Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Alessio, Torcinaro"'
Autor:
Francesca De Santa, Georgios Strimpakos, Nicole Marchetti, Giorgio Gargari, Alessio Torcinaro, Stefania Arioli, Diego Mora, Carla Petrella, Stefano Farioli-Vecchioli
Publikováno v:
Microbiome, Vol 12, Iss 1, Pp 1-19 (2024)
Abstract Background Intestinal microbial composition not only affects the health of the gut but also influences centrally mediated systems involved in mood, through the “gut-brain” axis, a bidirectional communication between gut microbiota and th
Externí odkaz:
https://doaj.org/article/10f796cd15274f609602796181dbdad7
Autor:
Alessio Torcinaro, Donato Cappetta, Francesca De Santa, Marialucia Telesca, Massimiliano Leigheb, Liberato Berrino, Konrad Urbanek, Antonella De Angelis, Elisabetta Ferraro
Publikováno v:
Metabolites, Vol 12, Iss 7, p 663 (2022)
Sarcopenia is defined as the loss of muscle mass associated with reduced strength leading to poor quality of life in elderly people. The decline of skeletal muscle performance is characterized by bioenergetic impairment and severe oxidative stress, a
Externí odkaz:
https://doaj.org/article/2760b7f860784684acb77881e121e08c
Publikováno v:
Diagnostics, Vol 12, Iss 3, p 561 (2022)
Adult skeletal muscle is capable of active and efficient differentiation in the event of injury in both physiological and pathological conditions, such as in Duchenne muscular dystrophy (DMD). DMD is characterized by different features, such as conti
Externí odkaz:
https://doaj.org/article/9ba13849bcfe4d2cbdcf8c409cd84ad1
Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy
Autor:
Barbora Malecova, Sole Gatto, Usue Etxaniz, Magda Passafaro, Amy Cortez, Chiara Nicoletti, Lorenzo Giordani, Alessio Torcinaro, Marco De Bardi, Silvio Bicciato, Francesca De Santa, Luca Madaro, Pier Lorenzo Puri
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-12 (2018)
Fibro-adipogenic progenitors (FAPs) resident in skeletal muscle are involved in both regeneration and maladaptive processes. Here, the authors identify subpopulations of FAPs with biological activities implicated in physiological muscle repair that a
Externí odkaz:
https://doaj.org/article/a4ca33e25f2e4918b9bcaecc28dae436
Publikováno v:
Brain Sciences, Vol 11, Iss 9, p 1245 (2021)
Sarcopenia, a geriatric syndrome involving loss of muscle mass and strength, is often associated with the early phases of Alzheimer’s disease (AD). Pathological hallmarks of AD including amyloid β (Aβ) aggregates which can be found in peripheral
Externí odkaz:
https://doaj.org/article/3cb5f8404afc4a2e9ecfe9f56ab2d07c
Autor:
Giuliana Gatti, Laura Vilardo, Carla Musa, Chiara Di Pietro, Fabrizio Bonaventura, Ferdinando Scavizzi, Alessio Torcinaro, Barbara Bucci, Raffaele Saporito, Ivan Arisi, Francesca De Santa, Marcello Raspa, Loredana Guglielmi, Igea D’Agnano
Publikováno v:
Biomedicines, Vol 9, Iss 10, p 1343 (2021)
Nuclear lamina components have long been regarded as scaffolding proteins, forming a dense fibrillar structure necessary for the maintenance of the nucleus shape in all the animal kingdom. More recently, mutations, aberrant localisation and deregulat
Externí odkaz:
https://doaj.org/article/5a5822597810477bb0b9dd4c20cc581a
Autor:
Luca Madaro, Alessio Torcinaro, Marco De Bardi, Federica F Contino, Mattia Pelizzola, Giuseppe R Diaferia, Giulia Imeneo, Marina Bouchè, Pier Lorenzo Puri, Francesca De Santa
Publikováno v:
PLoS Genetics, Vol 15, Iss 10, p e1008408 (2019)
Satellite cells (SCs) are muscle stem cells that remain quiescent during homeostasis and are activated in response to acute muscle damage or in chronic degenerative conditions such as Duchenne Muscular Dystrophy. The activity of SCs is supported by s
Externí odkaz:
https://doaj.org/article/2259e8adf494489592bd33d5d7548504
Publikováno v:
Diagnostics; Volume 12; Issue 3; Pages: 561
Adult skeletal muscle is capable of active and efficient differentiation in the event of injury in both physiological and pathological conditions, such as in Duchenne muscular dystrophy (DMD). DMD is characterized by different features, such as conti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c104346e827b0c5a3d1be322efe98d17
Autor:
Michela Gloriani, Luisa Pieroni, Cristiana Valle, Cyril Quessada, Silvia Scaricamazza, Elisabetta Ferraro, Giacomo Giacovazzo, Gabriella Dobrowolny, Hao Wang, Valentina Nesci, Antonio Musarò, Niccolò Candelise, Cinzia Volonté, Illari Salvatori, Shyuan T. Ngo, Jean-Philippe Loeffler, Alberto Ferri, Frédérique René, Tesfaye Wolde Tefera, Susanna Amadio, Aniello Primiano, Andrea Urbani, Elisa Lepore, Alessio Torcinaro, Frederik J. Steyn, Roberto Coccurello
Publikováno v:
British journal of pharmacology 179 (2022): 1732–1752. doi:10.1111/bph.15738
info:cnr-pdr/source/autori:Silvia Scaricamazza, Illari Salvatori, Susanna Amadio, Valentina Nesci, Alessio Torcinaro, Giacomo Giacovazzo, Aniello Primiano, Michela Gloriani, Niccolò Candelise, Luisa Pieroni, Jean-Philippe Loeffler, Frederique Renè, Cyril Quessada, Tesfaye W Tefera, Hao Wang, Frederik J Steyn, Shyuan T Ngo, Gabriella Dobrowolny, Elisa Lepore, Andrea Urbani, Antonio Musarò, Cinzia Volonté, Elisabetta Ferraro, Roberto Coccurello, Cristiana Valle, Alberto Ferri/titolo:Repurposing of Trimetazidine for Amyotrophic Lateral Sclerosis: a study in SOD1 G93A mice/doi:10.1111%2Fbph.15738/rivista:British journal of pharmacology/anno:2022/pagina_da:1732/pagina_a:1752/intervallo_pagine:1732–1752/volume:179
info:cnr-pdr/source/autori:Silvia Scaricamazza, Illari Salvatori, Susanna Amadio, Valentina Nesci, Alessio Torcinaro, Giacomo Giacovazzo, Aniello Primiano, Michela Gloriani, Niccolò Candelise, Luisa Pieroni, Jean-Philippe Loeffler, Frederique Renè, Cyril Quessada, Tesfaye W Tefera, Hao Wang, Frederik J Steyn, Shyuan T Ngo, Gabriella Dobrowolny, Elisa Lepore, Andrea Urbani, Antonio Musarò, Cinzia Volonté, Elisabetta Ferraro, Roberto Coccurello, Cristiana Valle, Alberto Ferri/titolo:Repurposing of Trimetazidine for Amyotrophic Lateral Sclerosis: a study in SOD1 G93A mice/doi:10.1111%2Fbph.15738/rivista:British journal of pharmacology/anno:2022/pagina_da:1732/pagina_a:1752/intervallo_pagine:1732–1752/volume:179
Background and purpose: Amyotrophic lateral sclerosis (ALS), a neurodegenerative disease characterized by the degeneration of upper and lower motor neurons, progressive wasting and paralysis of voluntary muscles is currently incurable despite intense
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a8a38f2d23b43968f6a89d83159402a
Autor:
Silvia, Scaricamazza, Illari, Salvatori, Susanna, Amadio, Valentina, Nesci, Alessio, Torcinaro, Giacomo, Giacovazzo, Aniello, Primiano, Michela, Gloriani, Niccolò, Candelise, Luisa, Pieroni, Jean-Philippe, Loeffler, Frederique, Renè, Cyril, Quessada, Tesfaye W, Tefera, Hao, Wang, Frederik J, Steyn, Shyuan T, Ngo, Gabriella, Dobrowolny, Elisa, Lepore, Andrea, Urbani, Antonio, Musarò, Cinzia, Volonté, Elisabetta, Ferraro, Roberto, Coccurello, Cristiana, Valle, Alberto, Ferri
Publikováno v:
British journal of pharmacology. 179(8)
Amyotrophic lateral sclerosis (ALS), a neurodegenerative disease characterized by the degeneration of upper and lower motor neurons, progressive wasting and paralysis of voluntary muscles and is currently incurable. Although considered to be a pure m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9a1744b242571d105bb20e5161e5b41
https://pubmed.ncbi.nlm.nih.gov/34783031
https://pubmed.ncbi.nlm.nih.gov/34783031