Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa.
about
Synthetic biology and therapeutic strategies for the degenerating brain: Synthetic biology approaches can transform classical cell and gene therapies, to provide new cures for neurodegenerative diseasesGene therapy of inherited retinal degenerations: prospects and challengesA comprehensive review of retinal gene therapyFunctional and molecular characterization of rod-like cells from retinal stem cells derived from the adult ciliary epitheliumOptogenetic therapy for retinitis pigmentosa.Gene augmentation for adRP mutations in RHO.Gene therapy for PRPH2-associated ocular disease: challenges and prospectsVector platforms for gene therapy of inherited retinopathies.Recombinant vectors based on porcine adeno-associated viral serotypes transduce the murine and pig retinaThe Krüppel-associated box repressor domain can induce reversible heterochromatization of a mouse locus in vivo.Gene therapy of inherited retinopathies: a long and successful road from viral vectors to patients.Rhodopsin targeted transcriptional silencing by DNA-binding.Allele-Specific Inhibition of Rhodopsin With an Antisense Oligonucleotide Slows Photoreceptor Cell DegenerationNrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice.Gene-based therapies for dominantly inherited retinopathies.Clinical and Rehabilitative Management of Retinitis Pigmentosa: Up-to-Date.Gene therapy in animal models of autosomal dominant retinitis pigmentosaGene therapies for inherited retinal disorders.Gene therapy to rescue retinal degeneration caused by mutations in rhodopsin.In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy in the S334ter-3 Rat Model of Autosomal Dominant Retinitis Pigmentosa.A designed zinc-finger transcriptional repressor of phospholamban improves function of the failing heart.Gene delivery to the retina: from mouse to man.Long-term rescue of retinal structure and function by rhodopsin RNA replacement with a single adeno-associated viral vector in P23H RHO transgenic mice.In vivo Editing of the Human Mutant Rhodopsin Gene by Electroporation of Plasmid-based CRISPR/Cas9 in the Mouse Retina.Targeting and silencing of rhodopsin by ectopic expression of the transcription factor KLF15.Designer epigenome modifiers enable robust and sustained gene silencing in clinically relevant human cells.
P2860
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P2860
Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Zinc-finger-based transcriptio ...... dominant retinitis pigmentosa.
@ast
Zinc-finger-based transcriptio ...... dominant retinitis pigmentosa.
@en
type
label
Zinc-finger-based transcriptio ...... dominant retinitis pigmentosa.
@ast
Zinc-finger-based transcriptio ...... dominant retinitis pigmentosa.
@en
prefLabel
Zinc-finger-based transcriptio ...... dominant retinitis pigmentosa.
@ast
Zinc-finger-based transcriptio ...... dominant retinitis pigmentosa.
@en
P2093
P2860
P50
P356
P1476
Zinc-finger-based transcriptio ...... dominant retinitis pigmentosa.
@en
P2093
Ciro Bonetti
Claudio Mussolino
Daniela Sanges
Elena Marrocco
Germana Meroni
Umberto Di Vicino
P2860
P304
P356
10.1002/EMMM.201000119
P577
2011-01-26T00:00:00Z