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YUHSpace1. College of Medicine (의과대학)Dept. of Anatomy (해부학교실)1. Journal Papers

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Issue DateTitleJournal Title
2019Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing THERANOSTICS
2013Genetic analysis of the CHD7 gene in Korean patients with CHARGE syndromeGENE
2017Identification of evidence for autoimmune pathology of bilateral sudden sensorineural hearing loss using proteomic analysisCLINICAL IMMUNOLOGY
2020Inhibition of Pendrin by a small molecule reduces Lipopolysaccharide-induced acute Lung Injury THERANOSTICS
2020Investigation of intact mouse cochleae using two-photon laser scanning microscopyMICROSCOPY RESEARCH AND TECHNIQUE
2021LCCL peptide cleavage after noise exposure exacerbates hearing loss and is associated with the monocyte infiltration in the cochleaHEARING RESEARCH
2021Neutrophils infiltrate into the spiral ligament but not the stria vascularis in the cochlea during lipopolysaccharide-induced inflammation THERANOSTICS
2012Nonsyndromic X-linked hearing loss.FRONTIERS IN BIOSCIENCE
2011Pou3f4 deficiency causes defects in otic fibrocytes and stria vascularis by different mechanismsBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
2018Progressive hearing loss in vitamin A-deficient mice which may be protected by the activation of cochlear melanocyte SCIENTIFIC REPORTS
2014The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss OPEN BIOLOGY
2021Three-Dimensional Distribution of Cochlear Macrophages in the Lateral Wall of Cleared Cochlea CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY
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