Zobrazeno 1 - 10
of 75
pro vyhledávání: '"ilaria piano"'
Autor:
Ilaria Piano, Arianna Votta, Patrizia Colucci, Francesca Corsi, Sara Vitolo, Chiara Cerri, Dario Puppi, Michele Lai, José Fernando Maya-Vetencourt, Massimiliano Leigheb, Chiara Gabellini, Elisabetta Ferraro
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-17 (2023)
Abstract Microglia chronic activation is a hallmark of several neurodegenerative diseases, including the retinal ones, possibly contributing to their etiopathogenesis. However, some microglia sub-populations have anti-inflammatory and neuroprotective
Externí odkaz:
https://doaj.org/article/d09e8042757b484b95e07469451601b6
Publikováno v:
Pharmaceuticals, Vol 16, Iss 9, p 1307 (2023)
A mechanism shared by most neurodegenerative diseases, like Alzheimer’s disease (AD) and Parkinson’s disease (PD), is neuroinflammation. It has been shown to have a link between cognitive impairment and retinal function under neuroinflammatory co
Externí odkaz:
https://doaj.org/article/68c7717e4ef24ea396601432d46bd791
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Rhodopsin (RHO) mutations are responsible for 25–40% of the dominant cases of retinitis pigmentosa (RP) with different severity and progression rates. The Tvrm4 mice, heterozygous for an I307N dominant mutation of RHO, display a normal retinal phen
Externí odkaz:
https://doaj.org/article/bc2dcf6ac29f4a7faf4b94524e965d02
Autor:
Mattia Di Paolo, Francesca Corsi, Maria Maggi, Luca Nardi, Silvia Bisti, Ilaria Piano, Claudia Gargini
Publikováno v:
Molecules, Vol 28, Iss 4, p 1699 (2023)
Saffron treatment is a broad-spectrum therapy used for several retinal diseases, and its effectiveness depends on a particular molecular composition (REPRON® saffron). Its production requires specific crops and procedures that, together with low yie
Externí odkaz:
https://doaj.org/article/476ef2f356964c22ac9c43e7f74bcdb8
Autor:
Felicia D'Andrea, Stefania Sartini, Ilaria Piano, Matteo Franceschi, Luca Quattrini, Lorenzo Guazzelli, Lidia Ciccone, Elisabetta Orlandini, Claudia Gargini, Concettina La Motta, Susanna Nencetti
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 35, Iss 1, Pp 1194-1205 (2020)
Aldose reductase is a key enzyme in the development of long term diabetic complications and its inhibition represents a viable therapeutic solution for people affected by these pathologies. Therefore, the search for effective aldose reductase inhibit
Externí odkaz:
https://doaj.org/article/2b923e0da4124b2f977b2ce22fca760a
Autor:
Lorenzo Chiaverini, Damiano Cirri, Iogann Tolbatov, Francesca Corsi, Ilaria Piano, Alessandro Marrone, Alessandro Pratesi, Tiziano Marzo, Diego La Mendola
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 14, p 7505 (2022)
Ammonium trichloro (dioxoethylene-O,O′) tellurate (AS101) is a potent immunomodulator prodrug that, in recent years, entered various clinical trials and was tested for a variety of potential therapeutic applications. It has been demonstrated that A
Externí odkaz:
https://doaj.org/article/0afb0799b4d04d379e190b2ebf08239b
Autor:
Andrea Bacci, Francesca Corsi, Massimiliano Runfola, Simona Sestito, Ilaria Piano, Clementina Manera, Giuseppe Saccomanni, Claudia Gargini, Simona Rapposelli
Publikováno v:
Pharmaceuticals, Vol 15, Iss 6, p 688 (2022)
Overproduction of reactive oxygen species (ROS) and alterations in metallostasis are common and related hallmarks in several neurodegenerative diseases (NDDs). Nature-based derivatives always represent an attractive tool in MTDL drug design, especial
Externí odkaz:
https://doaj.org/article/01cccc83f1664f2b81c758eca66ebccf
Autor:
Ilaria Piano, Vanessa D’Antongiovanni, Elena Novelli, Martina Biagioni, Michele Dei Cas, Rita Clara Paroni, Riccardo Ghidoni, Enrica Strettoi, Claudia Gargini
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
Tvrm4 mice, a model of autosomal dominant retinitis pigmentosa (RP), carry a mutation of Rhodopsin gene that can be activated by brief exposure to very intense light. Here, we test the possibility of an anatomical, metabolic, and functional recovery
Externí odkaz:
https://doaj.org/article/21e647d62a5f44b8af2b66c8bc7fe739
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
Abstract Hallmarks of Retinitis Pigmentosa (RP), a family of genetic diseases, are a typical rod-cone-degeneration with initial night blindness and loss of peripheral vision, followed by decreased daylight sight and progressive visual acuity loss up
Externí odkaz:
https://doaj.org/article/3508d26868994ba39d4081781f0b86d3
Autor:
Antonio Falasconi, Martina Biagioni, Elena Novelli, Ilaria Piano, Claudia Gargini, Enrica Strettoi
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
Retinal degeneration 9 (rd9) mice carry a mutation in the retina specific “Retinitis Pigmentosa GTPase Regulator (RPGR)” Open Reading Frame (ORF) 15 gene, located on the X chromosome and represent a rare model of X-linked Retinitis Pigmentosa (XL
Externí odkaz:
https://doaj.org/article/eeb855e263f9471bb082e6bc571ea841