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Experimental & Molecular Medicine|March 31, 2025
Systematic genetic assessment of hearing loss using whole-genome sequencing identifies pathogenic variantsJung Ah Kim, Seung Hyun Jang, Sun Yung Joo, et al.
Hearing Research|December 24, 2019
P2RX2 and P2RX4 receptors mediate cation absorption in transitional cells and supporting cells of the utricular maculaJunhui Jeong, Jin Young Kim, Hansol Hong, et al.
Clinical and Experimental Otorhinolaryngology|August 1, 2020
Three-Dimensional Distribution of Cochlear Macrophages in the Lateral Wall of Cleared CochleaSeong Hoon Bae, Sang Hyun Kwak, Jee Eun Yoo, et al.
The Laryngoscope|January 25, 2020
Clinical Experience of Vibroplasty With Direct Coupling to the Oval Window Without Use of a CouplerSang Hyun Kwak, Young Min Moon, Gi-Sung Nam, et al.
Scientific Reports|September 29, 2025
Leveraging underrepresented population data improves interpretation of genetic variants associated with hearing lossSun Young Joo, Seung Hyun Jang, Jung Ah Kim, et al.
BMC Medical Genetics|April 3, 2019
The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case reportGi-Sung Nam, John Hoon Rim, Jae Young Choi, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 6, 2023
Audiogram Configuration, Molecular Etiology, and Outcome of Cochlear Implantation in Postlingual Auditory Neuropathy Spectrum DisorderYehree Kim, Jae Joon Han, Jayoung Oh, et al.
Nature Communications|April 26, 2016
The HSP70 co-chaperone DNAJC14 targets misfolded pendrin for unconventional protein secretionJinsei Jung, Jiyoon Kim, Shin Hye Roh, et al.
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