[1] |
Marler S, Sanders KB, Veenstra-VanderWeele J. N-acetylcysteine as treatment for self-injurious behavior in a child with autism[J]. J Child Adolesc Psychopharmacol, 2014, 24(4): 231-234.
|
[2] |
Stutzman D, Dopheide J. Acetylcysteine for treatment of autism spectrum disorder symptoms[J]. Am J Health Syst Pharm, 2015, 72(22): 1956-1959.
|
[3] |
Chen YW, Lin HC, Ng MC, et al. Activation of mGluR2/3 underlies the effects of N-acetylcystein on amygdala-associated autism-like phenotypes in a valproate-induced rat model of autism[J]. Front Behav Neurosci, 2014, 8: 219.
|
[4] |
陈亦岚, 文敏, 周波, 等. 孤独症大鼠前额叶皮质中Notch相关蛋白的表达[J]. 中国儿童保健杂志, 2016, 24(3): 260-263.
|
[5] |
Wei J, Zhang L, Ren L, et al. Endosulfan inhibits proliferation through the Notch signaling pathway in human umbilical vein endothelial cells[J]. Environ Pollut, 2017, 221: 26-36.
|
[6] |
Yao M, Gao F, Wang X, et al. Nox4 is involved in high glucose-induced apoptosis in renal tubular epithelial cells via Notch pathway[J]. Mol Med Rep, 2017, 15(6): 4319-4325.
|
[7] |
Sosa-Díaz N, Bringas ME, Atzori M, et al. Prefrontal cortex, hippocampus, and basolateral amygdala plasticity in a rat model of autism spectrum[J]. Synapse, 2014, 68(10): 468-473.
|
[8] |
Bailey A, Luthert P, Bolton P, et al. Autism and megalencephaly[J]. Lancet, 1993, 341(8854): 1225-1226.
|
[9] |
Wang Z, Xu L, Zhu X, et al. Demethylation of specific Wnt/beta-catenin pathway genes and its upregulationin rat brain induced by prenatal valproate exposure[J]. Anat Rec (Hoboken), 2010, 293(11): 1947-1953.
|
[10] |
Zhang Y, Cui W, Zhai Q, et al. N-acetylcysteine ameliorates repetitive/stereotypic behavior due to its antioxidant properties without activation of the canonical Wnt pathway in a valproic acid-induced rat model of autism[J]. Mol Med Rep, 2017, 16(2): 2233-2240.
|
[11] |
Vulto-van Silfhout AT, de Brouwer AF, de Leeuw N, et al. A 380-kb duplication in 7p22.3 encompassing the LFNG gene in a boy with asperger syndrome[J]. Mol Syndromol, 2012, 2(6): 245-250.
|
[12] |
Wise A, Tenezaca L, Fernandez RW, et al. Drosophila mutants of the autism candidate gene neurobeachin (rugose) exhibit neuro-developmental disorders, aberrant synaptic properties, altered locomotion, and impaired adult social behavior and activity patterns[J]. J Neurogenet, 2015, 29(2-3): 135-143.
|
[13] |
Yatim A, Benne C, Sobhian B, et al. NOTCH1 nuclear interactome reveals key regulators of its transcriptional activity and oncogenic function[J]. Mol Cell, 2012, 48(3): 445-458.
|
[14] |
Tuand K, Stijnen P, Volders K, et al. Nuclear localization of the autism candidate gene neurobeachin and functional interaction with the NOTCH1 intracellular domain indicate a role in regulating transcription[J]. PLoS One, 2016, 11(3): e0151954.
|
[15] |
Niesmann K, Breuer D, Brockhaus J, et al. Dendritic spine formation and synaptic function require neurobeachin[J]. Nat Commun, 2011, 2: 557.
|
[16] |
刘瑶, 赵晓云, 韩颖, 等. 脑缺血后处理对脑缺血再灌注大鼠Notch1信号通路及学习记忆功能的影响[J]. 中国医科大学学报, 2017, 46(11): 984-989.
|
[17] |
Borghese L, Dolezalova D, Opitz T, et al. Inhibition of notch signaling in human embryonic stem cell-derived neural stem cells delays G1/S phase transition and accelerates neuronal differentiation in vitro and in vivo[J]. Stem Cells, 2010, 28(5): 955-964.
|