Axonal sprouting in the dorsal cochlear nucleus affects gap-prepulse inhibition following noise exposure

por Han, Kyu-Hee, Mun, Seog-Kyun, Sohn, Seonyong, Piao, Xian-Yu, Park, Ilyong, Chang, Munyoung
Publicado 2019

Losartan Prevents Maladaptive Auditory-Somatosensory Plasticity After Hearing Loss via Transforming Growth Factor-β Signaling Suppression

por Mun, Seog-Kyun, Han, Kyu-Hee, Baek, Jong Tae, Ahn, Suk-Won, Cho, Hyun Sang, Chang, Mun Young
Publicado 2019

Role of microRNA-375-3p-mediated regulation in tinnitus development

por Han, Kyu-Hee, Cho, Hyeeun, Han, Kyeo-Rye, Mun, Seog-Kyun, Kim, Young-Kook, Park, Ilyong, Chang, Munyoung
Publicado 2021

Establishment of a Flexible Real-Time Polymerase Chain Reaction-Based Platform for Detecting Prevalent Deafness Mutations Associated with Variable Degree of Sensorineural Hearing L...

por Han, Kyu-Hee, Kim, Ah Reum, Kim, Min Young, Ahn, Soyeon, Oh, Seung-Ha, Song, Ju Hun, Choi, Byung Yoon
Publicado 2016

Multiphasic analysis of whole exome sequencing data identifies a novel mutation of ACTG1 in a nonsyndromic hearing loss family

por Park, Gibeom, Gim, Jungsoo, Kim, Arheum, Han, Kyu-Hee, Kim, Hyo-Sang, Oh, Seung-Ha, Park, Taesung, Park, Woong-Yang, Choi, ByungYoon
Publicado 2013

Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population

por Kim, So Young, Kim, Ah Reum, Han, Kyu Hee, Kim, Min Young, Jeon, Eun-Hee, Koo, Ja-Won, Oh, Seung Ha, Choi, Byung Yoon
Publicado 2015

Prevalence of p.V37I Variant of GJB2 in Mild or Moderate Hearing Loss in a Pediatric Population and the Interpretation of Its Pathogenicity

por Kim, So Young, Park, Gibeom, Han, Kyu-Hee, Kim, Ahreum, Koo, Ja-Won, Chang, Sun O., Oh, Seung Ha, Park, Woong-Yang, Choi, Byung Yoon
Publicado 2013

Diagnostic Application of Targeted Resequencing for Familial Nonsyndromic Hearing Loss

por Choi, Byung Yoon, Park, Gibeom, Gim, Jungsoo, Kim, Ah Reum, Kim, Bong-Jik, Kim, Hyo-Sang, Park, Joo Hyun, Park, Taesung, Oh, Seung-Ha, Han, Kyu-Hee, Park, Woong-Yang
Publicado 2013

ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathy

por Han, Kyu-Hee, Oh, Doo-Yi, Lee, Seungmin, Lee, Chung, Han, Jin Hee, Kim, Min Young, Park, Hye-Rim, Park, Moo Kyun, Kim, Nayoung K. D., Lee, Jaekwang, Yi, Eunyoung, Kim, Jong-Min, Kim, Jeong-Whun, Chae, Jong-Hee, Oh, Seung Ha, Park, Woong-Yang, Choi, Byung Yoon
Publicado 2017