Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Lorenzo Preti"'
Autor:
Elena Marchesi, Valentina Gentili, Daria Bortolotti, Lorenzo Preti, Paolo Marchetti, Virginia Cristofori, Anna Fantinati, Roberta Rizzo, Claudio Trapella, Daniela Perrone, Maria Luisa Navacchia
Publikováno v:
ACS Omega, Vol 8, Iss 47, Pp 45078-45087 (2023)
Externí odkaz:
https://doaj.org/article/3e015baece9c4e2fb2c91e2e72a011a0
Autor:
Elena Marchesi, Elisabetta Melloni, Fabio Casciano, Elena Pozza, Roberto Argazzi, Carmela De Risi, Lorenzo Preti, Daniela Perrone, Maria Luisa Navacchia
Publikováno v:
Molecules, Vol 29, Iss 14, p 3383 (2024)
Herein, we report the synthesis of a new hybrid compound based on a 2′-deoxyuridine nucleoside conjugated with a NO photo-donor moiety (dU-t-NO) via CuAAC click chemistry. Hybrid dU-t-NO, as well as two previously reported 2′-deoxyadenosine based
Externí odkaz:
https://doaj.org/article/304fe710d7984b7f8c515a743a68d86f
Autor:
Valentina Venturi, Elena Marchesi, Daniela Perrone, Valentina Costa, Martina Catani, Simona Aprile, Lindomar Alberto Lerin, Federico Zappaterra, Pier Paolo Giovannini, Lorenzo Preti
Publikováno v:
Molecules, Vol 29, Iss 6, p 1305 (2024)
Ursodeoxycholic acid (UDCA) and acetoacetate are natural compounds present in the human intestine and blood, respectively. A number of studies highlighted that besides their well-known primary biological roles, both compounds possess the ability to i
Externí odkaz:
https://doaj.org/article/eca37f5df30646c3b896a276b4314dc9
Autor:
Elena Marchesi, Rita Cortesi, Lorenzo Preti, Paola Rimessi, Maddalena Sguizzato, Matteo Bovolenta, Daniela Perrone
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 8, p 4270 (2022)
Our groups previously reported that conjugation at 3′-end with ursodeoxycholic acid (UDCA) significantly enhanced in vitro exon skipping properties of ASO 51 oligonucleotide targeting the human DMD exon 51. In this study, we designed a series of li
Externí odkaz:
https://doaj.org/article/b17d8f2ac4b74ac193dc561235532d8f
Autor:
Simone Sprio, Massimiliano Dapporto, Lorenzo Preti, Elisa Mazzoni, Maria Rosa Iaquinta, Fernanda Martini, Mauro Tognon, Nicola M. Pugno, Elisa Restivo, Livia Visai, Anna Tampieri
Publikováno v:
Frontiers in Materials, Vol 7 (2020)
In the present work, hydroxyapatite (HA) nanoparticles doped with Mg2+, Sr2+, and Zn2+ ions are developed by wet neutralization method and then sintered at 1,250°C to obtain bulk consolidated materials. Physicochemical and microstructural analyses s
Externí odkaz:
https://doaj.org/article/b5eb15432890429f8ffd33a5ce3b847f
Autor:
Elisabetta Melloni, Elena Marchesi, Lorenzo Preti, Fabio Casciano, Erika Rimondi, Arianna Romani, Paola Secchiero, Maria Luisa Navacchia, Daniela Perrone
Publikováno v:
Molecules, Vol 27, Iss 2, p 471 (2022)
Chenodeoxycholic acid and ursodeoxycholic acid (CDCA and UDCA, respectively) have been conjugated with paclitaxel (PTX) anticancer drugs through a high-yield condensation reaction. Bile acid-PTX hybrids (BA-PTX) have been investigated for their pro-a
Externí odkaz:
https://doaj.org/article/1c36930ecea9485f9412a96da63b2339
Autor:
Elena Marchesi, Matteo Bovolenta, Lorenzo Preti, Massimo L. Capobianco, Kamel Mamchaoui, Monica Bertoldo, Daniela Perrone
Publikováno v:
Molecules, Vol 26, Iss 24, p 7662 (2021)
Steric blocking antisense oligonucleotides (ASO) are promising tools for splice modulation such as exon-skipping, although their therapeutic effect may be compromised by insufficient delivery. To address this issue, we investigated the synthesis of a
Externí odkaz:
https://doaj.org/article/4032b6268bc14cc3a6b11fd7e41653ff
Publikováno v:
Molecules, Vol 26, Iss 11, p 3100 (2021)
The click azide = alkyne 1,3-dipolar cycloaddition (click chemistry) has become the approach of choice for bioconjugations in medicinal chemistry, providing facile reaction conditions amenable to both small and biological molecules. Many nucleoside a
Externí odkaz:
https://doaj.org/article/d4881a18eb624502b04bd7fe0912b13a
A Graded Multifunctional Hybrid Scaffold with Superparamagnetic Ability for Periodontal Regeneration
Autor:
Simone Sprio, Elisabetta Campodoni, Monica Sandri, Lorenzo Preti, Tobias Keppler, Frank A. Müller, Nicola M. Pugno, Anna Tampieri
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 11, p 3604 (2018)
The regeneration of dental tissues is a still an unmet clinical need; in fact, no therapies have been completely successful in regenerating dental tissue complexes such as periodontium, which is also due to the lack of scaffolds that are able to guid
Externí odkaz:
https://doaj.org/article/5786be6026f441758ac9f56269797656
Autor:
Olga Bortolini, Costanza Leonardi, Paolo Dambruoso, Arianna Brandolese, Eleonora Polo, Graziano Di Carmine, Alessandro Massi, Daniele Ragno, Lorenzo Preti
Publikováno v:
Advanced synthesis & catalysis
363 (2021): 5473–5485. doi:10.1002/adsc.202100757
info:cnr-pdr/source/autori:Leonardi, Costanza; Brandolese, Arianna; Preti, Lorenzo; Bortolini, Olga; Polo, Eleonora; Dambruoso, Paolo; Ragno, Daniele; Di Carmine, Graziano; Massi, Alessandro/titolo:Expanding the Toolbox of Heterogeneous Asymmetric Organocatalysts: Bifunctional Cyclopropenimine Superbases for Enantioselective Catalysis in Batch and Continuous Flow/doi:10.1002%2Fadsc.202100757/rivista:Advanced synthesis & catalysis (Print)/anno:2021/pagina_da:5473/pagina_a:5485/intervallo_pagine:5473–5485/volume:363
363 (2021): 5473–5485. doi:10.1002/adsc.202100757
info:cnr-pdr/source/autori:Leonardi, Costanza; Brandolese, Arianna; Preti, Lorenzo; Bortolini, Olga; Polo, Eleonora; Dambruoso, Paolo; Ragno, Daniele; Di Carmine, Graziano; Massi, Alessandro/titolo:Expanding the Toolbox of Heterogeneous Asymmetric Organocatalysts: Bifunctional Cyclopropenimine Superbases for Enantioselective Catalysis in Batch and Continuous Flow/doi:10.1002%2Fadsc.202100757/rivista:Advanced synthesis & catalysis (Print)/anno:2021/pagina_da:5473/pagina_a:5485/intervallo_pagine:5473–5485/volume:363
A strategy for the immobilization of chiral 2,3-bisaminocyclopropenium salt (pre-catalyst) onto polystyrene and silica supports is presented together with a suitable procedure for the conversion into the corresponding cyclopropenimine superbase catal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b7c97efe78a330a4e822073c1731184
http://www.cnr.it/prodotto/i/465961
http://www.cnr.it/prodotto/i/465961