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Mengnan Tian
Mengnan Tian
Vanderbilt University Medical Center
Protein subunit
Biology
Molecular biology
Stop codon
Mutant
4
Papers
92
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Overexpressing wild‐type γ2 subunits rescued the seizure phenotype in Gabrg2+/Q390X Dravet syndrome mice
2017
Epilepsia
Xuan Huang
Chengwen Zhou
Mengnan Tian
Jing-Qiong Kang
Wangzhen Shen
Kelienne M. Verdier
Aurea Pimenta
Robert L. Macdonald
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Citations (15)
Impaired surface αβγ GABAA receptor expression in familial epilepsy due to a GABRG2 frameshift mutation
2013
Neurobiology of Disease
Mengnan Tian
Davide Mei
Elena Freri
Ciria C. Hernandez
Tiziana Granata
Wangzhen Shen
Robert L. Macdonald
Renzo Guerrini
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Citations (18)
The GABRG2 Nonsense Mutation, Q40X, Associated with Dravet Syndrome Activated NMD and Generated a Truncated Subunit That was Partially Rescued by aminoglycoside-Induced Stop Codon Read-through
2012
Neurobiology of Disease
Xuan Huang
Mengnan Tian
Ciria C. Hernandez
Ningning Hu
Robert L. Macdonald
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Citations (29)
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