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dc.creatorMcEnery, Kayla Anne Filan
dc.date.accessioned2013-06-04T16:14:15Z
dc.date.available2013-06-04T16:14:15Z
dc.date.created2013-05
dc.date.issued2013-02-04
dc.date.submittedMay 2013
dc.identifier.urihttps://hdl.handle.net/1969.1/148875
dc.description.abstractStroke is the fourth leading cause of death worldwide. Low levels of IGF-1, a known neuroprotectant, correspond to aging and increased severity of stroke. We have previously demonstrated that there is an inverse relationship between the presence of anti-let7f or anti-miR-1 and levels of IGF-1. Further, the localization of let-7f was found to be within the microglial cell population. We hypothesize that let7f and miR-1 directly bind to the 3’ UTR region of IGF-1. Microglial cells (EOC-20) will be transfected with an IGF-1 clone with a luciferase tag. IGF-1 synthesis following treatment with antagomirs to either miR-1 or let7f will be tested by a luciferase assay.en
dc.format.mimetypeapplication/pdf
dc.subjectmicroRNA, MiRNA, IGF-1, strokeen
dc.titleMicroRNA Regulation of IGF-1en
dc.typeThesisen
thesis.degree.departmentBiochemistry/Biophysicsen
thesis.degree.disciplineBiochemistryen
thesis.degree.grantorHonors and Undergraduate Researchen
dc.contributor.committeeMemberSohrabji , Farida
dc.type.materialtexten
dc.date.updated2013-06-04T16:14:15Z


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