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177Noa Stern, Dan Thomas Major, Hugo Emilio Gottlieb, Daniel Weizman and Bilha Fischer.
What is the conformation of physiologically-active dinucleoside polyphosphates in solution? Conformational analysis of free dinucleoside polyphosphates by NMR and molecular dynamics simulations, Org. Biomol. Chem., 2010, 8, 4637. Nikolai B. Ulyanov and Thomas L. James.
RNA structural motifs that entail hydrogen bonds involving sugar–phosphate backbone atoms of RNA, New J. Chem., 2010, 34, 910. Katarzyna Wrobel, Crescencio Rodríguez Flores, Qilin Chan and Kazimierz Wrobel.
Ribonucleoside labeling with Os(vi): A methodological approach to evaluation of RNA methylation by HPLC-ICP-MS, Metallomics, 2010, 2, 140. Gaku Fukuhara and Yoshihisa Inoue.
Oligosaccharide sensing with chromophore-modified curdlan in aqueous media, Chem. Commun., 2010, 46, 9128. Johan Sjöström, Johan Mattsson, Rikard Bergman, Erik Johansson, Karin Josefsson, David Svantesson and Jan Swenson.
Dielectric secondary relaxation of water in aqueous binary glass-formers, Phys. Chem. Chem. Phys., 2010, 12, 10452. Dorota A. Adamiak, Jan Milecki, Ryszard W. Adamiak and Wojciech Rypniewski.
The hydration and unusual hydrogen bonding in the crystal structure of an RNA duplex containing alternating CG base pairs, New J. Chem., 2010, 34, 903. Ian R. Greig.
The analysis of enzymic free energy relationships using kinetic and computational models, Chem. Soc. Rev., 2010, 39, 2272. Alfonso Fernández-Botello, Bert P. Operschall, Antonín Holy, Virtudes Moreno and Helmut Sigel.
Metal ion-binding properties of 9-[(2-phosphonomethoxy)ethyl]-2-aminopurine (PME2AP), an isomer of the antiviral nucleotide analogue 9-[(2-phosphonomethoxy)ethyl]adenine (PMEA). Steric guiding of metal ion-coordination by the purine-amino group, Dalton Trans., 2010, 39, 6344. Takashi Kobayashi, Hikaru Kuramochi, Tadashi SuzukiCurrent address: Department of Chemistry and Biological Science, Aoyama Gakuin University, Fuchinobe, Sagamihara-shi, Kanagawa 229-8558, Japan. and Teijiro Ichimura.
Triplet formation of 6-azauridine and singlet oxygen sensitization with UV light irradiation, Phys. Chem. Chem. Phys., 2010, 12, 5140.