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Drug Target miRNA

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Cover of 'Drug Target miRNA'

Table of Contents

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    Book Overview
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    Chapter 1 miRNA Targeting Drugs: The Next Blockbusters?
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    Chapter 2 Functional Analysis of miRNAs Using the DIANA Tools Online Suite.
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    Chapter 3 Non-nucleotide Modification of Anti-miRNA Oligonucleotides.
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    Chapter 4 Quantification of Oligonucleotide Association with miRNA-Argonaute Complexes In Vitro.
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    Chapter 5 Determination of Anti-miR Association with miRNA/Argonaute Complexes In Vivo.
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    Chapter 6 Competitive Argonaute-Based RNA Immunoprecipitation for Investigation of Transcriptomic Response to Anti-miR.
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    Chapter 7 Assessing Anti-miR Pharmacology with miRNA Polysome Shift Assay.
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    Chapter 8 Evaluating Synergistic Effects of miR-34a Mimics in Combination with Other Therapeutic Agents in Cultured Non-Small Cell Lung Cancer Cells.
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    Chapter 9 Assessing the Off-Target Effects of miRNA Inhibitors on Innate Immune Toll-Like Receptors.
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    Chapter 10 Design of Multimodal Small Molecules Targeting miRNAs Biogenesis: Synthesis and In Vitro Evaluation.
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    Chapter 11 Machine Learning Approaches Toward Building Predictive Models for Small Molecule Modulators of miRNA and Its Utility in Virtual Screening of Molecular Databases.
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    Chapter 12 Identification of Small Molecule Modulators of MicroRNA by Library Screening.
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    Chapter 13 Rapid Generation of miRNA Inhibitor Leads by Bioinformatics and Efficient High-Throughput Screening Methods.
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    Chapter 14 Drug Target miRNA
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    Chapter 15 Small Molecules Targeting the miRNA-Binding Domain of Argonaute 2: From Computer-Aided Molecular Design to RNA Immunoprecipitation.
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    Chapter 16 Surface Plasmon Resonance: A Useful Strategy for the Identification of Small Molecule Argonaute 2 Protein Binders.
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    Chapter 17 Antagonists of the miRNA-Argonaute 2 Protein Complex: Anti-miR-AGOs.
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    Chapter 18 Elucidating Mechanisms of Molecular Recognition Between Human Argonaute and miRNA Using Computational Approaches.
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    Chapter 19 Kinetic Analysis of Target RNA Binding and Slicing by Human Argonaute 2 Protein.
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    Chapter 20 Site-Specific Fluorescent Labeling of Argonaute for FRET-Based Bio-Assays.
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    Chapter 21 Single-Molecule Fluorescence Energy Transfer Assays for the Characterization of Reaction Pathways of miRNA-Argonaute Complex.
Attention for Chapter 2: Functional Analysis of miRNAs Using the DIANA Tools Online Suite.
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Chapter title
Functional Analysis of miRNAs Using the DIANA Tools Online Suite.
Chapter number 2
Book title
Drug Target miRNA
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6563-2_2
Pubmed ID
Book ISBNs
978-1-4939-6561-8, 978-1-4939-6563-2
Authors

Ioannis S. Vlachos, Artemis G. Hatzigeorgiou

Editors

Marco F. Schmidt

Abstract

microRNAs (miRNAs) are central regulators of gene expression. They are actively studied for their involvement in numerous physiological and pathological conditions but also as diagnostic biomarkers or promising therapeutic targets. The increased complexity of the miRNA interactomes hinders straightforward interpretation of miRNA expression differences between states and conditions. To this end, functional analysis web servers process and combine experimental and in silico data, enabling researchers to uncover targeted pathways and transcriptional mechanisms that are hidden within numerous interactions and vast expression datasets. DIANA-tools ( www.microrna.gr ) is a web server hosting state-of-the-art utilities and databases for miRNA functional investigation. Available utilities cover a wide scope of different needs and research scenarios, rendering DIANA website a one-stop-shop for miRNA analyses. The most commonly utilized databases and algorithms include DIANA-microT-CDS, DIANA-TarBase v7.0, DIANA-lncBase v2.0, DIANA-miRGen v3.0, DIANA-miRPath v3.0, and DIANA-mirExTra v2.0.In the presented protocol, we will utilize different online tools in order to explore miRNA functions and to identify probable targets of interest for downstream analyses and wet lab experiments. The combined use of different applications from the DIANA suite can shed light to numerous different aspects of miRNA regulation and regulatory function, without the necessity for extensive bioinformatics expertise or computational infrastructure.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 37 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 3%
Unknown 36 97%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 22%
Student > Ph. D. Student 6 16%
Student > Bachelor 4 11%
Other 2 5%
Unspecified 2 5%
Other 5 14%
Unknown 10 27%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 19%
Agricultural and Biological Sciences 4 11%
Computer Science 3 8%
Medicine and Dentistry 3 8%
Unspecified 2 5%
Other 7 19%
Unknown 11 30%