YUHSpace

BROWSE

YUHSpace1. College of Medicine (의과대학)Dept. of Laboratory Medicine (진단검사의학교실)1. Journal Papers

Browsing "1. Journal Papers" by Author : 4658

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
가 나 다 라 마 바 사 아 자 차 카 타 파 하
or enter first few letters:
  • Sort by:
  • In order:
  • Results/Page
  • Authors/Record:

Showing results 1 to 13 of 13

This table browses all dspace content
Issue DateTitleJournal Title
2014A Drug-Repositioning Screening Identifies Pentetic Acid as a Potential Therapeutic Agent for Suppressing the Elastase-Mediated Virulence of Pseudomonas aeruginosaANTIMICROBIAL AGENTS AND CHEMOTHERAPY
2013A novel synonymous mutation causing complete skipping of exon 16 in the SLC26A4 gene in a Korean family with hearing lossBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
2021Activation of KCNQ4 as a Therapeutic Strategy to Treat Hearing Loss INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
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
2013Dissemination of metallo-β-lactamase-producing Pseudomonas aeruginosa of sequence type 235 in Asian countriesJOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
2020Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory RehabilitationEAR AND HEARING
2022In vivo outer hair cell gene editing ameliorates progressive hearing loss in dominant-negative Kcnq4 murine model THERANOSTICS
2014Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations.LARYNGOSCOPE
2015Non-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
2022OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin AUTOPHAGY
2019Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency Scientific Reports
2019The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report BMC MEDICAL GENETICS
1
  • License
    sherpa_romeo
    sherpa_juliet

OAK

DSpace Software Copyright © 2002-2017 Duraspace Yonsei University Medical Library All right Reserves. / TEL:02-2228-2915 /
YUHSpace는 국립중앙도서관 OAK 보급사업으로 구축되었습니다.

Browse

Links