Showing results (11-20 of 19) with videos related to
Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Cell Reports|July 19, 2018
Dual Function of USP14 Deubiquitinase in Cellular Proteasomal Activity and Autophagic FluxEunkyoung Kim, Seoyoung Park, Jung Hoon Lee, et al.Scientific Reports|August 3, 2023
Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspectsSang-Yeon Lee, Min Young Kim, Jin Hee Han, et al.Journal of Alzheimer'S Disease : JAD|September 21, 2020
Proteasome Activity in the Plasma as a Novel Biomarker in Mild Cognitive Impairment with Chronic TinnitusYejin Yun, Sang-Yeon Lee, Won Hoon Choi, et al.BMC Medical Genomics|December 9, 2023
Novel autosomal dominant TMC1 variants linked to hearing loss: insight into protein-lipid interactionsSung Ho Cho, Yejin Yun, Dae Hee Lee, et al.Scientific Reports|July 21, 2023
Phenotypic and molecular basis of SIX1 variants linked to non-syndromic deafness and atypical branchio-otic syndrome in South KoreaSomin Lee, Yejin Yun, Ju Hyuen Cha, et al.Proceedings of the National Academy of Sciences of the United States of America|July 30, 2020
Aggresomal sequestration and STUB1-mediated ubiquitylation during mammalian proteaphagy of inhibited proteasomesWon Hoon Choi, Yejin Yun, Seoyoung Park, et al.Cell Reports|June 29, 2023
ECPAS/Ecm29-mediated 26S proteasome disassembly is an adaptive response to glucose starvationWon Hoon Choi, Yejin Yun, Insuk Byun, et al.Cell Reports. Medicine|July 1, 2025
Comprehensive genetic profiling of sensorineural hearing loss using an integrative diagnostic approachSang-Yeon Lee, Seungbok Lee, Seongyeol Park, et al.Molecular Therapy. Nucleic Acids|August 6, 2024
Discovery of novel disease-causing mutation in <i>SSBP1</i> and its correction using adenine base editor to improve mitochondrial functionJu Hyuen Cha, Seok-Hoon Lee, Yejin Yun, et al.Pageof 2