Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Silvia Santoro"'
Autor:
Giulia Donato, Tiziana Caspanello, Massimo De Majo, Marisa Masucci, Diego Iannelli, Silvia Santoro, Alessandra Caprì, Nicola Maria Iannelli, Maria Grazia Pennisi
Publikováno v:
Veterinary Sciences, Vol 11, Iss 1, p 39 (2024)
Domperidone is used as an immunomodulatory drug for Leishmania infantum infection and disease in dogs. However, a pro-arrhythmic side effect, caused by prolonged QT intervals, is reported in humans. This pilot study evaluated the corrected QT (QTc) i
Externí odkaz:
https://doaj.org/article/8a105c1651924d4f9aadb01a0da4bdb9
Autor:
Milena Ślęczkowska, Kaalindi Misra, Silvia Santoro, Monique M. Gerrits, Janneke G. J. Hoeijmakers
Publikováno v:
Biomedicines, Vol 11, Iss 10, p 2680 (2023)
Neuropathic pain (NP) is a typical symptom of peripheral nerve disorders, including painful neuropathy. The biological mechanisms that control ion channels are important for many cell activities and are also therapeutic targets. Disruption of the cel
Externí odkaz:
https://doaj.org/article/1fc93650b37148679eea92ac8e45e0ee
Autor:
Silvia Santoro, Costanza Paganin, Sara Gilardi, Tarcisio Brignoli, Giovanni Bertoni, Silvia Ferrara
Publikováno v:
mBio, Vol 14, Iss 1 (2023)
ABSTRACT Behind the pathogenic lifestyle of Pseudomonas aeruginosa exists a complex regulatory network of intertwined switches at both the transcriptional and posttranscriptional levels. Major players that mediate translation regulation of several ge
Externí odkaz:
https://doaj.org/article/3a4663a85d114ff5b0b9ade2e3b195df
Autor:
Federica Cerri, Francesco Gentile, Ferdinando Clarelli, Silvia Santoro, Yuri Matteo Falzone, Giorgia Dina, Alessandro Romano, Teuta Domi, Laura Pozzi, Raffaella Fazio, Paola Podini, Melissa Sorosina, Paola Carrera, Federica Esposito, Nilo Riva, Chiara Briani, Tiziana Cavallaro, Massimo Filippi, Angelo Quattrini
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Although inflammation appears to play a role in neurolymphomatosis (NL), the mechanisms leading to degeneration in the peripheral nervous system are poorly understood. The purpose of this exploratory study was to identify molecular pathways underlyin
Externí odkaz:
https://doaj.org/article/cc6f17e7176d4a779b5afbb6b7aa98d8
Autor:
Antonino Giordano, Ferdinando Clarelli, Miryam Cannizzaro, Elisabetta Mascia, Silvia Santoro, Melissa Sorosina, Laura Ferrè, Letizia Leocani, Federica Esposito
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundRehabilitation is fundamental for progressive multiple sclerosis (MS), but predictive biomarkers of motor recovery are lacking, making patient selection difficult. Motor recovery depends on synaptic plasticity, in which the Brain-Derived Ne
Externí odkaz:
https://doaj.org/article/1dd0df52c2e24cecafadb5d361367f7e
Autor:
Ferdinando Clarelli, Nadia Barizzone, Eleonora Mangano, Miriam Zuccalà, Chiara Basagni, Santosh Anand, Melissa Sorosina, Elisabetta Mascia, Silvia Santoro, PROGEMUS, PROGRESSO, Franca Rosa Guerini, Eleonora Virgilio, Antonio Gallo, Alessandro Pizzino, Cristoforo Comi, Vittorio Martinelli, Giancarlo Comi, Gianluca De Bellis, Maurizio Leone, Massimo Filippi, Federica Esposito, Roberta Bordoni, Filippo Martinelli Boneschi, Sandra D'Alfonso, P Crociani, D Vecchio, P Ragonese, A Gajofatto, E Scarpini, A Bertolotto, D Caputo, C Gasperini, F Granella, S Cordera, P Cavallo, R Cavallo, R Bergamaschi, G Ristori, C Solaro, F Martinelli, F Passantino, M Pugliatti, A Gallo, L Brambilla, C Clerico, F Capone, F Esposito, G Liberatore, M Rodegher, p Rossi, M Radaelli, L Moiola, B Colombo, A Ghezzi, A Annovazzi, R Capra, G Coniglio, M. P Amato, B Nacmias, G Tedeschi, A D’Ambrosio, P Cavalla, F Patti, E D’Amico, D Galimberti, P Gallo, M Atzori, L Grimaldi, S Bucello, G Mancardi, E Capello
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Genome-wide association studies identified over 200 risk loci for multiple sclerosis (MS) focusing on common variants, which account for about 50% of disease heritability. The goal of this study was to investigate whether low-frequency and rare funct
Externí odkaz:
https://doaj.org/article/68d0393bd32c4e15a1437e3e4fc9a308
Publikováno v:
Frontiers in Microbiology, Vol 12 (2021)
Pseudomonas aeruginosa is one of the most critical opportunistic pathogens in humans, able to cause both lethal acute and chronic lung infections. In previous work, we indicated that the small RNA ErsA plays a role in the regulatory network of P. aer
Externí odkaz:
https://doaj.org/article/95ddcd266ea34869abac329c64208e69
Autor:
Cyndi Mangano, Francesco Macrì, Simona Di Pietro, Michela Pugliese, Silvia Santoro, Nicola M. Iannelli, Giuseppe Mazzullo, Rosalia Crupi, Massimo De Majo
Publikováno v:
BMC Veterinary Research, Vol 15, Iss 1, Pp 1-9 (2019)
Abstract Background Nodular lymphoid hyperplasia (NLH) is one of the most common non-neoplastic splenic lesions in dogs, especially in old ones, showing a splenic enlargement. More recent studies have been focused on Contrast Enhanced Ultrasonography
Externí odkaz:
https://doaj.org/article/a26becf417b5438b91b70d7a8bed241f
Autor:
Rowida Almomani, Margherita Marchi, Maurice Sopacua, Patrick Lindsey, Erika Salvi, Bart de Koning, Silvia Santoro, Stefania Magri, Hubert J M Smeets, Filippo Martinelli Boneschi, Rayaz A Malik, Dan Ziegler, Janneke G J Hoeijmakers, Gidon Bönhof, Sulayman Dib-Hajj, Stephen G Waxman, Ingemar S J Merkies, Giuseppe Lauria, Catharina G Faber, Monique M Gerrits, on behalf on the PROPANE Study Group
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0248250 (2021)
[This corrects the article DOI: 10.1371/journal.pone.0238467.].
Externí odkaz:
https://doaj.org/article/c1c1cc67202f46d9a15f002a4e227929
Autor:
Rowida Almomani, Margherita Marchi, Maurice Sopacua, Patrick Lindsey, Erika Salvi, Bart de Koning, Silvia Santoro, Stefania Magri, Hubert J M Smeets, Filippo Martinelli Boneschi, Rayaz R Malik, Dan Ziegler, Janneke G J Hoeijmakers, Gidon Bönhof, Sulayman Dib-Hajj, Stephen G Waxman, Ingemar S J Merkies, Giuseppe Lauria, Catharina G Faber, Monique M Gerrits, on behalf on the PROPANE Study Group
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0238467 (2020)
Resolving the genetic architecture of painful neuropathy will lead to better disease management strategies. We aimed to develop a reliable method to re-sequence multiple genes in a large cohort of painful neuropathy patients at low cost. In this stud
Externí odkaz:
https://doaj.org/article/a140dd09be1741a88891ab27a803a8de