• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Consensus miRNA expression profiles derived from interplatform normalization of microarray data.基于芯片间标准化的共识 miRNA 表达谱。
RNA. 2010 Jan;16(1):16-25. doi: 10.1261/rna.1688110. Epub 2009 Nov 30.
2
Modified least-variant set normalization for miRNA microarray.miRNA 微阵列的修正最小变异集归一化
RNA. 2010 Dec;16(12):2293-303. doi: 10.1261/rna.2345710. Epub 2010 Oct 27.
3
An optimized isolation and labeling platform for accurate microRNA expression profiling.一种用于精确微小RNA表达谱分析的优化分离和标记平台。
RNA. 2005 Sep;11(9):1461-70. doi: 10.1261/rna.2610405. Epub 2005 Jul 25.
4
Effect of various normalization methods on Applied Biosystems expression array system data.各种标准化方法对Applied Biosystems表达阵列系统数据的影响。
BMC Bioinformatics. 2006 Dec 15;7:533. doi: 10.1186/1471-2105-7-533.
5
Comparison of microarray platforms for measuring differential microRNA expression in paired normal/cancer colon tissues.比较微阵列平台在配对正常/癌症结肠组织中测量差异 microRNA 表达的性能。
PLoS One. 2012;7(9):e45105. doi: 10.1371/journal.pone.0045105. Epub 2012 Sep 13.
6
Identification and target prediction of miRNAs specifically expressed in rat neural tissue.大鼠神经组织中特异性表达的微小RNA的鉴定与靶标预测
BMC Genomics. 2009 May 9;10:214. doi: 10.1186/1471-2164-10-214.
7
Statistical Methods for Identifying Biomarkers from miRNA Profiles of Cancers.从癌症的微小RNA谱中识别生物标志物的统计方法
Methods Mol Biol. 2019;1882:261-286. doi: 10.1007/978-1-4939-8879-2_24.
8
MicroRNA expression profiling in cancer from a bioinformatics prospective.从生物信息学角度看癌症中的微小RNA表达谱分析
Expert Rev Mol Diagn. 2007 Nov;7(6):787-92. doi: 10.1586/14737159.7.6.787.
9
Reproducibility of quantitative RT-PCR array in miRNA expression profiling and comparison with microarray analysis.定量逆转录聚合酶链反应(RT-PCR)芯片在微小RNA(miRNA)表达谱分析中的可重复性及与微阵列分析的比较
BMC Genomics. 2009 Aug 28;10:407. doi: 10.1186/1471-2164-10-407.
10
The beagle dog MicroRNA tissue atlas: identifying translatable biomarkers of organ toxicity.比格犬微小RNA组织图谱:识别可转化的器官毒性生物标志物。
BMC Genomics. 2016 Aug 17;17:649. doi: 10.1186/s12864-016-2958-x.

引用本文的文献

1
Brain cell-specific origin of circulating microRNA biomarkers in experimental temporal lobe epilepsy.实验性颞叶癫痫中循环微小RNA生物标志物的脑细胞特异性起源
Front Mol Neurosci. 2023 Sep 22;16:1230942. doi: 10.3389/fnmol.2023.1230942. eCollection 2023.
2
Optimized workflow to modify microRNA expression in primary human intravascular cells.优化工作流程以修饰原代人血管细胞中的 microRNA 表达。
BMC Immunol. 2023 Feb 15;24(1):5. doi: 10.1186/s12865-023-00540-9.
3
A Bioinformatics Approach to MicroRNA-Sequencing Analysis Based on Human Saliva Samples of Patients with Endometriosis.基于子宫内膜异位症患者唾液样本的 miRNA 测序分析的生物信息学方法。
Int J Mol Sci. 2022 Jul 21;23(14):8045. doi: 10.3390/ijms23148045.
4
Endometriosis Associated-miRNome Analysis of Blood Samples: A Prospective Study.血液样本中子宫内膜异位症相关微小RNA组分析:一项前瞻性研究。
Diagnostics (Basel). 2022 May 5;12(5):1150. doi: 10.3390/diagnostics12051150.
5
MicroRNome analysis generates a blood-based signature for endometriosis.MicroRNome 分析生成基于血液的子宫内膜异位症特征。
Sci Rep. 2022 Mar 8;12(1):4051. doi: 10.1038/s41598-022-07771-7.
6
Salivary MicroRNA Signature for Diagnosis of Endometriosis.用于诊断子宫内膜异位症的唾液微小RNA特征
J Clin Med. 2022 Jan 26;11(3):612. doi: 10.3390/jcm11030612.
7
Clues for Improving the Pathophysiology Knowledge for Endometriosis Using Plasma Micro-RNA Expression.利用血浆微小RNA表达改善子宫内膜异位症病理生理学知识的线索
Diagnostics (Basel). 2022 Jan 12;12(1):175. doi: 10.3390/diagnostics12010175.
8
Prospective Study on Plasma MicroRNA-4286 and Incident Acute Coronary Syndrome.血浆 microRNA-4286 与新发急性冠状动脉综合征的前瞻性研究。
J Am Heart Assoc. 2021 Mar 16;10(6):e018999. doi: 10.1161/JAHA.120.018999. Epub 2021 Mar 10.
9
A narrative review of the roles of the miR-15/107 family in heart disease: lessons and prospects for heart disease.miR-15/107家族在心脏病中作用的叙述性综述:心脏病的经验教训与前景
Ann Transl Med. 2021 Jan;9(1):66. doi: 10.21037/atm-20-6073.
10
MicroRNA-15a Regulates the Differentiation of Intramuscular Preadipocytes by Targeting , and in Chickens.miR-15a 通过靶向 和 调控肌内前体脂肪细胞分化。
Int J Mol Sci. 2019 Aug 20;20(16):4063. doi: 10.3390/ijms20164063.

本文引用的文献

1
C19MC microRNAs are processed from introns of large Pol-II, non-protein-coding transcripts.C19MC微小RNA由大型RNA聚合酶II的内含子加工而来,这些内含子来自非蛋白质编码转录本。
Nucleic Acids Res. 2009 Jun;37(10):3464-73. doi: 10.1093/nar/gkp205. Epub 2009 Apr 1.
2
Impact of normalization on miRNA microarray expression profiling.标准化对miRNA微阵列表达谱的影响。
RNA. 2009 Mar;15(3):493-501. doi: 10.1261/rna.1295509. Epub 2009 Jan 28.
3
Chromatin structure analyses identify miRNA promoters.染色质结构分析可鉴定出微小RNA启动子。
Genes Dev. 2008 Nov 15;22(22):3172-83. doi: 10.1101/gad.1706508.
4
Genome-scale spatiotemporal analysis of Caenorhabditis elegans microRNA promoter activity.秀丽隐杆线虫微小RNA启动子活性的全基因组时空分析。
Genome Res. 2008 Dec;18(12):2005-15. doi: 10.1101/gr.083055.108. Epub 2008 Nov 3.
5
MicroRNA (miRNA) cloning analysis reveals sex differences in miRNA expression profiles between adult mouse testis and ovary.微小RNA(miRNA)克隆分析揭示了成年小鼠睾丸和卵巢之间miRNA表达谱的性别差异。
Reproduction. 2008 Dec;136(6):811-22. doi: 10.1530/REP-08-0349. Epub 2008 Sep 4.
6
Highly sensitive and specific microRNA expression profiling using BeadArray technology.使用微珠芯片技术进行高灵敏度和特异性的微小RNA表达谱分析。
Nucleic Acids Res. 2008 Aug;36(14):e87. doi: 10.1093/nar/gkn387. Epub 2008 Jun 25.
7
Normalization of microRNA expression levels in quantitative RT-PCR assays: identification of suitable reference RNA targets in normal and cancerous human solid tissues.定量逆转录聚合酶链反应分析中微小RNA表达水平的标准化:在正常和癌性人类实体组织中鉴定合适的参考RNA靶标
RNA. 2008 May;14(5):844-52. doi: 10.1261/rna.939908. Epub 2008 Mar 28.
8
Reproducibility of microarray data: a further analysis of microarray quality control (MAQC) data.微阵列数据的可重复性:对微阵列质量控制(MAQC)数据的进一步分析。
BMC Bioinformatics. 2007 Oct 25;8:412. doi: 10.1186/1471-2105-8-412.
9
Characterization of microRNA expression profiles in normal human tissues.正常人体组织中微小RNA表达谱的特征分析
BMC Genomics. 2007 Jun 12;8:166. doi: 10.1186/1471-2164-8-166.
10
The multifunctional RNA-binding protein hnRNP A1 is required for processing of miR-18a.多功能RNA结合蛋白hnRNP A1是miR-18a加工所必需的。
Nat Struct Mol Biol. 2007 Jul;14(7):591-6. doi: 10.1038/nsmb1250. Epub 2007 Jun 10.

基于芯片间标准化的共识 miRNA 表达谱。

Consensus miRNA expression profiles derived from interplatform normalization of microarray data.

机构信息

Functional Genomics Unit, Institute of Genomics and Integrative Biology, Council of Scientific and Industrial Research (CSIR), Delhi 110 007, India.

出版信息

RNA. 2010 Jan;16(1):16-25. doi: 10.1261/rna.1688110. Epub 2009 Nov 30.

DOI:10.1261/rna.1688110
PMID:19948767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2802026/
Abstract

Eukaryotic gene expression is controlled at the post-transcriptional level by small noncoding RNAs called microRNAs (miRNA). miRNAs play important roles during early development and participate in gene regulatory circuits in the cell. Different high-throughput expression analysis methods including microarrays, bead-based detection, and small RNA cloning have been applied to quantitatively detect miRNAs in various tissues, cell types, and biological conditions. High-throughput expression data was collected from public repositories and processed to create a database of miRNA expression profiles. Several commonly used normalization methods were compared to identify suitable methods for cross-platform comparison of high-throughput miRNA expression data. The database provides interlaboratory and interplatform validated reference expression levels for miRNAs. The normalized expression profiles were validated by querying for well-established features of miRNA expression. Firstly, expression profiles of several tissue-specific miRNAs showed good agreement between the database and previously reported profiles. We have also identified a set of miRNAs that are constitutively expressed across mammalian tissues. Secondly, we used the database to compare the expression patterns of miRNAs belonging to the let-7 family, where the divergence in expression patterns implies that they may have diversified functionally. Lastly, we compared expression profiles of intronic and clustered miRNAs. Expression profiles of intronic miRNAs and clustered miRNAs showed either very good, or in certain cases, very poor correlation with the host gene. Interplatform comparison of miRNA expression profiles thus provides a resource of consensus expression profiles that can be used in the future for studying miRNA function and regulation.

摘要

真核生物基因表达在转录后水平受到称为 microRNAs (miRNA) 的小非编码 RNA 的调控。miRNA 在早期发育中发挥重要作用,并参与细胞中的基因调控回路。微阵列、基于珠的检测和小 RNA 克隆等不同的高通量表达分析方法已被用于定量检测各种组织、细胞类型和生物条件下的 miRNA。从公共存储库中收集了高通量表达数据,并进行处理以创建 miRNA 表达谱数据库。比较了几种常用的归一化方法,以确定适用于高通量 miRNA 表达数据跨平台比较的方法。该数据库提供了 miRNA 实验室间和平台间验证的参考表达水平。通过查询 miRNA 表达的既定特征来验证归一化表达谱。首先,数据库中几个组织特异性 miRNA 的表达谱与先前报道的表达谱很好地一致。我们还鉴定了一组在哺乳动物组织中持续表达的 miRNA。其次,我们使用该数据库比较了属于 let-7 家族的 miRNA 的表达模式,其中表达模式的差异表明它们可能具有功能多样化。最后,我们比较了内含子和簇 miRNA 的表达谱。内含子 miRNA 和簇 miRNA 的表达谱与宿主基因具有很好的相关性,或者在某些情况下,相关性很差。miRNA 表达谱的跨平台比较因此提供了共识表达谱资源,可用于未来研究 miRNA 功能和调控。