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dc.contributor.advisorSwaroop, Anand
dc.contributor.authorTurner, Brian C.
dc.date.accessioned2011-09-26T15:42:31Z
dc.date.available2011-09-26T15:42:31Z
dc.date.issued2002
dc.identifier.urihttp://hdl.handle.net/10920/23546
dc.descriptionv, 31 p.en_US
dc.description.abstractMacular degeneration is a classification of eye diseases that includes many different, specific forms. Age-related macular degeneration (AMD) is one particular disease form and is one of the most frequently occurring, affecting over 30 percent of the United States population over 75 years of age. AMD consists of two types, geographic atrophy (dry), and choroidal neovascularization (wet), which is exceedingly worse and can lead to blindness. The disease has proven to be highly complex, and the overall causes and pathology of this disease are still unknown. Many risk factors are associated with AMD including smoking and hypertension; however, age is the most common risk factor. Although the specific pathology and causes of AMD are still unknown, it is thought to have significant ties to the retinal pigment epithelium (RPE), a one-ceIl-thick layer located between the retina and choroid tissues. This layer maintains the blood-brain barrier and is imperative to the maintenance of the retina Currently there is relatively little knowledge about the RPE, the genes expressed in its cells, and their expression levels. However, it is hypothesized that gene mutation in RPE cells could be responsible for AMD as well as other macular dystrophies. Polymerase Chain Reaction (PCR) technology was used to compare gene expression in RPE cells to gene expression in cells of various other human tissues in order to identify genes with specific expression within RPE cells. Three genes were found to show expression in RPE cells, but not in the other human tissues. This data suggests that these three genes could be RPE-specific.en_US
dc.description.sponsorshipSensory Gene Microarray Node. Center for Retinal and Macular Degeneration. W.K. Kellogg Eye Center. University of Michigan. Ann Arbor, Michigan.
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.publisherKalamazoo Collegeen_US
dc.relation.ispartofKalamazoo College Biology Senior Individualized Projects Collection
dc.relation.ispartofseriesSenior Individualized Projects. Biology;
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.
dc.titleIdentification of Retinal Pigment Epithelium-Specific Clonesen_US
dc.typeThesisen_US
KCollege.Access.ContactIf you are not a current Kalamazoo College student, faculty, or staff member, email dspace@kzoo.edu to request access to this thesis.


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  • Biology Senior Individualized Projects [1405]
    This collection includes Senior Individualized Projects (SIP's) completed in the Biology Department. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

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