Targeting ATM ameliorates mutant Huntingtin toxicity in cell and animal models of Huntington's disease.
第一作者:
Xiao-Hong,Lu
第一单位:
Center for Neurobehavioral Genetics, Semel Institute for Neuroscience & Human Behavior, University of California, Los Angeles (UCLA), Los Angeles, CA 90095, USA. Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA. UCLA Brain Research Institute, Los Angeles, CA 90095, USA.
作者:
医学主题词
成年人(Adult);老年人(Aged);动物(Animals);行为, 动物(Behavior, Animal);脑(Brain);细胞系(Cell Line);细胞保护(Cytoprotection);疾病模型, 动物(Disease Models, Animal);黑腹果蝇(Drosophila melanogaster);基因剂量(Gene Dosage);基因敲低技术(Gene Knockdown Techniques);组蛋白类(Histones);人类(Humans);杭廷顿病(Huntington Disease);诱导多能干细胞(Induced Pluripotent Stem Cells);小鼠, 神经学突变型(Mice, Neurologic Mutants);中年人(Middle Aged);吗啉类(Morpholines);突变蛋白质类(Mutant Proteins);神经组织蛋白质类(Nerve Tissue Proteins);神经元(Neurons);氧化性应激(Oxidative Stress);死后变化(Postmortem Changes);血清素质膜转运蛋白质类(Serotonin Plasma Membrane Transport Proteins);信号传导(Signal Transduction);噻吨类(Thioxanthenes)
DOI
10.1126/scitranslmed.3010523
PMID
25540325
发布时间
2020-10-28
基金项目
R01 NS084298/NS/NINDS NIH HHS/United States
P50 AG16570/AG/NIA NIH HHS/United States
NS42179/NS/NINDS NIH HHS/United States
R01 NS074312/NS/NINDS NIH HHS/United States
R01 NS049501/NS/NINDS NIH HHS/United States
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Science translational medicine
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