Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations - Wikidata - wikimedia - TriplyDB

Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations

Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations

http://www.wikidata.org/entity/Q35229775

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A novel adeno-associated viral variant for efficient and selective intravitreal transduction of rat Müller cells 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 Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year Promising and delivering gene therapies for vision loss Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration.Retinal pigment epithelium defects in humans and mice with mutations in MYO7A: imaging melanosome-specific autofluorescence.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 Cone degeneration following rod ablation in a reversible model of retinal degeneration.Macular function in macular degenerations: repeatability of microperimetry as a potential outcome measure for ABCA4-associated retinopathy trials.Quantifying Fundus Autofluorescence in Patients With Retinitis Pigmentosa A comparison of visual field sensitivity to photoreceptor thickness in retinitis pigmentosa.Quantitative Analysis of Retinal Structure Using Spectral-Domain Optical Coherence Tomography in RPGR-Associated Retinopathy Whole exome sequencing reveals genetic predisposition in a large family with retinitis pigmentosa Real-time imaging of rabbit retina with retinal degeneration by using spectral-domain optical coherence tomography Cone photoreceptor packing density and the outer nuclear layer thickness in healthy subjects.Natural History of the Central Structural Abnormalities in Choroideremia: A Prospective Cross-Sectional Study.The transition zone between healthy and diseased retina in patients with retinitis pigmentosa Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations.Correlation of outer nuclear layer thickness with cone density values in patients with retinitis pigmentosa and healthy subjects.Distinct characteristics of inferonasal fundus autofluorescence patterns in stargardt disease and retinitis pigmentosa.Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model Genotypic and phenotypic characterization of P23H line 1 rat model.Autofluorescence imaging with near-infrared excitation:normalization by reflectance to reduce signal from choroidal fluorophores.Retinal disease course in Usher syndrome 1B due to MYO7A mutations Retinal histopathology in eyes from patients with autosomal dominant retinitis pigmentosa caused by rhodopsin mutations.Autosomal recessive retinitis pigmentosa caused by mutations in the MAK gene.TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular cones.Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal Degeneration.Cobalamin C Deficiency Shows a Rapidly Progressing Maculopathy With Severe Photoreceptor and Ganglion Cell Loss.Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindness Factors Affecting Perceptual Threshold in Argus II Retinal Prosthesis Subjects Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations.Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.A Comparison of Methods for Tracking Progression in X-Linked Retinitis Pigmentosa Using Frequency Domain OCT.Proceedings of the First International Optogenetic Therapies for Vision Symposium.Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndrome.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.Electronic restoration of vision in those with photoreceptor degenerations.

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P2860

Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations

http://www.wikidata.org/entity/Q35229775

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2008 nî lūn-bûn

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2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2008 թվականի ապրիլին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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Retinal laminar architecture i ...... ed by Rhodopsin gene mutations

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Retinal laminar architecture i ...... ed by Rhodopsin gene mutations

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Retinal laminar architecture i ...... ed by Rhodopsin gene mutations

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Retinal laminar architecture i ...... ed by Rhodopsin gene mutations

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Retinal laminar architecture i ...... ed by Rhodopsin gene mutations

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Investigative Ophthalmology & Visual Science

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Retinal laminar architecture i ...... ed by Rhodopsin gene mutations

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Alejandro J Roman

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Alexander Sumaroka

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Anjani Naidu

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Artur V Cideciyan

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D Alan White

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Elizabeth A M Windsor

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Shalesh Kaushal

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Sharon B Schwartz

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Tomas S Aleman

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P2860

Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chain

Ectopic expression of a microbial-type rhodopsin restores visual responses in mice with photoreceptor degeneration

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa

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

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

Retinitis pigmentosa

In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosa

Retinal degeneration in the nervous mutant mouse. IV. Inner retinal changes.

Mutant rhodopsin transgene expression on a null background.

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1580-1590

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10.1167/IOVS.07-1110

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4

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Samuel G. Jacobson

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5467743

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3179264

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