Long-term rescue of retinal structure and function by rhodopsin RNA replacement with a single adeno-associated viral vector in P23H RHO transgenic mice.
about
Gene therapy of inherited retinal degenerations: prospects and challengesA comprehensive review of retinal gene therapySuccessful subretinal delivery and monitoring of MicroBeads in miceAdvancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano SymposiumPotential of Small Molecule-Mediated Reprogramming of Rod Photoreceptors to Treat Retinitis PigmentosaCLINICAL PROGRESS IN INHERITED RETINAL DEGENERATIONS: GENE THERAPY CLINICAL TRIALS AND ADVANCES IN GENETIC SEQUENCING.Gene augmentation for adRP mutations in RHO.Gene therapy for PRPH2-associated ocular disease: challenges and prospectsVector platforms for gene therapy of inherited retinopathies.Repair of rhodopsin mRNA by spliceosome-mediated RNA trans-splicing: a new approach for autosomal dominant retinitis pigmentosa.Trans-Corneal Subretinal Injection in Mice and Its Effect on the Function and Morphology of the Retina.A High-Throughput Drug Screening Strategy for Detecting Rhodopsin P23H Mutant Rescue and Degradation.Gene therapy of inherited retinopathies: a long and successful road from viral vectors to patients.Non-viral therapeutic approaches to ocular diseases: An overview and future directionsAssessment of visual function and retinal structure following acute light exposure in the light sensitive T4R rhodopsin mutant dogAdvances in gene therapy technologies to treat retinitis pigmentosa.Gene therapy approaches for the treatment of retinal disordersRecombinant AAV as a platform for translating the therapeutic potential of RNA interference.Long-term Characterization of Retinal Degeneration in Royal College of Surgeons Rats Using Spectral-Domain Optical Coherence TomographyGene therapy in animal models of autosomal dominant retinitis pigmentosaSmall-interfering RNAs (siRNAs) as a promising tool for ocular therapy.Gene therapies for inherited retinal disorders.Recent advances of stem cell therapy for retinitis pigmentosa.AAV Delivery of GRP78/BiP Promotes Adaptation of Human RPE Cell to ER Stress.Viral vectors for therapy of neurologic diseases.Gene therapy to rescue retinal degeneration caused by mutations in rhodopsin.Caspase-7 ablation modulates UPR, reprograms TRAF2-JNK apoptosis and protects T17M rhodopsin mice from severe retinal degeneration.Gene therapy to treat inherited and complex retinal degenerative diseasesWild-type opsin does not aggregate with a misfolded opsin mutant.Autosomal recessive retinitis pigmentosa E150K opsin mice exhibit photoreceptor disorganization.Recent Advancements in Gene Therapy for Hereditary Retinal Dystrophies.Clustered Regularly Interspaced Short Palindromic Repeats-Based Genome Surgery for the Treatment of Autosomal Dominant Retinitis Pigmentosa.
P2860
Q27009261-A294FB58-59A4-4CB0-B481-FA78FC1939C9Q27023914-90153609-4BE6-439F-956A-33D11110BC4FQ27317308-0E782F77-9379-4B75-9A11-C36E028260DAQ27694625-7355CE02-899F-4F71-A9AB-1850253C84DAQ28818084-65699395-246B-4D85-8B7E-080E1D004646Q33782257-827B7D87-7447-4E8F-8227-D3DAF32A6D67Q34083185-29F436AC-A017-47A6-BFF1-9FC9FAF007CAQ34400262-626F18DF-3856-4C26-B2B5-33AD3DFD80F9Q34561531-61B41189-4485-4816-95B1-BDDDBA4B330FQ35594834-4C8FBA8C-E535-4B6D-89C7-9184DD855AC7Q35759030-B8F45F67-EB45-4F12-8D7D-C13042BB0CF1Q36009841-78541C81-B530-484C-B61B-0A764DDDB361Q36147481-FAFB07CC-A812-4394-85E3-71EFA126DD23Q36425890-D4E485C4-C588-4DD6-B41D-5F4628F94BF8Q37217166-7DF25EFE-AAF0-4920-9702-2632C89E9A1DQ37427526-5439D236-F8CD-4520-8DE4-325D02089145Q37481357-619456E2-819B-4AA1-B8CD-82641458259EQ37696045-95960ABD-F9F6-4005-9379-39823F4A4E65Q37715259-1B565493-3826-42F6-8A0C-C3F2D2D74F1FQ38053151-48756C74-5E6B-4A04-84AA-018B91386FDEQ38128390-EDD9F403-97B7-4179-B5DF-D3CB295ED072Q38221905-A45D5F50-FC3C-4B20-B77E-3B5A82C86744Q38241625-96E651BB-5D8D-469D-B88F-81175AC37133Q38646084-68AE11DA-F061-4C72-B07A-E5C23EEFCE41Q38746238-17A069B5-97C0-4D74-8459-C26582470F56Q38907972-886B80CA-23B5-4851-953E-F301993EC493Q39495823-B044DBA8-A7DA-4B9A-BEE3-C04922722ECDQ41855514-9E77569A-7B8A-4FAE-9779-C98FA3BE3D36Q41881511-294A0DD5-FA2B-4379-8B8D-0FEF4A711387Q42438771-E40039A7-D4E6-4022-A3D5-C9A2E039BB88Q47554759-0B4DD7E9-81A2-4AF4-85B6-6334FDDA927DQ54212285-149B5A94-9024-40A5-BED8-702BA447BC9E
P2860
Long-term rescue of retinal structure and function by rhodopsin RNA replacement with a single adeno-associated viral vector in P23H RHO transgenic mice.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Long-term rescue of retinal st ...... r in P23H RHO transgenic mice.
@en
Long-term rescue of retinal st ...... r in P23H RHO transgenic mice.
@nl
type
label
Long-term rescue of retinal st ...... r in P23H RHO transgenic mice.
@en
Long-term rescue of retinal st ...... r in P23H RHO transgenic mice.
@nl
prefLabel
Long-term rescue of retinal st ...... r in P23H RHO transgenic mice.
@en
Long-term rescue of retinal st ...... r in P23H RHO transgenic mice.
@nl
P2860
P50
P356
P1433
P1476
Long-term rescue of retinal st ...... or in P23H RHO transgenic mice
@en
P2093
Brian Rossmiller
P2860
P304
P356
10.1089/HUM.2011.213
P577
2012-03-28T00:00:00Z