Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Silvia Ghirga"'
Autor:
Lorenzo Barolo, Ylenia Gigante, Lorenza Mautone, Silvia Ghirga, Alessandro Soloperto, Alessandra Giorgi, Francesca Ghirga, Martina Pitea, Alessio Incocciati, Francesco Mura, Giancarlo Ruocco, Alberto Boffi, Paola Baiocco, Silvia Di Angelantonio
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract Tauopathies, including Alzheimer’s disease and Frontotemporal Dementia, are debilitating neurodegenerative disorders marked by cognitive decline. Despite extensive research, achieving effective treatments and significant symptom management
Externí odkaz:
https://doaj.org/article/d69b351b7e094759bfd10aa20ce9dd0f
Autor:
Natalia Pediconi, Ylenia Gigante, Silvia Cama, Martina Pitea, Lorenza Mautone, Giancarlo Ruocco, Silvia Ghirga, Silvia Di Angelantonio
Publikováno v:
Frontiers in Aging Neuroscience, Vol 15 (2023)
IntroductionAmyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the progressive loss of motor neuron function. Although ophthalmic deficits are not considered a classic symptom of ALS, recent studies suggest that
Externí odkaz:
https://doaj.org/article/e264dc78efba44eb88e37d4ea331e430
Autor:
Alessandro Soloperto, Deborah Quaglio, Paola Baiocco, Isabella Romeo, Mattia Mori, Matteo Ardini, Caterina Presutti, Ida Sannino, Silvia Ghirga, Antonia Iazzetti, Rodolfo Ippoliti, Giancarlo Ruocco, Bruno Botta, Francesca Ghirga, Silvia Di Angelantonio, Alberto Boffi
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-15 (2022)
Abstract Numerous studies have shown a strong correlation between the number of neurofibrillary tangles of the tau protein and Alzheimer's disease progression, making the quantitative detection of tau very promising from a clinical point of view. How
Externí odkaz:
https://doaj.org/article/ea4bc56ead7f4f7b80769aef5c5bb896
Autor:
Carlo Brighi, Federico Salaris, Alessandro Soloperto, Federica Cordella, Silvia Ghirga, Valeria de Turris, Maria Rosito, Pier Francesca Porceddu, Chiara D’Antoni, Angelo Reggiani, Alessandro Rosa, Silvia Di Angelantonio
Publikováno v:
Cell Death and Disease, Vol 12, Iss 5, Pp 1-22 (2021)
Abstract Fragile X syndrome (FXS) is a neurodevelopmental disorder, characterized by intellectual disability and sensory deficits, caused by epigenetic silencing of the FMR1 gene and subsequent loss of its protein product, fragile X mental retardatio
Externí odkaz:
https://doaj.org/article/0351c777a3714b9bbe0d47abd6b491b8
Autor:
Federica Cordella, Laura Ferrucci, Chiara D’Antoni, Silvia Ghirga, Carlo Brighi, Alessandro Soloperto, Ylenia Gigante, Davide Ragozzino, Paola Bezzi, Silvia Di Angelantonio
Publikováno v:
Life, Vol 12, Iss 11, p 1884 (2022)
Maintaining the excitability of neurons and circuits is fundamental for healthy brain functions. The global compensatory increase in excitatory synaptic strength, in response to decreased activity, is one of the main homeostatic mechanisms responsibl
Externí odkaz:
https://doaj.org/article/e1710a768b27486dae22e28491f06bb6
Publikováno v:
Entropy, Vol 23, Iss 9, p 1185 (2021)
The comprehension of neuronal network functioning, from most basic mechanisms of signal transmission to complex patterns of memory and decision making, is at the basis of the modern research in experimental and computational neurophysiology. While me
Externí odkaz:
https://doaj.org/article/0b71c4ffafed4986924e3d05bed28a51
Autor:
Valeria de Turris, Pier Francesca Porceddu, Alessandro Soloperto, Silvia Di Angelantonio, Silvia Ghirga, Carlo Brighi, Federica Cordella, Federico Salaris, Maria Rosito, Alessandro Rosa, Chiara D’Antoni, Angelo Reggiani
Publikováno v:
Cell Death & Disease
Cell Death and Disease, Vol 12, Iss 5, Pp 1-22 (2021)
Cell Death and Disease, Vol 12, Iss 5, Pp 1-22 (2021)
Fragile X syndrome (FXS) is a neurodevelopmental disorder, characterized by intellectual disability and sensory deficits, caused by epigenetic silencing of the FMR1 gene and subsequent loss of its protein product, fragile X mental retardation protein
Autor:
Silvia Ghirga, S. Di Angelantonio, Pier Francesca Porceddu, Alessandro Rosa, Alessandro Soloperto, Federico Salaris, Federica Cordella, Maria Rosito, Carlo Brighi, Angelo Reggiani, V. de Turris
Fragile X syndrome (FXS) is a neurodevelopmental disorder, characterized by intellectual disability and sensory deficits, caused by epigenetic silencing of the FMR1 gene and subsequent loss of its protein product, fragile X mental retardation protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edb8fd5e454d2b8d5f91e7efaefd3d8b
https://doi.org/10.1101/2020.11.12.379800
https://doi.org/10.1101/2020.11.12.379800
Autor:
Francesca Pagani, Marco Leonetti, Silvia Ghirga, Silvia Di Angelantonio, Maria Rosito, Giancarlo Ruocco
Publikováno v:
Journal of the Optical Society of America. A, Optics, image science, and vision. 37(4)
It has been recently demonstrated that the exposure of naive neuronal cells to light—at the basis of optogenetic techniques and calcium imaging measurements—may alter neuronal firing. Indeed, understanding the effect of light on nongenetically mo
Publikováno v:
Adaptive Optics and Wavefront Control for Biological Systems VI.