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Transcriptional profiling of differentially vulnerable motor neurons at pre-symptomatic stage in the Smn2b/- mouse model of spinal muscular atrophy

机译:脊髓性肌萎缩的Smn2b /-小鼠模型在症状前阶段的差异脆弱运动神经元的转录谱

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摘要

IntroductionThe term motor neuron disease encompasses a spectrum of disorders in which motor neurons are the lost. Importantly, while some motor neurons are lost early in disease and others remain intact at disease end-stage. This creates a valuable experimental paradigm to investigate the factors that regulate motor neuron vulnerability. Spinal muscular atrophy is a childhood motor neuron disease caused by mutations or deletions in the SMN1 gene. Here, we have performed transcriptional analysis on differentially vulnerable motor neurons from an intermediate mouse model of Spinal muscular atrophy at a presymptomatic time point.
机译:简介运动神经元疾病一词涵盖了运动神经元丢失的一系列疾病。重要的是,尽管某些运动神经元在疾病早期丢失,而另一些在疾病末期仍保持完整。这创建了一个有价值的实验范例,以研究调节运动神经元易损性的因素。脊髓性肌萎缩症是由SMN1基因突变或缺失引起的儿童运动神经元疾病。在这里,我们在症状发生前的某个时间点对来自脊髓性肌萎缩症的中级小鼠模型的易受伤害的运动神经元进行了转录分析。

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