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dc.contributor.authorYildirim, A
dc.contributor.authorAkkus, M
dc.contributor.authorNergiz, Y
dc.contributor.authorYuruker, S
dc.date.accessioned2019-12-12T06:24:57Z
dc.date.available2019-12-12T06:24:57Z
dc.date.issued2004
dc.identifier.issn0379-5284
dc.identifier.urihttps://doi.org/
dc.identifier.urihttp://hdl.handle.net/11655/16223
dc.description.abstractObjective: Milky spots in the human omental tissue are known to be consisting of lymphocytes, macrophages and mast cells. Our goal was to evaluate the relationship of lymphoid cells and macrophages with vasculature and stromal components. Methods: In this study we examined the biopsy specimens obtained from the adult patients whom were operated for different purposes in the General Surgery Department of Dicle University Hospital, Ankara, Turkey. We used CD31 as an endothelial cell marker, CD36 which is known to react with microvascular endothelium and adipocytes, and CD44 which is a hyaluronic acid receptor using an indirect immunoperoxidase technique. Results: We observed that CD31 was mainly reactive with vascular endothelial cells and platelets, CD36 was reactive with microvascular endothelium and adipocytes and CD44 was mainly expressed by the endothelial cells of high endothelial venules, fibroblasts in stromal compartments and by large mononuclear cells. Conclusion: We determined the structural and immunophenotypic features of omental lymphoid tissue components stressing vascular and stromal elements, and we briefly discussed the significance of the expression of these molecules in the determined locations.
dc.language.isoen
dc.publisherSaudi Med J
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGeneral & Internal Medicine
dc.titleImmunohistochemical Analysis Of Cd31, Cd36, And Cd44 Antigens In Human Omentum
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalSaudi Medical Journal
dc.contributor.departmentHistoloji ve Embriyoloji
dc.identifier.volume25
dc.identifier.issue3
dc.identifier.startpage308
dc.identifier.endpage312
dc.description.indexWoS


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