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本文引用的文献

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Control of T(reg) and T(H)17 cell differentiation by the aryl hydrocarbon receptor.芳烃受体对调节性T细胞和辅助性T细胞17分化的调控
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Proteomic analysis of active multiple sclerosis lesions reveals therapeutic targets.对活动性多发性硬化症病灶的蛋白质组学分析揭示了治疗靶点。
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Human Metabolome Database: completing the 'human parts list'.人类代谢组数据库:完善“人类部件清单”。
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The biology of interleukin-2.白细胞介素-2的生物学特性
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Dysregulated Epstein-Barr virus infection in the multiple sclerosis brain.多发性硬化症大脑中爱泼斯坦-巴尔病毒感染失调
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Monocyte-derived dendritic cells in multiple sclerosis: the effect of bacterial infection.多发性硬化症中单核细胞衍生的树突状细胞:细菌感染的影响
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Multiple sclerosis: a complicated picture of autoimmunity.多发性硬化症:自身免疫的复杂情况。
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8
Induction of antigen-specific tolerance in multiple sclerosis after immunization with DNA encoding myelin basic protein in a randomized, placebo-controlled phase 1/2 trial.在一项随机、安慰剂对照的1/2期试验中,用编码髓鞘碱性蛋白的DNA免疫后诱导多发性硬化症患者产生抗原特异性耐受性。
Arch Neurol. 2007 Oct;64(10):1407-15. doi: 10.1001/archneur.64.10.nct70002. Epub 2007 Aug 13.
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Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes.大规模基因精细定位及基因型-表型关联研究表明,1型糖尿病中白细胞介素2受体A(IL2RA)区域存在多态性。
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10
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis.白细胞介素7受体α链(IL7R)显示出与多发性硬化症的等位基因关联和功能关联。
Nat Genet. 2007 Sep;39(9):1083-91. doi: 10.1038/ng2103. Epub 2007 Jul 29.

用于多发性硬化症研究的系统生物学方法。

Systems biology approaches for the study of multiple sclerosis.

作者信息

Quintana Francisco J, Farez Mauricio F, Weiner Howard L

机构信息

Center for Neurologic Diseases, Harvard Medical School, Boston, MA 02115, USA.

出版信息

J Cell Mol Med. 2008 Aug;12(4):1087-93. doi: 10.1111/j.1582-4934.2008.00375.x. Epub 2008 May 26.

DOI:10.1111/j.1582-4934.2008.00375.x
PMID:18505469
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3865652/
Abstract

Multiple sclerosis (MS) is a progressive neurological disease caused by an autoimmune attack to the central nervous system (CNS). MS is thought to result from a complex interaction between genetic and environmental factors. In this review we analyze the contribution of genomics, trancriptomics and proteomics in delineating these factors, as well as their utility for the monitoring of disease progression, the identification of new targets for therapeutic intervention and the early detection of individuals at risk.

摘要

多发性硬化症(MS)是一种由针对中枢神经系统(CNS)的自身免疫攻击引起的进行性神经疾病。MS被认为是遗传因素和环境因素之间复杂相互作用的结果。在本综述中,我们分析了基因组学、转录组学和蛋白质组学在阐明这些因素方面的作用,以及它们在监测疾病进展、确定治疗干预新靶点和早期发现高危个体方面的效用。