Clinical characteristics and current therapies for inherited retinal degenerations
about
Gene therapy of inherited retinal degenerations: prospects and challengesDiagnostic exome sequencing in 266 Dutch patients with visual impairment.RPGR: Its role in photoreceptor physiology, human disease, and future therapies.The Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome.Induced Pluripotent Stem Cell Therapies for Degenerative Disease of the Outer Retina: Disease Modeling and Cell Replacement.Construction of a plasmid for human brain-derived neurotrophic factor and its effect on retinal pigment epithelial cell viability.Neuroprotective Strategy in Retinal Degeneration: Suppressing ER Stress-Induced Cell Death via Inhibition of the mTOR Signal.Reorganization of early visual cortex functional connectivity following selective peripheral and central visual loss.Long-term Characterization of Retinal Degeneration in Royal College of Surgeons Rats Using Spectral-Domain Optical Coherence TomographyIdentification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell Subtypes.Whole exome sequencing using Ion Proton system enables reliable genetic diagnosis of inherited retinal dystrophies.Hereditary Retinal Dystrophy.Anosmia-A Clinical Review.Gene Therapy and Stem Cell Transplantation in Retinal Disease: The New Frontier.Microglial phagocytosis and activation underlying photoreceptor degeneration is regulated by CX3CL1-CX3CR1 signaling in a mouse model of retinitis pigmentosa.A Method for the Isolation and Culture of Adult Rat Retinal Pigment Epithelial (RPE) Cells to Study Retinal Diseases.Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration Families.The clinical implications of molecular monitoring and analyses of inherited retinal diseases.A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration.Recent Advancements in Gene Therapy for Hereditary Retinal Dystrophies.Design and In Vitro Use of Antisense Oligonucleotides to Correct Pre-mRNA Splicing Defects in Inherited Retinal Dystrophies.Early Microglia Activation Precedes Photoreceptor Degeneration in a Mouse Model of CNGB1-Linked Retinitis Pigmentosa.Managing Bardet–Biedl Syndrome—Now and in the Future.Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration FamiliesCombination of cGMP analogue and drug delivery system provides functional protection in hereditary retinal degeneration.Novel variants identified with next-generation sequencing in Polish patients with cone-rod dystrophy.
P2860
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P2860
Clinical characteristics and current therapies for inherited retinal degenerations
description
2014 nî lūn-bûn
@nan
2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Clinical characteristics and current therapies for inherited retinal degenerations
@en
type
label
Clinical characteristics and current therapies for inherited retinal degenerations
@en
prefLabel
Clinical characteristics and current therapies for inherited retinal degenerations
@en
P2860
P1476
Clinical characteristics and current therapies for inherited retinal degenerations
@en
P2093
Katia Marazova
P2860
P304
P356
10.1101/CSHPERSPECT.A017111
P577
2014-10-16T00:00:00Z