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首页> 外文期刊>Journal of Neuroscience Research >Gene expression profiling of 12633 genes in Alzheimer hippocampal CA1: Transcription and neurotrophic factor down-regulation and up-regulation of apoptotic and pro-inflammatory signaling.
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Gene expression profiling of 12633 genes in Alzheimer hippocampal CA1: Transcription and neurotrophic factor down-regulation and up-regulation of apoptotic and pro-inflammatory signaling.

机译:阿尔茨海默病海马CA1中12633个基因的基因表达谱:转录和神经营养因子下调以及凋亡和促炎信号的上调。

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Alterations in transcription, RNA editing, translation, protein processing, and clearance are a consistent feature of Alzheimer's disease (AD) brain. To extend our initial study (Alzheimer Reports [2000] 3:161-167), RNA samples isolated from control and AD hippocampal cornu ammonis 1 (CA1) were analyzed for 12633 gene and expressed sequence tag (EST) expression levels using DNA microarrays (HG-U95Av2 Genechips; Affymetrix, Santa Clara, CA). Hippocampal CA1 tissues were carefully selected from several hundred potential specimens obtained from domestic and international brain banks. To minimize the effects of individual differences in gene expression, RNA of high spectral quality (A(260/280) >/= 1.9) was pooled from CA1 of six control or six AD subjects. Results were compared as a group; individual gene expression patterns for the most-changed RNA message levels were also profiled. There were no significant differences in age, postmortem interval (mean
机译:转录,RNA编辑,翻译,蛋白质加工和清除的改变是阿尔茨海默氏病(AD)大脑的一贯特征。为了扩展我们的初步研究(Alzheimer Reports [2000] 3:161-167),使用DNA微阵列芯片分析了从对照和AD海马角膜氨化蛋白1(CA1)分离的RNA样品中的12633个基因并表达了序列标签(EST)表达水平( HG-U95Av2基因芯片; Affymetrix,加利福尼亚州圣克拉拉)。海马CA1组织是从数百家从国内外脑库获得的潜在标本中精心挑选的。为了最小化基因表达中个体差异的影响,从六个对照或六个AD受试者的CA1中收集了高光谱质量的RNA(A(260/280)> / = 1.9)。将结果作为一组进行比较;还分析了变化最大的RNA信息水平的单个基因表达模式。两组大脑的年龄,死后间隔(平均

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