(Q45886746)

17 December 2017

title

Retinal optogenetic therapies: clinical criteria for candidacy (English)

1 reference

17 December 2017

1 reference

1

1 reference

17 December 2017

author name string

A Sumaroka

series ordinal

2

1 reference

17 December 2017

X Luo

series ordinal

3

1 reference

17 December 2017

A V Cideciyan

series ordinal

4

1 reference

17 December 2017

publication date

13 May 2013

1 reference

17 December 2017

published in

Clinical Genetics

1 reference

17 December 2017

volume

84

1 reference

17 December 2017

issue

2

1 reference

17 December 2017

page(s)

175-182

1 reference

17 December 2017

From channelrhodopsins to optogenetics

cites work

1 reference

Microbial rhodopsins in the spotlight

21 January 2018

1 reference

Optogenetic neuromodulation.

21 January 2018

1 reference

Nanomedicine for the treatment of retinal and optic nerve diseases

21 January 2018

1 reference

Optogenetic approaches to restoring visual function in retinitis pigmentosa.

21 January 2018

1 reference

Treatment possibilities for retinitis pigmentosa

21 January 2018

1 reference

Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination

21 January 2018

1 reference

Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success

21 January 2018

1 reference

Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations

21 January 2018

1 reference

Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations

21 January 2018

1 reference

CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.

21 January 2018

1 reference

Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetate

21 January 2018

1 reference

Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations

21 January 2018

1 reference

Anatomical correlates to the bands seen in the outer retina by optical coherence tomography: literature review and model

21 January 2018

1 reference

Canine and human visual cortex intact and responsive despite early retinal blindness from RPE65 mutation

21 January 2018

1 reference

Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis

21 January 2018

1 reference

Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model

21 January 2018

1 reference

Morphometric study of the displacement of retinal ganglion cells subserving cones within the human fovea.

21 January 2018

1 reference

Topography of ganglion cells in human retina.

21 January 2018

1 reference

Intravitreal injection of AAV2 transduces macaque inner retina

21 January 2018

1 reference

The genomic, biochemical, and cellular responses of the retina in inherited photoreceptor degenerations and prospects for the treatment of these disorders

21 January 2018

1 reference

Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait

21 January 2018

1 reference

A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi Jews

21 January 2018

1 reference

Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa

21 January 2018

1 reference

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population

21 January 2018

1 reference

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

21 January 2018

1 reference

Mutations in the CRB1 gene cause Leber congenital amaurosis

21 January 2018

1 reference

CRB1 mutations in inherited retinal dystrophies

21 January 2018

1 reference

RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expression

21 January 2018

1 reference

Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations

21 January 2018

1 reference

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 ciliopathy

21 January 2018

1 reference

Differential macular morphology in patients with RPE65-, CEP290-, GUCY2D-, and AIPL1-related Leber congenital amaurosis

21 January 2018

1 reference

Genetic reactivation of cone photoreceptors restores visual responses in retinitis pigmentosa

21 January 2018

1 reference

Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy

21 January 2018

1 reference

Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement

21 January 2018

1 reference

Interim results from the international trial of Second Sight's visual prosthesis

21 January 2018

1 reference

Morphometric analysis of macular photoreceptors and ganglion cells in retinas with retinitis pigmentosa

21 January 2018

1 reference

Leber congenital amaurosis: genes, proteins and disease mechanisms

21 January 2018

1 reference

A review and update on the current status of stem cell therapy and the retina

21 January 2018

1 reference

Remodeling of the Human Retina in Choroideremia: Rab Escort Protein 1 (REP-1) Mutations

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12165

1 reference

17 December 2017

1 reference

17 December 2017