Zobrazeno 1 - 10
of 106
pro vyhledávání: '"Ivana Pibiri"'
Autor:
Federica Corrao, Maria Grazia Zizzo, Marco Tutone, Raffaella Melfi, Ignazio Fiduccia, Pietro Salvatore Carollo, Aldo Di Leonardo, Gaetano Caldara, Riccardo Perriera, Andrea Pace, Beatrice Belmonte, Selene Sammataro, Ivana Pibiri, Laura Lentini
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 156, Iss , Pp 113886- (2022)
Stop mutations cause 11% of the genetic diseases, due to the introduction of a premature termination codon (PTC) in the mRNA, followed by the production of a truncated protein. A promising therapeutic approach is the suppression therapy by Translatio
Externí odkaz:
https://doaj.org/article/96d8fcb1f02b48969527e8b5b31f7c6a
Autor:
Carla Rizzo, Ignazio Fiduccia, Silvestre Buscemi, Antonio Palumbo Piccionello, Andrea Pace, Ivana Pibiri
Publikováno v:
Applied Sciences, Vol 13, Iss 5, p 2947 (2023)
The synthesis and thermotropic behaviour of some di-alkyloxy-phenyl-1,2,4-triazolium trifluoromethane-sulfonate salts bearing a seven-carbon atom perfluoroalkyl chain on the cation is herein described. The fluorinated salts presenting a 1,2,4-triazol
Externí odkaz:
https://doaj.org/article/59fc3313fb764233b288cc7a44a069d3
Publikováno v:
Molecules, Vol 28, Iss 4, p 1968 (2023)
The wreck of the Punic ship exhibited at the Archaeological Park of Lilybaeum (Marsala, Italy) is a unique example in the world. In this paper, the investigation of some metal finds (30 nails and 3 fragments of sheathings) belonging to the wreck of t
Externí odkaz:
https://doaj.org/article/44bbb20ce0e0441ca89704feb0536ce9
Autor:
Valentino Bezzerri, Laura Lentini, Martina Api, Elena Marinelli Busilacchi, Vincenzo Cavalieri, Antonella Pomilio, Francesca Diomede, Anna Pegoraro, Simone Cesaro, Antonella Poloni, Andrea Pace, Oriana Trubiani, Giuseppe Lippi, Ivana Pibiri, Marco Cipolli
Publikováno v:
Biomedicines, Vol 10, Iss 4, p 886 (2022)
Shwachman-Diamond syndrome (SDS) is one of the most commonly inherited bone marrow failure syndromes (IBMFS). In SDS, bone marrow is hypocellular, with marked neutropenia. Moreover, SDS patients have a high risk of developing myelodysplastic syndrome
Externí odkaz:
https://doaj.org/article/c80e994022c74243b1e23ca59487fc1f
Autor:
Melina S. Weber, Margit Schulze, Giuseppe Lazzara, Antonio Palumbo Piccionello, Andrea Pace, Ivana Pibiri
Publikováno v:
Applied Sciences, Vol 11, Iss 21, p 10347 (2021)
The synthesis and characterization of a new class of 1,2,4-oxadiazolylpyridinium as a cationic scaffold for fluorinated ionic liquid crystals is herein described. A series of 12 fluorinated heterocyclic salts based on a 1,2,4-oxadiazole moiety, conne
Externí odkaz:
https://doaj.org/article/91832627f5564b988935720d342cd96a
Publikováno v:
Nanomaterials, Vol 11, Iss 7, p 1717 (2021)
Interest in the development of graphene-based materials for advanced applications is growing, because of the unique features of such nanomaterials and, above all, of their outstanding versatility, which enables several functionalization pathways that
Externí odkaz:
https://doaj.org/article/a3b1afc4719348ffb58a27ea8a730ba2
Publikováno v:
Heliyon, Vol 5, Iss 6, Pp e01963- (2019)
The readthrough of nonsense mutations by small molecules like Ataluren is considered a novel therapeutic approach to overcome the gene defect in several genetic diseases as cystic fibrosis (CF). This pharmacological approach suppresses translation te
Externí odkaz:
https://doaj.org/article/2155e2d78ffc48e1b819bd302e0d337e
Autor:
Simona Rubino, Rosa Alduina, Patrizia Cancemi, Maria Assunta Girasolo, Vita Di Stefano, Santino Orecchio, Silvestre Buscemi, Ivana Pibiri
Publikováno v:
Molecules, Vol 25, Iss 19, p 4487 (2020)
Two mononuclear Pd(II) complexes [PdCl2(pfptp)] (1) and [PdCl2(pfhtp)] (2), with ligands 2-(3-perfluoropropyl-1-methyl-1,2,4-triazole-5yl)-pyridine (pfptp) and 2-(3-perfluoroheptyl-1-methyl-1,2,4-triazole-5yl)-pyridine (pfhtp), were synthesized and s
Externí odkaz:
https://doaj.org/article/e96037a7bb84447188a836cb17dcbdf6
Autor:
Pietro Salvatore Carollo, Marco Tutone, Giulia Culletta, Ignazio Fiduccia, Federica Corrao, Ivana Pibiri, Maria Grazia Zizzo, Raffaella Melfi, Andrea Pace, Anna Maria Almerico, Laura Lentini
Cystic Fibrosis (CF) is an autosomal recessive genetic disease caused by mutations in the CFTR gene, coding for the CFTR chloride channel. About 10% of the CFTR gene mutations are "stop" mutations, which generate a Premature Termination Codon (PTC),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3658::eb735107b3e0709e99f592758810dbef
https://hdl.handle.net/10447/592653
https://hdl.handle.net/10447/592653
Autor:
Lentini, Pietro Salvatore Carollo, Marco Tutone, Giulia Culletta, Ignazio Fiduccia, Federica Corrao, Ivana Pibiri, Aldo Di Leonardo, Maria Grazia Zizzo, Raffaella Melfi, Andrea Pace, Anna Maria Almerico, Laura
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 11; Pages: 9609
Cystic Fibrosis (CF) is an autosomal recessive genetic disease caused by mutations in the CFTR gene, coding for the CFTR chloride channel. About 10% of the CFTR gene mutations are “stop” mutations that generate a premature termination codon (PTC)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::02572dabb4baa176d3e4760ea1d5c11b