Zobrazeno 1 - 10
of 125
pro vyhledávání: '"ROVIELLO GN"'
Publikováno v:
International Journal of Nanomedicine, Vol Volume 13, Pp 2613-2629 (2018)
Domenica Musumeci,1,2 Valentina Roviello,3 Giovanni N Roviello1 1CNR-Institute of Biostructure and Bioimaging, Naples, Italy; 2Department of Chemical Sciences, University of Naples Federico II, Naples, Italy; 3Analytical Chemistry for the Environment
Externí odkaz:
https://doaj.org/article/939641a3a84c4d64a8c6cdb80a87d991
Publikováno v:
International Journal of Nanomedicine, Vol Volume 11, Pp 5897-5904 (2016)
Giovanni N Roviello,1 Caterina Vicidomini,1 Vincenzo Costanzo,1 Valentina Roviello2 1CNR Istituto di Biostrutture e Bioimmagini, Via Mezzocannone site and Headquarters, 2Centro Regionale di Competenza (CRdC) Tecnologie, Via Nuova Agnano, Napoli, Ital
Externí odkaz:
https://doaj.org/article/052bdc7c2d7e426f8cd229891315c9bf
Publikováno v:
International Journal Of Molecular Sciences
Publikováno v:
Journal of medicinal chemistry (Online) 54 (2011): 2095–2101.
info:cnr-pdr/source/autori:Roviello GN, Di Gaetano S, Capasso D, Franco S, Crescenzo C, Bucci EM, Pedone C./titolo:RNA-binding and viral reverse transcriptase inhibitory activity of a novelcationic diamino acid-based peptide./doi:/rivista:Journal of medicinal chemistry (Online)/anno:2011/pagina_da:2095/pagina_a:2101/intervallo_pagine:2095–2101/volume:54
info:cnr-pdr/source/autori:Roviello GN, Di Gaetano S, Capasso D, Franco S, Crescenzo C, Bucci EM, Pedone C./titolo:RNA-binding and viral reverse transcriptase inhibitory activity of a novelcationic diamino acid-based peptide./doi:/rivista:Journal of medicinal chemistry (Online)/anno:2011/pagina_da:2095/pagina_a:2101/intervallo_pagine:2095–2101/volume:54
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::41b6bd43ca0a71d56f2aee8e4c716d73
https://publications.cnr.it/doc/212396
https://publications.cnr.it/doc/212396
Publikováno v:
Amino acids (Wien, Print) 39 (2010): 45–57.
info:cnr-pdr/source/autori:Roviello GN; Benedetti E; Pedone C; Bucci EM/titolo:Nucleobase-containing peptides: an overview of their characteristic features and applications/doi:/rivista:Amino acids (Wien, Print)/anno:2010/pagina_da:45/pagina_a:57/intervallo_pagine:45–57/volume:39
info:cnr-pdr/source/autori:Roviello GN; Benedetti E; Pedone C; Bucci EM/titolo:Nucleobase-containing peptides: an overview of their characteristic features and applications/doi:/rivista:Amino acids (Wien, Print)/anno:2010/pagina_da:45/pagina_a:57/intervallo_pagine:45–57/volume:39
Reports on nucleobase-containing chiral peptides (both natural and artificial) and achiral pseudopeptides are reviewed. Their synthesis, structural features, DNA and RNA-binding ability, as well as some other interesting applications which make them
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::f9d57a2fce110f7cf547785c55745099
http://www.cnr.it/prodotto/i/14150
http://www.cnr.it/prodotto/i/14150
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Akademický článek
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Publikováno v:
RSC advances 6 (2016): 27607–27613. doi:10.1039/c6ra00294c
info:cnr-pdr/source/autori:Roviello G.N.; Roviello V.; Autiero I.; Saviano M./titolo:Solid phase synthesis of TyrT, a thymine-tyrosine conjugate with poly(A) RNA-binding ability/doi:10.1039%2Fc6ra00294c/rivista:RSC advances/anno:2016/pagina_da:27607/pagina_a:27613/intervallo_pagine:27607–27613/volume:6
Rsc Advances
info:cnr-pdr/source/autori:Roviello G.N.; Roviello V.; Autiero I.; Saviano M./titolo:Solid phase synthesis of TyrT, a thymine-tyrosine conjugate with poly(A) RNA-binding ability/doi:10.1039%2Fc6ra00294c/rivista:RSC advances/anno:2016/pagina_da:27607/pagina_a:27613/intervallo_pagine:27607–27613/volume:6
Rsc Advances
TyrT nucleoamino amide interacts with poly(A) RNA.
The present work deals with the synthesis and characterization of a novel nucleoamino acid derivative based on a l-tyrosine moiety to which a thymine nucleobase was anchored by means of an amide
The present work deals with the synthesis and characterization of a novel nucleoamino acid derivative based on a l-tyrosine moiety to which a thymine nucleobase was anchored by means of an amide