| OverviewOur laboratory is 
        interested in understanding underlying mechanisms of ocular angiogenesis 
        and the abnormalities in this process that lead to retinal vascular disease. 
        Since abnormal angiogenesis is frequently the final common pathway leading 
        to the vast majority of diseases that result in catastrophic loss of vision, 
        we are also interested in understanding mechanisms of retinal degeneration 
        that lead to ocular angiogenesis. This aspect of our program focuses on 
        the role of polytopic membrane proteins of visual importance that are 
        mutated in certain inherited retinal degenerations. While most of our 
        effort is devoted to understanding ocular angiogenesis, the role of abnormal 
        membrane protein targeting and integration provides an alternate approach 
        to identifying potential therapeutic avenues to treating diseases for 
        which there are currently no effective treatments. Finally, a third component 
        of our research program focuses on developing physiologically relevant 
        animal models of ocular angiogenesis and drug delivery systems useful 
        in the treatment of human retinal neovascular and degenerative diseases.
 
   
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