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本文引用的文献

1
Microarray-based approach identifies microRNAs and their target functional patterns in polycystic kidney disease.基于微阵列的方法可识别多囊肾病中的微小RNA及其靶标功能模式。
BMC Genomics. 2008 Dec 23;9:624. doi: 10.1186/1471-2164-9-624.
2
Mechanistic insights into the link between a polymorphism of the 3'UTR of the SLC7A1 gene and hypertension.SLC7A1基因3'非翻译区多态性与高血压之间联系的机制性见解。
Hum Mutat. 2009 Mar;30(3):328-33. doi: 10.1002/humu.20891.
3
Comprehensive analysis of microRNA expression patterns in renal biopsies of lupus nephritis patients.狼疮性肾炎患者肾活检中微小RNA表达模式的综合分析。
Rheumatol Int. 2009 May;29(7):749-54. doi: 10.1007/s00296-008-0758-6. Epub 2008 Nov 8.
4
The emerging role of microRNAs in cardiac remodeling and heart failure.微小RNA在心脏重塑和心力衰竭中的新作用。
Circ Res. 2008 Nov 7;103(10):1072-83. doi: 10.1161/CIRCRESAHA.108.183087.
5
Most mammalian mRNAs are conserved targets of microRNAs.大多数哺乳动物的信使核糖核酸是微小核糖核酸的保守靶标。
Genome Res. 2009 Jan;19(1):92-105. doi: 10.1101/gr.082701.108. Epub 2008 Oct 27.
6
MicroRNA15a modulates expression of the cell-cycle regulator Cdc25A and affects hepatic cystogenesis in a rat model of polycystic kidney disease.微小RNA15a调节细胞周期调节因子Cdc25A的表达,并影响多囊肾病大鼠模型中的肝囊肿形成。
J Clin Invest. 2008 Nov;118(11):3714-24. doi: 10.1172/JCI34922. Epub 2008 Oct 23.
7
Toward microRNA-based therapeutics for heart disease: the sense in antisense.迈向基于微小RNA的心脏病治疗:反义中的意义。
Circ Res. 2008 Oct 24;103(9):919-28. doi: 10.1161/CIRCRESAHA.108.183426.
8
Microarray analysis of micro-ribonucleic acid expression in primary immunoglobulin A nephropathy.原发性免疫球蛋白A肾病中微小核糖核酸表达的微阵列分析
Saudi Med J. 2008 Oct;29(10):1388-93.
9
Genome-wide microRNA expression profiling in renal cell carcinoma: significant down-regulation of miR-141 and miR-200c.肾细胞癌全基因组微小RNA表达谱分析:miR-141和miR-200c显著下调
J Pathol. 2008 Dec;216(4):418-27. doi: 10.1002/path.2437.
10
MicroRNA-directed transcriptional gene silencing in mammalian cells.哺乳动物细胞中微小RNA介导的转录基因沉默
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微小RNA:肾脏与血压研究的新前沿

MicroRNA: a new frontier in kidney and blood pressure research.

作者信息

Liang Mingyu, Liu Yong, Mladinov Domagoj, Cowley Allen W, Trivedi Hariprasad, Fang Yi, Xu Xialian, Ding Xiaoqiang, Tian Zhongmin

机构信息

Dept. of Physiology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

出版信息

Am J Physiol Renal Physiol. 2009 Sep;297(3):F553-8. doi: 10.1152/ajprenal.00045.2009. Epub 2009 Apr 1.

DOI:10.1152/ajprenal.00045.2009
PMID:19339633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2739705/
Abstract

MicroRNA (miRNA) has emerged rapidly as a major new direction in many fields of research including kidney and blood pressure research. A mammalian genome encodes several hundred miRNAs. These miRNAs potentially regulate the expression of thousands of proteins. miRNA expression profiles differ substantially between the kidney and other organs as well as between kidney regions. miRNAs may be functionally important in models of diabetic nephropathy, podocyte development, and polycystic disease. miRNAs may be involved in the regulation of arterial blood pressure, including possible involvement in genetic elements of hypertension. Studies of miRNAs could generate diagnostic biomarkers for kidney disease and new mechanistic insights into the complex regulatory networks underlying kidney disease and hypertension. Further progress in the understanding of miRNA biogenesis and action and technical improvements for target identification and miRNA manipulation will be important for studying miRNAs in renal function and blood pressure regulation.

摘要

微小RNA(miRNA)已迅速成为包括肾脏和血压研究在内的许多研究领域的一个主要新方向。哺乳动物基因组编码数百种miRNA。这些miRNA可能调控数千种蛋白质的表达。肾脏与其他器官之间以及肾脏不同区域之间的miRNA表达谱存在很大差异。miRNA在糖尿病肾病、足细胞发育和多囊性疾病模型中可能具有重要功能。miRNA可能参与动脉血压的调节,包括可能参与高血压的遗传因素。对miRNA的研究可以产生肾脏疾病的诊断生物标志物,并为肾脏疾病和高血压潜在的复杂调控网络提供新的机制性见解。在理解miRNA生物合成和作用方面取得进一步进展,以及在靶标识别和miRNA操作方面的技术改进,对于研究miRNA在肾功能和血压调节中的作用至关重要。