Hye-youn Kim
Seoul, Republic of Korea
Last Updated: 09/26/2026
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Found 15 publications
MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss.
Journal: Experimental & molecular medicine
Published: March 04, 2024
Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.
Journal: Journal of Korean medical science
Published: June 15, 2023
Prostaglandin F2α analogue, bimatoprost ameliorates colistin-induced nephrotoxicity.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: May 01, 2023
LRRC6 regulates biogenesis of motile cilia by aiding FOXJ1 translocation into the nucleus.
Journal: Cell communication and signaling : CCS
Published: December 26, 2022
Overlooked KCNQ4 variants augment the risk of hearing loss.
Journal: Experimental & molecular medicine
Published: August 16, 2022
Clinical Heterogeneity Associated with MYO7A Variants Relies on Affected Domains.
Journal: Biomedicines
Published: March 08, 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
Microbiome analysis reveals that Ralstonia is responsible for decreased renal function in patients with ulcerative colitis.
Journal: Clinical and translational medicine
Published: October 29, 2020
Heterogeneity of MYO15A variants significantly determine the feasibility of acoustic stimulation with hearing aid and cochlear implant.
Journal: Hearing research
Published: July 27, 2020
Last Updated: 09/26/2026