Retinal optogenetic therapies: clinical criteria for candidacy. - Wikidata - wikimedia - TriplyDB

Retinal optogenetic therapies: clinical criteria for candidacy.

Retinal optogenetic therapies: clinical criteria for candidacy.

http://www.wikidata.org/entity/Q45886746

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Optogenetic approaches to retinal prosthesis Therapeutic potential of optogenetic neuromodulation Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion Cells.Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy.Improvement in vision: a new goal for treatment of hereditary retinal degenerations Halting progressive neurodegeneration in advanced retinitis pigmentosa Let There Be Light: Gene and Cell Therapy for Blindness.Advances in Gene Therapy for Diseases of the Eye.Red-shifted channelrhodopsin stimulation restores light responses in blind mice, macaque retina, and human retina.Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene.Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutations.Aberrant protein trafficking in retinal degenerations: The initial phase of retinal remodeling.Shining Light on the Sprout of Life: Optogenetics Applications in Stem Cell Research and Therapy.A New Promoter Allows Optogenetic Vision Restoration with Enhanced Sensitivity in Macaque Retina.Long-term restoration of visual function in end-stage retinal degeneration using subretinal human melanopsin gene therapy.Comparison of 5-year progression of retinitis pigmentosa involving the posterior pole among siblings by means of SD-OCT: a retrospective study.Cochlear Gene Therapy for Sensorineural Hearing Loss: Current Status and Major Remaining Hurdles for Translational Success.

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Retinal optogenetic therapies: clinical criteria for candidacy.

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2013 nî lūn-bûn

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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2013年學術文章

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Retinal optogenetic therapies: clinical criteria for candidacy.

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Retinal optogenetic therapies: clinical criteria for candidacy.

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Retinal optogenetic therapies: clinical criteria for candidacy.

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Retinal optogenetic therapies: clinical criteria for candidacy.

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Retinal optogenetic therapies: clinical criteria for candidacy.

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Clinical Genetics

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Retinal optogenetic therapies: clinical criteria for candidacy.

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A Sumaroka

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A V Cideciyan

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X Luo

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P2860

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Interim results from the international trial of Second Sight's visual prosthesis.

A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi Jews

Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination

Mutations in the CRB1 gene cause Leber congenital amaurosis

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population

Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis

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 retinal ciliopathy

Optogenetic neuromodulation.

Morphometric study of the displacement of retinal ganglion cells subserving cones within the human fovea.

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175-182

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10.1111/CGE.12165

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2

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84

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Samuel G. Jacobson

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236204755

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