Zobrazeno 1 - 10
of 255
pro vyhledávání: '"Ghirga, P"'
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:
Mattia Mori, Francesca Ghirga, Beatrice Amato, Luca Secco, Deborah Quaglio, Isabella Romeo, Marta Gambirasi, Alberta Bergamo, Sonia Covaceuszach, Riccardo Sgarra, Bruno Botta, Guidalberto Manfioletti
Publikováno v:
ACS Omega, Vol 8, Iss 36, Pp 32424-32431 (2023)
Externí odkaz:
https://doaj.org/article/53d81a7b3be24d8483ab60c73cf116db
Akademický článek
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Autor:
María Balsera-Manzanero, Francesca Ghirga, Ana Ruiz-Molina, Mattia Mori, Jerónimo Pachón, Bruno Botta, Elisa Cordero, Deborah Quaglio, Javier Sánchez-Céspedes
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2024)
Regardless of the clinical impact of human adenovirus (HAdV) infections in the healthy population and its high morbidity in immunosuppressed patients, a specific treatment is still not yet available. In this study, we screened the CM1407 COST Action
Externí odkaz:
https://doaj.org/article/16017175d6df4b659d48d030b5b66d11
Autor:
Alessandro Falsini, Gaia Giuntini, Mattia Mori, Francesca Ghirga, Deborah Quaglio, Antonino Cucinotta, Federica Coppola, Irene Filippi, Antonella Naldini, Bruno Botta, Fabio Carraro
Publikováno v:
Pharmaceuticals, Vol 17, Iss 2, p 227 (2024)
Melanoma is the principal cause of death in skin cancer due to its ability to invade and cause metastasis. Hypoxia, which characterises the tumour microenvironment (TME), plays an important role in melanoma development, as cancer cells can adapt and
Externí odkaz:
https://doaj.org/article/3cbc55a18b1a4bdab49b40f3076dabf2
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
An ideal imaging system provides a spatial resolution that is ultimately dictated by the numerical aperture (NA) of the illumination and collection optics. In biological tissue, resolution is further affected by scattering limiting the penetration de
Externí odkaz:
http://arxiv.org/abs/1804.01511
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:
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
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.