检索结果 - Jacobson, Samuel G.

Leber Congenital Amaurosis (LCA): Potential for Improvement of Vision 由 Cideciyan, Artur V., Jacobson, Samuel G.

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Autofluorescence Imaging With Near-Infrared Excitation: Normalization by Reflectance to Reduce Signal From Choroidal Fluorophores 由 Cideciyan, Artur V., Swider, Malgorzata, Jacobson, Samuel G.

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Retinal Pigment Epithelium Defects in Humans and Mice with Mutations in MYO7A: Imaging Melanosome-Specific Autofluorescence 由 Gibbs, Daniel, Cideciyan, Artur V., Jacobson, Samuel G., Williams, David S.

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In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development 由 Cheng, Hong, Aleman, Tomas S., Cideciyan, Artur V., Khanna, Ritu, Jacobson, Samuel G., Swaroop, Anand

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Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front 由 Cideciyan, Artur V., Swider, Malgorzata, Schwartz, Sharon B., Stone, Edwin M., Jacobson, Samuel G.

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Late-Onset Retinal Degeneration caused by C1QTNF5 Mutation: Sub-Retinal Pigment Epithelium Deposits and Visual Consequences 由 Jacobson, Samuel G., Cideciyan, Artur V., Sumaroka, Alexander, Roman, Alejandro J., Wright, Alan F.

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Functional Rescue of Retinal Degeneration-Associated Mutant RPE65 Proteins 由 Jin, Minghao, Li, Songhua, Hu, Jane, Jin, Heather H., Jacobson, Samuel G., Bok, Dean

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Macular Rod Function in Retinitis Pigmentosa Measured With Scotopic Microperimetry 由 Krishnan, Arun K., Roman, Alejandro J., Swider, Malgorzata, Jacobson, Samuel G., Cideciyan, Artur V.

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Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man 由 Cideciyan, Artur V., Zhao, Xinyu, Nielsen, Lori, Khani, Shahrokh C., Jacobson, Samuel G., Palczewski, Krzysztof

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Evidence for retinal remodelling in retinitis pigmentosa caused by PDE6B mutation 由 Jacobson, Samuel G, Sumaroka, Alexander, Aleman, Tomas S, Cideciyan, Artur V, Danciger, Michael, Farber, Debora B

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Reply to Townes-Anderson: RPE65 gene therapy does not alter the natural history of retinal degeneration 由 Cideciyan, Artur V., Jacobson, Samuel G., Beltran, William A., Hauswirth, William W., Aguirre, Gustavo D.

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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 由 Maeda, Tadao, Cideciyan, Artur V., Maeda, Akiko, Golczak, Marcin, Aleman, Tomas S., Jacobson, Samuel G., Palczewski, Krzysztof

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Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II 由 Yan, Denise, Ouyang, Xiaomei, Patterson, D Michael, Du, Li Lin, Jacobson, Samuel G, Liu, Xue-Zhong

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Temperature-sensitive retinoid isomerase activity of RPE65 mutants associated with Leber Congenital Amaurosis 由 Li, Songhua, Hu, Jane, Jin, Robin J., Aiyar, Ashok, Jacobson, Samuel G., Bok, Dean, Jin, Minghao

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Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrast 由 Roman, Alejandro J., Cideciyan, Artur V., Matsui, Rodrigo, Sheplock, Rebecca, Schwartz, Sharon B., Jacobson, Samuel G.

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Foveal Therapy in Blue Cone Monochromacy: Predictions of Visual Potential From Artificial Intelligence 由 Sumaroka, Alexander, Cideciyan, Artur V., Sheplock, Rebecca, Wu, Vivian, Kohl, Susanne, Wissinger, Bernd, Jacobson, Samuel G.

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Childhood-onset genetic cone-rod photoreceptor diseases and underlying pathobiology 由 Garafalo, Alexandra V., Sheplock, Rebecca, Sumaroka, Alexander, Roman, Alejandro J., Cideciyan, Artur V., Jacobson, Samuel G.

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Association of the Asn306Ser variant of the SP4 transcription factor and an intronic variant in the β-subunit of transducin with digenic disease 由 Gao, Yong-Qing, Danciger, Michael, Özgül, Riza Köksal, Gribanova, Yekaterina E., Jacobson, Samuel G., Farber, Debora B.

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Harmonin in the Murine Retina and the Retinal Phenotypes of Ush1c-Mutant Mice and Human USH1C 由 Williams, David S., Aleman, Tomas S., Lillo, Concepción, Lopes, Vanda S., Hughes, Louise C., Stone, Edwin M., Jacobson, Samuel G.

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Intervisit Variability of Visual Parameters in Leber Congenital Amaurosis Caused by RPE65 Mutations 由 Roman, Alejandro J., Cideciyan, Artur V., Schwartz, Sharon B., Olivares, Melani B., Heon, Elise, Jacobson, Samuel G.

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