Kyung S. Oh
Seoul, Republic of Korea
Last Updated: 09/26/2026
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Found 8 publications
HAP1 interaction with KCNQ4 attenuates channel surface expression and function.
Journal: Molecules and cells
Published: October 01, 2025
Reverse translational approach to clarify the strong potency of enavogliflozin, a novel sodium-glucose cotransporter 2 inhibitor.
Journal: The Journal of pharmacology and experimental therapeutics
Published: March 19, 2025
TMEM145 is a key stereociliary component in the link structures of outer hair cells and mediates the secretion of stereocilin and tubby.
Journal: Nature communications
Published: February 12, 2025
Antisense oligonucleotide therapy mitigates autosomal dominant progressive hearing loss in a murine model of human DFNA2.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: January 21, 2025
Overlooked KCNQ4 variants augment the risk of hearing loss.
Journal: Experimental & molecular medicine
Published: August 16, 2022
OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin.
Journal: Autophagy
Published: March 07, 2022
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
Showing 1-8 of 8
Last Updated: 09/26/2026