| 1. |
Guan JS, Haggarty SJ, Giacometti E, et al. HDAC2 negatively regulates memory formation and synaptic plasticity. Nature, 2009, 459(7243): 55-60.
|
| 2. |
Huang Y, Zhao F, Wang L, et al. Increased expression ofhistone deacetylases 2 in temporal lobe epilepsy: a study of epileptic patients and rat models. Synapse, 2012, 66(2): 151-159.
|
| 3. |
Xi ZQ, Sun JJ, Wang XF, et al. HSPBAPI is found extensively in the anterior temporal neocortex of patients with intractable epilepsy. Synapse, 2007, 61(9): 741-747.
|
| 4. |
Senner CE. The role of DNA methylation in mammalian development. Reprod Biomed Online, 2011, 22(6): 529-535.
|
| 5. |
Urdinguio RG, Fernandez AF, Lopez Nieva P, et al. Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome. Epigenetics, 2010, 5 (2): 656-663.
|
| 6. |
Roth TL, Zoladz PR, Sweatt JD, et al. Epigenetic modification of hippocampal BDNF DNA in adult rats in an animal model of post-traumatic stress disorder. J Psychiatr Res, 2011, 45(7): 919-926.
|
| 7. |
Kobow K, Jeske I, Hildebraudt M, et al. Increased reelin promoter methylation is associated with granule cell dispersion in human temporal lobe epilepsy. J Neuropathol Exp Neurol, 2009, 68(4): 356-364.
|
| 8. |
Imenez Mateos EM, Bray I, Sanz Rodriguez A, et al. miRNA Expression profile after status epilepticus and hippocampal neuroprotection by targeting miR-132. Am J Pathol, 2011, 179 (5): 2519-2532.
|
| 9. |
Mercer TR, Dinger ME, Mattick JS. Long noncoding RNAs: insights into functions. Nat Rev Genet, 2009, 10(3): 155-159.
|
| 10. |
Halil AM, Faghihi MA, Modarresi F, et al. A novel RNA transcrpt with antiapoptotic function is silenced in fragile X syndrome. PLoS One, 2008, 3(1): e1486.
|
| 11. |
Ladd PD, Smith LE, Rabaia NA, et al. An antisense transcript spanning the CGG repeat region of FMRI is upregulated in premutation Cal Tiers but silenced in full mutation individuals. Hum Mol Genet, 2007, 16(24): 3174-3187.
|
| 12. |
P Kwan, MJ Brodie. Early identification of refractory epilepsy. N Engl J Med, 2000, 342(20): 314-319.
|
| 13. |
I Najm, L Jehi, A Palmini, et al. Temporal patterns and mechanisms of epilepsy surgery failure. Epilepsia, 2013, 54(3): 772-782.
|
| 14. |
SF Berkovic, IE Scheffer. Genetics of the epilepsies. Epilepsia, 2001, 42(Suppl 5): 16-23.
|
| 15. |
AJ Becker, J Chen, A Zien, et al. Correlated stage-and subfield-associated hippocampal gene expression patterns in experimental and human temporal lobe epilepsy. Eur J Neurosci, 2003, 18(2): 2792-2802.
|
| 16. |
M Majores, J Eils, OD Wiestler, et al. Molecular profiling of temporal lobe epilepsy: comparison of data from human tissue samples and animal models. Epilepsy Res, 2004, 60(4): 173-178.
|
| 17. |
K Kobow, I Blumcke. The methylation hypothesis: do epigenetic chromatin modifications play a role in epileptogenesis?. Epilepsia, 2011, 52(Suppl 4): 15-19.
|
| 18. |
SF Miller-Delaney, K Bryan, S Das, et al. Differential DNA methylation profilesof coding and non-coding genes define hippocampal sclerosis in human temporal lobe epilepsy. Brain, 2005, 138(5): 616-631.
|
| 19. |
C Nervi, E De Marinis, G Codacci-Pisanelli. Epigenetic treatment of solid tumours: a review of clinical trials. Clin Epigenet, 2015, 7(1): 127.
|
| 20. |
M Szyf. Prospects for the development of epigenetic drugs for CNS conditions. Nat Rev Drug Discov, 2015, 14(5): 461-474.
|
| 21. |
K Kobow, A Kaspi, KN Harikrishnan, et al. Deep sequencing reveals increased DNA methylation in chronic rat epilepsy. Acta Neuropathol, 2013, 126(5): 741-756.
|
| 22. |
SF Berkovic, JC Mulley, IE Scheffer, et al. Human epilepsies: interaction of genetic and acquired factors. Trends Neurosci, 2006, 29(6): 391-397.
|
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