Browsing by Yonsei Author : Jung, Jinsei

Name:
Jung, Jinsei [정진세] http://orcid.org/0000-0003-1906-6969
Department :
College of Medicine (의과대학) - Dept. of Otorhinolaryngology (이비인후과학교실)
Y-HRN :
(Yonsei Health Research Network)
Scopus ID :
(55546452200)

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Issue DateTitleJournal Title
2020DNAJC14 Ameliorates Inner Ear Degeneration in the DFNB4 Mouse Model MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT
2020Regulation of CFTR Bicarbonate Channel Activity by WNK1: Implications for Pancreatitis and CFTR-Related Disorders CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY
2020Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory RehabilitationEAR AND HEARING
2020P2RX2 and P2RX4 receptors mediate cation absorption in transitional cells and supporting cells of the utricular maculaHEARING RESEARCH
2019Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairmentExperimental and Molecular Medicine
2019The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report BMC MEDICAL GENETICS
2019Long-Term Changes in Video Head Impulse and Caloric Tests in Patients with Unilateral Vestibular Neuritis Korean Journal of Otorhinolaryngology-Head and Neck Surgery
2019Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants Clinical and Experimental Otorhinolaryngology
2019Clinical Characteristics of Bilateral Meniere's Disease in a Single Asian Ethnic GroupLARYNGOSCOPE
2019Cleaved Cochlin Sequesters Pseudomonas aeruginosa and Activates Innate Immunity in the Inner EarCELL HOST & MICROBE
2019A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activatorsHUMAN MUTATION
2019Meta-analysis of Delayed Facial Palsy Following Middle Ear SurgeryOTOLOGY & NEUROTOLOGY
2019Is Early Progression to Bilateral Involvement in Menière's Disease a Poor Prognostic Indicator?OTOLOGY & NEUROTOLOGY
2019Lessons From an Analysis of Newborn Hearing Screening Data for Children With Cochlear ImplantsOTOLOGY & NEUROTOLOGY
2019Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing THERANOSTICS
2019Effect of Specific Retinoic Acid Receptor Agonists on Noise-Induced Hearing Loss International Journal of Environmental Research and Public Health
2019Outcomes and Predictive Factors of Electroacoustic Stimulation Rehabilitation in Children With Limited Low-Frequency HearingOtology & Neurotology
2019Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency Scientific Reports
2019Extended-duration deafness is correlated with better subjective satisfaction in CROS-tBAHI recipientsClinical Otolaryngology
2019Feasibility of Revision Cochlear Implant Surgery for Better Speech Comprehension Journal of Audiology & Otology
2019Effects of self-reported hearing or vision impairment on depressive symptoms: a population-based longitudinal studyEPIDEMIOLOGY AND PSYCHIATRIC SCIENCES
2019A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunctionEUROPEAN JOURNAL OF MEDICAL GENETICS
2018Vibrant Soundbridge can improve the most comfortable listening level in sensorineural hearing loss: Our experience with 61 patients.CLINICAL OTOLARYNGOLOGY
2018Benefits of Bimodal Hearing With Cochlear and Middle Ear Implants: Preliminary Results in Four Patients.OTOLOGY & NEUROTOLOGY
2018Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss SCIENTIFIC REPORTS
2017ANO9/TMEM16J promotes tumourigenesis via EGFR and is a novel therapeutic target for pancreatic cancerBRITISH JOURNAL OF CANCER
2017Audiologic Gain of Incus Short Process Vibroplasty With Conventional Incus Long Process Vibroplasty: A Retrospective Analysis of 36 PatientsOTOLOGY & NEUROTOLOGY
2017Effects of Saccular Function on Recovery of Subjective Dizziness After Vestibular RehabilitationOTOLOGY & NEUROTOLOGY
2017Evaluation of Maximal Speech Intelligibility With Vibrant Soundbridge in Patients With Sensorineural Hearing LossOTOLOGY & NEUROTOLOGY
2017Discrepancies between video head impulse and caloric tests in patients with enlarged vestibular aqueduct.LARYNGOSCOPE
2017Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report BMC MEDICAL GENETICS
2017Hearing Preservation During Cochlear Implantation and Electroacoustic Stimulation in Patients With SLC26A4 MutationsOTOLOGY & NEUROTOLOGY
2017Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population SCIENTIFIC REPORTS
2017Resistance to hypertension and high Cl- excretion in humans with SLC26A4 mutationsCLINICAL GENETICS
2017Benefits of active middle ear implants in mixed hearing loss: Stapes versus round windowLARYNGOSCOPE
2017β1- and β2-adrenergic stimulation-induced electrogenic transport by human endolymphatic sac epithelium and its clinical implications. SCIENTIFIC REPORTS
2016Ventilation tube insertion is not effective to the treatment of hearing impairment in pediatric patients with Cornelia de Lange syndromeAMERICAN JOURNAL OF OTOLARYNGOLOGY
2016Pore dilatation increases the bicarbonate permeability of CFTR, ANO1 and glycine receptor anion channels.JOURNAL OF PHYSIOLOGY-LONDON
2016The HSP70 co-chaperone DNAJC14 targets misfolded pendrin for unconventional protein secretion. NATURE COMMUNICATIONS
2016Vestibular function is associated with residual low-frequency hearing loss in patients with bi-allelic mutations in the SLC26A4 geneHEARING RESEARCH
2016Audiologic limitations of Vibrant Soundbridge device: Is the contralateral hearing aid fitting indispensable?LARYNGOSCOPE
2016Is dehydration test using isosorbide useful in Meniere's disease?ACTA OTO-LARYNGOLOGICA
2015Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposurePFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
2015Electrogenic transport and K(+) ion channel expression by the human endolymphatic sac epithelium SCIENTIFIC REPORTS
2015Genetic aspects and clinical characteristics of familial Meniere's disease in a South Korean populationLARYNGOSCOPE
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
2015Novel COCH p.V123E Mutation, Causative of DFNA9 Sensorineural Hearing Loss and Vestibular Disorder, Shows Impaired Cochlin Post-Translational Cleavage and SecretionHUMAN MUTATION
2015Does calmodulin regulate the bicarbonate permeability of ANO1/TMEM16A or not? JOURNAL OF GENERAL PHYSIOLOGY
2014Shank2 mutant mice display a hypersecretory response to cholera toxinJOURNAL OF PHYSIOLOGY-LONDON
2014Mechanisms of CFTR Functional Variants That Impair Regulated Bicarbonate Permeation and Increase Risk for Pancreatitis but Not for Cystic Fibrosis. PLOS GENETICS
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