Limbal Stem Cell Markers

dc.contributor.authorEkici, Cemal
dc.contributor.authorDeğirmenci, Çumali
dc.date.accessioned2021-11-30T14:10:53Z
dc.date.available2021-11-30T14:10:53Z
dc.date.issued2016
dc.departmentİnönü Üniversitesien_US
dc.description.abstractAbstract: Limbal stem cell deficiency has an important position among corneal blindness, it is the second most common cause of blindness in the worldwide. Hyperemia in the eye, watering of the eyes, chronic pain attacks, blepharospasm, low vision, conjunctivalization, neovascularization, and fibrovascular pannus are observed in patients and these lowering their quality of life significantly. Keratolimbal allografts, conjunctivolimbal allografts and eccentric corneal grafts were used in the treatment of these pathologies. However, as a result of the recent studies, genes and markers that belong to stem cells such as p63 gene, ABCG2, ABCB5, Vimentin, K19 and connexin were defined and thus limbal stem cells were successfully reproduced. Today, the treatment of these diseases is possible by reproducing the stem cells in a small limbal biopsy using various methods. This approach is still current and still developing. In this study we aimed to review limbal stem cell’s genes, markers and current treatment modalitiesen_US
dc.identifier.citationEKİCİ C,DEĞİRMENCİ C (2016). Limbal Stem Cell Markers. Medicine Science, 5(1), 233 - 243.en_US
dc.identifier.endpage243en_US
dc.identifier.issn2147-0634
dc.identifier.issue1en_US
dc.identifier.startpage233en_US
dc.identifier.trdizinid260994en_US
dc.identifier.urihttps://hdl.handle.net/11616/43561
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/260994
dc.identifier.volume5en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofMedicine Scienceen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleLimbal Stem Cell Markersen_US
dc.typeArticleen_US

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