Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Tiziana Alberio"'
Autor:
Tiziana Alberio, Mariam Shallak, Amruth Kaleem Basha Shaik, Roberto Sergio Accolla, Greta Forlani
Publikováno v:
Viruses, Vol 16, Iss 8, p 1176 (2024)
The different susceptibility to HIV-1 infection in U937 cells—permissive (Plus) or nonpermissive (Minus)—is linked to the expression in Minus cells of interferon (IFN)-γ inducible antiviral factors such as tripartite motif-containing protein 22
Externí odkaz:
https://doaj.org/article/13b4e13188304443b69abc8f85e8f1b4
Autor:
Mariam Shallak, Tiziana Alberio, Mauro Fasano, Maria Monti, Ilaria Iacobucci, Julien Ladet, Franck Mortreux, Roberto S. Accolla, Greta Forlani
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Adult T-cell leukemia/lymphoma (ATL) is a T-cell lymphoproliferative neoplasm caused by the human T-cell leukemia virus type 1 (HTLV-1). Two viral proteins, Tax-1 and HBZ play important roles in HTLV-1 infectivity and in HTLV-1-associated pathologies
Externí odkaz:
https://doaj.org/article/401e1068b2264f0f86bc77d4eebebdb7
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 7, p 6268 (2023)
Mitochondrial dysfunction and vesicular trafficking alterations have been implicated in the pathogenesis of several neurodegenerative diseases. It has become clear that pathogenetic pathways leading to neurodegeneration are often interconnected. Inde
Externí odkaz:
https://doaj.org/article/62073ac63ad8403cae19f1ac470034f6
Publikováno v:
Biomedicines, Vol 10, Iss 9, p 2297 (2022)
The growing number of patients affected by neurodegenerative disorders represents a huge problem for healthcare systems, human society, and economics. In this context, omics strategies are crucial for the identification of molecular factors involved
Externí odkaz:
https://doaj.org/article/37f08af9815d48088d015050a8a94194
Autor:
Alessandra Zito, Marta Lualdi, Paola Granata, Dario Cocciadiferro, Antonio Novelli, Tiziana Alberio, Rosario Casalone, Mauro Fasano
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Gene set enrichment analysis (GSEA) is a powerful tool to associate a disease phenotype to a group of genes/proteins. GSEA attributes a specific weight to each gene/protein in the input list that depends on a metric of choice, which is usually repres
Externí odkaz:
https://doaj.org/article/f5d1ee5b7a4742b78f4c1544eebc8d94
Autor:
Mara Zilocchi, Ilaria Colugnat, Marta Lualdi, Monica Meduri, Federica Marini, Victor Corasolla Carregari, Mohamed Taha Moutaoufik, Sadhna Phanse, Luisa Pieroni, Mohan Babu, Barbara Garavaglia, Mauro Fasano, Tiziana Alberio
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Mutations in PARK2 gene are the most frequent cause of familial forms of Parkinson’s disease (PD). This gene encodes Parkin, an E3 ubiquitin ligase involved in several cellular mechanisms, including mitophagy. Parkin loss-of-function is responsible
Externí odkaz:
https://doaj.org/article/51ceb95f2cac41d79ea02df87249d100
Autor:
Tiziana Alberio, Greta Forlani, Marta Lualdi, Giovanna Tosi, Roberto S. Accolla, Mauro Fasano
Publikováno v:
Journal of Translational Medicine, Vol 16, Iss 1, Pp 1-13 (2018)
Abstract Background Fibrinogen is a central player in the blood coagulation cascade and one of the most abundant plasma proteins. This glycoprotein also triggers important events (e.g., cell spreading, the respiratory burst and degranulation) in neut
Externí odkaz:
https://doaj.org/article/73021201f9704d3cbf83497994eef84d
Autor:
Marta Lualdi, Adeena Shafique, Edoardo Pedrini, Luisa Pieroni, Viviana Greco, Massimo Castagnola, Giorgia Cucina, Lucia Corrado, Alice Di Pierro, Fabiola De Marchi, Lara Camillo, Claudia Colombrita, Marianna D’Anca, Tiziana Alberio, Sandra D’Alfonso, Mauro Fasano
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 19, p 10385 (2021)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive degeneration of the corticospinal motor neurons, which ultimately leads to death. The repeat expansion in chromosome 9 open reading frame 72 (C9ORF72) rep
Externí odkaz:
https://doaj.org/article/826ae3a32da74839afdfdd893bea1ce8
Autor:
Marta Lualdi, Maurizio Ronci, Mara Zilocchi, Federica Corno, Emily S. Turilli, Mauro Sponchiado, Antonio Aceto, Tiziana Alberio, Mauro Fasano
Publikováno v:
Frontiers in Aging Neuroscience, Vol 11 (2019)
Parkinson’s disease (PD) is the second most frequent neurodegenerative disease worldwide and the availability of early biomarkers and novel biotargets represents an urgent medical need. The main pathogenetic hallmark of PD is the specific loss of n
Externí odkaz:
https://doaj.org/article/6a450c8179904753b92af01846627428
Publikováno v:
EuPA Open Proteomics, Vol 10, Iss C, Pp 24-27 (2016)
The mitochondrial human proteome project (mt-HPP) was initiated by the Italian HPP group as a part of both the chromosome-centric initiative (C-HPP) and the “biology and disease driven” initiative (B/D-HPP). In recent years several reports highli
Externí odkaz:
https://doaj.org/article/4dccbf8ebf634cdc9ed490cafa18be47