Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination von Jacobson, Samuel G., Cideciyan, Artur V., Aleman, Tomas S., Pianta, Michael J., Sumaroka, Alexander, Schwartz, Sharon B., Smilko, Elaine E., Milam, Ann H., Sheffield, Val C., Stone, Edwin M.

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Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate von Haider, Neena B., Jacobson, Samuel G., Cideciyan, Artur V., Swiderski, Ruth, Streb, Luan M., Searby, Charles, Beck, Gretel, Hockey, Robin, Hanna, David B., Gorman, Susan, Duhl, David, Carmi, Rivka, Bennett, Jean, Weleber, Richard G., Fishman, Gerald A., Wright, Alan F., Stone, Edwin M., Sheffield, Val C.

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Neuroendocrine profiling in inherited stress-induced arterial hypertension rat strain with stress-sensitive arterial hypertension von Markel, A L, Redina, O E, Gilinsky, M A, Dymshits, G M, Kalashnikova, E V, Khvorostova, Yu V, Fedoseeva, L A, Jacobson, G S

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Psychophysical Evidence for Rod Vulnerability in Age-Related Macular Degeneration von Owsley, Cynthia, Jackson, Gregory R, Cideciyan, Artur V, Huang, Yijun, Fine, Stuart L, Ho, Allen C, Maguire, Maureen G, Lolley, Virginia, Jacobson, Samuel G

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Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel von Kohl, Susanne, Marx, Tim, Giddings, Ian, Jägle, Herbert, Jacobson, Samuel G., Apfelstedt-Sylla, Eckhart, Zrenner, Eberhart, Sharpe, Lindsay T., Wissinger, Bernd

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Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration von Jacobson, Samuel G., Sumaroka, Alexander, Aleman, Tomas S., Cideciyan, Artur V., Schwartz, Sharon B., Roman, Alejandro J., McInnes, Roderick R., Sheffield, Val C., Stone, Edwin M., Swaroop, Anand, Wright, Alan F.

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An Analysis of Allelic Variation in the ABCA4 Gene von Webster, Andrew R, Heon, Elise, Lotery, Andrew J, Vandenburgh, Kimberlie, Casavant, Thomas L, Oh, Kean T, Beck, Gretel, Fishman, Gerald A, Lam, Byron L, Levin, Alex, Heckenlively, John R, Jacobson, Samuel G, Weleber, Richard G, Sheffield, Val C, Stone, Edwin M

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Genetics and Phenotypes of RPE65 Mutations in Inherited Retinal Degeneration von Thompson, Debra A, Gyurus, Peter, Fleischer, Laura L, Bingham, Eve L, McHenry, Christina L, Apfelstedt-Sylla, Eckart, Zrenner, Eberhart, Lorenz, Birgit, Richards, Julia E, Jacobson, Samuel G, Sieving, Paul A, Gal, Andreas

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Relation of optical coherence tomography to microanatomy in normal and rd chickens von Huang, Y, Cideciyan, AV, Papastergiou, GI, Banin, E, Semple-Rowland, SL, Milam, AH, Jacobson, SG

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Macular Pigment and Lutein Supplementation in Retinitis Pigmentosa and Usher Syndrome von Aleman, Tomas S, Duncan, Jacque L, Bieber, Michelle L, de Castro, Elaine, Marks, Daniel A, Gardner, Leigh M, Steinberg, Janet D, Cideciyan, Artur V, Maguire, Maureen G, Jacobson, Samuel G

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Retinal optogenetic therapies: clinical criteria for candidacy von Jacobson, S G, Sumaroka, A, Luo, X, Cideciyan, A V

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De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis von Freund, Carol L., Wang, Qing-Ling, Chen, Shiming, Muskat, Brenda L., Wiles, Carmella D., Sheffield, Val C., Jacobson, Samuel G., Mclnnes, Roderick R., Zack, Donald J., Stone, Edwin M.

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Allelic Variation in the VMD2 Gene in Best Disease and Age-Related Macular Degeneration von Lotery, Andrew J, Munier, Francis L, Fishman, Gerald A, Weleber, Richard G, Jacobson, Samuel G, Affatigato, Louisa M, Nichols, Brian E, Schorderet, Daniel F, Sheffield, Val C, Stone, Edwin M

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Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetate von Maeda, Tadao, Cideciyan, Artur V., Maeda, Akiko, Golczak, Marcin, Aleman, Tomas S., Jacobson, Samuel G., Palczewski, Krzysztof

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Disease Expression of RP1 Mutations Causing Autosomal Dominant Retinitis Pigmentosa von Jacobson, Samuel G, Cideciyan, Artur V, Iannaccone, Alessandro, Weleber, Richard G, Fishman, Gerald A, Maguire, Albert M, Affatigato, Louisa M, Bennett, Jean, Pierce, Eric A, Danciger, Michael, Farber, Debora B, Stone, Edwin M

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Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosa von Petters, Robert M., Alexander, Curtis A., Wells, Kevin D., Collins, E. Bruce, Sommer, Jeffrey R., Blanton, Maria R., Rojas, Guadalupe, Hao, Ying, Flowers, William L., Banin, Eyal, Cideciyan, Artur V., Jacobson, Samuel G., Wong, Fulton

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A Nonsense Mutation in a Novel Gene Is Associated With Retinitis Pigmentosa in a Family Linked to the RP1 Locus von Guillonneau, Xavier, Piriev, Natik I., Danciger, Michael, Kozak, Christine A., Cideciyan, Artur V., Jacobson, Samuel G., Farber, Debora B.

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Rhodopsin Mutations in Autosomal Dominant Retinitis Pigmentosa von Sung, Ching-Hwa, Davenport, Carol M., Hennessey, Jill C., Maumenee, Irene H., Jacobson, Samuel G., Heckenlively, John R., Nowakowski, Rodney, Fishman, Gerald, Gouras, Peter, Nathans, Jeremy

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Autoantibodies against retinal bipolar cells in cutaneous melanoma- associated retinopathy von Milam, AH, Saari, JC, Jacobson, SG, Lubinski, WP, Feun, LG, Alexander, KR

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Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic wavelets von Aleman, T S, Lam, B L, Cideciyan, A V, Sumaroka, A, Windsor, E A M, Roman, A J, Schwartz, S B, Stone, E M, Jacobson, S G

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