Mouse models of human ocular disease for translational research von Krebs, Mark P, Collin, Gayle B, Hicks, Wanda L, Yu, Minzhong, Charette, Jeremy R, Shi, Lan Ying, Wang, Jieping, Naggert, Jürgen K, Peachey, Neal S, Nishina, Patsy M

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Elevation of 20-carbon long chain bases due to a mutation in serine palmitoyltransferase small subunit b results in neurodegeneration von Zhao, Lihong, Spassieva, Stefka, Gable, Kenneth, Gupta, Sita D., Shi, Lan-Ying, Wang, Jieping, Bielawski, Jacek, Hicks, Wanda L., Krebs, Mark P., Naggert, Juergen, Hannun, Yusuf A., Dunn, Teresa M., Nishina, Patsy M.

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Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model von Weatherly, Sonia M, Collin, Gayle B, Charette, Jeremy R, Stone, Lisa, Damkham, Nattaya, Hyde, Lillian F, Peterson, James G, Hicks, Wanda, Carter, Gregory W, Naggert, Jürgen K, Krebs, Mark P, Nishina, Patsy M

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Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss von Collin, Gayle B, Gogna, Navdeep, Chang, Bo, Damkham, Nattaya, Pinkney, Jai, Hyde, Lillian F, Stone, Lisa, Naggert, Jürgen K, Nishina, Patsy M, Krebs, Mark P

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Single-Cell RNA Sequencing Reveals Molecular Features of Heterogeneity in the Murine Retinal Pigment Epithelium von Pandey, Ravi S, Krebs, Mark P, Bolisetty, Mohan T, Charette, Jeremy R, Naggert, Jürgen K, Robson, Paul, Nishina, Patsy M, Carter, Gregory W

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A Dpagt1 Missense Variant Causes Degenerative Retinopathy without Myasthenic Syndrome in Mice von Hyde, Lillian F, Kong, Yang, Zhao, Lihong, Rao, Sriganesh Ramachandra, Wang, Jieping, Stone, Lisa, Njaa, Andrew, Collin, Gayle B, Krebs, Mark P, Chang, Bo, Fliesler, Steven J, Nishina, Patsy M, Naggert, Jürgen K

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A Splicing Mutation in Slc4a5 Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction von Collin, Gayle B, Shi, Lanying, Yu, Minzhong, Akturk, Nurten, Charette, Jeremy R, Hyde, Lillian F, Weatherly, Sonia M, Pera, Martin F, Naggert, Jürgen K, Peachey, Neal S, Nishina, Patsy M, Krebs, Mark P

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Molecular Mechanisms of Rhodopsin Retinitis Pigmentosa and the Efficacy of Pharmacological Rescue von Krebs, Mark P., Holden, David C., Joshi, Parth, Clark, Charles L., Lee, Andrew H., Kaushal, Shalesh

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Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity von Saksens, Nicole T M, Krebs, Mark P, Schoenmaker-Koller, Frederieke E, Hicks, Wanda, Yu, Minzhong, Shi, Lanying, Rowe, Lucy, Collin, Gayle B, Charette, Jeremy R, Letteboer, Stef J, Neveling, Kornelia, van Moorsel, Tamara W, Abu-Ltaif, Sleiman, De Baere, Elfride, Walraedt, Sophie, Banfi, Sandro, Simonelli, Francesca, Cremers, Frans P M, Boon, Camiel J F, Roepman, Ronald, Leroy, Bart P, Peachey, Neal S, Hoyng, Carel B, Nishina, Patsy M, den Hollander, Anneke I

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A mouse model of cone photoreceptor function loss (cpfl9) with degeneration due to a mutation in Gucy2e von Naggert, Anna S E N, Collin, Gayle B, Wang, Jieping, Krebs, Mark P, Chang, Bo

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Retinoids Assist the Cellular Folding of the Autosomal Dominant Retinitis Pigmentosa Opsin Mutant P23H von Noorwez, Syed M., Malhotra, Ritu, McDowell, J. Hugh, Smith, Karen A., Krebs, Mark P., Kaushal, Shalesh

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A High-Throughput Screening Method for Small-Molecule Pharmacologic Chaperones of Misfolded Rhodopsin von Noorwez, Syed M, Ostrov, David A, McDowell, J. Hugh, Krebs, Mark P, Kaushal, Shalesh

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Optimization of bacteriorhodopsin for bioelectronic devices von Wise, Kevin J, Gillespie, Nathan B, Stuart, Jeffrey A, Krebs, Mark P, Birge, Robert R

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Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAs von Soundararajan, Ramani, Won, Jungyeon, Stearns, Timothy M, Charette, Jeremy R, Hicks, Wanda L, Collin, Gayle B, Naggert, Jürgen K, Krebs, Mark P, Nishina, Patsy M

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Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation von Collin, Gayle B, Hubmacher, Dirk, Charette, Jeremy R, Hicks, Wanda L, Stone, Lisa, Yu, Minzhong, Naggert, Jürgen K, Krebs, Mark P, Peachey, Neal S, Apte, Suneel S, Nishina, Patsy M

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Using Vascular Landmarks to Orient 3D Optical Coherence Tomography Images of the Mouse Eye von Krebs, Mark P.

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Mouse Models of NMNAT1 -Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease von Greenwald, Scott H, Charette, Jeremy R, Staniszewska, Magdalena, Shi, Lan Ying, Brown, Steve D.M, Stone, Lisa, Liu, Qin, Hicks, Wanda L, Collin, Gayle B, Bowl, Michael R, Krebs, Mark P, Nishina, Patsy M, Pierce, Eric A

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Enhanced retinal pigment epithelium regeneration after injury in MRL/MpJ mice von Xia, Huiming, Krebs, Mark P., Kaushal, Shalesh, Scott, Edward W.

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Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1 rd8 mouse model von Weatherly, Sonia M, Gayle B. Collin, Charette, Jeremy R, Lisa Stone, Nattaya Damkham, Lillian F. Hyde, James G. Peterson, Hicks, Wanda, Gregory W. Carter, Jürgen K. Naggert, Mark P. Krebs, Patsy M. Nishina

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Bright-Field Imaging and Optical Coherence Tomography of the Mouse Posterior Eye von Krebs, Mark P., Xiao, Mei, Sheppard, Keith, Hicks, Wanda, Nishina, Patsy M.

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