• A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study
• A Novel Exon 2 Deletion Mutation in the <em>GRXCR1</em> Gene Associated With Non-Syndromic Hearing Loss: A Case Report and Review of Literatures
• Allele-Specific Small Interfering RNA Corrects Aberrant Cellular Phenotype in Keratitis-Ichthyosis-Deafness Syndrome Keratinocytes
• Analysis between phenotypes and genotypes of inner ear malformation
• Analysis of Genetic Variations in Connexin 26 ( <em>GJB2</em> ) Gene among Nonsyndromic Hearing Impairment: Familial Study
• Analysis of Genetic Variations in Connexin 26 ( GJB2 ) Gene among Nonsyndromic Hearing Impairment: Familial Study
• Auditory Detection Thresholds and Cochlear Resistivity Differ Between Pediatric Cochlear Implant Listeners With Enlarged Vestibular Aqueduct and Those With Connexin-26 Mutations
• Classical Vohwinkel syndrome with heterozygous p.Asp66His mutation in GJB2 gene: Second Asian case
• Congenital Middle Ear Malformation with Common Deafness Gene Mutation Analysis: A Review of 813 Profound Sensorineural Hearing Loss Child Patients
• Connexin 43 and Connexin 26 Involvement in the Ponatinib-Induced Cardiomyopathy: Sex-Related Differences in a Murine Model
• Developmental abnormalities in supporting cell phalangeal processes and cytoskeleton in the <em>Gjb2</em> knockdown mouse model
• Establishment of an iPSC line (JTUi002-A) from a patient with Waardenburg syndrome caused by a SOX10 mutation and carrying a GJB2 mutation
• G59S mutation in the GJB2 gene in a Chinese family with classic Vohwinkel syndrome
• Inducible knockout of syncytin-a leads to poor placental glucose transport in mice
• More than keratitis, ichthyosis, and deafness: Multisystem effects of lethal GJB2 mutations
• Precise control of ion channel and gap junction expression is required for patterning of the regenerating axolotl limb
• Targeted Next-Generation Sequencing Identifies Separate Causes of Hearing Loss in One Deaf Family and Variable Clinical Manifestations for the p.R161C Mutation in <em>SOX10</em>
• Torticollis in children with enlarged vestibular aqueducts