Adipose-Derived Stem Cell Coculturing Stimulates Integrin-Mediated Extracellular Matrix Adhesion of Melanocytes by Upregulating Growth Factors

por Kim, Hyangmi, Yi, Nayoung, Do, Byung-Rok, Lee, Ai-Young
Publicado 2019

SorCS1 inhibits amyloid-β binding to neurexin and rescues amyloid-β–induced synaptic pathology

por Lee, Alfred Kihoon, Yi, Nayoung, Khaled, Husam, Feller, Benjamin, Takahashi, Hideto
Publicado 2023

Central auditory maturation and behavioral outcomes after cochlear implantation in prelingual auditory neuropathy spectrum disorder related to OTOF variants (DFNB9): Lessons from p...

por Lee, Sang-Yeon, Han, Jin Hee, Song, Hoo-Kang, Kim, Namju Justin, Yi, Nayoung, Kyong, Jeong-Sug, Choi, Byung Yoon
Publicado 2021

Major Contribution of GREB1L Alterations to Severe Inner Ear Malformation Largely in a Non-mendelian Fashion

por Kim, Bong Jik, Jeon, Hyoungwon, Lee, Sang-Yeon, Yi, Nayoung, Han, Jin Hee, Seo, Go Hun, Oh, Seung-Ha, Choi, Byung Yoon
Publicado 2022

Efficacy of cochlear implants in children with borderline hearing who have already achieved significant language development with hearing aids

por Kim, Young Seok, Kim, Yehree, Lee, Seung Jae, Han, Jin Hee, Yi, Nayoung, Yoo, Hyo Soon, Carandang, Marge, Lee, Sang-Yeon, Kim, Bong Jik, Choi, Byung Yoon
Publicado 2022

Improving genetic diagnosis by disease-specific, ACMG/AMP variant interpretation guidelines for hearing loss

por Kim, So Young, Kim, Bong Jik, Oh, Doo Yi, Han, Jin Hee, Yi, Nayoung, Kim, Namju Justin, Park, Moo Kyun, Keum, Changwon, Seo, Go Hun, Choi, Byung Yoon
Publicado 2022

α-Synuclein Preformed Fibrils Bind to β-Neurexins and Impair β-Neurexin-Mediated Presynaptic Organization

por Feller, Benjamin, Fallon, Aurélie, Luo, Wen, Nguyen, Phuong Trang, Shlaifer, Irina, Lee, Alfred Kihoon, Chofflet, Nicolas, Yi, Nayoung, Khaled, Husam, Karkout, Samer, Bourgault, Steve, Durcan, Thomas M., Takahashi, Hideto
Publicado 2023

Powerful use of automated prioritization of candidate variants in genetic hearing loss with extreme etiologic heterogeneity

por Kim, So Young, Lee, Seungmin, Seo, Go Hun, Kim, Bong Jik, Oh, Doo Yi, Han, Jin Hee, Park, Moo Kyun, Lee, So min, Kim, Bonggi, Yi, Nayoung, Kim, Namju Justin, Koh, Doo Hyun, Hwang, Sohyun, Keum, Changwon, Choi, Byung Yoon
Publicado 2021

Full etiologic spectrum of pediatric severe to profound hearing loss of consecutive 119 cases

por Kim, Young Seok, Kim, Yoonjoong, Jeon, Hyoung Won, Yi, Nayoung, Lee, Sang-Yeon, Kim, Yehree, Han, Jin Hee, Kim, Min Young, Kim, Bo Hye, Choi, Hyeong Yun, Carandang, Marge, Koo, Ja-Won, Kim, Bong Jik, Bae, Yun Jung, Choi, Byung Yoon
Publicado 2022

Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss

por Lee, Sang-Yeon, Choi, Hyun Been, Park, Mina, Choi, Il Soon, An, Jieun, Kim, Ami, Kim, Eunku, Kim, Nahyun, Han, Jin Hee, Kim, Min young, Lee, Seung min, Oh, Doo-Yi, Kim, Bong Jik, Yi, Nayoung, Kim, Nayoung, K. D., Lee, Chung, Park, Woong-Yang, Koh, Young Ik, Gee, Heon Yung, Cho, Hyun Sung, Kang, Tong Mook, Choi, Byung Yoon
Publicado 2021