Zobrazeno 1 - 5
of 5
pro vyhledávání: '"F. P. R. Nilson"'
Publikováno v:
Journal of Biochemical and Biophysical Methods. 26:1-26
Pure 1'#,2',3',4'#,5',5''-2H6-ribonucleoside derivatives 10-14, 1'#,2',2'',3',4'#,5',5''-2H7-2'-deoxynucleoside blocks 15-18 and their natural-abundance counterparts were used to assemble partially deuterated ribonucleotide-dimers (* indicates deuter
Publikováno v:
ChemInform. 24
Autor:
Tatiana Maltseva, S.-I. Yamakage, C. Glemarec, A. Foeldesi, F. P. R. Nilson, Jyoti Chattopadhyaya
Publikováno v:
ChemInform. 28
Autor:
F. P. R. Nilson, András Földesi, Tatiana Maltseva, Jyoti Chattopadhyaya, S.-I. Yamakage, P. Agback
Publikováno v:
Scopus-Elsevier
Selective incorporation of the stereospecifically deuteriated sugar moieties (> 97 atom % 2H enhancements at H2', H2'', H3' and H5'/5'' sites, approximately 85 atom % 2H enhancement at H4' and approximately 20 atom % 2H enhancement at H1') in DNA and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9ee5343a0d3b70236c13b9a2d798dd8
https://europepmc.org/articles/PMC307998/
https://europepmc.org/articles/PMC307998/
Autor:
Tatiana Maltseva, András Földesi, F. P. R. Nilson, Jyoti Chattopadhyaya, C. Glemarec, S.-I. Yamakage
Publikováno v:
Scopus-Elsevier
The present state-of-the-art of the Uppsala “NMR-window” concept (see refs 1-4, 7-8 & 10-11) developed for the high-field NMR conformational studies on the solution structure of large, biologically functional DNAs and RNAs is summarised. The use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c62aa15025d353b57fa6cd99b82c4e3b
http://www.scopus.com/inward/record.url?eid=2-s2.0-0030820558&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0030820558&partnerID=MN8TOARS