Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome
Author:
Publisher
Elsevier BV
Subject
Neurology
Reference35 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999
2. Rett syndrome neuropathology review 2000;Armstrong;Brain Dev.,2001
3. Neuropathology of Rett syndrome;Armstrong;Ment. Retard. Dev. Disabil. Res. Rev.,2002
4. Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents;Belichenko;NeuroReport,1994
5. Altered development of glutamate and GABA receptors in the basal ganglia of girls with Rett syndrome;Blue;Exp. Neurol.,1999
Cited by 272 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. LTP is Absent in the CA1 Region of the Hippocampus of Male and Female Rett Syndrome Mouse Models;Neuroscience;2024-01
2. Purkinje-cell-specific MeCP2 deficiency leads to motor deficits and autistic-like behavior due to aberrations in PTP1B-TrkB-SK signaling;Cell Reports;2023-12
3. Adenosinergic System and BDNF Signaling Changes as a Cross-Sectional Feature of RTT: Characterization of Mecp2 Heterozygous Mouse Females;International Journal of Molecular Sciences;2023-11-13
4. Neuronal MeCP2 in the dentate gyrus regulates mossy fiber sprouting of mice with temporal lobe epilepsy;Neurobiology of Disease;2023-11
5. Activity-induced MeCP2 phosphorylation regulates retinogeniculate synapse refinement;Proceedings of the National Academy of Sciences;2023-10-23
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3