Jae Y. Choi
Seoul, Republic of Korea
Last Updated: 09/26/2026
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Found 17 publications
MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss.
Journal: Experimental & molecular medicine
Published: March 04, 2024
Overlooked KCNQ4 variants augment the risk of hearing loss.
Journal: Experimental & molecular medicine
Published: August 16, 2022
Purinergic signaling in the peripheral vestibular system.
Journal: Purinergic signalling
Published: October 06, 2021
COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype-genotype study.
Journal: Human genetics
Published: April 20, 2021
Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluation.
Journal: Human genetics
Published: March 25, 2021
Novel pendrin inhibitor attenuates airway hyperresponsiveness and mucin expression in experimental murine asthma.
Journal: The Journal of allergy and clinical immunology
Published: November 30, 2018
Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment.
Journal: Experimental & molecular medicine
Published: October 22, 2018
microRNA-183 is Essential for Hair Cell Regeneration after Neomycin Injury in Zebrafish.
Journal: Yonsei medical journal
Published: June 12, 2017
Last Updated: 09/26/2026