Browsing by Yonsei Author : Kim, Hye-Youn

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Name:
Kim, Hye-Youn [김혜연]
orcid http://orcid.org/0000-0003-2090-6427
Department :
College of Medicine (의과대학) - Dept. of Pharmacology (약리학교실)

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Showing results 1 to 14 of 14

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Issue DateTitleJournal Title
2023Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss JOURNAL OF KOREAN MEDICAL SCIENCE
2023Prostaglandin F2α analogue, bimatoprost ameliorates colistin-induced nephrotoxicity BIOMEDICINE & PHARMACOTHERAPY
2023LRRC6 regulates biogenesis of motile cilia by aiding FOXJ1 translocation into the nucleus CELL COMMUNICATION AND SIGNALING
2023Overlooked KCNQ4 variants augment the risk of hearing loss EXPERIMENTAL AND MOLECULAR MEDICINE
2023Disease modeling of ADAMTS9-related nephropathy using kidney organoids reveals its roles in tubular cells and podocytes FRONTIERS IN MEDICINE
2022OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin AUTOPHAGY
2022COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype-genotype studyHUMAN GENETICS
2022Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluation HUMAN GENETICS
2022Clinical Heterogeneity Associated with MYO7A Variants Relies on Affected Domains BIOMEDICINES
2021Plasma Membrane Localized GCaMP-MS4A12 by Orai1 Co-Expression Shows Thapsigargin- and Ca 2+-Dependent Fluorescence Increases MOLECULES AND CELLS
2021Microbiome analysis reveals that Ralstonia is responsible for decreased renal function in patients with ulcerative colitis CLINICAL AND TRANSLATIONAL MEDICINE
2020PLCE1 Regulates the Migration, Proliferation, and Differentiation of Podocytes EXPERIMENTAL AND MOLECULAR MEDICINE
2019Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairmentExperimental and Molecular Medicine
2018ZMYND10 stabilizes intermediate chain proteins in the cytoplasmic pre-assembly of dynein arms PLOS GENETICS
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