Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Elisa Pozzi"'
Autor:
Emilia Cirillo, Antonietta Tarallo, Elisabetta Toriello, Annamaria Carissimo, Giuliana Giardino, Antonio De Rosa, Carla Damiano, Annarosa Soresina, Raffaele Badolato, Rosa Maria Dellepiane, Lucia A. Baselli, Maria Carrabba, Giovanna Fabio, Patrizia Bertolini, Davide Montin, Francesca Conti, Roberta Romano, Elisa Pozzi, Giulio Ferrero, Roberta Roncarati, Manuela Ferracin, Alfredo Brusco, Giancarlo Parenti, Claudio Pignata
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionAtaxia telangiectasia (AT) is a rare disorder characterized by neurodegeneration, combined immunodeficiency, a predisposition to malignancies, and high clinical variability. Profiling of microRNAs (miRNAs) may offer insights into the unde
Externí odkaz:
https://doaj.org/article/fcaa1e5e99644d8590fe1280ba7fae17
Autor:
Angelo Robotto, Carlotta Olivero, Elisa Pozzi, Claudia Strumia, Camilla Crasà, Cristina Fedele, Maddalena Derosa, Massimo Di Martino, Stefania Latino, Giada Scorza, Andrea Civra, David Lembo, Paola Quaglino, Enrico Brizio, Denis Polato
Publikováno v:
PLoS ONE, Vol 19, Iss 5 (2024)
Externí odkaz:
https://doaj.org/article/d48afb3a8dcc4351b917a696fe0a892a
Autor:
Elisa Rubino, Silvia Boschi, Elisa Giorgio, Elisa Pozzi, Andrea Marcinnò, Erica Gallo, Fausto Roveta, Alberto Grassini, Alfredo Brusco, Innocenzo Rainero
Publikováno v:
Neurobiology of Pain, Vol 11, Iss , Pp 100089- (2022)
Recent studies suggested that epigenetic mechanisms, including DNA methylation, may be involved in migraine pathogenesis. The calcitonin gene-related peptide (CGRP), encoded by calcitonin gene-related peptide 1 (CALCA) gene, plays a key role in the d
Externí odkaz:
https://doaj.org/article/718dd2e683bf494c85d056664dc4b3e0
Autor:
Cecilia Mancini, Eriola Hoxha, Luisa Iommarini, Alessandro Brussino, Uwe Richter, Francesca Montarolo, Claudia Cagnoli, Roberta Parolisi, Diana Iulia Gondor Morosini, Valentina Nicolò, Francesca Maltecca, Luisa Muratori, Giulia Ronchi, Stefano Geuna, Francesca Arnaboldi, Elena Donetti, Elisa Giorgio, Simona Cavalieri, Eleonora Di Gregorio, Elisa Pozzi, Marta Ferrero, Evelise Riberi, Giorgio Casari, Fiorella Altruda, Emilia Turco, Giuseppe Gasparre, Brendan J. Battersby, Anna Maria Porcelli, Enza Ferrero, Alfredo Brusco, Filippo Tempia
Publikováno v:
Neurobiology of Disease, Vol 124, Iss , Pp 14-28 (2019)
Spinocerebellar ataxia 28 is an autosomal dominant neurodegenerative disorder caused by missense mutations affecting the proteolytic domain of AFG3L2, a major component of the mitochondrial m-AAA protease. However, little is known of the underlying p
Externí odkaz:
https://doaj.org/article/fb3744284a404bcf85efa0b2b018e6b8
Autor:
Stefania Squadrone, Paola Brizio, Cecilia Mancini, Elisa Pozzi, Simona Cavalieri, Maria Cesarina Abete, Alfredo Brusco
Publikováno v:
Neurobiology of Disease, Vol 81, Iss , Pp 162-167 (2015)
Transition metals are cofactors for a wide range of vital enzymes and are directly or indirectly involved in the response against reactive oxygen species (ROS), which can damage cellular components. Their altered homeostasis has been studied in neuro
Externí odkaz:
https://doaj.org/article/37a6e5c9f7b848ebb946b4cbc8a74fe3
Autor:
Francesca Monari, Giulia Pedrielli, Patrizia Vergani, Elisa Pozzi, Federico Mecacci, Caterina Serena, Isabella Neri, Fabio Facchinetti
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0155761 (2016)
OBJECTIVE:To evaluate outcome in the pregnancy following a stillbirth (SB) by a placental vascular disorders. STUDY DESIGN:A prospective, observational, multicenter study was conducted in woman with a history of stillbirth (> 22 weeks) between 2005 a
Externí odkaz:
https://doaj.org/article/ac443d0ecc8c498293e2f1ecbe4efd64
Autor:
Enza Ferrero, Eleonora Di Gregorio, Marta Ferrero, Erika Ortolan, Young-Ah Moon, Antonella Di Campli, Lisa Pavinato, Cecilia Mancini, Debasmita Tripathy, Marta Manes, Eriola Hoxha, Chiara Costanzi, Elisa Pozzi, Matteo Rossi Sebastiano, Nico Mitro, Filippo Tempia, Donatella Caruso, Barbara Borroni, Manuela Basso, Michele Sallese, Alfredo Brusco
Fatty acid elongase ELOVL5 is part of a protein family of multipass transmembrane proteins that reside in the endoplasmic reticulum where they regulate long-chain fatty acid elongation. A missense variant (c.689G > T p.Gly230Val) in ELOVL5 causes Spi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f91e8071f8c8ed9a156ba4239a4c896
https://hdl.handle.net/2318/1904432
https://hdl.handle.net/2318/1904432
Autor:
Simona Cavalieri, Stefania Augeri, Maria Vinciguerra, Ada Funaro, Evelise Riberi, Marta Ferrero, Cecilia Mancini, Lorenzo Nanetti, Elisa Giorgio, Caterina Mariotti, F. Bianchi, Eleonora Di Gregorio, Alfredo Brusco, Vincenzo Costanzo, Nicola Lo Buono, Maria Paola Sassi, Elisa Pozzi
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
Short term treatment with low doses of glucocorticoid analogues has been shown to ameliorate neurological symptoms in Ataxia–Telangiectasia (A–T), a rare autosomal recessive multisystem disease that mainly affects the cerebellum, immune system, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d28f3a51063956e09f01d082838e43b2
https://doi.org/10.1038/s41598-020-77352-z
https://doi.org/10.1038/s41598-020-77352-z
Autor:
Elvira Sondo, Edoardo Della Sala, Marta Ferrero, Martina Lorenzati, Cristina Morerio, Alfredo Brusco, Pietro Cortelli, Nicoletta Pedemonte, Emanuela Pesce, Elisa Giorgio, Elisa Pozzi, Giusy Borrelli, Annalisa Buffo
Publikováno v:
Human mutationREFERENCES. 42(1)
In genetic diseases, the most prevalent mechanism of pathogenicity is an altered expression of dosage-sensitive genes. Drugs that restore physiological levels of these genes should be effective in treating the associated conditions. We developed a sc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57a0259d6a429c9991b11fe86596c83b
https://pubmed.ncbi.nlm.nih.gov/33252173
https://pubmed.ncbi.nlm.nih.gov/33252173
Autor:
Marta Ferrero, G. De Michele, Elisa Pozzi, Gabriella Silvestri, L. Pradotto, Elisa Giorgio, Simona Cavalieri, Elisa Rubino, Cecilia Mancini, Filippo M. Santorelli, Antonella Antenora, Anna Rubegni, Alfredo Brusco, Melissa Barghigiani, Siro Bagnoli, Fabio Sirchia, Alessandro Mauro, Alessandro Filla, Patrizia Ferrero, S. Piacentini, Laura Orsi, Maurizio Zibetti, E. Di Gregorio, Paolo Prontera, Pasquale Nigro, Alessandra Tessa, Evelise Riberi
Background and purpose Hereditary ataxias are heterogeneous groups of neurodegenerative disorders, characterized by cerebellar syndromes associated with dysarthria, oculomotor and corticospinal signs, neuropathy and cognitive impairment. Recent repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f22badd62e6dfb7eea28f5a6eeed26e
http://hdl.handle.net/2318/1678964
http://hdl.handle.net/2318/1678964