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Retinoschisin
Program Nr: 1 from the 2004 ASHG Annual Meeting Mutations in A
1 Supporting Information for a Microrna Network Regulates
Subterranean Mammals Show Convergent Regression in Ocular Genes and Enhancers, Along with Adaptation to Tunneling
Avian Binocularity and Adaptation to Nocturnal Environments: Genomic Insights Froma Highly Derived Visual Phenotype Rui Borges Universidade Do Porto - Portugal
University of London Thesis
The Role of Chx10 in the Development of the Vertebrate Retina
Ligand-Specific Transcriptional Mechanisms Underlie Aryl Hydrocarbon Receptor-Mediated Developmental Toxicity of Oxygenated Pahs
The Plasminogen Protein Is Associated with High Myopia As
Studies on the Interaction Between Retinoschisin and the Retinal Na/K-Atpase
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Liquid Biopsy of Vitreous Reveals an Abundant Vesicle Population Consistent with the Size and Morphology of Exosomes
X-Linked Juvenile Retinoschisis
Null Retinoschisin-Protein Expression from an RS1 C354del1-Ins18 Mutation Causing Progressive and Severe XLRS in a Cross-Sectional Family Study
From Gene Identification and Functional Characterization to Genome Editing Approaches for Inherited Retinal Disorders Elise Orhan Le Gac De Lansalut
Product Description SALSA® MLPA® Probemix P488-B1 RS1 to Be Used with the MLPA General Protocol
Summary of Research Activites by Key Approach and Resource
Identification of Synaptic PPT1 Substrates Highlight Roles of Depalmitoylation in Disulfide Bond Formation and Synaptic Function
PROGRAM AOPT-2019 Page 121
Top View
Proteomic Insight Into the Pathogenesis of CAPN5- Vitreoretinopathy Received: 13 February 2019 Gabriel Velez1,2,3, Jing Yang1,2, Angela S
Rhodopsin Mutations Leading to Retinitis Pigmentosa
Integrative Subcellular Proteomic Analysis Allows Accurate Prediction of Human Disease-Causing Genes
X-Linked Juvenile Retinoschisis: Clinical Diagnosis, Genetic Analysis, and Molecular Mechanisms