Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Nicoletta, Loberto"'
Autor:
Giulia Lunghi, Erika Di Biase, Emma Veronica Carsana, Alexandre Henriques, Noelle Callizot, Laura Mauri, Maria Grazia Ciampa, Luigi Mari, Nicoletta Loberto, Massimo Aureli, Sandro Sonnino, Michael Spedding, Elena Chiricozzi, Maria Fazzari
Publikováno v:
FEBS Open Bio, Vol 13, Iss 12, Pp 2324-2341 (2023)
Alterations in glycosphingolipid metabolism have been linked to the pathophysiological mechanisms of amyotrophic lateral sclerosis (ALS), a neurodegenerative disease affecting motor neurons. Accordingly, administration of GM1, a sialic acid‐contain
Externí odkaz:
https://doaj.org/article/bc90ee2630b94cd7baec16a20f019b9f
Autor:
Dorina Dobi, Nicoletta Loberto, Rosaria Bassi, Anna Pistocchi, Giulia Lunghi, Anna Tamanini, Massimo Aureli
Publikováno v:
FEBS Open Bio, Vol 13, Iss 9, Pp 1601-1614 (2023)
Cystic fibrosis (CF) is the most common inherited, life‐limiting disorder in Caucasian populations. It is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR), which lead to an impairment of protei
Externí odkaz:
https://doaj.org/article/cf41b81ef2a64b609a257945b0ae668e
Autor:
Marco Cafora, Noemi Poerio, Francesca Forti, Nicoletta Loberto, Davide Pin, Rosaria Bassi, Massimo Aureli, Federica Briani, Anna Pistocchi, Maurizio Fraziano
Publikováno v:
Frontiers in Microbiology, Vol 13 (2022)
Multi drug resistant (MDR) bacteria are insensitive to the most common antibiotics currently in use. The spread of antibiotic-resistant bacteria, if not contained, will represent the main cause of death for humanity in 2050. The situation is even mor
Externí odkaz:
https://doaj.org/article/381f8ec2e51e4526a1525df4727771a7
Autor:
Maria Fazzari, Giulia Lunghi, Alexandre Henriques, Noëlle Callizot, Maria Grazia Ciampa, Laura Mauri, Simona Prioni, Emma Veronica Carsana, Nicoletta Loberto, Massimo Aureli, Luigi Mari, Sandro Sonnino, Elena Chiricozzi, Erika Di Biase
Publikováno v:
Biomedicines, Vol 11, Iss 5, p 1305 (2023)
Past evidence has shown that the exogenous administration of GM1 ganglioside slowed neuronal death in preclinical models of Parkinson’s disease, a neurodegenerative disorder characterized by the progressive loss of dopamine-producing neurons: howev
Externí odkaz:
https://doaj.org/article/8a1943fc716f42f4923a8d9f878d1326
Autor:
Giulia Lunghi, Emma Veronica Carsana, Nicoletta Loberto, Laura Cioccarelli, Simona Prioni, Laura Mauri, Rosaria Bassi, Stefano Duga, Letizia Straniero, Rosanna Asselta, Giulia Soldà, Alessio Di Fonzo, Emanuele Frattini, Manuela Magni, Nara Liessi, Andrea Armirotti, Elena Ferrari, Maura Samarani, Massimo Aureli
Publikováno v:
Cells, Vol 11, Iss 15, p 2343 (2022)
β-glucocerebrosidase is a lysosomal hydrolase involved in the catabolism of the sphingolipid glucosylceramide. Biallelic loss of function mutations in this enzyme are responsible for the onset of Gaucher disease, while monoallelic β-glucocerebrosid
Externí odkaz:
https://doaj.org/article/0c02205b205142f68964b014a1490b02
Autor:
Nara Liessi, Valeria Tomati, Valeria Capurro, Nicoletta Loberto, Mar Garcia-Aloy, Pietro Franceschi, Massimo Aureli, Nicoletta Pedemonte, Andrea Armirotti
Publikováno v:
Journal of Cystic Fibrosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2809ce64dbccce8eb943f503c26c188
https://doi.org/10.1016/j.jcf.2023.04.012
https://doi.org/10.1016/j.jcf.2023.04.012
Autor:
Nicoletta Loberto, Alessia Brix, Anna Pistocchi, Federica Briani, Francesca Forti, Marco Cafora, Massimo Aureli
Publikováno v:
Journal of Cystic Fibrosis. 20:1046-1052
Cystic Fibrosis (CF), one of the most frequent hereditary diseases due to mutations in the CFTR gene, causes mortality in humans mainly due to infection in the respiratory system. However, besides the massive inflammatory response triggered by chroni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec9f6bb0d9d1294155ad6cafec8897a5
https://doi.org/10.1016/j.jcf.2020.11.017
https://doi.org/10.1016/j.jcf.2020.11.017
Autor:
Domitilla Schiumarini, Nicoletta Loberto, Giulia Mancini, Rosaria Bassi, Paola Giussani, Elena Chiricozzi, Maura Samarani, Silvia Munari, Anna Tamanini, Giulio Cabrini, Giuseppe Lippi, Maria Cristina Dechecchi, Sandro Sonnino, Massimo Aureli
Publikováno v:
Mediators of Inflammation, Vol 2017 (2017)
Cystic fibrosis (CF) is the most common autosomal genetic recessive disease caused by mutations of gene encoding for the cystic fibrosis transmembrane conductance regulator. Patients with CF display a wide spectrum of symptoms, the most severe being
Externí odkaz:
https://doaj.org/article/af2909c0c2a44a82ba88345b7d4a22fa
Autor:
Aureli, Giulia Lunghi, Emma Veronica Carsana, Nicoletta Loberto, Laura Cioccarelli, Simona Prioni, Laura Mauri, Rosaria Bassi, Stefano Duga, Letizia Straniero, Rosanna Asselta, Giulia Soldà, Alessio Di Fonzo, Emanuele Frattini, Manuela Magni, Nara Liessi, Andrea Armirotti, Elena Ferrari, Maura Samarani, Massimo
Publikováno v:
Cells; Volume 11; Issue 15; Pages: 2343
β-glucocerebrosidase is a lysosomal hydrolase involved in the catabolism of the sphingolipid glucosylceramide. Biallelic loss of function mutations in this enzyme are responsible for the onset of Gaucher disease, while monoallelic β-glucocerebrosid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::0152f3a5a2c6159c75ff3dc9e50bc084
Autor:
Emma Veronica Carsana, Giulia Lunghi, Simona Prioni, Laura Mauri, Nicoletta Loberto, Alessandro Prinetti, Fabio Andrea Zucca, Rosaria Bassi, Sandro Sonnino, Elena Chiricozzi, Stefano Duga, Letizia Straniero, Rosanna Asselta, Giulia Soldà, Maura Samarani, Massimo Aureli
Niemann-Pick type A disease (NPA) is a rare lysosomal storage disorder caused by mutations in the gene coding for the lysosomal enzyme acid sphingomyelinase (ASM). ASM deficiency leads to the consequent accumulation of its uncatabolized substrate, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::970f1ce630e730724c630707fe382554
https://hdl.handle.net/2434/944971
https://hdl.handle.net/2434/944971
