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首页> 外文期刊>Genomics Data >Analytical sequence to study G-CSF effect on the transcriptome of isolated spinal motoneurons from {SOD1} {G93A} mice, an animal model for amyotrophic lateral sclerosis
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Analytical sequence to study G-CSF effect on the transcriptome of isolated spinal motoneurons from {SOD1} {G93A} mice, an animal model for amyotrophic lateral sclerosis

机译:分析序列研究G-CSF对来自 {SOD1 } {G93A }小鼠(一种肌萎缩性侧索硬化的动物模型)分离的脊髓运动神经元转录组的影响的分析序列

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Abstract Granulocyte-colony stimulating factor (G-CSF) has been recently identified as a neurotrophic factor able to preserve motor functions, rescue motor units and extent survival in an animal model of amyotrophic lateral sclerosis, the {SOD1} {G93A} mice. To gain insight into the mode of action of G-CSF, we have recently performed gene expression profiling on isolated lumbar motoneurons from {SOD1G93A} mice, and shown that G-CSF re-adjusted gene expression in motoneurons of symptomatic {SOD1G93A} mice and modulates genes related to neuromuscular function (Henriques et al., 2015). Here, we provide quality controls for the microarray experiment (GO accession number GSE60856) and describe the experimental strategy.
机译:摘要粒细胞集落刺激因子(G-CSF)最近被鉴定为一种能够在肌萎缩性侧索硬化动物模型中维持神经功能,挽救运动单位并延长存活率的神经营养因子,即 {SOD1 } {G93A } 老鼠。为了深入了解G-CSF的作用方式,我们最近对 {SOD1G93A }小鼠分离出的腰部运动神经元进行了基因表达谱分析,并表明G-CSF重新调整了症状性 {SOD1G93A的运动神经元中的基因表达小鼠并调节与神经肌肉功能相关的基因(Henriques等,2015)。在这里,我们提供了微阵列实验(GO登记号GSE60856)的质量控制并描述了实验策略。

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