Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jong Jin Ro"'
Autor:
Anders Dahlén, Byeang Hyean Kim, Anita C. Jones, Tom Brown, Moa Sandberg Wranne, Mattias Bood, Anders Foller Füchtbauer, Déborah L M Rupert, Rachel S. Fisher, Morten Grøtli, Fredrik Höök, Sangamesh Sarangamath, Marcus Wilhelmsson, Steven W. Magennis, Jong Jin Ro, Afaf H. El-Sagheer
Publikováno v:
Bood, M, Füchtbauer, A F, Wranne, M S, Ro, J J, Sarangamath, S, El-sagheer, A H, Rupert, D L M, Fisher, R S, Magennis, S W, Jones, A C, Höök, F, Brown, T, Kim, B H, Dahlén, A, Wilhelmsson, L M & Grøtli, M 2018, ' Pentacyclic adenine: a versatile and exceptionally bright fluorescent DNA base analogue ', Chemical Science, vol. 9, no. 14, pp. 3494-3502 . https://doi.org/10.1039/C7SC05448C
Emissive base analogs are powerful tools for probing nucleic acids at the molecular level. Herein we describe the development and thorough characterization of pentacyclic adenine (pA), a versatile base analog with exceptional fluorescence properties.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb6e1e0fa5c9f3ba57f43b759b407bc0
https://doi.org/10.1039/c7sc05448c
https://doi.org/10.1039/c7sc05448c
Publikováno v:
Chemical Communications. 54:7471-7474
Herein, we describe an extended version of a fluorescence probe for detecting miRNAs through the novel application of a PyA-cluster system. By testing various (CG)n sequences in the middle of the oligonucleotide strand of the probe, we obtained an op
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::246ca14440d9d0b182623fd2c924f11e
https://doi.org/10.1039/c8cc03982h
https://doi.org/10.1039/c8cc03982h
Publikováno v:
RSC advances. 8(14)
We have developed hybridization-sensitive fluorescent oligonucleotide probes that, in the presence of quencher strands, undergo efficient fluorescence quenching through the formation of partial DNA/DNA duplexes. In the presence of target RNA, rapid d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d096c046a662d26c032aff6e59f95fba
https://pubmed.ncbi.nlm.nih.gov/35539109
https://pubmed.ncbi.nlm.nih.gov/35539109
Publikováno v:
Methods and Applications in Fluorescence. 6:015004
2'-deoxyfuranouridine derivatives presenting various aryl groups have been synthesized through Cu(I)-catalyzed intramolecular cyclizations. Moreover, corresponding pyrrolo-dC derivatives have been synthesized and both families of compounds thoroughly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8c4f0b8dc3b0f2a7fc881efe71a6959
https://doi.org/10.1088/2050-6120/aa8e19
https://doi.org/10.1088/2050-6120/aa8e19
Fluorescence properties of 6-aryl-2′-deoxy-furanouridine and –pyrrolocytidine and their derivatives.
Publikováno v:
Methods & Applications in Fluorescence; Jan2018, Vol. 6 Issue 1, p1-1, 1p