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Molecular Therapy : the Journal of the American Society of Gene Therapy|September 3, 2025
Antisense oligonucleotide therapy mitigates autosomal dominant progressive hearing loss in a murine model of human DFNA2Seung Hyun Jang, Jae Won Roh, Kyung Seok Oh, et al.Molecular Therapy. Methods & Clinical Development|January 8, 2020
DNAJC14 Ameliorates Inner Ear Degeneration in the DFNB4 Mouse ModelHye Ji Choi, Hyun Jae Lee, Jin Young Choi, et al.Pflugers Archiv : European Journal of Physiology|January 30, 2015
Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposureHyun Jong Kim, Ikhyun Jun, Jae Seok Yoon, et al.Cells|September 28, 2023
Novel Variant in CEP250 Causes Protein Mislocalization and Leads to Nonsyndromic Autosomal Recessive Type of Progressive Hearing LossMinjin Kang, Jung Ah Kim, Mee Hyun Song, et al.Proceedings of the National Academy of Sciences of the United States of America|May 3, 2020
Distinct roles of stereociliary links in the nonlinear sound processing and noise resistance of cochlear outer hair cellsWoongsu Han, Jeong-Oh Shin, Ji-Hyun Ma, et al.Journal of Medical Genetics|April 22, 2026
Rare missense variants in MYO7A and OTOP2 genes in a South Korean Meniere's disease cohortMai T Pham, Pablo Cruz-Granados, Prathamesh T Nadar-Ponniah, et al.Scientific Reports|July 2, 2024
Vestibular hair cells are more prone to damage by excessive acceleration insult in the mouse with KCNQ4 dysfunctionHansol Hong, Eun Ji Koo, Yesai Park, et al.Journal of Clinical Medicine|April 13, 2024
Characterization of Vestibular Phenotypes in Patients with Genetic Hearing LossJi Hyuk Han, Seong Hoon Bae, Sun Young Joo, et al.Theranostics|November 8, 2019
Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearingMin-A Kim, Sung Huhn Kim, Nari Ryu, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|September 10, 2023
Novel small molecule-mediated restoration of the surface expression and anion exchange activity of mutated pendrin causing Pendred syndrome and DFNB4Jinsei Jung, Shin Hye Noh, Sungwoo Jo, et al.Pageof 12