Antisense oligodeoxynucleotides: synthesis, biophysical and biological evaluation of oligodeoxynucleotides containing modified pyrimidines (original) (raw)
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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Antisense oligonuclotides with oxetane-constrained cytidine enhance heteroduplex stability, and elicit satisfactory RNase H response as well as showing improved …
Jyoti Chattopadhyaya
Org. Biomol. Chem …, 2002
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Oxetane modified antisense oligonucleotides promote RNase H cleavage of the complementary RNA strand in the hybrid duplex as efficiently as the native, and offer improved endonuclease resistance
Jyoti Chattopadhyaya
Journal of the Chemical Society, Perkin Transactions 2, 2001
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Chemically modified oligonucleotides with efficient RNase H response
Patrick Hrdlicka
Bioorganic & Medicinal Chemistry Letters, 2008
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2'-O-[2-[(N,N-dimethylamino)oxy]ethyl]-modified oligonucleotides inhibit expression of mRNA in vitro and in vivo
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Ramon Eritja
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Studies of a Chemically Modified Oligodeoxynucleotide Containing a 5-ATOM Amide Backbone Which Exhibits Improved Binding to Rna
George Minasov
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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
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Tetrahedron Letters, 1994
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Oxetane modified, conformationally constrained, antisense oligodeoxyribonucleotides function efficiently as gene silencing molecules
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2‘- O -[2-(Methylthio)ethyl]-Modified Oligonucleotide: An Analogue of 2‘- O -[2-(Methoxy)-ethyl]-Modified Oligonucleotide with Improved Protein Binding Properties and High Binding Affinity to Target RNA †
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Synthesis, Hybridization, and Nuclease Resistance Properties of 2'-O-AMINOOXYETHYL Modified Oligonucleotides
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Targeting RNA for Degradation with a (2', 5')-Oligoadenylate Antisense Chimera
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Functionalization of the 3′-Ends of DNA and RNA Strands with N-ethyl-N-coupled Nucleosides: A Promising Approach To Avoid 3′-Exonuclease-Catalyzed Hydrolysis of Therapeutic Oligonucleotides
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Antisense Recognition of the HER-2 mRNA: Effects of Phosphorothioate Substitution and Polyamines on DNA·RNA, RNA·RNA, and DNA·DNA Duplex Stability †
veena vijayanathan
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