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Transcriptional profiling of the postnatal brain of the Ts1Cje mouse model of Down syndrome

机译:唐氏综合征的Ts1Cje小鼠模型的出生后大脑的转录谱

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Abstract The Ts1Cje mouse model of Down syndrome (DS) has partial trisomy of mouse chromosome 16 (MMU16), which is syntenic to human chromosome 21 (HSA21). It develops various neuropathological features demonstrated by {DS} patients such as reduced cerebellar volume [1] and altered hippocampus-dependent learning and memory [2,3]. To understand the global gene expression effect of the partially triplicated {MMU16} segment on mouse brain development, we performed the spatiotemporal transcriptome analysis of Ts1Cje and disomic control cerebral cortex, cerebellum and hippocampus harvested at four developmental time-points: postnatal day (P)1, P15, {P30} and P84. Here, we provide a detailed description of the experimental and analysis procedures of the microarray dataset, which has been deposited in the Gene Expression Omnibus (GSE49050) database.
机译:摘要唐氏综合征(DS)的Ts1Cje小鼠模型具有小鼠16号染色体(MMU16)的部分三体性,与人类21号染色体(HSA21)具有同义性。它发展出{DS}患者所表现出的各种神经病理学特征,例如小脑体积减少[1]和海马依赖性学习和记忆改变[2,3]。为了解{MMU16}部分重复的部分对小鼠大脑发育的整体基因表达影响,我们进行了Ts1Cje时空转录组分析以及在四个发育时间点收获的二体性控制的大脑皮层,小脑和海马体:产后一天(P) 1,P15,{P30}和P84。在这里,我们提供了微阵列数据集的实验和分析程序的详细说明,该数据集已保存在“基因表达综合”(GSE49050)数据库中。

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