[-] Show simple item record

dc.contributor.advisorMohan, Rajiv R.eng
dc.contributor.authorGupta, Rangan, 1978-eng
dc.contributor.authorTandon, Ashisheng
dc.contributor.authorTovey, Jonathaneng
dc.contributor.authorSharma, Ajayeng
dc.contributor.corporatenameUniversity of Missouri--Columbia. School of Medicineeng
dc.contributor.meetingnameHealth Sciences Research Day (2010 : University of Missouri)eng
dc.date.issued2010eng
dc.description.abstractTransforming growth factor [beta] (TGFb) is known to cause fibrosis in the cornea following injury and/or infection. Effective reduction in corneal fibrosis has been reported by inhibiting TGFb activity. However, associated molecular mechanism is still unknown. The aim of study was to test the hypothesis that the alteration in SMAD signaling is a novel approach for treating corneal fibrosis using an established in vitro model.eng
dc.format.extent1 pageeng
dc.identifier.urihttp://hdl.handle.net/10355/9414
dc.languageEnglisheng
dc.relation.ispartofcommunityUniversity of Missouri--Columbia. Health Sciences Research Dayeng
dc.rightsOpenAccess.eng
dc.rights.licenseThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.eng
dc.subjectmyofibroblastseng
dc.subjectanti-fibrotic therapieseng
dc.subject.FASTEye -- Diseaseseng
dc.subject.FASTTransforming growth factors-betaeng
dc.subject.FASTFibrosiseng
dc.titleSMAD-signaling inhibition : potential for developing newer treatments for corneal fibrosis [abstract]eng
dc.typeAbstracteng


Files in this item

[PDF]

This item appears in the following Collection(s)

[-] Show simple item record