Literature DB >> 14647331

Approaches for the sequence-specific knockdown of mRNA.

Lisa J Scherer1, John J Rossi.   

Abstract

Over the past 25 years there have been thousands of published reports describing applications of antisense nucleic acid derivatives for targeted inhibition of gene function. The major classes of antisense agents currently used by investigators for sequence-specific mRNA knockdowns are antisense oligonucleotides (ODNs), ribozymes, DNAzymes and RNA interference (RNAi). Whatever the method, the problems for effective application are remarkably similar: efficient delivery, enhanced stability, minimization of off-target effects and identification of sensitive sites in the target RNAs. These challenges have been in existence from the first attempts to use antisense research tools, and need to be met before any antisense molecule can become widely accepted as a therapeutic agent.

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Year:  2003        PMID: 14647331     DOI: 10.1038/nbt915

Source DB:  PubMed          Journal:  Nat Biotechnol        ISSN: 1087-0156            Impact factor:   54.908


  122 in total

1.  siRNA-aptamer chimeras on nanoparticles: preserving targeting functionality for effective gene silencing.

Authors:  Vaishali Bagalkot; Xiaohu Gao
Journal:  ACS Nano       Date:  2011-09-21       Impact factor: 15.881

2.  Efficient RNA interference depends on global context of the target sequence: quantitative analysis of silencing efficiency using Eulerian graph representation of siRNA.

Authors:  Petr Pancoska; Zdenek Moravek; Ute M Moll
Journal:  Nucleic Acids Res       Date:  2004-03-01       Impact factor: 16.971

3.  Surfection: a new platform for transfected cell arrays.

Authors:  Fu-Hsiung Chang; Chien-Hsin Lee; Ming-Ta Chen; Chun-Chen Kuo; Yi-Lin Chiang; Chi-Ying Hang; Steve Roffler
Journal:  Nucleic Acids Res       Date:  2004-02-18       Impact factor: 16.971

Review 4.  RNA-based therapeutics: current progress and future prospects.

Authors:  John C Burnett; John J Rossi
Journal:  Chem Biol       Date:  2012-01-27

5.  siRNAs target sites selection of ezrin and the influence of RNA interference on ezrin expression and biological characters of osteosarcoma cells.

Authors:  XiFu Shang; YaoFei Wang; QiChun Zhao; KeRong Wu; Xu Li; XiaoFeng Ji; Rui He; WenZhi Zhang
Journal:  Mol Cell Biochem       Date:  2012-05       Impact factor: 3.396

6.  NPAS1 regulates branching morphogenesis in embryonic lung.

Authors:  Bernadette M Levesque; Shutang Zhou; Lin Shan; Pamela Johnston; Yanping Kong; Simone Degan; Mary E Sunday
Journal:  Am J Respir Cell Mol Biol       Date:  2006-11-16       Impact factor: 6.914

7.  RNAi-mediated silencing of the myo-inositol-1-phosphate synthase gene (GmMIPS1) in transgenic soybean inhibited seed development and reduced phytate content.

Authors:  Aline C S Nunes; Giovanni R Vianna; Florencia Cuneo; Jaime Amaya-Farfán; Guy de Capdeville; Elíbio L Rech; Francisco J L Aragão
Journal:  Planta       Date:  2006-01-04       Impact factor: 4.116

8.  Triple combination of siRNAs targeting TGFβ1, TGFβR2, and CTGF enhances reduction of collagen I and smooth muscle actin in corneal fibroblasts.

Authors:  Sriniwas Sriram; Paulette Robinson; Liya Pi; Alfred S Lewin; Gregory Schultz
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-12-17       Impact factor: 4.799

9.  Triblock copolymer-encapsulated nanoparticles with outstanding colloidal stability for siRNA delivery.

Authors:  Jian Qian; Xiaohu Gao
Journal:  ACS Appl Mater Interfaces       Date:  2013-01-15       Impact factor: 9.229

10.  Effective inhibition in animals of viral pathogenesis by a ribozyme derived from RNase P catalytic RNA.

Authors:  Yong Bai; Phong Trang; Hongjian Li; Kihoon Kim; Tianhong Zhou; Fenyong Liu
Journal:  Proc Natl Acad Sci U S A       Date:  2008-07-28       Impact factor: 11.205

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