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miRTarBase: a database curates experimentally validated microRNA-target interactions.

作者信息

Hsu Sheng-Da, Lin Feng-Mao, Wu Wei-Yun, Liang Chao, Huang Wei-Chih, Chan Wen-Ling, Tsai Wen-Ting, Chen Goun-Zhou, Lee Chia-Jung, Chiu Chih-Min, Chien Chia-Hung, Wu Ming-Chia, Huang Chi-Ying, Tsou Ann-Ping, Huang Hsien-Da

机构信息

Institute of Bioinformatics and Systems Biology, National Chiao Tung University, Hsin-Chu 300, Taiwan.

出版信息

Nucleic Acids Res. 2011 Jan;39(Database issue):D163-9. doi: 10.1093/nar/gkq1107. Epub 2010 Nov 10.


DOI:10.1093/nar/gkq1107
PMID:21071411
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3013699/
Abstract

MicroRNAs (miRNAs), i.e. small non-coding RNA molecules (∼22 nt), can bind to one or more target sites on a gene transcript to negatively regulate protein expression, subsequently controlling many cellular mechanisms. A current and curated collection of miRNA-target interactions (MTIs) with experimental support is essential to thoroughly elucidating miRNA functions under different conditions and in different species. As a database, miRTarBase has accumulated more than 3500 MTIs by manually surveying pertinent literature after data mining of the text systematically to filter research articles related to functional studies of miRNAs. Generally, the collected MTIs are validated experimentally by reporter assays, western blot, or microarray experiments with overexpression or knockdown of miRNAs. miRTarBase curates 3576 experimentally verified MTIs between 657 miRNAs and 2297 target genes among 17 species. miRTarBase contains the largest amount of validated MTIs by comparing with other similar, previously developed databases. The MTIs collected in the miRTarBase can also provide a large amount of positive samples to develop computational methods capable of identifying miRNA-target interactions. miRTarBase is now available on http://miRTarBase.mbc.nctu.edu.tw/, and is updated frequently by continuously surveying research articles.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/3013699/bb8d06847349/gkq1107f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/3013699/fce120dd10c5/gkq1107f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/3013699/c05911474579/gkq1107f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/3013699/bb8d06847349/gkq1107f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/3013699/fce120dd10c5/gkq1107f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/3013699/c05911474579/gkq1107f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/3013699/bb8d06847349/gkq1107f3.jpg

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本文引用的文献

[1]
miRSel: automated extraction of associations between microRNAs and genes from the biomedical literature.

BMC Bioinformatics. 2010-3-16

[2]
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Genome Biol. 2009-11-17

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Nucleic Acids Res. 2009-11-11

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Nucleic Acids Res. 2009-10-22

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Nat Protoc. 2009

[7]
miRecords: an integrated resource for microRNA-target interactions.

Nucleic Acids Res. 2009-1

[8]
The database of experimentally supported targets: a functional update of TarBase.

Nucleic Acids Res. 2009-1

[9]
miR2Disease: a manually curated database for microRNA deregulation in human disease.

Nucleic Acids Res. 2009-1

[10]
Widespread changes in protein synthesis induced by microRNAs.

Nature. 2008-9-4

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