Jianjun Wang

N-Terminal Mutant Huntingtin Associates with Mitochondria and Impairs Mitochondrial Trafficking

He Li, Shihua Li, Xiao-Jiang Li, 2008, The Journal of Neuroscience.

Gene therapy via canalostomy approach preserves auditory and vestibular functions in a mouse model of Jervell and Lange-Nielsen syndrome type 2

Jianjun Wang, Xi Lin, Xuewen Wu, 2021, Nature Communications.

Virally-expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice

Jianjun Wang, Xi Lin, Q. Chang, 2013, Gene Therapy.

Impaired ubiquitin–proteasome system activity in the synapses of Huntington's disease mice

A. Orr, Suzanne Tydlacka, Chuan-en Wang, 2008, The Journal of cell biology.

Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange-Nielsen deafness syndrome

Jianjun Wang, Xi Lin, Q. Chang, 2015, EMBO molecular medicine.

Combined examination of sequence and copy number variations in human deafness genes improves diagnosis for cases of genetic deafness

Jianjun Wang, Xi Lin, Huawei Li, 2014, BMC Ear, Nose and Throat Disorders.

De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome

Weiwei Guo, Ping Chen, Hui Jiang, 2014, Cell Research.

Virally Mediated Connexin 26 Expression in Postnatal Scala Media Significantly and Transiently Preserves Hearing in Connexin 30 Null Mice

Sun Myoung Kim, Jianjun Wang, Xi Lin, 2022, Frontiers in Cell and Developmental Biology.