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AIPL1
A Multistep Bioinformatic Approach Detects Putative Regulatory
(LCA9) for Leber's Congenital Amaurosis on Chromosome 1P36
Platform Abstracts
Whole Genome Sequencing in Cats, Identifies New Models for Blindness in AIPL1 and Somite Segmentation in HES7
Retinal Organoids Derived from Hipscs of an AIPL1-LCA
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Comprehensive Genotyping Reveals RPE65 As the Most Frequently Mutated Gene in Leber Congenital Amaurosis in Denmark
Gypenosides Alleviate Cone Cell Death in a Zebrafish Model
Development of Gene Therapy for the Treatment of Retinal Dystrophies Caused by Mutations in AIPL1
Mutant Screen for Reproduction Unveils Depression-Associated Piccolo's Control Over Reproductive Behavior
A Domestic Cat Whole Exome Sequencing Resource for Trait Discovery Alana R
Could Ion Channels-Encoding Or Related Genes Act As Modifier Of
Clinical and Functional Analyses of AIPL1 Variants Reveal Mechanisms
Current Concepts of Genotype-Phenotype Correlations
Leber Congenital Amaurosis Linked to AIPL1: a Mouse Model Reveals Destabilization of Cgmp Phosphodiesterase
Gene Expression in the Mouse Eye: an Online Resource for Genetics Using 103 Strains of Mice
Recurrent AIPL1 C.487C>T Truncating Variant in Leber Congenital
Complete Exon-Intron Structure of the RPGR-Interacting Protein (RPGRIP1) Gene Allows the Identification of Mutations Underlying Leber Congenital Amaurosis
Top View
AIPL1 Implicated in the Pathogenesis of Two Cases of Autosomal Recessive Retinal Degeneration
Whole Exome Sequencing Identifies Multiple Pathogenic Variants in a Large South
Generation, Transcriptome Profiling, and Functional Validation of Cone-Rich Human Retinal Organoids
The Phenotype of Leber Congenital Amaurosis in Patients with AIPL1 Mutations
Integrative Subcellular Proteomic Analysis Allows Accurate Prediction of Human Disease-Causing Genes
An Unusual Retinal Vascular Morphology in Connection with A
The Genecards Suite Gil Stelzer Gene Information Consolidation