Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Cecilia Delprete"'
Autor:
Rodrigo Zamith Cunha, Ester Grilli, Andrea Piva, Cecilia Delprete, Cecilia Franciosi, Marco Caprini, Roberto Chiocchetti
Publikováno v:
Molecules, Vol 29, Iss 19, p 4613 (2024)
The gustatory system is responsible for detecting and evaluating the palatability of the various chemicals present in food and beverages. Taste bud cells, located primarily on the tongue, communicate with the gustatory sensory neurons by means of neu
Externí odkaz:
https://doaj.org/article/2ad1aa957bd54a7a8dda41e2f4e1decd
Autor:
Rodrigo Zamith Cunha, Giulia Salamanca, Fanny Mille, Cecilia Delprete, Cecilia Franciosi, Giuliano Piva, Alessandro Gramenzi, Roberto Chiocchetti
Publikováno v:
Animals, Vol 13, Iss 18, p 2833 (2023)
The endocannabinoid system (ECS) has emerged as a potential therapeutic target in veterinary medicine due to its involvement in a wide range of physiological processes including pain, inflammation, immune function, and neurological function. Modulati
Externí odkaz:
https://doaj.org/article/b23d874dff5e435eaceeff0b3b9de2ca
Autor:
Azzurra Sargenti, Francesco Musmeci, Francesco Bacchi, Cecilia Delprete, Domenico Andrea Cristaldi, Federica Cannas, Simone Bonetti, Simone Pasqua, Daniele Gazzola, Delfina Costa, Federico Villa, Maria Raffaella Zocchi, Alessandro Poggi
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
To improve pathogenetic studies in cancer development and reliable preclinical testing of anti-cancer treatments, three-dimensional (3D) cultures, including spheroids, have been widely recognized as more physiologically relevant in vitro models of in
Externí odkaz:
https://doaj.org/article/777bc6df1c1e42dd8d43045d4d769064
Autor:
Domenico Andrea Cristaldi, Azzurra Sargenti, Simone Bonetti, Francesco Musmeci, Cecilia Delprete, Francesco Bacchi, Simone Pasqua, Carola Cavallo, Laura Bonsi, Francesco Alviano, Daniele Gazzola, Spartaco Santi
Publikováno v:
Micromachines, Vol 11, Iss 5, p 465 (2020)
Gathering precise information on mass density, size and weight of cells or cell aggregates, is crucial for applications in many biomedical fields with a specific focus on cancer research. Although few technical solutions have been presented for singl
Externí odkaz:
https://doaj.org/article/89af1e891ca24efe92f5f8a22f1decd3
Autor:
Simone Bonetti, Francesco Musmeci, Alessandro Poggi, Federico Villa, Daniele Gazzola, Francesco Bacchi, Maria Raffaella Zocchi, Federica Cannas, Domenico Andrea Cristaldi, Cecilia Delprete, Delfina Costa, Simone Pasqua, Azzurra Sargenti
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Frontiers in Immunology
Frontiers in Immunology
To improve pathogenetic studies in cancer development and reliable preclinical testing of anti-cancer treatments, three-dimensional (3D) cultures, including spheroids, have been widely recognized as more physiologically relevant in vitro models of in
Autor:
Cecilia Delprete, Laura Bonsi, Carola Cavallo, Spartaco Santi, Simone Pasqua, Simone Bonetti, Francesco Musmeci, Daniele Gazzola, Azzurra Sargenti, Francesco Alviano, Domenico Andrea Cristaldi, Francesco Bacchi
Publikováno v:
Micromachines, Vol 11, Iss 465, p 465 (2020)
Micromachines
Volume 11
Issue 5
Micromachines
Volume 11
Issue 5
Gathering precise information on mass density, size and weight of cells or cell aggregates, is crucial for applications in many biomedical fields with a specific focus on cancer research. Although few technical solutions have been presented for singl
Autor:
Francesco Formaggio, Roberto Rimondini, Cecilia Delprete, Leonardo Scalia, Emilio Merlo Pich, Rocco Liguori, Ferdinando Nicoletti, Marco Caprini
Publikováno v:
Molecular Pain. 18:174480692210870
Fabry disease (FD) is a X-linked lysosomal storage disorder caused by deficient function of the alpha-galactosidase A (α-GalA) enzyme. α-GalA deficiency leads to multisystemic clinical manifestations caused by the preferential accumulation of globo
Autor:
Juan Politei, Marco Caprini, Giovanni Dothel, Vincenzo Donadio, Martina Masotti, Roberto Rimondini, Rocco Liguori, Cecilia Delprete
Publikováno v:
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society. 31(3)
Background Fabry disease (FD) is a hereditary X-linked metabolic storage disorder characterized by deficient or absent lysosomal α-galactosidase A (α-Gal A) activity. This deficiency causes progressive accumulation of glycosphingolipids, primarily