Redesigning nucleic acids

التفاصيل البيبلوغرافية
العنوان: Redesigning nucleic acids
المؤلفون: Heike A. Held, J. J. Vögel, Andrew L. Roughton, Thomas R. Battersby, J. T. Kodra, Michael J. Lutz, Joseph Stackhouse, Krishnan P. Nambiar, Daniel Hutter, Klaus Schneider, Martin Egli, Joseph A. Piccirilli, Christophe Hammer, Simon E. Moroney, Steven A. Benner, Jennifer Horlacher, L. J. MacPherson, U. von Krosigk, Tuncer Arslan, D. K. Bäschlin, Clemens Richert, Jurgen G. Schmidt, Stefan Lutz, Simona C. Jurczyk, Bernd Eschgfäller, Christopher Switzer, Thomas F. Jenny, E. Müller, H. A. König, M. Blättler, Birgitte Hyrup, Zh. Huang
المصدر: Pure and Applied Chemistry. 70:263-266
بيانات النشر: Walter de Gruyter GmbH, 1998.
سنة النشر: 1998
مصطلحات موضوعية: Molecular Structure, Oligonucleotide, Chemistry, General Chemical Engineering, Oligonucleotides, RNA, DNA, General Chemistry, Computational biology, Catalysis, Phosphates, chemistry.chemical_compound, Nucleic Acids, Nucleic acid, Organic chemistry, Sulfones, Codon, Molecular Biology
الوصف: A research program has applied the tools of synthetic organic chemistry to systematically modify the structure of DNA and RNA oligonucleotides to learn more about the chemical principles underlying their ability to store and transmit genetic information. Oligonucleotides (as opposed to nucleosides) have long been overlooked by synthetic organic chemists as targets for structural modification. Synthetic chemistry has now yielded oligonucleotides with 12 replicatable letters, modified backbones, and new insight into why Nature chose the oligonucleotide structures that she did.
تدمد: 1365-3075
0033-4545
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b940b7d75ddb946ff93654a2ab04b0c1
https://doi.org/10.1351/pac199870020263
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....b940b7d75ddb946ff93654a2ab04b0c1
قاعدة البيانات: OpenAIRE