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Elife|October 11, 2017
Molecular architecture underlying fluid absorption by the developing inner earKeiji Honda, Sung Huhn Kim, Michael C Kelly, 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.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.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.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.JMIR Medical Informatics|December 10, 2021
Differential Biases and Variabilities of Deep Learning-Based Artificial Intelligence and Human Experts in Clinical Diagnosis: Retrospective Cohort and Survey StudyDongchul Cha, Chongwon Pae, Se A Lee, et al.International Journal of Pediatric Otorhinolaryngology|February 8, 2017
Prevalence of vestibular and balance disorders in children and adolescents according to age: A multi-center studyJong Dae Lee, Chang-Hee Kim, Seok Min Hong, et al.Scientific Reports|November 11, 2018
Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing lossJinsei Jung, Hyun Been Choi, Young Ik Koh, et al.Cell Host & Microbe|March 26, 2019
Cleaved Cochlin Sequesters Pseudomonas aeruginosa and Activates Innate Immunity in the Inner EarJinsei Jung, Jee Eun Yoo, Young Ho Choe, et al.Pageof 9