Accumulation of non-outer segment proteins in the outer segment underlies photoreceptor degeneration in Bardet–Biedl syndrome von Datta, Poppy, Allamargot, Chantal, Hudson, Joseph S., Andersen, Emily K., Bhattarai, Sajag, Drack, Arlene V., Sheffield, Val C., Seo, Seongjin

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AAV2/4-RS1 gene therapy in the retinoschisin knockout mouse model of X-linked retinoschisis von Scruggs, Brittni A, Bhattarai, Sajag, Helms, Megan, Cherascu, Ioana, Salesevic, Adisa, Stalter, Elliot, Laird, Joseph, Baker, Sheila A, Drack, Arlene V

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AAV2/4-RS1 gene therapy in the retinoschisin knockout mouse model of X-linked retinoschisis von Brittni A. Scruggs, Sajag Bhattarai, Megan Helms, Ioana Cherascu, Adisa Salesevic, Elliot Stalter, Joseph Laird, Sheila A. Baker, Arlene V. Drack

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Correlation between electroretinography, foveal anatomy and visual acuity in aniridia due to PAX6 mutations von Dangremond, Tucker, Wang, Kai, Helms, Megan, Bhattarai, Sajag, Pfeifer, Wanda, Drack, Arlene V.

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TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa and prevents obesity in Bardet-Biedl syndrome type 1 mice von Drack, Arlene V, Dumitrescu, Alina V, Bhattarai, Sajag, Gratie, Daniel, Stone, Edwin M, Mullins, Robert, Sheffield, Val C

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Progressive retinal degeneration of rods and cones in a Bardet-Biedl syndrome type 10 mouse model von Mayer, Sara K, Thomas, Jacintha, Helms, Megan, Kothapalli, Aishwarya, Cherascu, Ioana, Salesevic, Adisa, Stalter, Elliot, Wang, Kai, Datta, Poppy, Searby, Charles, Seo, Seongjin, Hsu, Ying, Bhattarai, Sajag, Sheffield, Val C, Drack, Arlene V

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Subretinal gene therapy delays vision loss in a Bardet-Biedl Syndrome type 10 mouse model von Hsu, Ying, Bhattarai, Sajag, Thompson, Jacob M., Mahoney, Angela, Thomas, Jacintha, Mayer, Sara K., Datta, Poppy, Garrison, Janelle, Searby, Charles C., Vandenberghe, Luk H., Seo, Seongjin, Sheffield, Val C., Drack, Arlene V.

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Investigating the role of Caspase-1 in a mouse model of Juvenile X-linked Retinoschisis von Gehrke, Ella J, Pandey, Araniko, Thompson, Jacob, Bhattarai, Sajag, Gurung, Prajwal, Hsu, Ying, Drack, Arlene V

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RNA interference-based therapy for spinocerebellar ataxia type 7 retinal degeneration von Ramachandran, Pavitra S, Bhattarai, Sajag, Singh, Pratibha, Boudreau, Ryan L, Thompson, Stewart, Laspada, Albert R, Drack, Arlene V, Davidson, Beverly L

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An osmolarity dependent mechanism partially ameliorates retinal cysts and rescues cone function in a mouse model of X-linked retinoschisis von Gehrke, Ella J, Thompson, Jacob, Kalmanek, Emily, Stanley, Sarah T, Laird, Joseph, Bhattarai, Sajag, Lobeck, Brianna, Mayer, Sara, Mahoney, Angela, Hassan, Salma, Hsu, Ying, Drack, Arlene

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Endothelial BBSome is essential for vascular, metabolic, and retinal functions von Jiang, Jingwei, Reho, John J., Bhattarai, Sajag, Cherascu, Ioana, Hedberg-Buenz, Adam, Meyer, Kacie J., Tayyari, Fariba, Rauckhorst, Adam J., Guo, Deng Fu, Morgan, Donald A., Taylor, Eric B., Anderson, Michael G., Drack, Arlene V., Rahmouni, Kamal

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Vitritis in Pediatric Genetic Retinal Disorders von Stunkel, Maria, BS, Bhattarai, Sajag, MS, Kemerley, Andrew, BS, Stone, Edwin M., MD, PhD, Wang, Kai, PhD, Mullins, Robert F., PhD, Drack, Arlene V., MD

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TRIP8b is required for maximal expression of HCN1 in the mouse retina von Pan, Yuan, Bhattarai, Sajag, Modestou, Modestos, Drack, Arlene V, Chetkovich, Dane M, Baker, Sheila A

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Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1 von Seo, Seongjin, Mullins, Robert F, Dumitrescu, Alina V, Bhattarai, Sajag, Gratie, Daniel, Wang, Kai, Stone, Edwin M, Sheffield, Val, Drack, Arlene V

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BBS mutations modify phenotypic expression of CEP290-related ciliopathies von Zhang, Yan, Seo, Seongjin, Bhattarai, Sajag, Bugge, Kevin, Searby, Charles C, Zhang, Qihong, Drack, Arlene V, Stone, Edwin M, Sheffield, Val C

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Electroretinogram abnormalities in FKRP-related limb–girdle muscular dystrophy (LGMDR9) von Hagedorn, Joshua L., Dunn, Taylor M., Bhattarai, Sajag, Stephan, Carrie, Mathews, Katherine D., Pfeifer, Wanda, Drack, Arlene V.

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Characterization of a novel porcine model of CLN3-Batten disease von Johnson, Tyler B., Sturdevant, David A., White, Katherine A., Drack, Arlene V., Bhattarai, Sajag, Rogers, Chris, Cooper, Jonathan D., Pearce, David A., Weimer, Jill M.

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α^sub 2^δ-4 Is Required for the Molecular and Structural Organization of Rod and Cone Photoreceptor Synapses von Kerov, Vasily, Laird, Joseph G, Joiner, Mei-ling, Knecht, Sharmon, Soh, Daniel, Hagen, Jussara, Gardner, Sarah H, Gutierrez, Wade, Yoshimatsu, Takeshi, Bhattarai, Sajag, Puthussery, Teresa, Artemyev, Nikolai O, Drack, Arlene V, Wong, Rachel O, Baker, Sheila A, Lee, Amy

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Correlation between electroretinography, foveal anatomy and visual acuity in albinism von Hu, Zhaohui, Wang, Kai, Bertsch, Morgan, Dunn, Taylor, Kehoe, Taylor, Kemerley, Andrew D., Helms, Megan, Bhattarai, Sajag, Pfeifer, Wanda, Scheetz, Todd E., Drack, Arlene V.

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A visually guided swim assay for mouse models of human retinal disease recapitulates the multi-luminance mobility test in humans von Hassan, Salma, Hsu, Ying, Mayer, Sara K, Thomas, Jacintha, Kothapalli, Aishwarya, Helms, Megan, Baker, Sheila A, Laird, Joseph G, Bhattarai, Sajag, Drack, Arlene V

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