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本文引用的文献

1
MicroRNA-127 modulates fetal lung development.微小RNA-127调节胎儿肺发育。
Physiol Genomics. 2009 May 13;37(3):268-78. doi: 10.1152/physiolgenomics.90268.2008. Epub 2009 Mar 17.
2
MicroRNA: a new frontier in kidney and blood pressure research.微小RNA:肾脏与血压研究的新前沿
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Proteomics joins the search for microRNA targets.蛋白质组学也加入了寻找微小RNA靶标的行列。
Cell. 2008 Aug 22;134(4):560-2. doi: 10.1016/j.cell.2008.08.008.
4
Dysregulation of microRNAs after myocardial infarction reveals a role of miR-29 in cardiac fibrosis.心肌梗死后微小RNA的失调揭示了miR-29在心脏纤维化中的作用。
Proc Natl Acad Sci U S A. 2008 Sep 2;105(35):13027-32. doi: 10.1073/pnas.0805038105. Epub 2008 Aug 22.
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MicroRNA and cardiac pathologies.微小RNA与心脏疾病
Physiol Genomics. 2008 Aug 15;34(3):239-42. doi: 10.1152/physiolgenomics.90254.2008. Epub 2008 Jun 10.
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Global identification of microRNA-target RNA pairs by parallel analysis of RNA ends.通过RNA末端平行分析对微小RNA-靶RNA对进行全局鉴定。
Nat Biotechnol. 2008 Aug;26(8):941-6. doi: 10.1038/nbt1417. Epub 2008 Jun 9.
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MicroRNA: basic mechanisms and transcriptional regulatory networks for cell fate determination.微小RNA:细胞命运决定的基本机制与转录调控网络
Cardiovasc Res. 2008 Sep 1;79(4):553-61. doi: 10.1093/cvr/cvn151. Epub 2008 Jun 6.
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Endogenous siRNA and miRNA targets identified by sequencing of the Arabidopsis degradome.通过对拟南芥降解组进行测序鉴定出的内源性小干扰RNA和微小RNA靶标。
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Functional meta-analysis of double connectivity in gene coexpression networks in mammals.哺乳动物基因共表达网络中双连通性的功能元分析。
Physiol Genomics. 2008 Jun 12;34(1):34-41. doi: 10.1152/physiolgenomics.00008.2008. Epub 2008 Apr 22.
10
Molecular networks in Dahl salt-sensitive hypertension based on transcriptome analysis of a panel of consomic rats.基于一组近交系大鼠转录组分析的Dahl盐敏感性高血压分子网络
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微小RNA:通往系统分子医学广阔范式的新入口。

MicroRNA: a new entrance to the broad paradigm of systems molecular medicine.

作者信息

Liang Mingyu

机构信息

Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA.

出版信息

Physiol Genomics. 2009 Jul 9;38(2):113-5. doi: 10.1152/physiolgenomics.00080.2009. Epub 2009 May 26.

DOI:10.1152/physiolgenomics.00080.2009
PMID:19470802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2712222/
Abstract

Systems molecular medicine is the science of combining systems biology with molecular analysis and intervention to address clinically relevant questions. MicroRNAs (miRNAs) appear particularly suitable to serve as hubs of regulatory networks underlying complex diseases. Clear experimental evidence for coordinated regulation of a large number of genes by miRNAs, however, is still rare. It leaves open several fundamental questions that are important for determining the value of miRNA in complex regulatory networks and in systems molecular medicine. Physiological genomics is a powerful approach for addressing these open questions.

摘要

系统分子医学是一门将系统生物学与分子分析及干预相结合以解决临床相关问题的科学。微小RNA(miRNA)似乎特别适合作为复杂疾病潜在调控网络的枢纽。然而,关于miRNA对大量基因进行协同调控的确切实验证据仍然很少。这留下了几个基本问题,这些问题对于确定miRNA在复杂调控网络和系统分子医学中的价值至关重要。生理基因组学是解决这些未决问题的有力方法。