Autofluorescence Imaging With Near-Infrared Excitation: Normalization by Reflectance to Reduce Signal From Choroidal Fluorophores

Por Cideciyan, Artur V., Swider, Malgorzata, Jacobson, Samuel G.
Publicado no Invest Ophthalmol Vis Sci (2015)

Retinal Pigment Epithelium Defects in Humans and Mice with Mutations in MYO7A: Imaging Melanosome-Specific Autofluorescence

Por Gibbs, Daniel, Cideciyan, Artur V., Jacobson, Samuel G., Williams, David S.
Publicado em 2009

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

Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front

Por Cideciyan, Artur V., Swider, Malgorzata, Schwartz, Sharon B., Stone, Edwin M., Jacobson, Samuel G.
Publicado no Invest Ophthalmol Vis Sci (2015)

Late-Onset Retinal Degeneration caused by C1QTNF5 Mutation: Sub-Retinal Pigment Epithelium Deposits and Visual Consequences

Por Jacobson, Samuel G., Cideciyan, Artur V., Sumaroka, Alexander, Roman, Alejandro J., Wright, Alan F.
Publicado no JAMA Ophthalmol (2014)

Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man

Por Cideciyan, Artur V., Zhao, Xinyu, Nielsen, Lori, Khani, Shahrokh C., Jacobson, Samuel G., Palczewski, Krzysztof
Publicado em 1998

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

Reply to Townes-Anderson: RPE65 gene therapy does not alter the natural history of retinal degeneration

Por Cideciyan, Artur V., Jacobson, Samuel G., Beltran, William A., Hauswirth, William W., Aguirre, Gustavo D.
Publicado em 2013

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

Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II

Por Yan, Denise, Ouyang, Xiaomei, Patterson, D Michael, Du, Li Lin, Jacobson, Samuel G, Liu, Xue-Zhong
Publicado no J Hum Genet (2009)

Temperature-sensitive retinoid isomerase activity of RPE65 mutants associated with Leber Congenital Amaurosis

Por Li, Songhua, Hu, Jane, Jin, Robin J., Aiyar, Ashok, Jacobson, Samuel G., Bok, Dean, Jin, Minghao
Publicado no J Biochem (2015)

Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrast

Por Roman, Alejandro J., Cideciyan, Artur V., Matsui, Rodrigo, Sheplock, Rebecca, Schwartz, Sharon B., Jacobson, Samuel G.
Publicado no BMC Ophthalmol (2015)

Mutations in the Cone Photoreceptor G-Protein α-Subunit Gene GNAT2 in Patients with Achromatopsia

Por Kohl, Susanne, Baumann, Britta, Rosenberg, Thomas, Kellner, Ulrich, Lorenz, Birgit, Vadalà, Maria, Jacobson, Samuel G., Wissinger, Bernd
Publicado em 2002

Association of the Asn306Ser variant of the SP4 transcription factor and an intronic variant in the β-subunit of transducin with digenic disease

Por Gao, Yong-Qing, Danciger, Michael, Özgül, Riza Köksal, Gribanova, Yekaterina E., Jacobson, Samuel G., Farber, Debora B.
Publicado em 2007

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

Intervisit Variability of Visual Parameters in Leber Congenital Amaurosis Caused by RPE65 Mutations

Por Roman, Alejandro J., Cideciyan, Artur V., Schwartz, Sharon B., Olivares, Melani B., Heon, Elise, Jacobson, Samuel G.
Publicado em 2013

Gene Augmentation for X-Linked Retinitis Pigmentosa Caused by Mutations in RPGR

Por Beltran, William A., Cideciyan, Artur V., Lewin, Alfred S., Hauswirth, William W., Jacobson, Samuel G., Aguirre, Gustavo D.
Publicado no Cold Spring Harb Perspect Med (2015)

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

Improvement and Decline in Vision with Gene Therapy in Childhood Blindness

Por Jacobson, Samuel G., Cideciyan, Artur V., Roman, Alejandro J., Sumaroka, Alexander, Schwartz, Sharon B., Heon, Elise, Hauswirth, William W.
Publicado no N Engl J Med (2015)

Improvement in vision: a new goal for treatment of hereditary retinal degenerations

Por Jacobson, Samuel G, Cideciyan, Artur V, Aguirre, Gustavo D, Roman, Alejandro J, Sumaroka, Alexander, Hauswirth, William W, Palczewski, Krzysztof
Publicado no Expert Opin Orphan Drugs (2015)