Zobrazeno 1 - 8
of 8
pro vyhledávání: '"G. N. ROVIELLO"'
Autor:
G. N. ROVIELLO, MUSUMECI, DOMENICA, G. MILANO, E. M. BUCCI, A. MESSERE, C. PEDONE, E. BENEDETTI, CALABRESE, MARIA LUCIA, MASSA, RITA
Publikováno v:
9th ISABC, Napoli, 2006
info:cnr-pdr/source/autori:Giovanni N. Roviello, Domenica Musumeci, Giovanna Milano, Enrico M. Bucci, Maria L. Calabrese, Anna Messere, Rita Massa, Carlo Pedone, and Ettore Benedetti/congresso_nome:9th ISABC/congresso_luogo:Napoli/congresso_data:2006/anno:2006/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:Giovanni N. Roviello, Domenica Musumeci, Giovanna Milano, Enrico M. Bucci, Maria L. Calabrese, Anna Messere, Rita Massa, Carlo Pedone, and Ettore Benedetti/congresso_nome:9th ISABC/congresso_luogo:Napoli/congresso_data:2006/anno:2006/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::eab3136e11de291ca2ac19fa859e3ce3
http://www.cnr.it/prodotto/i/77191
http://www.cnr.it/prodotto/i/77191
Publikováno v:
First IRBM Workshop on Medicinal & Organic Chemistry, Pomezia, 2008
info:cnr-pdr/source/autori:G. N. Roviello, D. Musumeci, C. Pedone, M. Castiglione and E. M. Bucci/congresso_nome:First IRBM Workshop on Medicinal & Organic Chemistry/congresso_luogo:Pomezia/congresso_data:2008/anno:2008/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:G. N. Roviello, D. Musumeci, C. Pedone, M. Castiglione and E. M. Bucci/congresso_nome:First IRBM Workshop on Medicinal & Organic Chemistry/congresso_luogo:Pomezia/congresso_data:2008/anno:2008/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::0176e682f19961580c1ffecb49b84c65
https://publications.cnr.it/doc/103921
https://publications.cnr.it/doc/103921
Autor:
Giovanni N. Roviello, Silvano Fumero, Margherita Valente, Enrico M. Bucci, Maria Moccia, Carlo Pedone, Roberto Sapio, Domenica Musumeci
Publikováno v:
Nucleosides, nucleotides & nucleic acids 26 (2007): 1447–1450. doi:10.1080/15257770701542330
info:cnr-pdr/source/autori:D. Musumeci; E.M. Bucci; M. Moccia; G.N. Roviello; R. Sapio; M. Valente; C. Pedone; S. Fumero/titolo:Bent oligonucleotide duplexes as HMGB1 inhibitors: a comparative study/doi:10.1080%2F15257770701542330/rivista:Nucleosides, nucleotides & nucleic acids/anno:2007/pagina_da:1447/pagina_a:1450/intervallo_pagine:1447–1450/volume:26
info:cnr-pdr/source/autori:D. Musumeci; E.M. Bucci; M. Moccia; G.N. Roviello; R. Sapio; M. Valente; C. Pedone; S. Fumero/titolo:Bent oligonucleotide duplexes as HMGB1 inhibitors: a comparative study/doi:10.1080%2F15257770701542330/rivista:Nucleosides, nucleotides & nucleic acids/anno:2007/pagina_da:1447/pagina_a:1450/intervallo_pagine:1447–1450/volume:26
In this work we explore the ability of a chimeric LNA/DNA bent duplex, in which the kink is induced by 2 unpaired adenines in the middle of one strand, to bind HMGB1, a protein involved in many inflammatory processes. The LNA/DNA duplex was compared
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c29163b58fc1d37093abc86c938ec9ff
https://doi.org/10.1080/15257770701542330
https://doi.org/10.1080/15257770701542330
Autor:
Maria Moccia, Roberto Sapio, Enrico M. Bucci, Margherita Valente, V Anrò, Giovanni N. Roviello, Domenica Musumeci
Publikováno v:
Nucleosides, Nucleotides & Nucleic Acids. 26:1047-1050
In this work a novel approach to identify new therapeutic targets consisting of serum proteins which contain an oligonucleotide binding domain is presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4092a16ddd2b88654ad4c0c2998dc5be
https://doi.org/10.1080/15257770701509602
https://doi.org/10.1080/15257770701509602
Publikováno v:
Acta Crystallographica Section E: Structure Reports
Acta crystallographica. Section E 69 (2013): o1526–o1527. doi:10.1107/S160053681302480X
info:cnr-pdr/source/autori:Roviello, Giuseppina; Borbone, Fabio; Carella, Antonio R.; Roviello, Giovanni N.; Tuzi, Angela/titolo:Dipentyl 2,6-diaminobenzo[1,2-b:4,5-b?]difuran-3,7-dicarboxylate/doi:10.1107%2FS160053681302480X/rivista:Acta crystallographica. Section E/anno:2013/pagina_da:o1526/pagina_a:o1527/intervallo_pagine:o1526–o1527/volume:69
Acta crystallographica. Section E 69 (2013): o1526–o1527. doi:10.1107/S160053681302480X
info:cnr-pdr/source/autori:Roviello, Giuseppina; Borbone, Fabio; Carella, Antonio R.; Roviello, Giovanni N.; Tuzi, Angela/titolo:Dipentyl 2,6-diaminobenzo[1,2-b:4,5-b?]difuran-3,7-dicarboxylate/doi:10.1107%2FS160053681302480X/rivista:Acta crystallographica. Section E/anno:2013/pagina_da:o1526/pagina_a:o1527/intervallo_pagine:o1526–o1527/volume:69
The title compound, C22H28N2O6, crystallizes with one half-molecule in the independent unit, the molecule being located on an inversion centre. The penthyl groups are in the all-trans conformation and an almost planar conformation of the whole mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd9d7fcc6e363e8375d6782a2bb192bd
https://pubmed.ncbi.nlm.nih.gov/24098215
https://pubmed.ncbi.nlm.nih.gov/24098215
Autor:
Enrico M. Bucci, Giovanni N. Roviello, Domenica Musumeci, Gennaro Piccialli, Giorgia Oliviero
Publikováno v:
Bioconjugate chemistry 23 (2012): 382–391. doi:10.1021/bc200305t
info:cnr-pdr/source/autori:Musumeci, Domenica; Oliviero, Giorgia; Roviello, Giovanni N.; Bucci, Enrico M.; Piccialli, Gennaro/titolo:G-quadruplex-forming oligonucleotide conjugated to magnetic nanoparticles: Synthesis, characterization, and enzymatic stability assays/doi:10.1021%2Fbc200305t/rivista:Bioconjugate chemistry/anno:2012/pagina_da:382/pagina_a:391/intervallo_pagine:382–391/volume:23
info:cnr-pdr/source/autori:Musumeci, Domenica; Oliviero, Giorgia; Roviello, Giovanni N.; Bucci, Enrico M.; Piccialli, Gennaro/titolo:G-quadruplex-forming oligonucleotide conjugated to magnetic nanoparticles: Synthesis, characterization, and enzymatic stability assays/doi:10.1021%2Fbc200305t/rivista:Bioconjugate chemistry/anno:2012/pagina_da:382/pagina_a:391/intervallo_pagine:382–391/volume:23
In the present work, we report the conjugation of superparamagnetic nanoparticles to a fluorescently labeled oligodeoxyribonucleotide (ODN) able to fold into stable unimolecular guanine quadruple helix under proper ion conditions by means of its thro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::945b43849c122b87411b8aa69817f204
https://pubmed.ncbi.nlm.nih.gov/22239558
https://pubmed.ncbi.nlm.nih.gov/22239558
Autor:
Carlo Pedone, Domenica Musumeci, Giovanni N. Roviello, Ettore Benedetti, M Castiglione, Enrico M. Bucci
Publikováno v:
Journal of peptide science
15 (2009): 155–160. doi:10.1002/psc.1072
info:cnr-pdr/source/autori:Roviello GN; Musumeci D; Castiglione M; Bucci EM; Pedone C; Benedetti E/titolo:Solid phase synthesis and RNA-binding studies of a serum-resistant nucleo-epsilon-peptide/doi:10.1002%2Fpsc.1072/rivista:Journal of peptide science (Print)/anno:2009/pagina_da:155/pagina_a:160/intervallo_pagine:155–160/volume:15
15 (2009): 155–160. doi:10.1002/psc.1072
info:cnr-pdr/source/autori:Roviello GN; Musumeci D; Castiglione M; Bucci EM; Pedone C; Benedetti E/titolo:Solid phase synthesis and RNA-binding studies of a serum-resistant nucleo-epsilon-peptide/doi:10.1002%2Fpsc.1072/rivista:Journal of peptide science (Print)/anno:2009/pagina_da:155/pagina_a:160/intervallo_pagine:155–160/volume:15
In the present work we report the synthesis of a new Fmoc-protected L-lysine-based nucleo-amino acid suitable for the solid phase assembly and its oligomerisation to the corresponding nucleo-e-peptide that we called e-lysPNA. The ability to bind comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0c17792bfcdd9bedeb26ac13ed2735c
http://hdl.handle.net/11588/565518
http://hdl.handle.net/11588/565518