Su T - Search Results

1

Clinical and Functional Features of Epilepsy-Associated In-Frame Deletion Variants in SCN1A.

Wang JY, Tang B, Sheng WX, Hua LD, Zeng Y, Fan CX, Deng WY, Gao MM, Zhu WW, He N, Su T. Wang JY, et al. Among authors: su t. Front Mol Neurosci. 2022 Mar 14;15:828846. doi: 10.3389/fnmol.2022.828846. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35359575 Free PMC article.

2

Study of antiepileptic effect of extracts from Acorus tatarinowii Schott.

Liao WP, Chen L, Yi YH, Sun WW, Gao MM, Su T, Yang SQ. Liao WP, et al. Among authors: su t. Epilepsia. 2005;46 Suppl 1:21-4. doi: 10.1111/j.0013-9580.2005.461007.x. Epilepsia. 2005. PMID: 15816974 Free article.

3

Immunohistochemical investigation of voltage-gated potassium channel-interacting protein 1 in normal rat brain and Pentylenettrazole-induced seizures.

Su T, Luo AH, Cong WD, Sun WW, Deng WY, Zhao QH, Zhang ZH, Liao WP. Su T, et al. Neurosci Bull. 2006 Jul;22(4):195-203. Neurosci Bull. 2006. PMID: 17704832

4

Identification of the promoter region and the 5'-untranslated exons of the human voltage-gated sodium channel Nav1.1 gene (SCN1A) and enhancement of gene expression by the 5'-untranslated exons.

Long YS, Zhao QH, Su T, Cai YL, Zeng Y, Shi YW, Yi YH, Chang HH, Liao WP. Long YS, et al. Among authors: su t. J Neurosci Res. 2008 Nov 15;86(15):3375-81. doi: 10.1002/jnr.21790. J Neurosci Res. 2008. PMID: 18655196

5

Altered expression of voltage-gated potassium channel 4.2 and voltage-gated potassium channel 4-interacting protein, and changes in intracellular calcium levels following lithium-pilocarpine-induced status epilepticus.

Su T, Cong WD, Long YS, Luo AH, Sun WW, Deng WY, Liao WP. Su T, et al. Neuroscience. 2008 Dec 2;157(3):566-76. doi: 10.1016/j.neuroscience.2008.09.027. Epub 2008 Sep 27. Neuroscience. 2008. PMID: 18930118

6

Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: associated with loss of function of Na(v) 1.1.

Liao WP, Shi YW, Long YS, Zeng Y, Li T, Yu MJ, Su T, Deng P, Lei ZG, Xu SJ, Deng WY, Liu XR, Sun WW, Yi YH, Xu ZC, Duan S. Liao WP, et al. Among authors: su t. Epilepsia. 2010 Sep;51(9):1669-78. doi: 10.1111/j.1528-1167.2010.02645.x. Epub 2010 Jun 7. Epilepsia. 2010. PMID: 20550552 Free article.

7

Early continuous inhibition of group 1 mGlu signaling partially rescues dendritic spine abnormalities in the Fmr1 knockout mouse model for fragile X syndrome.

Su T, Fan HX, Jiang T, Sun WW, Den WY, Gao MM, Chen SQ, Zhao QH, Yi YH. Su T, et al. Psychopharmacology (Berl). 2011 May;215(2):291-300. doi: 10.1007/s00213-010-2130-2. Epub 2010 Dec 23. Psychopharmacology (Berl). 2011. PMID: 21181121

8

Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes.

Liu XR, Wu M, He N, Meng H, Wen L, Wang JL, Zhang MP, Li WB, Mao X, Qin JM, Li BM, Tang B, Deng YH, Shi YW, Su T, Yi YH, Tang BS, Liao WP. Liu XR, et al. Among authors: su t. Genes Brain Behav. 2013 Mar;12(2):234-40. doi: 10.1111/gbb.12008. Epub 2012 Dec 21. Genes Brain Behav. 2013. PMID: 23190448 Free article.

9

The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype.

Meng H, Xu HQ, Yu L, Lin GW, He N, Su T, Shi YW, Li B, Wang J, Liu XR, Tang B, Long YS, Yi YH, Liao WP. Meng H, et al. Among authors: su t. Hum Mutat. 2015 Jun;36(6):573-80. doi: 10.1002/humu.22782. Epub 2015 Apr 13. Hum Mutat. 2015. PMID: 25754450

10

Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene.

Liu XR, Huang D, Wang J, Wang YF, Sun H, Tang B, Li W, Lai JX, He N, Wu M, Su T, Meng H, Shi YW, Li BM, Tang BS, Liao WP. Liu XR, et al. Among authors: su t. Neurol Genet. 2016 Mar 22;2(2):e66. doi: 10.1212/NXG.0000000000000066. eCollection 2016 Apr. Neurol Genet. 2016. PMID: 27123484 Free PMC article.

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