Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Valentina Matteo"'
Autor:
Ester De Leo, Anna Taranta, Roberto Raso, Marco Pezzullo, Michela Piccione, Valentina Matteo, Alessia Vitale, Francesco Bellomo, Bianca Maria Goffredo, Francesca Diomedi Camassei, Giusi Prencipe, Laura Rita Rega, Francesco Emma
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 178, Iss , Pp 117236- (2024)
In infantile nephropathic cystinosis, variants of the CTNS gene cause accumulation of cystine in lysosomes, causing progressive damage to most organs. Patients usually present before 1 year of age with signs of renal Fanconi syndrome. Cysteamine ther
Externí odkaz:
https://doaj.org/article/a142271262d54c4080ae960e68694d5f
Autor:
Marianna Nicoletta Rossi, Valentina Matteo, Francesca Diomedi-Camassei, Ester De Leo, Olivier Devuyst, Mohamed Lamkanfi, Ivan Caiello, Elena Loricchio, Francesco Bellomo, Anna Taranta, Francesco Emma, Fabrizio De Benedetti, Giusi Prencipe
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Cystinosis is a rare autosomal recessive disorder caused by mutations in the CTNS gene that encodes cystinosin, a ubiquitous lysosomal cystine/H+ antiporter. The hallmark of the disease is progressive accumulation of cystine and cystine crystals in v
Externí odkaz:
https://doaj.org/article/a1638def141045a1a1850f75b41d76d3
Autor:
Marianna Nicoletta Rossi, Silvia Federici, Andrea Uva, Chiara Passarelli, Camilla Celani, Ivan Caiello, Valentina Matteo, Stefano Petrocchi, Eva Piano Mortari, Fabrizio De Benedetti, Giusi Prencipe, Antonella Insalaco
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Haploinsufficiency of A20 (HA20) is an inflammatory disease caused by mutations in the TNFAIP3 gene classically presenting with Behcet’s-like disease. A20 acts as an inhibitor of inflammation through its effect on NF-kB pathway. Here we describe fo
Externí odkaz:
https://doaj.org/article/6301ae75e4224dad8f89196fa2535f31
Autor:
Antonia Pascarella, Claudia Bracaglia, Ivan Caiello, Alessia Arduini, Gian Marco Moneta, Marianna Nicoletta Rossi, Valentina Matteo, Manuela Pardeo, Fabrizio De Benedetti, Giusi Prencipe
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
ObjectiveTo investigate the activation of the IFNγ signaling pathway in monocytes of patients with secondary hemophagocytic lymphohistiocytosis (sHLH)/macrophage activation syndrome (MAS) and to evaluate whether levels of phosphorylated STAT1 repres
Externí odkaz:
https://doaj.org/article/e91c1633f52d433d87d580747317d549
Autor:
Francesco Nicita, Lorena Travaglini, Valentina Matteo, Chiara Aiello, Daniela Longo, Antonella Insalaco, Enrico Bertini, Giusi Prencipe
Publikováno v:
Annals of Neurology. 93:1041-1043
Autor:
Marianna Nicoletta, Rossi, Silvia, Federici, Andrea, Uva, Chiara, Passarelli, Camilla, Celani, Ivan, Caiello, Valentina, Matteo, Stefano, Petrocchi, Eva Piano, Mortari, Fabrizio, De Benedetti, Giusi, Prencipe, Antonella, Insalaco
Publikováno v:
Frontiers in immunology. 13
Haploinsufficiency of A20 (HA20) is an inflammatory disease caused by mutations in the
Autor:
Fabrizio De Benedetti, Marianna Nicoletta Rossi, Manuela Pardeo, Gian Marco Moneta, Antonia Pascarella, Ivan Caiello, Valentina Matteo, Claudia Bracaglia, Alessia Arduini, Giusi Prencipe
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology
Frontiers in Immunology
ObjectiveTo investigate the activation of the IFNγ signaling pathway in monocytes of patients with secondary hemophagocytic lymphohistiocytosis (sHLH)/macrophage activation syndrome (MAS) and to evaluate whether levels of phosphorylated STAT1 repres