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1. College of Medicine (의과대학)
Dept. of Laboratory Medicine (진단검사의학교실)
1. Journal Papers
Browsing "1. Journal Papers" by Author : 4658
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Showing results 1 to 13 of 13
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Issue Date
Title
Journal Title
2014
A Drug-Repositioning Screening Identifies Pentetic Acid as a Potential Therapeutic Agent for Suppressing the Elastase-Mediated Virulence of Pseudomonas aeruginosa
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
2013
A novel synonymous mutation causing complete skipping of exon 16 in the SLC26A4 gene in a Korean family with hearing loss
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
2021
Activation of KCNQ4 as a Therapeutic Strategy to Treat Hearing Loss
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
2022
COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype-genotype study
HUMAN GENETICS
2022
Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluation
HUMAN GENETICS
2013
Dissemination of metallo-β-lactamase-producing Pseudomonas aeruginosa of sequence type 235 in Asian countries
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
2020
Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation
EAR AND HEARING
2022
In vivo outer hair cell gene editing ameliorates progressive hearing loss in dominant-negative Kcnq4 murine model
THERANOSTICS
2014
Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations.
LARYNGOSCOPE
2015
Non-syndromic hearing loss caused by the dominant cis mutation R75Q with the recessive mutation V37I of the GJB2 (Connexin 26) gene
EXPERIMENTAL AND MOLECULAR MEDICINE
2022
OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin
AUTOPHAGY
2019
Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency
Scientific Reports
2019
The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report
BMC MEDICAL GENETICS
1
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