RNAi-Mediated Gene Suppression in a GCAP1(L151F) Cone-Rod Dystrophy Mouse Model

PLoS ONE - United States
doi 10.1371/journal.pone.0057676
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Public Library of Science (PLoS)

Related search

Spondylometaphyseal Dysplasia-Cone-Rod Dystrophy Syndrome

2020English

Novel CDHR1 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Novel C8ORF37 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Rod-Cone Dystrophy in Spinocerebellar Ataxia Type 1

Archives of Ophthalmology
2011English

Ophthalmic Features of Cone-Rod Dystrophy Caused by Pathogenic Variants in the ALMS1 Gene

Acta Ophthalmologica
MedicineOphthalmology
2017English

Autosomal Dominant Cone-Rod Dystrophy With Negative Electroretinogram.

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
1995English

176. AAV-Mediated Gene Therapy in Limb-Girdle Muscular Dystrophy 2I (LGMD2I) Mouse Model

Molecular Therapy
Molecular MedicineMolecular BiologyPharmacologyMedicineGeneticsDrug Discovery
2012English

Disruption of a Retinal Guanylyl Cyclase Gene Leads to Cone-Specific Dystrophy and Paradoxical Rod Behavior

Journal of Neuroscience
Neuroscience
1999English

Cone Phosphodiesterase-6γ’ Subunit Augments Cone PDE6 Holoenzyme Assembly and Stability in a Mouse Model Lacking Both Rod and Cone PDE6 Catalytic Subunits

Frontiers in Molecular Neuroscience
Molecular NeuroscienceMolecular BiologyCellular
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy