检索结果 - Alejandro J. Román
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Probing Mechanisms of Photoreceptor Degeneration in a New Mouse Model of the Common Form of Autosomal Dominant Retinitis Pigmentosa due to P23H Opsin Mutations 由 Sanae Sakami, Tadao Maeda, Grzegorz Bereta, Kiichiro Okano, Marcin Golczak, Alexander Sumaroka, Alejandro J. Román, Artur V. Cideciyan, Samuel G. Jacobson, Krzysztof Palczewski
出版 2011Artigo -
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Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retina... 由 Artur V. Cideciyan, Rivka A. Rachel, Tomas S. Alemán, Małgorzata Świder, Sharon Schwartz, Alexander Sumaroka, Alejandro J. Román, Edwin M. Stone, Samuel G. Jacobson, Anand Swaroop
出版 2011Artigo -
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<i>TULP1</i>Mutations Causing Early-Onset Retinal Degeneration: Preserved but Insensitive Macular Cones 由 Samuel G. Jacobson, Artur V. Cideciyan, Wei Huang, Alexander Sumaroka, Alejandro J. Román, Sharon Schwartz, Xunda Luo, Rebecca Sheplock, Joanna M. Dauber, Małgorzata Świder, Edwin M. Stone
出版 2014Artigo -
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Defective photoreceptor phagocytosis in a mouse model of enhanced S‐cone syndrome causes progressive retinal degeneration 由 Debarshi Mustafi, Brian M. Kevany, Christel Genoud, Kiichiro Okano, Artur V. Cideciyan, Alexander Sumaroka, Alejandro J. Román, Samuel G. Jacobson, Andreas Engel, Mark D. Adams, Krzysztof Palczewski
出版 2011Artigo -
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Durable vision improvement after a single treatment with antisense oligonucleotide sepofarsen: a case report 由 Artur V. Cideciyan, Samuel G. Jacobson, Allen C. Ho, Alexandra V. Garafalo, Alejandro J. Román, Alexander Sumaroka, Arun K. Krishnan, Małgorzata Świder, Michael R. Schwartz, Aniz Girach
出版 2021Artigo -
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Inner Retinal Abnormalities in X-linked Retinitis Pigmentosa with<i>RPGR</i>Mutations 由 Tomas S. Alemán, Artur V. Cideciyan, Alexander Sumaroka, Sharon Schwartz, Alejandro J. Román, Elizabeth A. M. Windsor, Janet D. Steinberg, Kari Branham, Mohammad Othman, Anand Swaroop, Samuel G. Jacobson
出版 2007Artigo -
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Retinal Laminar Architecture in Human Retinitis Pigmentosa Caused by<i>Rhodopsin</i>Gene Mutations 由 Tomas S. Alemán, Artur V. Cideciyan, Alexander Sumaroka, Elizabeth A. M. Windsor, Waldo Herrera, D. Alan White, Shalesh Kaushal, Anjani Naidu, Alejandro J. Román, Sharon Schwartz, Edwin M. Stone, Samuel G. Jacobson
出版 2008Artigo -
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ABCA4 disease progression and a proposed strategy for gene therapy 由 Artur V. Cideciyan, Małgorzata Świder, Tomas S. Alemán, Yaroslav Tsybovsky, Sharon Schwartz, Elizabeth A. M. Windsor, Alejandro J. Román, Alexander Sumaroka, Janet D. Steinberg, Samuel G. Jacobson, Edwin M. Stone, Krzysztof Palczewski
出版 2008Artigo -
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Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the <i>CEP290</i> Gene 由 Samuel G. Jacobson, Artur V. Cideciyan, Alexander Sumaroka, Alejandro J. Román, Jason Charng, Monica Lu, Windy Choi, Rebecca Sheplock, Małgorzata Świder, Mychajlo S. Kosyk, Sharon Schwartz, Edwin M. Stone, Gerald A. Fishman
出版 2017Artigo -
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EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression 由 David B. McGuigan, Elise Héon, Artur V. Cideciyan, Rinki Ratnapriya, Monica Lu, Alexander Sumaroka, Alejandro J. Román, Vaishnavi Batmanabane, Alexandra V. Garafalo, Edwin M. Stone, Anand Swaroop, Samuel G. Jacobson
出版 2017Artigo -
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Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement 由 Artur V. Cideciyan, Samuel G. Jacobson, William A. Beltran, Alexander Sumaroka, Małgorzata Świder, Simone Iwabe, Alejandro J. Román, Melani B. Olivares, Sharon Schwartz, András M. Komáromy, William W. Hauswirth, Gustavo D. Aguirre
出版 2013Artigo
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