tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalKuwait Medical Journaltr_TR
dc.contributor.buuauthorGök, Duygu Yurtsever-
dc.contributor.researcheridAAW-4867-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.subject.wosGeneral & internal medicineen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.contributor.scopusid57193446960tr_TR
dc.subject.scopusFemale Germline Stem Cell; Stem Cells; Germ Layersen_US
dc.subject.emtreeOctamer transcription factor 4en_US
dc.subject.emtreeStem cell factor receptoren_US
dc.subject.emtreeTranscription factor NANOGen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAge distributionen_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeAnimal cellen_US
dc.subject.emtreeAnimal tissueen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeEmbryonic stem cellen_US
dc.subject.emtreeEpitheliumen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeGranulosa cellen_US
dc.subject.emtreeImmunohistochemistryen_US
dc.subject.emtreeMouseen_US
dc.subject.emtreeNewbornen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreeOocyteen_US
dc.subject.emtreeOvaryen_US
dc.subject.emtreeOvary follicleen_US
dc.subject.emtreeOvary follicle developmenten_US
dc.subject.emtreeProtein expressionen_US
dc.subject.emtreeProtein localizationen_US
dc.subject.emtreePubertyen_US
dc.subject.emtreeNeverse transcription polymerase chain reactionen_US
dc.subject.emtreeTheca cellen_US
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