Disruption of the Blood–Aqueous Barrier and Lens Abnormalities in Mice Lacking Lysyl Oxidase-Like 1 (LOXL1)

PURPOSE. Exfoliation syndrome (ES) is commonly associated with glaucoma, premature cataracts, and other ocular and systemic pathologies. LOXL1 gene variants are significantly associated with ES; however, the role of the protein in ES development remains unclear. The purpose of this study was to char...

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Detalhes bibliográficos
Main Authors: Wiggs, Janey L., Pawlyk, Basil, Connolly, Edward, Adamian, Michael, Miller, Joan W., Pasquale, Louis R., Haddadin, Ramez I., Grosskreutz, Cynthia L., Rhee, Douglas J., Li, Tiansen
Formato: Artigo
Idioma:Inglês
Publicado em: The Association for Research in Vision and Ophthalmology 2014
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3920824/
https://ncbi.nlm.nih.gov/pubmed/24425853
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.13-13033
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