A Novel Mecp2<sup>Y120D</sup> Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome.
作者:
主题词
动物(Animals);行为, 动物(Behavior, Animal);脑(Brain);染色质(Chromatin);女(雌)性(Female);基因敲入技术(Gene Knock-In Techniques);人类(Humans);长寿(Longevity);男(雄)性(Male);记忆, 短时(Memory, Short-Term);甲基-CpG-结合蛋白质2(Methyl-CpG-Binding Protein 2);小鼠(Mice);小鼠, 近交C57BL(Mice, Inbred C57BL);模型, 生物学(Models, Biological);突变(Mutation);神经元(Neurons);表型(Phenotype);Rett综合征(Rett Syndrome)
DOI
10.1007/s12035-018-1412-2
PMID
30402709
发布时间
2021-12-09
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Molecular neurobiology
4838-4854页
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