Mengnan Tian

Research Associate


Research output per year

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Research Output

Overexpressing wild-type γ2 subunits rescued the seizure phenotype in Gabrg2+/Q390X Dravet syndrome mice

Huang, X., Zhou, C., Tian, M., Kang, J. Q., Shen, W., Verdier, K., Pimenta, A. & MacDonald, R. L., Aug 1 2017, In : Epilepsia. 58, 8, p. 1451-1461 11 p.

Research output: Contribution to journalArticle

Open Access
  • Impaired surface αβγ GABAA receptor expression in familial epilepsy due to a GABRG2 frameshift mutation

    Tian, M., Mei, D., Freri, E., Hernandez, C. C., Granata, T., Shen, W., Macdonald, R. L. & Guerrini, R., Feb 1 2013, In : Neurobiology of Disease. 50, 1, p. 135-141 7 p.

    Research output: Contribution to journalArticle

  • 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

    Huang, X., Tian, M., Hernandez, C. C., Hu, N. & MacDonald, R. L., Oct 1 2012, In : Neurobiology of Disease. 48, 1, p. 115-123 9 p.

    Research output: Contribution to journalArticle

  • Open Access