Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Manuela Antoniel"'
Autor:
Vittoria Cenni, Patrizia Sabatelli, Alberto Di Martino, Luciano Merlini, Manuela Antoniel, Stefano Squarzoni, Simona Neri, Spartaco Santi, Samuele Metti, Paolo Bonaldo, Cesare Faldini
Publikováno v:
Cells, Vol 13, Iss 5, p 378 (2024)
The pericellular matrix (PCM) is a specialized extracellular matrix that surrounds cells. Interactions with the PCM enable the cells to sense and respond to mechanical signals, triggering a proper adaptive response. Collagen VI is a component of musc
Externí odkaz:
https://doaj.org/article/c453625c018140808afd9f71a0119467
Autor:
Maria Sofia Falzarano, Rachele Rossi, Andrea Grilli, Mingyan Fang, Hana Osman, Patrizia Sabatelli, Manuela Antoniel, Zhiyuan Lu, Wenyan Li, Rita Selvatici, Cristina Al-Khalili, Francesca Gualandi, Silvio Bicciato, Silvia Torelli, Alessandra Ferlini
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Background: Neuromuscular disorders (NMDs) are a heterogeneous group of genetic diseases, caused by mutations in genes involved in spinal cord, peripheral nerve, neuromuscular junction, and muscle functions. To advance the knowledge of the pathologic
Externí odkaz:
https://doaj.org/article/73150439769649459f63a62da9f5f2a9
Autor:
Luciano Merlini, Patrizia Sabatelli, Manuela Antoniel, Valeria Carinci, Fabio Niro, Giuseppe Monetti, Annalaura Torella, Teresa Giugliano, Cesare Faldini, Vincenzo Nigro
Publikováno v:
Skeletal Muscle, Vol 9, Iss 1, Pp 1-7 (2019)
Abstract Background Myopalladin (MYPN) is a component of the sarcomere that tethers nebulin in skeletal muscle and nebulette in cardiac muscle to alpha-actinin at the Z lines. Autosomal dominant MYPN mutations cause hypertrophic, dilated, or restrict
Externí odkaz:
https://doaj.org/article/ce0333adde5d4243a33501124533fe99
Autor:
Roberto Toni, Giusy Di Conza, Fulvio Barbaro, Nicoletta Zini, Elia Consolini, Davide Dallatana, Manuela Antoniel, Enrico Quarantini, Marco Quarantini, Sara Maioli, Celeste Angela Bruni, Lisa Elviri, Silvia Panseri, Simone Sprio, Monica Sandri, Anna Tampieri
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Osteoporosis stems from an unbalance between bone mineral resorption and deposition. Among the numerous cellular players responsible for this unbalance bone marrow (BM) monocytes/macrophages, mast cells, T and B lymphocytes, and dendritic cells play
Externí odkaz:
https://doaj.org/article/a1be07e9b0d54867a9326895a3be554c
Autor:
Manuela Antoniel, Francesco Traina, Luciano Merlini, Davide Andrenacci, Domenico Tigani, Spartaco Santi, Vittoria Cenni, Patrizia Sabatelli, Cesare Faldini, Stefano Squarzoni
Publikováno v:
Cells, Vol 9, Iss 2, p 409 (2020)
Mutations in collagen VI genes cause two major clinical myopathies, Bethlem myopathy (BM) and Ullrich congenital muscular dystrophy (UCMD), and the rarer myosclerosis myopathy. In addition to congenital muscle weakness, patients affected by collagen
Externí odkaz:
https://doaj.org/article/fc04f7a1b3e24353bd94abb1520394d0
Autor:
Patrizia Sabatelli, Manuela Antoniel, Stefano Squarzoni, Vittoria Cenni, Domenico Tigani, Luciano Merlini, Spartaco Santi, Davide Andrenacci, Francesco Traina, Cesare Faldini
Publikováno v:
Cells, Vol 9, Iss 2, p 409 (2020)
Cells
Volume 9
Issue 2
Cells
Volume 9
Issue 2
Mutations in collagen VI genes cause two major clinical myopathies, Bethlem myopathy (BM) and Ullrich congenital muscular dystrophy (UCMD), and the rarer myosclerosis myopathy. In addition to congenital muscle weakness, patients affected by collagen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c5c47e143e1c6ca0b9ae9d584acb6b1
https://www.mdpi.com/2073-4409/9/2/409
https://www.mdpi.com/2073-4409/9/2/409
Autor:
Fabio Di Lisa, Ildikò Szabò, Kristen Jones, Valeria Petronilli, Barbara Spolaore, Federico Fogolari, Salvatore Antonucci, Manuela Antoniel, Paolo Bernardi, Michela Carraro, Giovanna Lippe, Michael Forte, Valentina Giorgio
The permeability transition pore (PTP) is a Ca2+‐dependent mitochondrial channel whose opening causes a permeability increase in the inner membrane to ions and solutes. The most potent inhibitors are matrix protons, with channel block at pH 6.5. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4899c05978e71ae94722b6b3293103bc
http://hdl.handle.net/11577/3254014
http://hdl.handle.net/11577/3254014
Autor:
Manuela Antoniel, Giovanna Lippe, Barbara Spolaore, Valeria Petronilli, Paolo Bernardi, Valentina Giorgio, Federico Fogolari, Michael Forte
The “Permeability transition” (PT) is one of the most studied events that may trigger cell death and is due to a Ca2+- and ROS-dependent opening of a nonspecific pore, called PTP, whose molecular nature has been long debated. Recently, our resear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df05c83e995140c03312f28bf567a635
http://hdl.handle.net/11390/1112861
http://hdl.handle.net/11390/1112861
Autor:
Federico Fogolari, Manuela Antoniel, Valentina Giorgio, Gary D. Glick, Paolo Bernardi, Giovanna Lippe
Publikováno v:
International Journal of Molecular Sciences, Vol 15, Iss 5, Pp 7513-7536 (2014)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
The oligomycin-sensitivity conferring protein (OSCP) of the mitochondrial FOF1 ATP synthase has long been recognized to be essential for the coupling of proton transport to ATP synthesis. Located on top of the catalytic F1 sector, it makes stable con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c95ba2e04f7861b97d98e67681836170
http://hdl.handle.net/11585/794386
http://hdl.handle.net/11585/794386
Autor:
Valeria Petronilli, Mario Zoratti, Valentina Giorgio, Astrid Fabbro, Ildikò Szabò, Manuela Antoniel, Paolo Bernardi, Giovanna Lippe, Sophia von Stockum, Gary D. Glick, Federico Fogolari, Michael Forte
Publikováno v:
Università degli Studi di Padova-IRIS
Here we define the molecular nature of the mitochondrial permeability transition pore (PTP), a key effector of cell death. The PTP is regulated by matrix cyclophilin D (CyPD), which also binds the lateral stalk of the F O F 1 ATP synthase. We show th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::125bb1f5a217feddca6e64e9a84f4215
http://hdl.handle.net/11577/2574105
http://hdl.handle.net/11577/2574105