| The GABRG2 nonsense mutation, Q40X, associated with Dravet syndrome activated NMD and generated a truncated subunit that was partially rescued by aminoglycoside-induced stop … X Huang, M Tian, CC Hernandez, N Hu, RL Macdonald Neurobiology of disease 48 (1), 115-123, 2012 | 55 | 2012 |
| The intronic GABRG2 mutation, IVS6+ 2T→ G, associated with childhood absence epilepsy altered subunit mRNA intron splicing, activated nonsense-mediated decay, and produced a … M Tian, RL Macdonald Journal of Neuroscience 32 (17), 5937-5952, 2012 | 43 | 2012 |
| Impaired surface αβγ GABAA receptor expression in familial epilepsy due to a GABRG2 frameshift mutation M Tian, D Mei, E Freri, CC Hernandez, T Granata, W Shen, RL Macdonald, ... Neurobiology of disease 50, 135-141, 2013 | 37 | 2013 |
| PAC proton-activated chloride channel contributes to acid-induced cell death in primary rat cortical neurons J Osei-Owusu, J Yang, M Del Carmen Vitery, M Tian, Z Qiu Channels 14 (1), 53-58, 2020 | 30 | 2020 |
| Overexpressing wild‐type γ2 subunits rescued the seizure phenotype in Gabrg2+/Q390X Dravet syndrome mice X Huang, C Zhou, M Tian, JQ Kang, W Shen, K Verdier, A Pimenta, ... Epilepsia 58 (8), 1451-1461, 2017 | 27 | 2017 |
| Functional characterization of epilepsy associated GABRG2 mutations M Tian | | 2012 |
| AAV vector-mediated canine mini-dystrophin gene expression in mdx mice B Wang, MN Tian, CP Qiao, T Zhu, J Li, X Xiao MOLECULAR THERAPY 7 (5), S101-S102, 2003 | | 2003 |
| CANINE MINI-DYSTROPHIN GENE TRANSFER IN MDX MICE AMELIORATES DYSTROPHIC PATHOLOGY AND PROTECTS MEMBRANE INTEGRITY B Wang, J Li, CP Qiao, LQ Zhou, MN Tian, T Zhu, J Bogan, J Kornegay, ... | | |
| CONSTRUCTION AND ANALYSIS OF TRUNCATED MUSCLE-SPECIFIC PROMOTERS B Wang, LQ Zhou, N Kotchey, T Zhu, MN Tian, XC Jiang, J Li, X Xiao | | |
