Seyoung Yu
Seoul, Republic of Korea
Last Updated: 09/26/2026
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Found 19 publications
Regenerative Role of Lrig1+ Cells in Kidney Repair.
Journal: Journal of the American Society of Nephrology : JASN
Published: March 06, 2024
The contribution of de novo coding mutations to meningomyelocele.
Journal: Nature
Published: February 24, 2024
Deep learning outperforms kidney organoid experts.
Journal: Kidney research and clinical practice
Published: August 07, 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
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
PLCE1 regulates the migration, proliferation, and differentiation of podocytes.
Journal: Experimental & molecular medicine
Published: October 03, 2019
ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid Treatment.
Journal: Journal of the American Society of Nephrology : JASN
Published: July 30, 2019
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
Last Updated: 09/26/2026