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CDH23
Comprehensive Sequence Analysis of Nine Usher Syndrome Genes in The
USHIC, CDH23 and TMIE
TMHS Is an Integral Component of the Mechanotransduction Machinery of Cochlear Hair Cells
Tip-Link Protein Protocadherin 15 Interacts with Transmembrane Channel-Like Proteins TMC1 and TMC2
Elucidating Biological Roles of Novel Murine Genes in Hearing Impairment in Africa
ADHD) Gene Networks in Children of Both African American and European American Ancestry
Frequency of Usher Syndrome in Two Pediatric Populations: Implications for Genetic Screening of Deaf and Hard of Hearing Children William J
Sensational Cadherins for Hearing and Balance
Structural Determinants of Protocadherin-15 Mechanics and Function in Hearing and Balance Perception
Identification of Novel Cadherin 23 Variants in a Chinese Family with Hearing Loss
Profound, Prelingual Nonsyndromic Deafness Maps to Chromosome 10Q21 and Is Caused by a Novel Missense Mutation in the Usher Syndrome Type IF Gene PCDH15
Regulation of PCDH15 Function in Mechanosensory Hair Cells by Alternative Splicing of the Cytoplasmic Domain Stuart W
A Novel Heterozygous Missense Variant (C.667G>T;P
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Partial USH2A Deletions Contribute to Usher Syndrome in Denmark
PDZD7-MYO7A Complex Identified in Enriched Stereocilia Membranes
An Innovative Strategy for the Molecular Diagnosis of Usher Syndrome Identifies Causal Biallelic Mutations in 93% of European Patients
CDH23 Gene Cadherin Related 23
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Discovery of CDH23 As a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans
High Prevalence of CDH23 Mutations in Patients with Congenital High
Advances in Drug Therapy for Usher Syndrome
Identification of Novel CDH23 Variants Causing Moderate to Profound
Frequency of Usher Syndrome Type 1 in Deaf Children by Massively Parallel DNA Sequencing
Structure of the N Terminus of Cadherin 23 Reveals a New Adhesion Mechanism for a Subset of Cadherin Superfamily Members
The Genetics of Usher Syndrome
A New Mouse Mutant of the Cdh23 Gene with Early-Onset Hearing Loss Facilitates Evaluation of Otoprotection Drugs
Gene and Stem Cell Therapy for Usher Syndrome
The Impact of Modern Technologies on Molecular Diagnostic Success Rates, with a Focus on Inherited Retinal Dystrophy and Hearing Loss
Comprehensive Analysis Via Exome Sequencing Uncovers Genetic Etiology in Autosomal Recessive Nonsyndromic Deafness in a Large Multiethnic Cohort
Cadherin) Mutations
Structural Determinants of Protocadherin-15 Elasticity and Function In
Whole Exome Sequencing Identifies Multiple Pathogenic Variants in a Large South
Molecular Mechanism of Cell-Cell Adhesion Mediated by Cadherin-23 G
Otoseq a Guide for Clinicians
Physical and Functional Interaction Between Protocadherin 15 and Myosin Viia in Mechanosensory Hair Cells
The P.P240L Variant of CDH23 and the Risk of Nonsyndromic Hearing Loss: a Meta-Analysis