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Blue cone monochromacy
Blue Cone Monochromacy: Visual Function and Efficacy Outcome Measures for Clinical Trials
Structure of Cone Photoreceptors
The Genetic Horizon Improving Clinical Sensitivity in Difficult-To-Sequence Genes for Rare Hereditary Disorders
Intermixing the OPN1LW and OPN1MW Genes Disrupts the Exonic Splicing Code Causing an Array of Vision Disorders
Progressive Cone and Cone-Rod Dystrophies
Visual Impairment Age-Related Macular
Causes of Color Blindness: Function and Failure of the Genes That Detect Color
The Alter Retina: Alternative Splicing of Retinal Genes in Health and Disease
Addressing the Needs of Students with Color Vision Deficiencies in the Elementary School Library
BCM&School-EN-Final 3
Cone Targeted Gene Therapy: Animal Models
Translational Retinal Research and Therapies
Color Vision Deficiency
The Cone Dysfunction Syndromes Jonathan Aboshiha,1,2 Adam M Dubis,1,2 Joseph Carroll,3 Alison J Hardcastle,1,2 Michel Michaelides1,2
Reading Performance in Blue Cone Monochromacy: Defining an Outcome Measure for a Clinical Trial
Blue Cone Monochromatism M Michaelides Et Al 3
Visual Function and Cortical Organization in Carriers of Blue Cone Monochromacy
Blue Cone Monochromacy Caused by the C203R Missense Mutation Or Large Deletion Mutations
Top View
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Quarterly Data Report the Alliance for Regenerative Medicine (ARM) Is the Preeminent Global Advocate for Regenerative and Advanced Therapies
Molecular Genetics of Human Blue Cone Monochromacy
3-18-2017 Snapshots of a Life in Science, Jeremy
Preclinical Studies Support Intravitreal Gene Therapy for Blue Cone Monochromacy
Thyroid Hormone Signaling Specifies Cone Subtypes in Human Retinal
2016 Impact Report Celebrating 35 Years of Research Excellence
Noninvasive Imaging of the Human Rod Photoreceptor Mosaic Using a Confocal Adaptive Optics Scanning Ophthalmoscope Alfredo Dubra Marquette University
Functional Photoreceptor Loss Revealed with Adaptive Optics: an Alternate Cause of Color Blindness
Recommendations for Genetic Testing of Inherited Eye Diseases Report of the American Academy of Ophthalmology Task Force on Genetic Testing
Blue Cone Monochromatism with Foveal Hypoplasia Caused by the Concomitant Effect of Variants in OPN1LW/OPN1MW and GPR143 Genes
The Limits of Visual Resolution by Ethan Andrew Rossi a Dissertation
High-Resolution Microarray Analysis Unravels Complex Xq28 Aberrations
(12) Patent Application Publication (10) Pub. No.: US 2015/0259395 A1 Chalberg Et Al
Active Opsin Loci Adopt Intrachromosomal Loops That Depend on the Photoreceptor Transcription Factor Network
The Cone Dystroph Ies M.P
Article (Published Version)
Moran Eye Center Faculty, Residents, Fellows at ARVO 2019 Workshops
843 a AAV. See Adeno-Associated Virus (AAV) ABCA4 Gene , 408–409
Curriculum Vitae
Cone Rod Dystrophy Precision Panel Overview Indications Clinical Utility
UC Berkeley UC Berkeley Electronic Theses and Dissertations
Cone Opsins, Colour Blindness and Cone Dystrophy: Genotype-Phenotype Correlations
AI-Based Structure-Function Correlation in Age-Related Macular Degeneration
Novel OPN1LW/OPN1MW Deletion Mutations in 2 Japanese Families with Blue Cone Monochromacy
Developing an Outcome Measure with High Luminance for Optogenetics Treatment of Severe Retinal Degenerations and for Gene Therapy of Cone Diseases
(Irds) in Canada
The Spectral Sensitivity of the Human Short-Wavelength Sensitive Cones Derived from Thresholds and Color Matches
A Review on Today's Burden Affecting the Quality of Life for Colour Blind
Bibliography 2013
Blue Cone Monochromacy Causes Deterioration in Visual Acuity And
Old Mystery Solved: Achromatopsia, the Fuur Genealogy in Retrospective Thomas Rosenberg1*, Jens V
A Systematic Review and Meta-Analyses of Interventional Clinical Trial Studies for Gene Therapies for the Inherited Retinal Degenerations (Irds)
Progressive Loss of Cones in Achromatopsia. an Imaging Study
Leber Congenital Amaurosis Due to GUCY2D Mutations: Longitudinal Analysis of Retinal Structure and Visual Function
X-Linked Cone Dystrophy Caused by Mutation of the Red and Green Cone Opsins
Understanding and Coping with Achromatopsia
Copy-Number Variation Is an Important Contributor to the Genetic Causality of Inherited Retinal Degenerations
SSBP1 Mutations Cause Mtdna Depletion Underlying a Complex Optic Atrophy Disorder
Clinical(Characterization(Of(Patients
Blue Cone Monochromatism: Clinical