Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice.
第一作者:
Jessica L,Haigh
第一单位:
Department of Psychiatry and Behavioral Sciences, University of California, Davis, Davis, CA, USA.;Department of Neurobiology, Physiology and Behavior, University of California, Davis, Davis, CA, USA.
作者:
医学主题词
动物(Animals);注意力(Attention);碱基序列(Base Sequence);脑(Brain);染色质(Chromatin);保守序列(Conserved Sequence);疾病模型, 动物(Disease Models, Animal);脑电描记术(Electroencephalography);癫痫(Epilepsy);进化, 分子(Evolution, Molecular);女(雌)性(Female);基因表达调控(Gene Expression Regulation);HEK293细胞(HEK293 Cells);杂合子(Heterozygote);纯合子(Homozygote);人类(Humans);男(雄)性(Male);迷宫学习(Maze Learning);记忆障碍(Memory Disorders);小鼠, 近交C57BL(Mice, Inbred C57BL);神经元(Neurons);表型(Phenotype);蛋白质结合(Protein Binding);调控序列, 核酸(Regulatory Sequences, Nucleic Acid);序列缺失(Sequence Deletion);存活率分析(Survival Analysis);温度(Temperature);反式激活因子类(Trans-Activators);小鼠(Mice)
DOI
10.1186/s13073-021-00884-0
PMID
33910599
发布时间
2024-02-26
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