Results 161 to 170 of about 11,432 (197)
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Enantio-oligodeoxyribonucleotides.
Nucleic acids symposium series, 1991As a sugar-modified oligonucleotide, a hexamer of 9-(2-deoxy-beta-L-erythro-pentafuranosyl)-9H-purin-6-amine, [L-(dAp)5dA], was synthesized by triester method. The L-hexamer was resistant to bovine spleen phosphodiesterase. UV absorption studies indicated that L-hexamer formed a complex with poly U but not with poly dT at 0 degrees C.
S, Fujimori, K, Shudo, Y, Hashimoto
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Structural requirements and applications of inhibitory oligodeoxyribonucleotides
Immunologic Research, 2007Synthetic oligodeoxyribonucleotides (ODN) bearing certain sequence characteristics mimic bacterial DNA by activating B cells and dendritic cells through Toll-like receptor (TLR) 9, an event that potentiates both humoral and cell-mediated immunity. ODN sharing some of the sequence characteristics of strong stimulatory (ST-) ODN, but substituting GGG for
Robert F, Ashman, Petar, Lenert
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Phosphite Synthesis of Oligodeoxyribonucleotides
Russian Chemical Reviews, 1988Data in the literature published between 1983 and 1986 on the synthesis of oligodeoxyribonucleotides from nucleoside derivatives of phosphorous acid are reviewed. Attention is mainly focused on the techniques employed for preparing initial monomers for condensation.
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Internalization of Oligodeoxyribonucleotides by Vibrio parahaemolyticus
Antisense Research and Development, 1993The bacterium Vibrio parahaemolyticus was tested for its ability to internalize unmodified as well as modified DNA oligomers without attempting to permeabilize the cells. These experiments were conducted to establish whether it may be feasible to employ antisense oligomers for control of gene expression in Vibrio species without heat-shocking or ...
L A, Chrisey +3 more
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The automated synthesis of oligodeoxyribonucleotides
Trends in Biotechnology, 1985Abstract Progress in science is a history of the synergistic relationship between technology and theory: growth in theoretical understanding requires and initiates technological change; technological advance opens up new areas of knowledge. The history of molecular genetics is but a single illustration of this process.
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Solid phase synthesis of cyclic oligodeoxyribonucleotides.
Tetrahedron Letters, 1987Abstract The polymer supported synthesis of cyclic oligomers of deoxycytidilic acid is described, by a method based on an oligonucleotide-solid phase linkage through the amino group of the base.
S. BARBATO +4 more
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Synthesis of Oligodeoxyribonucleotides Containing Oleylamine Moieties
Russian Journal of Bioorganic Chemistry, 2001A method for directional introduction of oleylamine residues to any position of oligodeoxyribonucleotides during their automated synthesis was developed. The presence of oleylamine residues in 3'- or 5'-terminal nucleotides was shown to have no effect on the thermodynamic stability of DNA duplexes formed by such oligonucleotides and the complementary ...
S Iu, Andreev +5 more
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Synthesis and Biochemical Evaluation of Phosphonoformate Oligodeoxyribonucleotides
Journal of the American Chemical Society, 2006Phosphonoformate oligodeoxyribonucleotides were prepared via a solid phase synthesis strategy. The first step in the preparation of appropriate synthons was condensation of bis(N,N-diisopropylamino)phosphine and diphenylmethylsilylethyl chloroformate in the presence of sodium metal to yield formic acid, [bis(N,N-diisopropylamino)phosphino]-beta ...
Christina M, Yamada +2 more
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Random mutagenesis using degenerate oligodeoxyribonucleotides
Gene, 1988An efficient method for random mutagenesis was applied to a 75-bp target sequence. The mutational changes in the target region are introduced by the technique of oligodeoxyribonucleotide(oligo)-directed, site-specific mutagenesis using mixtures of degenerate oligos.
Hübner P, Iida S, Arber W
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Use of an aminooxy linker for the functionalization of oligodeoxyribonucleotides
Bioorganic & Medicinal Chemistry Letters, 2001We describe the preparation of oligonucleotides containing a 5'-linker bearing an aminooxy group. Use of the trityl protecting group for the aminooxy moiety allows purification of the modified oligonucleotide by reverse phase HPLC and cleavage in mild acidic conditions. Derivatization with an aldehydic reporter group is efficient and rapid.
E, Defrancq, J, Lhomme
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