Optogenetic therapy for retinitis pigmentosa
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B. Roska | J. Sahel | S. Picaud | V. Busskamp | J A Sahel | S Picaud | V Busskamp | B Roska
[1] Russell G Foster,et al. Non-rod, non-cone photoreception in the vertebrates , 2002, Progress in Retinal and Eye Research.
[2] Ernst Bamberg,et al. Microbial rhodopsins in the spotlight , 2010, Current Opinion in Neurobiology.
[3] Tim Gollisch,et al. Eye Smarter than Scientists Believed: Neural Computations in Circuits of the Retina , 2010, Neuron.
[4] Weng Tao,et al. Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[5] F. Werblin,et al. Vertical interactions across ten parallel, stacked representations in the mammalian retina , 2001, Nature.
[6] Edward S Boyden,et al. Virally delivered channelrhodopsin-2 safely and effectively restores visual function in multiple mouse models of blindness. , 2011, Molecular therapy : the journal of the American Society of Gene Therapy.
[7] David R Williams,et al. Intravitreal injection of AAV2 transduces macaque inner retina. , 2011, Investigative ophthalmology & visual science.
[8] Patrick Degenaar,et al. Optobionic vision—a new genetically enhanced light on retinal prosthesis , 2009, Journal of neural engineering.
[9] W. Hauswirth,et al. Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial. , 2008, Human gene therapy.
[10] Tracey Warr,et al. Circuitry , 2001 .
[11] R. Masland,et al. Restoration of visual function in retinal degeneration mice by ectopic expression of melanopsin , 2008, Proceedings of the National Academy of Sciences.
[12] J. Nathans,et al. A Novel Signaling Pathway from Rod Photoreceptors to Ganglion Cells in Mammalian Retina , 1998, Neuron.
[13] C. Cepko,et al. Electroporation and RNA interference in the rodent retina in vivo and in vitro , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[14] Alfred Stett,et al. Subretinal electronic chips allow blind patients to read letters and combine them to words , 2010, Proceedings of the Royal Society B: Biological Sciences.
[15] E. Bamberg,et al. Ultra light-sensitive and fast neuronal activation with the Ca2+-permeable channelrhodopsin CatCh , 2011, Nature Neuroscience.
[16] R. Masland. The fundamental plan of the retina , 2001, Nature Neuroscience.
[17] B. Jones,et al. Neural remodeling in retinal degeneration , 2003, Progress in Retinal and Eye Research.
[18] A. J. Roman,et al. Normal central retinal function and structure preserved in retinitis pigmentosa. , 2010, Investigative ophthalmology & visual science.
[19] Douglas S Kim,et al. Light-activated channels targeted to ON bipolar cells restore visual function in retinal degeneration , 2008, Nature Neuroscience.
[20] A. Cideciyan,et al. Treatment possibilities for retinitis pigmentosa. , 2010, The New England journal of medicine.
[21] K. Deisseroth,et al. Circuit-breakers: optical technologies for probing neural signals and systems , 2007, Nature Reviews Neuroscience.
[22] P. Khaw,et al. Current approaches and future prospects for stem cell rescue and regeneration of the retina and optic nerve. , 2010, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.
[23] R. Ali,et al. Prospects for retinal gene replacement therapy. , 2009, Trends in genetics : TIG.
[24] Kimio Takeuchi,et al. Effect of Nilvadipine on Central Visual Field in Retinitis Pigmentosa: A 30-Month Clinical Trial , 2010, Ophthalmologica.
[25] Dirk Trauner,et al. LiGluR restores visual responses in rodent models of inherited blindness. , 2011, Molecular therapy : the journal of the American Society of Gene Therapy.
[26] A. D. den Hollander,et al. Molecular genetics of Leber congenital amaurosis. , 2002, Human molecular genetics.
[27] E. Boyden,et al. Multiple-Color Optical Activation, Silencing, and Desynchronization of Neural Activity, with Single-Spike Temporal Resolution , 2007, PloS one.
[28] B. Schobert,et al. Halorhodopsin is a light-driven chloride pump. , 1982, The Journal of biological chemistry.
[29] Jay Neitz,et al. Gene therapy for red-green colour blindness in adult primates , 2009, Nature.
[30] Feng Zhang,et al. Multimodal fast optical interrogation of neural circuitry , 2007, Nature.
[31] John G. Flannery,et al. A Novel Adeno-Associated Viral Variant for Efficient and Selective Intravitreal Transduction of Rat Müller Cells , 2009, PloS one.
[32] Edwin M Stone,et al. Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics , 2008, Proceedings of the National Academy of Sciences.
[33] Shomi S. Bhattacharya,et al. Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait , 2010, Nature Reviews Genetics.
[34] B. Roska,et al. Gene therapy in ophthalmology: validation on cultured retinal cells and explants from postmortem human eyes. , 2011, Human gene therapy.
[35] G. Miesenböck,et al. The Optogenetic Catechism , 2009, Science.
[36] S. Shoham,et al. Patterned Optical Activation of Retinal Ganglion Cells , 2007, 2007 29th Annual International Conference of the IEEE Engineering in Medicine and Biology Society.
[37] A. Milam,et al. Histopathology of the human retina in retinitis pigmentosa. , 1998, Progress in retinal and eye research.
[38] Eriko Sugano,et al. Channelrhodopsin-2 gene transduced into retinal ganglion cells restores functional vision in genetically blind rats. , 2010, Experimental eye research.
[39] E. Bamberg,et al. Channelrhodopsin-2, a directly light-gated cation-selective membrane channel , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[40] A. Milam,et al. Morphometric analysis of the extramacular retina from postmortem eyes with retinitis pigmentosa. , 1999, Investigative ophthalmology & visual science.
[41] Konrad Lehmann,et al. Visual Function in Mice with Photoreceptor Degeneration and Transgenic Expression of Channelrhodopsin 2 in Ganglion Cells , 2010, The Journal of Neuroscience.
[42] A. Dizhoor,et al. Ectopic Expression of a Microbial-Type Rhodopsin Restores Visual Responses in Mice with Photoreceptor Degeneration , 2006, Neuron.
[43] K. Deisseroth,et al. Millisecond-timescale, genetically targeted optical control of neural activity , 2005, Nature Neuroscience.
[44] P. Humphries,et al. On the genetics of retinitis pigmentosa and on mutation‐independent approaches to therapeutic intervention , 2002, The EMBO journal.
[45] B. Jones,et al. Retinal remodeling during retinal degeneration. , 2005, Experimental eye research.
[46] E. Zrenner. Will Retinal Implants Restore Vision ? , 2002 .
[47] Karl Deisseroth,et al. Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa , 2010, Science.
[48] J. Golden,et al. Safety and Efficacy of Subretinal Readministration of a Viral Vector in Large Animals to Treat Congenital Blindness , 2010, Science Translational Medicine.
[49] Nick Tyler,et al. Effect of gene therapy on visual function in Leber's congenital amaurosis. , 2008, The New England journal of medicine.
[50] K. Deisseroth,et al. Bi-stable neural state switches , 2009, Nature Neuroscience.
[51] R. Koenekoop. Why do Cone Photoreceptors Die in Rod-Specific Forms of Retinal Degenerations? , 2009, Ophthalmic genetics.
[52] Jean Bennett,et al. Gene Therapy for Leber's Congenital Amaurosis is Safe and Effective Through 1.5 Years After Vector Administration , 2009, Molecular therapy : the journal of the American Society of Gene Therapy.
[53] F. Werblin,et al. Differential Targeting of Optical Neuromodulators to Ganglion Cell Soma and Dendrites Allows Dynamic Control of Center-Surround Antagonism , 2011, Neuron.
[54] C. Cepko,et al. Stimulation of the insulin/mTOR pathway delays cone death in a mouse model of retinitis pigmentosa , 2009, Nature Neuroscience.
[55] Eberhart Zrenner,et al. Photoreceptor Cell Death Mechanisms in Inherited Retinal Degeneration , 2008, Molecular Neurobiology.
[56] Kathleen A. Marshall,et al. Safety and efficacy of gene transfer for Leber's congenital amaurosis. , 2008, The New England journal of medicine.
[57] José-Alain Sahel,et al. Rod-Derived Cone Viability Factor for Treating Blinding Diseases: From Clinic to Redox Signaling , 2010, Science Translational Medicine.
[58] J. Sahel,et al. Retinitis pigmentosa: rod photoreceptor rescue by a calcium-channel blocker in the rd mouse , 1999, Nature Medicine.
[59] Heinz Wässle,et al. Parallel processing in the mammalian retina , 2004, Nature Reviews Neuroscience.
[60] A. Vugler. PROGRESS TOWARD THE MAINTENANCE AND REPAIR OF DEGENERATING RETINAL CIRCUITRY , 2010, Retina.
[61] C. Mussolino,et al. Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa , 2011, EMBO molecular medicine.
[62] James Weiland,et al. Artificial vision: needs, functioning, and testing of a retinal electronic prosthesis. , 2009, Progress in brain research.
[63] Zhuo-Hua Pan,et al. Ectopic Expression of Multiple Microbial Rhodopsins Restores ON and OFF Light Responses in Retinas with Photoreceptor Degeneration , 2009, The Journal of Neuroscience.
[64] D. Baylor,et al. An alternative pathway for signal flow from rod photoreceptors to ganglion cells in mammalian retina. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[65] R. Masland,et al. Remodeling of cone photoreceptor cells after rod degeneration in rd mice. , 2009, Experimental eye research.
[66] Toru Ishizuka,et al. Visual Properties of Transgenic Rats Harboring the Channelrhodopsin-2 Gene Regulated by the Thy-1.2 Promoter , 2009, PloS one.