In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development

Por Cheng, Hong, Aleman, Tomas S., Cideciyan, Artur V., Khanna, Ritu, Jacobson, Samuel G., Swaroop, Anand
Publicado em 2006

Evidence for retinal remodelling in retinitis pigmentosa caused by PDE6B mutation

Por Jacobson, Samuel G, Sumaroka, Alexander, Aleman, Tomas S, Cideciyan, Artur V, Danciger, Michael, Farber, Debora B
Publicado em 2007

Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetate

Por Maeda, Tadao, Cideciyan, Artur V., Maeda, Akiko, Golczak, Marcin, Aleman, Tomas S., Jacobson, Samuel G., Palczewski, Krzysztof
Publicado em 2009

Harmonin in the Murine Retina and the Retinal Phenotypes of Ush1c-Mutant Mice and Human USH1C

Por Williams, David S., Aleman, Tomas S., Lillo, Concepción, Lopes, Vanda S., Hughes, Louise C., Stone, Edwin M., Jacobson, Samuel G.
Publicado em 2009

Subconjunctivally Implantable Hydrogels with Degradable and Thermoresponsive Properties for Sustained Release of Insulin to the Retina

Por Misra, Gauri P., Singh, Ravi S.J., Aleman, Tomas S., Jacobson, Samuel G., Gardner, Thomas W., Lowe, Tao L.
Publicado em 2009

Relationship Between Optic Nerve Appearance and Retinal Nerve Fiber Layer Thickness as Explored with Spectral Domain Optical Coherence Tomography

Por Aleman, Tomas S., Huang, Jiayan, Garrity, Sean T., Carter, Stuart B., Aleman, Wendy D., Ying, Gui-shuang, Tamhankar, Madhura A.
Publicado no Transl Vis Sci Technol (2014)

Reduced-illuminance autofluorescence imaging in ABCA4-associated retinal degenerations

Por Cideciyan, Artur V., Swider, Malgorzata, Aleman, Tomas S., Roman, Marisa I., Sumaroka, Alexander, Schwartz, Sharon B., Stone, Edwin M., Jacobson, Samuel G.
Publicado em 2007

In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosa

Por Cideciyan, Artur V., Jacobson, Samuel G., Aleman, Tomas S., Gu, Danian, Pearce-Kelling, Susan E., Sumaroka, Alexander, Acland, Gregory M., Aguirre, Gustavo D.
Publicado em 2005

Photoreceptor Layer Topography in Children with Leber Congenital Amaurosis Caused by RPE65 Mutations

Por Jacobson, Samuel G., Cideciyan, Artur V., Aleman, Tomas S., Sumaroka, Alexander, Windsor, Elizabeth A. M., Schwartz, Sharon B., Heon, Elise, Stone, Edwin M.
Publicado em 2008

AMD-like retinopathy associated with intravenous iron

Por Song, Delu, Kanu, Levi N., Li, Yafeng, Kelly, Kristen L., Bhuyan, Rupak K., Aleman, Tomas, Morgan, Jessica I. W., Dunaief, Joshua L.
Publicado no Exp Eye Res (2016)

Detailed Functional and Structural Phenotype of Bietti Crystalline Dystrophy Associated with Mutations in CYP4V2 Complicated by Choroidal Neovascularization

Por Fuerst, Nicole M., Serrano, Leona, Han, Grace, Morgan, Jessica I. W., Maguire, Albert M., Leroy, Bart P., Kim, Benjamin J., Aleman, Tomas S.
Publicado no Ophthalmic Genet (2016)

Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: Retained photoreceptors adjacent to retinal disorganization

Por Jacobson, Samuel G., Aleman, Tomas S., Cideciyan, Artur V., Sumaroka, Alexander, Schwartz, Sharon B., Windsor, Elizabeth A.M., Swider, Malgorzata, Herrera, Waldo, Stone, Edwin M.
Publicado em 2009

The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65

Por Lopes, Vanda S., Gibbs, Daniel, Libby, Richard T., Aleman, Tomas S., Welch, Darcy L., Lillo, Concepción, Jacobson, Samuel G., Radu, Roxana A., Steel, Karen P., Williams, David S.
Publicado em 2011

Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindness

Por Van Hooser, J. Preston, Aleman, Tomas S., He, Yu-Guang, Cideciyan, Artur V., Kuksa, Vladimir, Pittler, Steven J., Stone, Edwin M., Jacobson, Samuel G., Palczewski, Krzysztof
Publicado em 2000

Lentiviral Expression of Retinal Guanylate Cyclase-1 (RetGC1) Restores Vision in an Avian Model of Childhood Blindness

Por Williams, Melissa L, Coleman, Jason E, Haire, Shannon E, Aleman, Tomas S, Cideciyan, Artur V, Sokal, Izabel, Palczewski, Krzysztof, Jacobson, Samuel G, Semple-Rowland, Susan L
Publicado em 2006

Defining the Residual Vision in Leber Congenital Amaurosis Caused by RPE65 Mutations

Por Jacobson, Samuel G., Aleman, Tomas S., Cideciyan, Artur V., Roman, Alejandro J., Sumaroka, Alexander, Windsor, Elizabeth A. M., Schwartz, Sharon B., Heon, Elise, Stone, Edwin M.
Publicado em 2008

Macular Function in Macular Degenerations: Repeatability of Microperimetry as a Potential Outcome Measure for ABCA4-Associated Retinopathy Trials

Por Cideciyan, Artur V., Swider, Malgorzata, Aleman, Tomas S., Feuer, Willam J., Schwartz, Sharon B., Russell, Robert C., Steinberg, Janet D., Stone, Edwin M., Jacobson, Samuel G.
Publicado em 2012

SPATA7: Evolving Phenotype from Cone-Rod Dystrophy to Retinitis Pigmentosa

Por Matsui, Rodrigo, McGuigan, David B., Gruzensky, Michaela L., Aleman, Tomas S., Schwartz, Sharon B., Sumaroka, Alexander, Koenekoop, Robert K., Cideciyan, Artur V., Jacobson, Samuel G.
Publicado no Ophthalmic Genet (2016)

Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man

Por CIDECIYAN, ARTUR V., HAESELEER, FRANÇOISE, FARISS, ROBERT N., ALEMAN, TOMAS S., JANG, GEENG-FU, VERLINDE, CHRISTOPHE L. M. J., MARMOR, MICHAEL F., JACOBSON, SAMUEL G., PALCZEWSKI, KRZYSZTOF
Publicado em 2000

ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retina

Por Cideciyan, Artur V., Swider, Malgorzata, Aleman, Tomas S., Sumaroka, Alexander, Schwartz, Sharon B., Roman, Marisa I., Milam, Ann H., Bennett, Jean, Stone, Edwin M., Jacobson, Samuel G.
Publicado em 2005