Photoreceptor structure and function in patients with congenital achromatopsia. - Test2 - elhamkhani - TriplyDB

Photoreceptor structure and function in patients with congenital achromatopsia.

Photoreceptor structure and function in patients with congenital achromatopsia.

http://www.wikidata.org/entity/Q35247580

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Adaptive optics ophthalmoscopy.Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 Achromatopsia Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia Normal Perceptual Sensitivity Arising From Weakly Reflective Cone Photoreceptors AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.Repeatability of in vivo parafoveal cone density and spacing measurements.High-resolution images of retinal structure in patients with choroideremia.Adaptive optics retinal imaging--clinical opportunities and challenges Selective cone photoreceptor injury in acute macular neuroretinopathy Microscopic inner retinal hyper-reflective phenotypes in retinal and neurologic disease.In vivo imaging of human cone photoreceptor inner segments.A prospective longitudinal study of retinal structure and function in achromatopsia.Fluorescence adaptive optics scanning laser ophthalmoscope for detection of reduced cones and hypoautofluorescent spots in fundus albipunctatus CNGB3-achromatopsia clinical trial with CNTF: diminished rod pathway responses with no evidence of improvement in cone function Dark-adaptation functions in molecularly confirmed achromatopsia and the implications for assessment in retinal therapy trials.High-resolution adaptive optics retinal imaging of cellular structure in choroideremia.Phenotypic characteristics including in vivo cone photoreceptor mosaic in KCNV2-related "cone dystrophy with supernormal rod electroretinogram"Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone health Clinical characteristics and current therapies for inherited retinal degenerations Spectral-domain optical coherence tomography staging and autofluorescence imaging in achromatopsia.Flicker cone function in normal and day blind sheep: a large animal model for human achromatopsia caused by CNGA3 mutation cGMP/Protein Kinase G Signaling Suppresses Inositol 1,4,5-Trisphosphate Receptor Phosphorylation and Promotes Endoplasmic Reticulum Stress in Photoreceptors of Cyclic Nucleotide-gated Channel-deficient Mice.The fundus photo has met its match: optical coherence tomography and adaptive optics ophthalmoscopy are here to stay Endoplasmic reticulum stress-associated cone photoreceptor degeneration in cyclic nucleotide-gated channel deficiency.Cone and rod loss in Stargardt disease revealed by adaptive optics scanning light ophthalmoscopy.Multimodal Imaging of Photoreceptor Structure in Choroideremia.Achromatopsia caused by novel missense mutations in the CNGA3 gene.Normative reference ranges for the retinal nerve fiber layer, macula, and retinal layer thicknesses in children Reliability and Repeatability of Cone Density Measurements in Patients with Congenital Achromatopsia Transient photoreceptor deconstruction by CNTF enhances rAAV-mediated cone functional rescue in late stage CNGB3-achromatopsia.Automatic detection of modal spacing (Yellott's ring) in adaptive optics scanning light ophthalmoscope images.Rhodopsin F45L Allele Does Not Cause Autosomal Dominant Retinitis Pigmentosa in a Large Caucasian Family.Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia.Assessing Photoreceptor Structure in Retinitis Pigmentosa and Usher Syndrome.Retinal structure and function in achromatopsia: implications for gene therapy.Achromatopsia mutations target sequential steps of ATF6 activation.The morphology of human rod ERGs obtained by silent substitution stimulation.Gene replacement therapy for retinal CNG channelopathies.Adaptive optics imaging of the retina.

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P2860

Photoreceptor structure and function in patients with congenital achromatopsia.

http://www.wikidata.org/entity/Q35247580

description

2011 nî lūn-bûn

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2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Photoreceptor structure and function in patients with congenital achromatopsia.

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Photoreceptor structure and function in patients with congenital achromatopsia.

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Photoreceptor structure and function in patients with congenital achromatopsia.

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Photoreceptor structure and function in patients with congenital achromatopsia.

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prefLabel

Photoreceptor structure and function in patients with congenital achromatopsia.

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Photoreceptor structure and function in patients with congenital achromatopsia.

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Investigative Ophthalmology & Visual Science

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Photoreceptor structure and function in patients with congenital achromatopsia

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P2093

Adam M Dubis

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Daniela Maria O Bonci

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Gerald A Fishman

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Joseph Carroll

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Jungtae Rha

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Maureen Neitz

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Mohamed A Genead

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P2860

CNGA3 mutations in hereditary cone photoreceptor disorders

Gene therapy rescues cone function in congenital achromatopsia.

Longitudinal study of cone photoreceptors during retinal degeneration and in response to ciliary neurotrophic factor treatment

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel

Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases

Restoration of cone vision in a mouse model of achromatopsia

Cone photoreceptor function loss-3, a novel mouse model of achromatopsia due to a mutation in Gnat2

Applications of adaptive optics scanning laser ophthalmoscopy

Clinical value, normative retinal sensitivity values, and intrasession repeatability using a combined spectral domain optical coherence tomography/scanning laser ophthalmoscope microperimeter.

Quantitative analysis of OCT characteristics in patients with achromatopsia and blue-cone monochromatism.

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10.1167/IOVS.11-7762

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10

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Photoreceptor protein

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3183969

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