Comparative analysis of internal ribosomal entry sites as molecular tools for bicistronic expression.

No abstract is available for this paper.

• Publication year

  2014

• Venue

  Journal of Biotechnology

• Publication date

  2014-07-10

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/j.jbiotec.2014.03.033PMID 24709397
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• In vitro and in vivo comparison of viral and cellular internal ribosome entry sites for bicistronic vector expression

  2011cited by this paper
• A novel expression system of domain I of human beta2 glycoprotein I in Escherichia coli

  2006cited by this paper
• Translational efficiency of EMCV IRES in bicistronic vectors is dependent upon IRES sequence and gene location.

  2006cited by this paper
• Development of a new bicistronic retroviral vector with strong IRES activity

  2006cited by this paper
• Eukaryotic Translation Initiation Factor 4EAvailability Controls the Switch between Cap-Dependent andInternal Ribosomal Entry Site-MediatedTranslation

  2005cited by this paper
• Noninvasive monitoring of target gene expression by imaging reporter gene expression in living animals using improved bicistronic vectors.

  2005cited by this paper
• Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein

  2004cited by this paper
• High Translation Efficiency Is Mediated by the Encephalomyocarditis Virus Internal Ribosomal Entry Sites if the Natural Sequence Surrounding the Eleventh AUG Is Retained

  2002cited by this paper
• Composition and arrangement of genes define the strength of IRES-driven translation in bicistronic mRNAs.

  2001cited by this paper
• IRES-dependent second gene expression is significantly lower than cap-dependent first gene expression in a bicistronic vector.

  2000cited by this paper
• A 9-nt segment of a cellular mRNA can function as an internal ribosome entry site (IRES) and when present in linked multiple copies greatly enhances IRES activity.

  2000cited by this paper
• The sequence context of the initiation codon in the encephalomyocarditis virus leader modulates efficiency of internal translation initiation

  1992cited by this paper
• Encephalomyocarditis virus 3C protease: efficient cell-free expression from clones which link viral 5' noncoding sequences to the P3 region

  1986cited by this paper
• The nucleotide and deduced amino acid sequences of the encephalomyocarditis viral polyprotein coding region.

  1984cited by this paper
• The initiation of protein synthesis directed by the RNA from encephalomyocarditis virus.

  1973cited by this paper

• Simple improvements in vector design afford substantial gains in AAV delivery of aggregation-slowing Aβ variants

  2024cites this paper
• Cell factory engineering: Challenges and opportunities for synthetic biology applications

  2023cites this paper
• Assessment of the Anti-Amyloidogenic Properties of Essential Oils and Their Constituents in Cells Using a Whole-Cell Recombinant Biosensor

  2023cites this paper
• Reprogramming translation for gene therapy.

  2021cites this paper
• RNA-responsive elements for eukaryotic translational control

  2021cites this paper
• Expression vector cassette engineering for recombinant therapeutic production in mammalian cell systems

  2020cites this paper
• Heads or tails? Differential translational regulation in cercarial heads and tails of schistosome worms

  2019cites this paper
• Vector-related stratagems for enhanced monoclonal antibody production in mammalian cells.

  2019cites this paper
• Metabolic stability and persistence of expression of mRNA for nonviral gene delivery

  2018cites this paper
• HSPC280, a winged helix protein expressed in the subventricular zone of the developing ganglionic eminences, inhibits neuronal differentiation

  2016cites this paper