Mesyl phosphoramidate antisense oligonucleotides as an alternative to phosphorothioates with improved biochemical and biological properties (original ) (raw )Modified oligonucleotides: IV solid phase synthesis and preliminary evaluation of phosphorothioate RNA as potential antisense agents
Francois Morvan
Tetrahedron Letters, 1990
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The therapeutic potential of antisense oligonucleotides
Ramaswamy Narayanan
BioEssays, 1995
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RNase H-independent antisense activity of oligonucleotide N34P54 phosphoramidates
Sergei Gryaznov
Nucleic Acids Research - NAR
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Mixed-Backbone oligonucleotides as second-generation antisense agents with reduced phosphorothioate-related side effects
Carl Saxinger
Bioorganic & Medicinal Chemistry Letters, 1998
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Mesyl Phosphoramidate Oligonucleotides: A New Promising Type of Antisense Agents
Dmitry Stetsenko
2023
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Mixed backbone antisense oligonucleotides: design, biochemical and biological properties of oligonucleotides containing 24-54-ribo- and 34-54-deoxyribonucleotide segments
adrienne manning
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Mesyl phosphoramidate backbone modified antisense oligonucleotides targeting miR-21 with enhanced in vivo therapeutic potency
Valentin Vlasov
Proceedings of the National Academy of Sciences of the United States of America, 2020
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Oligonucleotide N3'-->P5' phosphoramidates as antisense agents
Sergei Gryaznov
Nucleic Acids Research, 1996
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Abstracts from the Fourth Annual NIH Symposium on Therapeutic Oligonucleotides: Antisense and DNA Chips
Igor Panyutin
Antisense and Nucleic Acid Drug Development, 2000
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Therapeutic implications of antisense oligonucleotides
M. Mazzei
International Journal of Clinical & Laboratory Research, 1992
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Antisense oligodeoxynucleotides: synthesis, biophysical and biological evaluation of oligodeoxynucleotides containing modified pyrimidines
Yogesh Sanghvi
Nucleic Acids Research, 1993
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Antisense Oligonucleotides, A Novel Developing Targeting Therapy
Palma Rocchi
Antisense Therapy [Working Title]
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Partial protection of oncogene, anti-sense oligodeoxynucleotides against serum nuclease degradation using terminal methylphosphonate groups
Hilmar Warenius
British journal of cancer, 1989
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Antisense Oligonucleotides: An Emerging Area in Drug Discovery and Development
Karishma Dhuri
Journal of Clinical Medicine
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Nuclear antisense effects of neutral, anionic and cationic oligonucleotide analogs
Ryszard Kole
Nucleic acids research, 2001
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The Combination of Mesyl-Phosphoramidate Inter-Nucleotide Linkages and 2′-O-Methyl in Selected Positions in the Antisense Oligonucleotide Enhances the Performance of RNaseH1 Active PS-ASOs
Lingdi Zhang
Nucleic Acid Therapeutics
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Comparison of different antisense strategies in mammalian cells using locked nucleic acids, 2'-O-methyl RNA, phosphorothioates and small interfering RNA
Jens Kurreck
Nucleic Acids Research, 2003
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Comparative inhibition of chloramphenicol acetyltransferase gene expression by antisense oligonucleotide analogues having alkyl phosphotriester, methylphosphonate and phosphorothioate linkages
Gerald Zon
Nucleic Acids Research, 1987
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Therapeutic antisense oligonucleotides against cancer: hurdling to the clinic
Pedro Moreno
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In vitro and in vivo properties of therapeutic oligonucleotides containing non-chiral 3′ and 5′ thiophosphate linkages
Erich Koller
Nucleic Acids Research, 2019
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Potent and nontoxic antisense oligonucleotides containing locked nucleic acids
Michael Ossipov
Proceedings of The National Academy of Sciences, 2000
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Antisense Oligonucleotides Containing Conformationally Constrained 2′,4′-( N Methoxy)aminomethylene and 2′,4′-Aminooxymethylene and 2′- O ,4′- C -Aminomethylene Bridged Nucleoside Analogues Show Improved Potency in Animal Models
Chris Black
Journal of Medicinal Chemistry, 2010
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Short Antisense Oligonucleotides with Novel 2′−4′ Conformationaly Restricted Nucleoside Analogues Show Improved Potency without Increased Toxicity in Animals
Guillermo Vasquez
Journal of Medicinal Chemistry, 2009
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Synthesis, biophysical properties and biological activity of second generation antisense oligonucleotides containing chiral phosphorothioate linkages
sam lee
Nucleic Acids Research, 2014
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Antisense oligonuclotides with oxetane-constrained cytidine enhance heteroduplex stability, and elicit satisfactory RNase H response as well as showing improved resistance to both exo and endonucleasesElectronic supplementary information (ESI) available: RNA cleavage kinetics. See http://www.rsc....
Jyoti Chattopadhyaya
Organic & Biomolecular Chemistry, 2002
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Oxetane modified, conformationally constrained, antisense oligodeoxyribonucleotides function efficiently as gene silencing molecules
Cezary Swider
Nucleic Acids Research, 2004
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