The efficacy of combination therapy for idiopathic sudden sensorineural hearing loss
Jung, Da Jung, Park, Ji Hye, Jang, Jeong Hun, Lee, Kyu-Yup
Published in The Laryngoscope (01.08.2016)
Published in The Laryngoscope (01.08.2016)
Get more information
Journal Article
Prediction of hearing outcomes in chronic otitis media patients underwent tympanoplasty using ossiculoplasty outcome parameter staging or middle ear risk indices
Jung, Da Jung, Lee, Hyun Ju, Hong, Ji Song, Kim, Dong Gyu, Mun, Jae Yeon, Bae, Jong-Won, Yoo, Myung Hoon, Lee, Kyu-Yup
Published in PloS one (29.07.2021)
Published in PloS one (29.07.2021)
Get full text
Journal Article
Modified U1 snRNA and antisense oligonucleotides rescue splice mutations in SLC26A4 that cause hereditary hearing loss
Lee, Byeonghyeon, Kim, Ye‐Ri, Kim, Sang‐Joo, Goh, Sung‐Ho, Kim, Jong‐Heun, Oh, Se‐Kyung, Baek, Jeong‐In, Kim, Un‐Kyung, Lee, Kyu‐Yup
Published in Human mutation (01.08.2019)
Published in Human mutation (01.08.2019)
Get full text
Journal Article
Association of metabolic syndrome with the incidence of hearing loss: A national population-based study
Jung, Da Jung, Han, Kyung Do, Cho, Yang-Sun, Rhee, Chae Seo, Lee, Kyu-Yup
Published in PloS one (26.07.2019)
Published in PloS one (26.07.2019)
Get full text
Journal Article
Mitochondrial redox system: A key target of antioxidant therapy to prevent acquired sensorineural hearing loss
Baek, Jeong-In, Kim, Ye-Ri, Lee, Kyu-Yup, Kim, Un-Kyung
Published in Frontiers in pharmacology (31.03.2023)
Published in Frontiers in pharmacology (31.03.2023)
Get full text
Journal Article
Efficacy of the Bonebridge BCI602 for Adult Patients with Single-sided Deafness: A Prospective Multicenter Study
Kim, Hantai, Park, Moo Kyun, Park, Shi Nae, Cho, Hyong-Ho, Choi, Jae Young, Lee, Chi Kyou, Lee, Il-Woo, Moon, Il Joon, Jung, Jae Yun, Jung, Jinsei, Lee, Kyu-Yup, Oh, Jeong-Hoon, Park, Hong Ju, Seo, Jae-Hyun, Song, Jae-Jin, Ha, Jungho, Jang, Jeong Hun, Choung, Yun-Hoon
Published in Otolaryngology-head and neck surgery (01.02.2024)
Published in Otolaryngology-head and neck surgery (01.02.2024)
Get more information
Journal Article
Pannexin 3 is required for normal progression of skeletal development in vertebrates
Oh, Se-Kyung, Shin, Jeong-Oh, Baek, Jeong-In, Lee, Jinwook, Bae, Jae Woong, Ankamerddy, Harinarayana, Kim, Myoung-Jin, Huh, Tae-Lin, Ryoo, Zae-Young, Kim, Un-Kyung, Bok, Jinwoong, Lee, Kyu-Yup
Published in The FASEB journal (01.11.2015)
Published in The FASEB journal (01.11.2015)
Get more information
Journal Article
Galangin prevents aminoglycoside-induced ototoxicity by decreasing mitochondrial production of reactive oxygen species in mouse cochlear cultures
Kim, Ye-Ri, Kim, Min-A, Cho, Hyun-Ju, Oh, Se-Kyung, Lee, In-Kyu, Kim, Un-Kyung, Lee, Kyu-Yup
Published in Toxicology letters (14.03.2016)
Published in Toxicology letters (14.03.2016)
Get full text
Journal Article
Alpha-lipoic acid protects against cisplatin-induced ototoxicity via the regulation of MAPKs and proinflammatory cytokines
Kim, Jeongho, Cho, Hyun-Ju, Sagong, Borum, Kim, Se-Jin, Lee, Jae-Tae, So, Hong-Seob, Lee, In-Kyu, Kim, Un-Kyung, Lee, Kyu-Yup, Choo, Yon-Sik
Published in Biochemical and biophysical research communications (27.06.2014)
Published in Biochemical and biophysical research communications (27.06.2014)
Get full text
Journal Article
Protective effect of berberine chloride against cisplatin-induced ototoxicity
Kim, Jong-Heun, Baek, Jeong-In, Lee, In-Kyu, Kim, Un-Kyung, Kim, Ye-Ri, Lee, Kyu-Yup
Published in Genes & genomics (01.01.2022)
Published in Genes & genomics (01.01.2022)
Get full text
Journal Article
Identification of Pathogenic Mechanisms of COCH Mutations, Abolished Cochlin Secretion, and Intracellular Aggregate Formation: Genotype-Phenotype Correlations in DFNA9 Deafness and Vestibular Disorder
Bae, Seung-Hyun, Robertson, Nahid G., Cho, Hyun-Ju, Morton, Cynthia C., Jung, Da Jung, Baek, Jeong-In, Choi, Soo-Young, Lee, Jaetae, Lee, Kyu-Yup, Kim, Un-Kyung
Published in Human mutation (01.12.2014)
Published in Human mutation (01.12.2014)
Get full text
Journal Article
Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing
Kim, Min-A, Kim, Sung Huhn, Ryu, Nari, Ma, Ji-Hyun, Kim, Ye-Ri, Jung, Jinsei, Hsu, Chuan-Jen, Choi, Jae Young, Lee, Kyu-Yup, Wangemann, Philine, Bok, Jinwoong, Kim, Un-Kyung
Published in Theranostics (01.01.2019)
Published in Theranostics (01.01.2019)
Get full text
Journal Article
Consensus Statements on the Definition, Classification, and Diagnostic Tests for Tinnitus: A Delphi Study Conducted by the Korean Tinnitus Study Group
Choo, Oak-Sung, Kim, Hantai, Lee, Seung Jae, Kim, So Young, Lee, Kyu-Yup, Lee, Ho Yun, Moon, In Seok, Seo, Jae-Hyun, Rah, Yoon Chan, Song, Jae-Jun, Nam, Eui-Cheol, Park, Shi Nae, Song, Jae-Jin, Shim, Hyun Joon
Published in Journal of Korean medical science (05.02.2024)
Published in Journal of Korean medical science (05.02.2024)
Get full text
Journal Article
Association between a High-Potassium Diet and Hearing Thresholds in the Korean Adult Population
Jung, Da Jung, Lee, Jae Young, Cho, Kyu Hyang, Lee, Kyu-Yup, Do, Jun Young, Kang, Seok Hui
Published in Scientific reports (04.07.2019)
Published in Scientific reports (04.07.2019)
Get full text
Journal Article
Therapeutic potential of the mitochondria-targeted antioxidant MitoQ in mitochondrial-ROS induced sensorineural hearing loss caused by Idh2 deficiency
Kim, Ye-Ri, Baek, Jeong-In, Kim, Sung Hwan, Kim, Min-A, Lee, Byeonghyeon, Ryu, Nari, Kim, Kyung-Hee, Choi, Deok-Gyun, Kim, Hye-Min, Murphy, Michael P, Macpherson, Greg, Choo, Yeon-Sik, Bok, Jinwoong, Lee, Kyu-Yup, Park, Jeen-Woo, Kim, Un-Kyung
Published in Redox biology (01.01.2019)
Published in Redox biology (01.01.2019)
Get full text
Journal Article
Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families
Baek, Jeong-In, Oh, Se-Kyung, Kim, Dong-Bin, Choi, Soo-Young, Kim, Un-Kyung, Lee, Kyu-Yup, Lee, Sang-Heun
Published in Orphanet journal of rare diseases (03.09.2012)
Published in Orphanet journal of rare diseases (03.09.2012)
Get full text
Journal Article