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Results: 1-17 |
Results: 17

Authors: Torigoe, H Obika, S Imanishi, T
Citation: H. Torigoe et al., Promotion of triplex formation by 2 '-O,4 '-C-methylene bridged nucleic acid (2 ',4 '-BNA) modification: Thermodynamic and kinetic studies, NUCLEOS NUC, 20(4-7), 2001, pp. 1235-1238

Authors: Obika, S Hari, Y Sekiguchi, M Imanishi, T
Citation: S. Obika et al., A 2',4'-bridged nucleic acid containing 2-pyridone as a nucleobase: Efficient recognition of a C center dot G interruption by tripler formation with a pyrimidine motif, ANGEW CHEM, 40(11), 2001, pp. 2079-2081

Authors: Obika, S Onoda, M Morita, K Andoh, J Koizumi, M Imanishi, T
Citation: S. Obika et al., 3 '-Amino-2 ',4 '-BNA: novel bridged nucleic acids having an N3 '-> P5 ' phosphoramidate linkage, CHEM COMMUN, (19), 2001, pp. 1992-1993

Authors: Obika, S Uneda, T Sugimoto, T Nanbu, D Minami, T Doi, T Imanishi, T
Citation: S. Obika et al., 2 '-O,4 '-C-methylene bridged nucleic acid (2 ',4 '-BNA): Synthesis and triplex-forming properties, BIO MED CH, 9(4), 2001, pp. 1001-1011

Authors: Obika, S Yu, W Shimoyama, A Uneda, T Miyashita, K Doi, T Imanishi, T
Citation: S. Obika et al., Symmetrical cationic triglycerides: An efficient synthesis and applicationto gene transfer, BIO MED CH, 9(2), 2001, pp. 245-254

Authors: Torigoe, H Hari, Y Sekiguchi, M Obika, S Imanishi, T
Citation: H. Torigoe et al., 2 '-O,4 '-C-methylene bridged nucleic acid modification promotes pyrimidine motif tripler DNA formation at physiological pH - Thermodynamic and kinetic studies, J BIOL CHEM, 276(4), 2001, pp. 2354-2360

Authors: Obika, S Hari, Y Sugimoto, T Sekiguchi, M Imanishi, T
Citation: S. Obika et al., Triplex-forming enhancement with high sequence selectivity by single 2 '-O,4 '-C-methylene bridged nucleic acid (2 ',4 '-BNA) modification, TETRAHEDR L, 41(46), 2000, pp. 8923-8927

Authors: Obika, S Hari, Y Morio, K Imanishi, T
Citation: S. Obika et al., Synthesis of conformationally locked C-nucleosides having a 2,5-dioxabicyclo[2.2.1]heptane ring system, TETRAHEDR L, 41(2), 2000, pp. 215-219

Authors: Obika, S Hari, Y Morio, K Imanishi, T
Citation: S. Obika et al., Tripler formation by an oligonucleotide containing conformationally lockedC-nucleoside, 5-(2-O,4-C-methylene-beta-D-ribofuranosyl)oxazole, TETRAHEDR L, 41(2), 2000, pp. 221-224

Authors: Obika, S
Citation: S. Obika, Syntheses and properties of conformationally restrained nucleosides and oligonucleotides analogues, YAKUGAKU ZA, 120(2), 2000, pp. 147-158

Authors: Obika, S Morio, K Hari, Y Imanishi, T
Citation: S. Obika et al., Facile synthesis and conformation of 3 '-O,4 '-C-methyleneribonucleosides, CHEM COMMUN, (23), 1999, pp. 2423-2424

Authors: Obika, S Morio, K Hari, Y Imanishi, T
Citation: S. Obika et al., Preparation and properties of 2 ',5 '-linked oligonucleotide analogues containing 3 '-O,4 '-C-methyleneribonucleosides, BIOORG MED, 9(4), 1999, pp. 515-518

Authors: Obika, S Yu, W Shimoyama, A Uneda, T Minami, T Miyashita, K Doi, T Imanishi, T
Citation: S. Obika et al., Properties of cationic liposomes composed of cationic lipid YKS-220 havingan ester linkage: Adequate stability, high transfection efficiency, and low cytotoxicity, BIOL PHAR B, 22(2), 1999, pp. 187-190

Authors: Obika, S Andoh, J Sugimoto, T Miyashita, K Imanishi, T
Citation: S. Obika et al., Synthesis of a conformationally locked AZT analogue, 3 '-azido-3 '-deoxy-2'-O,4 '-C-methylene-5-methyluridine, TETRAHEDR L, 40(35), 1999, pp. 6465-6468

Authors: Imanishi, T Obika, S
Citation: T. Imanishi et S. Obika, Syntheses and properties of novel conformationally restrained nucleoside analogues, J SYN ORG J, 57(11), 1999, pp. 969-980

Authors: Yu, W Shimoyama, A Uneda, T Obika, S Miyashita, K Doi, T Imanishi, T
Citation: W. Yu et al., Gene transfer mediated by YKS-220 cationic particles: Convenient and efficient gene delivery reagent, J BIOCHEM, 125(6), 1999, pp. 1034-1038

Authors: Obika, S Nishiyama, T Tatematsu, S Nishimoto, M Miyashita, K Imanishi, T
Citation: S. Obika et al., Studies on novel and chiral 1,4-dihydropyridines. VI. Preparation of a polymer-supported 1,4-dihydropyridine having a chiral sulfinyl group and its application to biomimetic reduction, HETEROCYCLE, 49, 1998, pp. 261-267
Risultati: 1-17 |