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Journal ArticleDOI

Morpholino antisense oligomers: the case for an RNase H-independent structural type.

James Summerton
- 10 Dec 1999 - 
- Vol. 1489, Iss: 1, pp 141-158
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TLDR
In cell-free and cultured-cell systems where one wishes to block the translation of a messenger RNA coding for a normal protein, RNase H-independent morpholino antisense oligos provide complete resistance to nucleases, generally good targeting predictability, generally high in-cell efficacy, excellent sequence specificity, and very preliminary results suggest they may exhibit little non-antisense activity.
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This article is published in Biochimica et Biophysica Acta.The article was published on 1999-12-10. It has received 689 citations till now. The article focuses on the topics: RNase P & RNase H.

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Citations
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Journal ArticleDOI

Inhibition of enterovirus 71 infection by antisense octaguanidinium dendrimer-conjugated morpholino oligomers

TL;DR: It is suggested that IRES-targeting vivo- MOs are good antiviral candidates for treating early EV-71 infection, and vivo-MO-2 is a more favorable candidate with broader antiviral spectrum against enteroviruses and are refractory to antiviral resistance.
Journal ArticleDOI

Innovative Therapeutic and Delivery Approaches Using Nanotechnology to Correct Splicing Defects Underlying Disease

TL;DR: This review focuses primarily on therapeutic approaches targeting splicing, and highlights nanotechnology-based gene delivery applications that address the challenges and barriers facing nucleic acid-based therapeutics.
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RNA-Targeting Splicing Modifiers: Drug Development and Screening Assays

TL;DR: A review of RNA splicing modifiers can be found in this article, where the authors discuss the role of small molecules as important warheads in the arsenal for regulating the splicing of essential pathogenic genes.
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Vertebrate homologues of Frodo are dynamically expressed during embryonic development in tissues undergoing extensive morphogenetic movements.

TL;DR: Highly conserved dynamic expression patterns of Frodo homologues indicate a similar function for these proteins in different vertebrates.
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The zebrafish band 4.1 member Mir is involved in cell movements associated with gastrulation.

TL;DR: Results indicate that Mir is essential for embryonic development and that its role in early embryonic development likely involves calcium-dependent mechanisms essential during the extensive cell movements associated with gastrulation.
References
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Journal ArticleDOI

Cpg motifs in bacterial dna trigger direct b-cell activation

TL;DR: The potent immune activation by CpG oligon nucleotides has impli-cations for the design and interpretation of studies using 'antisense' oligonucleotides and points to possible new applications as adjuvants.
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The third helix of the Antennapedia homeodomain translocates through biological membranes

TL;DR: It is reported here that a polypeptide of 16 amino acids in length corresponding to the third helix of the homeodomain deleted of its N-terminal glutamate is still capable of translocating through the membrane, suggesting an energy-independent mechanism of translocation not involving classical endocytosis.
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Morpholino antisense oligomers: design, preparation, and properties.

TL;DR: An overview of the design, preparation, and properties of Morpholino oligos, a novel antisense structural type that solves the sequence specificity problem and provides high and predictable activity in cells.
Journal ArticleDOI

Intercellular trafficking and protein delivery by a herpesvirus structural protein.

Gillian Elliott, +1 more
- 24 Jan 1997 - 
TL;DR: It is shown that the HSV-1 structural protein VP22 has the remarkable property of intercellular transport, which is so efficient that following expression in a subpopulation the protein spreads to every cell in a monolayer, where it concentrates in the nucleus and binds chromatin.
Journal ArticleDOI

Evaluation of 2'-modified oligonucleotides containing 2'-deoxy gaps as antisense inhibitors of gene expression

TL;DR: The use of a previously described 17-mer phosphorothioate for structure-function analysis of 2'-sugar modifications and the results demonstrate the importance of target affinity in the action of antisense oligonucleotides and of RNase H as a mechanism by which these compounds exert their effects.
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