Changes in tear biomarker levels in keratoconus after corneal collagen crosslinking by Jose Ignacio Recalde, Juan Antonio Duran, Iñaki Rodriguez-Agirretxe, Iñaki Rodriguez-Agirretxe, Javier Soria, Miguel Angel Sanchez-Tena, Xandra Pereiro, Tatiana Suarez, Arantxa Acera

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Genomic/proteomic analyses of dexamethasone-treated human trabecular meshwork cells reveal a role for GULP1 and ABR in phagocytosis by Jennifer A. Faralli, Harini Desikan, Jennifer Peotter, Nitin Kanneganti, Benjamin Weinhaus, Mark S. Filla, Donna M. Peters

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Attenuation of corneal myofibroblast development through nanoparticle-mediated soluble transforming growth factor-β type II receptor (sTGFβRII) gene transfer by Sharma, Ajay, Rodier, Jason T., Tandon, Ashish, Klibanov, Alexander M., Mohan, Rajiv R.

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Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa by Fiorentino, A, Yu, J, Arno, G, Pontikos, N, Halford, S, Broadgate, S, Michaelides, M, Carss, K, Raymond, F, Cheetham, M, Webster, A, Downes, S, Hardcastle, A, NIHR-BioResource Rare Diseases Consortium, UK Inherited Retinal Dystrophy Consortium

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