Published in Laryngoscope on September 01, 2002
Gap junctions and cochlear homeostasis. J Membr Biol (2006) 1.41
Connexin26 is responsible for anionic molecule permeability in the cochlea for intercellular signalling and metabolic communications. Eur J Neurosci (2005) 1.36
Distinct and gradient distributions of connexin26 and connexin30 in the cochlear sensory epithelium of guinea pigs. J Comp Neurol (2006) 1.30
Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment. Clin Genet (2005) 1.30
Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease. Mol Cell Neurosci (2007) 1.24
Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models. Brain Res (2009) 1.20
Cellular characterization of Connexin26 and Connnexin30 expression in the cochlear lateral wall. Cell Tissue Res (2008) 1.13
Post-translational modifications of connexin26 revealed by mass spectrometry. Biochem J (2009) 1.00
Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness. Front Cell Neurosci (2015) 0.97
A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean population. PLoS One (2013) 0.91
3p-- syndrome defines a hearing loss locus in 3p25.3. Hear Res (2007) 0.88
Functional evaluation of GJB2 variants in nonsyndromic hearing loss. Mol Med (2011) 0.85
Green tea prevents down-regulation of gap junction intercellular communication in human keratinocytes treated with PMA. Eur Arch Otorhinolaryngol (2010) 0.79
Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2. Sci Rep (2016) 0.75
A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall. Neurobiol Dis (2017) 0.75
Antimicrobial activity of innate immune molecules against Streptococcus pneumoniae, Moraxella catarrhalis and nontypeable Haemophilus influenzae. BMC Infect Dis (2004) 1.63
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians. Hum Genet (2003) 1.61
Cisplatin cytotoxicity of auditory cells requires secretions of proinflammatory cytokines via activation of ERK and NF-kappaB. J Assoc Res Otolaryngol (2007) 1.25
Immortalization of normal adult human middle ear epithelial cells using a retrovirus containing the E6/E7 genes of human papillomavirus type 16. Ann Otol Rhinol Laryngol (2002) 1.20
Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population. J Hum Genet (2008) 1.17
Pathogenic effects of a novel mutation (c.664_681del) in KCNQ4 channels associated with auditory pathology. Biochim Biophys Acta (2010) 1.09
Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families. BMC Med Genet (2013) 1.07
Evidence that cisplatin-induced auditory damage is attenuated by downregulation of pro-inflammatory cytokines via Nrf2/HO-1. J Assoc Res Otolaryngol (2008) 1.06
A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss. Biochem Biophys Res Commun (2010) 1.05
Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome. Laryngoscope (2006) 0.97
Expression of hepatocyte growth factor and c-Met in hypopharyngeal squamous cell carcinoma. Acta Otolaryngol (2006) 0.96
Cisplatin ototoxicity involves cytokines and STAT6 signaling network. Cell Res (2011) 0.92
Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss. Int J Mol Med (2008) 0.91
Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein. Physiol Genomics (2009) 0.90
Different functional consequences of two missense mutations in the GJB2 gene associated with non-syndromic hearing loss. Hum Mutat (2009) 0.90
Three cases of Waardenburg syndrome type 2 in a Korean family. Korean J Ophthalmol (2004) 0.89
Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation. PLoS One (2012) 0.89
Intranasal extrusion of the endovascular coil after occluding internal carotid artery for massive nasopharyngeal bleeding. Otolaryngol Head Neck Surg (2005) 0.86
Functional evaluation of GJB2 variants in nonsyndromic hearing loss. Mol Med (2011) 0.85
Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing. BMC Med Genet (2014) 0.85
Genetic Screening of GJB2 and SLC26A4 in Korean Cochlear Implantees: Experience of Soree Ear Clinic. Clin Exp Otorhinolaryngol (2012) 0.85
Panel 4: Recent advances in otitis media in molecular biology, biochemistry, genetics, and animal models. Otolaryngol Head Neck Surg (2013) 0.83
Various causes and clinical characteristics in vertigo in children with normal eardrums. Int J Pediatr Otorhinolaryngol (2003) 0.82
Expression of water channel proteins (aquaporins) in the rat Eustachian tube and middle ear mucosa. Acta Otolaryngol (2007) 0.79
Limitations of hearing screening in newborns with PDS mutations. Int J Pediatr Otorhinolaryngol (2013) 0.79
Identification and functional characterization of novel compound heterozygotic mutations in the TECTA gene. Gene (2011) 0.78
Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations. Laryngoscope (2013) 0.78
Nucleoplasm staining patterns and cell cycle-associated expression of Ki-67 in middle ear cholesteatoma. Am J Otolaryngol (2005) 0.78
Drug synergism of antihypertensive action in combination of telmisartan with lercanidipine in spontaneous hypertensive rats. Arch Pharm Res (2010) 0.77
A novel synonymous mutation causing complete skipping of exon 16 in the SLC26A4 gene in a Korean family with hearing loss. Biochem Biophys Res Commun (2012) 0.76
A novel missense variant in the DIAPH1 gene in a Korean family with autosomal dominant nonsyndromic hearing loss. Genes Genet Syst (2016) 0.75
Immortalization of rat eustachian tube epithelial cells by adenovirus 12-simian virus 40 hybrid virus. Ann Otol Rhinol Laryngol (2002) 0.75
Expression of female sex hormone receptors in human middle-ear cholesteatomas. J Laryngol Otol (2005) 0.75
Expression of beta-defensins in human middle ear cholesteatoma. Acta Otolaryngol (2003) 0.75
3D micro-CT images of ossicles destroyed by middle ear cholesteatoma. Acta Otolaryngol (2004) 0.75
Genome-wide SNP-based linkage analysis for ADNSHL families identifies novel susceptibility loci with positive evidence for linkage. Genes Genet Syst (2011) 0.75