Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Federica, Tiberio"'
Autor:
Noah Giacon, Ettore Lo Cascio, Valeria Pennacchietti, Flavio De Maio, Giulia Santarelli, Diego Sibilia, Federica Tiberio, Maurizio Sanguinetti, Wanda Lattanzi, Angelo Toto, Alessandro Arcovito
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract The COVID-19 pandemic caused by SARS-CoV-2 has highlighted the urgent need for innovative antiviral strategies to fight viral infections. Although a substantial part of the overall effort has been directed at the Spike protein to create an e
Externí odkaz:
https://doaj.org/article/1ddadc7741ce42c7a61846415285a350
Autor:
Lorena Di Pietro, Flavia Giacalone, Elvira Ragozzino, Valentina Saccone, Federica Tiberio, Marco De Bardi, Mario Picozza, Giovanna Borsellino, Wanda Lattanzi, Enrico Guadagni, Sara Bortolani, Giorgio Tasca, Enzo Ricci, Ornella Parolini
Publikováno v:
Cell Death and Disease, Vol 13, Iss 9, Pp 1-13 (2022)
Abstract Muscle-resident non-myogenic mesenchymal cells play key roles that drive successful tissue regeneration within the skeletal muscle stem cell niche. These cells have recently emerged as remarkable therapeutic targets for neuromuscular disorde
Externí odkaz:
https://doaj.org/article/f13d6ca451c54f9fa0f9979eb21ed3c4
Autor:
Lorena Di Pietro, Marta Barba, Daniela Palacios, Federica Tiberio, Chiara Prampolini, Mirko Baranzini, Ornella Parolini, Alessandro Arcovito, Wanda Lattanzi
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract RUNX2 encodes the master bone transcription factor driving skeletal development in vertebrates, and playing a specific role in craniofacial and skull morphogenesis. The anatomically modern human (AMH) features sequence changes in the RUNX2 l
Externí odkaz:
https://doaj.org/article/0bf8edca908b4d4fb42a7584593ca882
Autor:
Federica Tiberio, Ilaria Cacciotti, Paolo Frassanito, Giuseppina Nocca, Gianpiero Tamburrini, Alessandro Arcovito, Wanda Lattanzi
Publikováno v:
Applied Sciences, Vol 11, Iss 6, p 2649 (2021)
Craniosynostosis (CS) is the second most prevalent craniofacial congenital malformation due to the premature fusion of skull sutures. CS care requires surgical treatment of variable complexity, aimed at resolving functional and cosmetic defects resul
Externí odkaz:
https://doaj.org/article/1e1a4348a0ca453587aa2226e8bbebdc
Autor:
Filomena, Lo Vecchio, Elisabetta, Tabolacci, Veronica, Nobile, Maria Grazia, Pomponi, Roberta, Pietrobono, Giovanni, Neri, Simona, Amenta, Ettore, Candida, Cristina, Grippaudo, Ettore, Lo Cascio, Alessia, Vita, Federica, Tiberio, Alessandro, Arcovito, Wanda, Lattanzi, Maurizio, Genuardi, Pietro, Chiurazzi
Publikováno v:
Genes. 13(7)
Craniosynostosis are a heterogeneous group of genetic conditions characterized by the premature fusion of the skull bones. The most common forms of craniosynostosis are Crouzon, Apert and Pfeiffer syndromes. They differ from each other in various add
Publikováno v:
Genes, Vol 12, Iss 1073, p 1073 (2021)
Genes
Genes
Craniosynostosis (CS) is the second most prevalent inborn craniofacial malformation; it results from the premature fusion of cranial sutures and leads to dimorphisms of variable severity. CS is clinically heterogeneous, as it can be either a sporadic
Autor:
Wanda Lattanzi, Giuseppina Nocca, Gianpiero Tamburrini, Alessandro Arcovito, Paolo Frassanito, Federica Tiberio, Ilaria Cacciotti
Publikováno v:
Applied Sciences, Vol 11, Iss 2649, p 2649 (2021)
Craniosynostosis (CS) is the second most prevalent craniofacial congenital malformation due to the premature fusion of skull sutures. CS care requires surgical treatment of variable complexity, aimed at resolving functional and cosmetic defects resul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5977c0f3799dc9c3b7783e020dbf6133
http://hdl.handle.net/10807/177111
http://hdl.handle.net/10807/177111
Autor:
Monica Rinaldi, Wanda Lattanzi, Ornella Parolini, Chiara Prampolini, Gabriele Ciasca, Daniela Fioretti, Giordano Perini, Valentina Palmieri, Jacopo Gervasoni, Aniello Primiano, Federica Tiberio, Marcello D'Ascenzo, Massimiliano Papi, Marco De Spirito
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 17
International Journal of Molecular Sciences, Vol 21, Iss 6301, p 6301 (2020)
International journal of molecular sciences
21 (2020): 1–17. doi:10.3390/ijms21176301
info:cnr-pdr/source/autori:Perini G.; Palmieri V.; Ciasca G.; D'ascenzo M.; Gervasoni J.; Primiano A.; Rinaldi M.; Fioretti D.; Prampolini C.; Tiberio F.; Lattanzi W.; Parolini O.; Spirito M.D.; Papi M./titolo:Graphene quantum dots' surface chemistry modulates the sensitivity of glioblastoma cells to chemotherapeutics/doi:10.3390%2Fijms21176301/rivista:International journal of molecular sciences (Print)/anno:2020/pagina_da:1/pagina_a:17/intervallo_pagine:1–17/volume:21
Volume 21
Issue 17
International Journal of Molecular Sciences, Vol 21, Iss 6301, p 6301 (2020)
International journal of molecular sciences
21 (2020): 1–17. doi:10.3390/ijms21176301
info:cnr-pdr/source/autori:Perini G.; Palmieri V.; Ciasca G.; D'ascenzo M.; Gervasoni J.; Primiano A.; Rinaldi M.; Fioretti D.; Prampolini C.; Tiberio F.; Lattanzi W.; Parolini O.; Spirito M.D.; Papi M./titolo:Graphene quantum dots' surface chemistry modulates the sensitivity of glioblastoma cells to chemotherapeutics/doi:10.3390%2Fijms21176301/rivista:International journal of molecular sciences (Print)/anno:2020/pagina_da:1/pagina_a:17/intervallo_pagine:1–17/volume:21
Recent evidence has shown that graphene quantum dots (GQDs) are capable of crossing the blood&ndash
brain barrier, the barrier that reduces cancer therapy efficacy. Here, we tested three alternative GQDs&rsquo
surface chemistries on two neu
brain barrier, the barrier that reduces cancer therapy efficacy. Here, we tested three alternative GQDs&rsquo
surface chemistries on two neu