Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Federica Albanese"'
Autor:
Satra Nim, Darren M. O’Hara, Carles Corbi-Verge, Albert Perez-Riba, Kazuko Fujisawa, Minesh Kapadia, Hien Chau, Federica Albanese, Grishma Pawar, Mitchell L. De Snoo, Sophie G. Ngana, Jisun Kim, Omar M. A. El-Agnaf, Enrico Rennella, Lewis E. Kay, Suneil K. Kalia, Lorraine V. Kalia, Philip M. Kim
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-19 (2023)
Abstract Accumulation of α-synuclein into toxic oligomers or fibrils is implicated in dopaminergic neurodegeneration in Parkinson’s disease. Here we performed a high-throughput, proteome-wide peptide screen to identify protein-protein interaction
Externí odkaz:
https://doaj.org/article/5d9353322078445d81d882610543e049
Autor:
Francesco Longo, Sameer Aryal, Paul G. Anastasiades, Marta Maltese, Corey Baimel, Federica Albanese, Joanna Tabor, Jeffrey D. Zhu, Mauricio M. Oliveira, Denise Gastaldo, Claudia Bagni, Emanuela Santini, Nicolas X. Tritsch, Adam G. Carter, Eric Klann
Publikováno v:
Cell Reports, Vol 42, Iss 8, Pp 112901- (2023)
Summary: Individuals with fragile X syndrome (FXS) are frequently diagnosed with autism spectrum disorder (ASD), including increased risk for restricted and repetitive behaviors (RRBs). Consistent with observations in humans, FXS model mice display d
Externí odkaz:
https://doaj.org/article/dc43b9ea499f4df290879ca6923d0caf
Autor:
Carla Bizzarri, Germana Antonella Giannone, Jacopo Gervasoni, Sabina Benedetti, Federica Albanese, Luca Dello Strologo, Isabella Guzzo, Mafalda Mucciolo, Francesca Diomedi Camassei, Francesco Emma, Marco Cappa, Ottavia Porzio
Publikováno v:
JCRPE, Vol 13, Iss 3, Pp 347-352 (2021)
We describe a 46,XX girl with Denys-Drash syndrome, showing both kidney disease and genital abnormalities, in whom a misdiagnosis of hyperandrogenism was made. A 15 year-old girl was affected by neonatal nephrotic syndrome, progressing to end stage k
Externí odkaz:
https://doaj.org/article/a2602538bac643a586c21dfc759aadad
Autor:
Salvatore Novello, Daniela Mercatelli, Federica Albanese, Chiara Domenicale, Alberto Brugnoli, Elisabetta D'Aversa, Silvia Vantaggiato, Sandra Dovero, Valentina Murtaj, Luca Presotto, Monica Borgatti, Derya R. Shimshek, Erwan Bezard, Rosa Maria Moresco, Sara Belloli, Michele Morari
Publikováno v:
Neurobiology of Disease, Vol 162, Iss , Pp 105579- (2022)
The G2019S mutation of LRRK2 represents a risk factor for idiopathic Parkinson's disease. Here, we investigate whether LRRK2 kinase activity regulates susceptibility to the environmental toxin 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine (MPTP). G201
Externí odkaz:
https://doaj.org/article/055453400ae74341863a1b9645ff1160
Autor:
Sebastiano Cicco, Marialuisa Sveva Marozzi, Carmen Alessandra Palumbo, Elisabetta Sturdà, Antonio Fusillo, Flavio Scarilli, Federica Albanese, Claudia Morelli, Davide Fiore Bavaro, Lucia Diella, Annalisa Saracino, Fabrizio Pappagallo, Antonio Giovanni Solimando, Gianfranco Lauletta, Roberto Ria, Angelo Vacca
Publikováno v:
Medicina, Vol 59, Iss 2, p 203 (2023)
Background and Objectives: COVID-19 induces massive systemic inflammation. Researchers have spent much time and effort finding an excellent and rapid image tool to evaluate COVID-19 patients. Since the pandemic’s beginning, lung ultrasound (LUS) ha
Externí odkaz:
https://doaj.org/article/94101ceff61847b483b2e1cdf508e93f
Autor:
Federica Albanese, Daniela Mercatelli, Luca Finetti, Giulia Lamonaca, Sara Pizzi, Derya R. Shimshek, Giovanni Bernacchia, Michele Morari
Publikováno v:
Neurobiology of Disease, Vol 159, Iss , Pp 105487- (2021)
Mutations in leucine-rich repeat kinase 2 (LRRK2) are associated with Parkinson's disease. LRRK2 modulates the autophagy-lysosome pathway (ALP), a clearance process subserving the quality control of cellular proteins and organelles. Since dysfunction
Externí odkaz:
https://doaj.org/article/c6ad653294774569ab0c5e0a0a79c526
Autor:
Chiara Domenicale, Daniela Mercatelli, Federica Albanese, Salvatore Novello, Fabrizio Vincenzi, Katia Varani, Michele Morari
Publikováno v:
Biomedicines, Vol 10, Iss 4, p 881 (2022)
The G2019S mutation in leucine rich-repeat kinase 2 (LRRK2) is a major cause of familial Parkinson’s disease. We previously reported that G2019S knock-in mice manifest dopamine transporter dysfunction and phosphoSerine129 α-synuclein (pSer129 α-s
Externí odkaz:
https://doaj.org/article/88edc5deace04944ab64ff00ad54ec70
Autor:
Luca Finetti, Stefano Civolani, Daniele Mirandola, Lorenzo Benetti, Santolo Francati, Federica Albanese, Felicia Menicucci, Marco Michelozzi, Maria Grazia Bellardi, Maria Luisa Dindo, Giovanni Bernacchia
Publikováno v:
Insects, Vol 13, Iss 3, p 280 (2022)
Drosophila suzukii (Matsumara) is an herbivorous pest whose control in the field with conventional chemical is particularly difficult and has important drawbacks. Here, we investigated the insecticidal properties of hydrolate from Monarda didyma, sca
Externí odkaz:
https://doaj.org/article/0f791a9037654c5ba56fd82f3b5d51de
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
Autophagy is a highly conserved process by which long-lived macromolecules, protein aggregates and dysfunctional/damaged organelles are delivered to lysosomes for degradation. Autophagy plays a crucial role in regulating protein quality control and c
Externí odkaz:
https://doaj.org/article/8325ed79f82645158cd4a0e2ab425546
Autor:
Maria Regoni, Letizia Zanetti, Stefano Comai, Daniela Mercatelli, Salvatore Novello, Federica Albanese, Laura Croci, Gian Giacomo Consalez, Andrea Ciammola, Flavia Valtorta, Michele Morari, Jenny Sassone
Publikováno v:
Biomedicines, Vol 9, Iss 5, p 514 (2021)
Mutations in the PARK2 gene encoding the protein parkin cause autosomal recessive juvenile parkinsonism (ARJP), a neurodegenerative disease characterized by early dysfunction and loss of dopamine (DA) neurons in the substantia nigra pars compacta (SN
Externí odkaz:
https://doaj.org/article/12033736213a4a09a364896d9ec296cc