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对多发性硬化症患者的 microRNA 和 mRNA 表达谱进行筛选,以揭示新的致病步骤并鉴定潜在的生物标志物。

MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkers.

机构信息

Institute of Experimental Neurology (INSPE), and Department of Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Via Olgettina 58, 20132 Milan, Italy.

出版信息

Neurosci Lett. 2012 Feb 2;508(1):4-8. doi: 10.1016/j.neulet.2011.11.006. Epub 2011 Nov 7.

Abstract

Identification of novel targets and biomarkers, such as microRNAs, is extremely helpful to understand the pathogenetic mechanisms in a disease like multiple sclerosis (MS). We tested the expression profile of 1145 microRNAs in peripheral blood mononuclear cells (PBMCs) of 19 MS patients and 14 controls, and we further explored their function by performing a whole-genome mRNA profiling in same subjects and using bioinformatic prediction tool. A total of 104 miRNAs have been identified as deregulated in MS patients; 2/10 which ranked highest (let-7g and miR-150) have been validated in a replication sample, leading to the identification of putative target genes.

摘要

鉴定新的靶点和生物标志物,如 microRNAs,对于理解多发性硬化症(MS)等疾病的发病机制非常有帮助。我们检测了 19 名 MS 患者和 14 名对照者外周血单个核细胞(PBMCs)中 1145 种 microRNAs 的表达谱,并通过对同一受试者进行全基因组 mRNA 谱分析和使用生物信息预测工具进一步探索了它们的功能。共鉴定出 104 种在 MS 患者中失调的 microRNAs;其中排名最高的 2 种(let-7g 和 miR-150)在复制样本中得到了验证,从而确定了可能的靶基因。

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