Analysis of Autofluorescent retinal images and measurement of atrophic lesion growth in Stargardt disease von Chen, B., Tosha, C., Gorin, M.B., Nusinowitz, S.

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Differential expression and function of ABCG1 and ABCG4 during development and aging von Bojanic, Dragana D, Tarr, Paul T, Gale, Greg D, Smith, Desmond J, Bok, Dean, Chen, Bryan, Nusinowitz, Steven, Lövgren-Sandblom, Anita, Björkhem, Ingemar, Edwards, Peter A

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The visual evoked potential in the mouse—Origins and response characteristics von Ridder, W.H., Nusinowitz, S.

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Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene von Chang, B., Hawes, N.L., Pardue, M.T., German, A.M., Hurd, R.E., Davisson, M.T., Nusinowitz, S., Rengarajan, K., Boyd, A.P., Sidney, S.S., Phillips, M.J., Stewart, R.E., Chaudhury, R., Nickerson, J.M., Heckenlively, J.R., Boatright, J.H.

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Retinal degeneration mutants in the mouse von Chang, B., Hawes, N.L., Hurd, R.E., Davisson, M.T., Nusinowitz, S., Heckenlively, J.R.

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Mizuo–Nakamura phenomenon with a negative waveform ERG von Yuan, A, Nusinowitz, S, Sarraf, D

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Retinal Function in X-linked Ocular Albinism (OA1) von Nusinowitz, S., Sarraf, D.

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Temporal response properties of the primary and secondary rod-signaling pathways in normal and Gnat2 mutant mice von Nusinowitz, S., Ridder, W.H., Ramirez, J.

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Disrupted compaction of CNS myelin in an OSP/Claudin-11 and PLP/DM20 double knockout mouse von Chow, E., Mottahedeh, J., Prins, M., Ridder, W., Nusinowitz, S., Bronstein, J.M.

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Mouse models of ocular diseases von CHANG, B., HAWES, N.L., HURD, R.E., WANG, J., HOWELL, D., DAVISSON, M.T., RODERICK, T.H., NUSINOWITZ, S., HECKENLIVELY, J.R.

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Cortical visual function in the rd12 mouse model of Leber Congenital Amarousis (LCA) after gene replacement therapy to restore retinal function von Nusinowitz, S., Ridder, W.H., Pang, J.J., Chang, B., Noorwez, S.M., Kaushal, S., Hauswirth, W.W., Heckenlively, J.R.

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Retinal Degeneration 6 (rd6): A New Mouse Model for Human Retinitis Punctata Albescens von Hawes, Norman L, Chang, Bo, Hageman, Gregory S, Nusinowitz, Steven, Nishina, Patsy M, Schneider, Bobbie S, Smith, Richard S, Roderick, Thomas H, Davisson, Muriel T, Heckenlively, John R

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Rescue of retinal degeneration by intravitreally injected adult bone marrow-derived lineage-negative hematopoietic stem cells von Otani, Atsushi, Dorrell, Michael Ian, Kinder, Karen, Moreno, Stacey K, Nusinowitz, Steven, Banin, Eyal, Heckenlively, John, Friedlander, Martin

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Reductions in Serum Vitamin A Arrest Accumulation of Toxic Retinal Fluorophores: A Potential Therapy for Treatment of Lipofuscin-Based Retinal Diseases von Radu, Roxana A, Han, Yun, Bui, Tam V, Nusinowitz, Steven, Bok, Dean, Lichter, Jay, Widder, Ken, Travis, Gabriel H, Mata, Nathan L

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Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23- his mutation von Birch, DG, Hood, DC, Nusinowitz, S, Pepperberg, DR

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Differential expression and function of ABCG1 and ABCG4 during development and aging[S] von Bojanic, Dragana D., Tarr, Paul T., Gale, Greg D., Smith, Desmond J., Bok, Dean, Chen, Bryan, Nusinowitz, Steven, Lövgren-Sandblom, Anita, Björkhem, Ingemar, Edwards, Peter A.

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Treatment with Isotretinoin Inhibits Lipofuscin Accumulation in a Mouse Model of Recessive Stargardt's Macular Degeneration von Radu, Roxana A., Mata, Nathan L., Nusinowitz, Steven, Liu, Xinran, Sieving, Paul A., Travis, Gabriel H.

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Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis von Pang, Ji-jing, Chang, Bo, Kumar, Ashok, Nusinowitz, Steven, Noorwez, Syed M, Li, Jie, Rani, Asha, Foster, Thomas C, Chiodo, Vince A, Doyle, Thomas, Li, Huashi, Malhotra, Ritu, Teusner, Jacqueline T, McDowell, J Hugh, Min, Seok-Hong, Li, Qiuhong, Kaushal, Shalesh, Hauswirth, William W

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The nob2 mouse, a null mutation in Cacnalf : Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses von BO CHANG, HECKENLIVELY, John R, MCCALL, Maureen A, MORGANS, Catherine W, NUSINOWITZ, Steve, PEACHEY, Neal S, RICE, Dennis S, VESSEY, Kirstan A, GREGG, Ronald G, BAYLEY, Philippa R, BRECHA, Nicholas C, DAVISSON, Muriel T, HAWES, Norm L, HIRANO, Arlene A, HURD, Ronald E, IKEDA, Akihiro, JOHNSON, Britt A

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Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA) von Pang, Ji-Jing, Chang, Bo, Hawes, Norman L, Hurd, Ronald E, Davisson, Muriel T, Li, Jie, Noorwez, Syed M, Malhotra, Ritu, McDowell, J Hugh, Kaushal, Shalesh, Hauswirth, William W, Nusinowitz, Steven, Thompson, Debra A, Heckenlively, John R

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