Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy - Wikidata - awgldk - TriplyDB

Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy

Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy

http://www.wikidata.org/entity/Q34373332

about

Advances in understanding the molecular basis of the first steps in color vision In vivo imaging of human cone photoreceptor inner segments.Outer retinal structure after closed-globe blunt ocular trauma.Dark-adaptation functions in molecularly confirmed achromatopsia and the implications for assessment in retinal therapy trials.Curing color blindness--mice and nonhuman primates Changes in outer retinal microstructures during six month period in eyes with acute zonal occult outer retinopathy-complex Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variants Blue cone monochromacy: visual function and efficacy outcome measures for clinical trials.Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone health Autofluorescence imaging with near-infrared excitation:normalization by reflectance to reduce signal from choroidal fluorophores.Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrast TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular cones.ASSESSING PHOTORECEPTOR STRUCTURE ASSOCIATED WITH ELLIPSOID ZONE DISRUPTIONS VISUALIZED WITH OPTICAL COHERENCE TOMOGRAPHY.Evaluating Descriptive Metrics of the Human Cone Mosaic Developing an Outcome Measure With High Luminance for Optogenetics Treatment of Severe Retinal Degenerations and for Gene Therapy of Cone Diseases Cone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency.Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia.Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations.EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression.Quantitative Assessment of Microstructural Changes of the Retina in Infants With Congenital Zika Syndrome.Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy.The cone dysfunction syndromes.Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutation.Imaging Lenticular Autofluorescence in Older Subjects.Adaptive optics imaging of inherited retinal diseases.Non-invasive assessment of human cone photoreceptor function.Photoreceptor disruption and vision loss associated with central serous retinopathy.Human L- and M-opsins restore M-cone function in a mouse model for human blue cone monochromacy.FREQUENT SUBCLINICAL MACULAR CHANGES IN COMBINED BRAF/MEK INHIBITION WITH HIGH-DOSE HYDROXYCHLOROQUINE AS TREATMENT FOR ADVANCED METASTATIC BRAF MUTANT MELANOMA: Preliminary Results From a Phase I/II Clinical Treatment Trial.BEST1 gene therapy corrects a diffuse retina-wide microdetachment modulated by light exposure.A 73,128 bp de novo deletion encompassing the OPN1LW/OPN1MW gene cluster in sporadic Blue Cone Monochromacy: a case report.Residual Cone Structure in Patients With X-Linked Cone Opsin Mutations

P2860

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P2860

Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy

http://www.wikidata.org/entity/Q34373332

description

2013 nî lūn-bûn

@nan

2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2013年の論文

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2013年論文

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2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

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2013年論文

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2013年论文

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name

Human cone visual pigment dele ...... eptors to warrant gene therapy

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Human cone visual pigment dele ...... eptors to warrant gene therapy

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Human cone visual pigment dele ...... eptors to warrant gene therapy

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Human cone visual pigment dele ...... eptors to warrant gene therapy

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Human cone visual pigment dele ...... eptors to warrant gene therapy

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Human cone visual pigment dele ...... eptors to warrant gene therapy

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Human cone visual pigment dele ...... eptors to warrant gene therapy

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Human cone visual pigment dele ...... eptors to warrant gene therapy

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Human cone visual pigment dele ...... eptors to warrant gene therapy

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Human Gene Therapy

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Human cone visual pigment dele ...... eptors to warrant gene therapy

@en

P2093

Alexander Sumaroka

http://www.w3.org/2001/XMLSchema#string

Anthony T Moore

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Artur V Cideciyan

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Bernd Wissinger

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Jessica C Gardner

http://www.w3.org/2001/XMLSchema#string

Joseph Carroll

http://www.w3.org/2001/XMLSchema#string

Megan Land

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Michel Michaelides

http://www.w3.org/2001/XMLSchema#string

Robert A Sisk

http://www.w3.org/2001/XMLSchema#string

Sharon B Schwartz

http://www.w3.org/2001/XMLSchema#string

P2860

Visual function and cortical organization in carriers of blue cone monochromacy

Molecular genetics of human color vision: the genes encoding blue, green, and red pigments

Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial

The genetics of normal and defective color vision

Safety and efficacy of gene transfer for Leber's congenital amaurosis

Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture)

Molecular genetics of inherited variation in human color vision

Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration.

Retinal pigment epithelium defects in humans and mice with mutations in MYO7A: imaging melanosome-specific autofluorescence.

Imaging outer segment renewal in living human cone photoreceptors.

P304

993-1006

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scholarly article

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10.1089/HUM.2013.153

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12

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24

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Samuel G. Jacobson

Robert B Hufnagel

Alison J Hardcastle

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2013-10-30T00:00:00Z

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257073516

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24067079

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Photoreceptor protein

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3868405

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