Therapeutic applications of ribozymes and riboswitches : methods and protocols /
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Imprint: | New York : Humana Press, [2014] ©2014 |
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Description: | 1 online resource (xi, 278 pages) : illustrations (some color) |
Language: | English |
Series: | Methods in Molecular Biology, 1940-6029 ; 1103 Methods in molecular biology (Clifton, N.J.) ; v. 1103. |
Subject: | |
Format: | E-Resource Book |
URL for this record: | http://pi.lib.uchicago.edu/1001/cat/bib/11219868 |
Table of Contents:
- Identification of regulatory RNA in bacterial genomes by genome-scale mapping of transcription start sites
- Screening inhibitory potential of anti-HIV RT RNA aptamers
- Design and evaluation of clinically relevant SOFA-HDV ribozymes targeting HIV RNA
- Directing RNase P-mediated cleavage of target mRNAs by engineered external guide sequences in cultured cells
- Design and analysis of hammerhead ribozyme activity against an artificial gene target
- Knockdown strategies for the study of proprotein convertases and proliferation in prostate cancer cells
- Use of tumor-targeting trans-splicing ribozyme for cancer treatment
- Characterization of hairpin ribozyme reactions
- Finding instances of riboswitches and ribozymes by homology search of structured RNA with infernal
- Structure-based virtual screening for the identification of RNA- binding ligands
- Probing riboswitch binding sites with molecular docking, focused libraries, and in-line probing assays
- Discovery of small molecule modifiers of micrornas for the treatment of HCV infection
- Bacterial flavin mononucleotide riboswitches as targets for flavin analogs
- Construction and application of riboswitch-based sensors that detect metabolites within bacterial cells
- Screening assays to identify artificial glmS ribozyme activators
- Analysis of riboswitch structure and ligand binding using small-angle X-ray scattering (SAXS)
- Use of SHAPE to select 2AP substitution sites for RNA-ligand interactions and dynamics studies
- Cell internalization SELEX: In vitro selection for molecules that internalize into cells
- DNA electronic switches based on analyte-responsive aptamers.