Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations
about
A novel adeno-associated viral variant for efficient and selective intravitreal transduction of rat Müller cellsTreatment 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 trialHuman RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 yearPromising and delivering gene therapies for vision lossDefective 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 ciliopathyCone 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 PigmentosaA 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 RetinopathyWhole exome sequencing reveals genetic predisposition in a large family with retinitis pigmentosaReal-time imaging of rabbit retina with retinal degeneration by using spectral-domain optical coherence tomographyCone 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 pigmentosaProbing 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 modelGenotypic 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 mutationsRetinal 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 mutantscGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindnessFactors Affecting Perceptual Threshold in Argus II Retinal Prosthesis SubjectsComplexity 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.
P2860
Q21142728-6C966AC4-F5F8-4A2A-BE4E-AD24100E1D99Q24608049-BDB4605E-25B7-4101-BCE0-4D88D6A4BE3AQ24634801-99FCD5E4-D072-4EC9-B0EA-02423FAC028DQ27007079-9C84FDE1-99B2-490F-A68B-D13241C6D711Q30464083-D5A59AB9-1FC2-4050-8171-3447F236A326Q30494855-E8A00CEA-0AE7-4F9B-8D17-DF879467BCDCQ30498337-F7D9A010-9E07-4144-AAE6-F13674B9E8AEQ30498458-1CC095BA-479C-4296-AA84-4EF2476D653EQ30512453-87BB5DA7-03D8-4CFC-A199-E9C6206BC066Q30843751-711902CF-AF1B-4B0F-A041-889A5D50E837Q33539517-C8A7F61F-0F83-4988-84C9-ED1A05CF1995Q33746411-17E14B57-10A8-429F-AD67-8E31F21270D7Q33914788-4BA6AB26-1465-4A0D-8B05-AC71F6D535D0Q34257191-DF63655A-BD4C-40C1-B2A3-7842C6F7AEF2Q34262858-52055393-5E6E-4858-979E-2FE83134A77EQ34547527-5700F112-4A56-4DFA-8834-E10FC4166B87Q34646569-371A42CE-40A5-43FE-B87C-BC2DFE0EA145Q34695879-0EE2701F-8809-44FF-98CC-EB98360C38BDQ34977143-6F5C8C87-440A-44B3-B278-6B61298DDBC6Q35000428-3CBAFBA1-9CBA-4618-A537-B3DE75D714CAQ35221208-EA850E06-F282-4AA5-B873-876C8AC4DE6BQ35640993-FA6B65F0-20C2-4C71-83EB-CDE8C2F854AEQ35682509-5539A642-E686-4113-A8A2-B2A35766933DQ35687907-5E55DFFE-D069-463E-9068-E7B0D092B64CQ35706943-523978BB-A075-477F-ABE7-BEC730060DE8Q35925194-5AD44328-7E9D-40E9-8F29-4E8E906DE662Q36086392-B18B00B7-7B35-4AA3-B0D5-BE5EBE68C0B5Q36098417-33D6506D-42E2-4125-9564-BB14E3DFD372Q36380253-597D1EDA-7B78-43E1-AE4E-D07F6BEE81BFQ36709692-3255D66C-0A67-4279-9DBA-01D4F75A7AE1Q37137455-2FF96D26-58FD-4492-9C13-D2CBDF834879Q37149422-FD893ECC-C482-4197-9CF9-0AD91807D233Q37275303-99F4CD16-4421-4B44-BD45-A997443538A5Q37323334-B95A29F3-2701-4B50-996B-CB9DF8586D27Q37386265-C6B14904-12D5-42A3-85A9-86E993C8DE4FQ37386268-3C6497FB-FD25-4CF8-9025-CBDD3D7E48ECQ37635389-7ECE9279-B5D3-4859-B7B8-C3686FBE17DBQ37641855-E02C75F4-A8CC-4AD5-8DBF-8A84777FFA23Q37671070-C319EAE9-CB09-4731-A2B3-FEEC073F23C1Q38028649-0E964F63-56F8-4A28-8A74-425BDF96228D
P2860
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations
description
2008 nî lūn-bûn
@nan
2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Retinal laminar architecture i ...... ed by Rhodopsin gene mutations
@ast
Retinal laminar architecture i ...... ed by Rhodopsin gene mutations
@en
type
label
Retinal laminar architecture i ...... ed by Rhodopsin gene mutations
@ast
Retinal laminar architecture i ...... ed by Rhodopsin gene mutations
@en
prefLabel
Retinal laminar architecture i ...... ed by Rhodopsin gene mutations
@ast
Retinal laminar architecture i ...... ed by Rhodopsin gene mutations
@en
P2093
P2860
P50
P356
P1476
Retinal laminar architecture i ...... ed by Rhodopsin gene mutations
@en
P2093
Alejandro J Roman
Alexander Sumaroka
Anjani Naidu
Artur V Cideciyan
D Alan White
Elizabeth A M Windsor
Shalesh Kaushal
Sharon B Schwartz
Tomas S Aleman
P2860
P304
P356
10.1167/IOVS.07-1110
P407
P577
2008-04-01T00:00:00Z