Zobrazeno 1 - 10
of 114
pro vyhledávání: '"Enrico Cappelli"'
Autor:
Niccolò DeCarlo, Ciro Romano, Gianluca Granero, Fabrizio D'amico, Enrico Cappelli, Gianluca Fabbri
Publikováno v:
GEOmedia, Vol 28, Iss 3 (2024)
The article explores the integration of the Digital Twin concept with Federated Learning techniques for monitoring critical infrastructure. This approach allows for local data processing and knowledge transfer between different infrastructures, minim
Externí odkaz:
https://doaj.org/article/112b28fa647449a8b105f3efa7cb345c
Autor:
Maurizio Miano, Nadia Bertola, Alice Grossi, Gianluca Dell’Orso, Stefano Regis, Marta Rusmini, Paolo Uva, Diego Vozzi, Francesca Fioredda, Elena Palmisani, Michela Lupia, Marina Lanciotti, Federica Grilli, Fabio Corsolini, Luca Arcuri, Maria Carla Giarratana, Isabella Ceccherini, Carlo Dufour, Enrico Cappelli, Silvia Ravera
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 4, p 2083 (2024)
Serine/arginine-rich splicing factors (SRSFs) are a family of proteins involved in RNA metabolism, including pre-mRNA constitutive and alternative splicing. The role of SRSF proteins in regulating mitochondrial activity has already been shown for SRS
Externí odkaz:
https://doaj.org/article/fd9ec858ee1b44499e20b5d0a0a5353c
Autor:
Maurizio Miano, Nadia Bertola, Alice Grossi, Gianluca Dell’orso, Stefano Regis, Francesca Fioredda, Michela Lupia, Marina Lanciotti, Elena Palmisani, Maria Carla Giarratana, Luca Arcuri, Fabio Corsolini, Marta Rusmini, Paolo Uva, Diego Vozzi, Isabella Ceccherini, Silvia Ravera, Enrico Cappelli, Carlo Dufour
Publikováno v:
HemaSphere, Vol 7, p e48553f7 (2023)
Externí odkaz:
https://doaj.org/article/d0651111c3114e90917657b5b832f927
Autor:
Ilaria Persico, Giorgia Fontana, Michela Faleschini, Melania Eva Zanchetta, Daniele Ammeti, Enrico Cappelli, Fabio Corsolini, Clara Mosa, Angela Guarina, Massimo Bogliolo, Jordi Surrallés, Carlo Dufour, Piero Farruggia, Anna Savoia, Roberta Bottega
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Fanconi anemia (FA) is a genome instability condition that drives somatic mosaicism in up to 25% of all patients, a phenomenon now acknowledged as a good prognostic factor. Herein, we describe the case of P1, a FA proband carrying a spl
Externí odkaz:
https://doaj.org/article/c362a4450ed34036b2c2c9e8d32928b8
Autor:
Nadia Bertola, Stefano Regis, Silvia Bruno, Andrea Nicola Mazzarello, Martina Serra, Michela Lupia, Federica Sabatini, Fabio Corsolini, Silvia Ravera, Enrico Cappelli
Publikováno v:
Antioxidants, Vol 12, Iss 5, p 1100 (2023)
Fanconi anemia (FA) is a rare genetic disease characterized by a dysfunctional DNA repair and an oxidative stress accumulation due to defective mitochondrial energy metabolism, not counteracted by endogenous antioxidant defenses, which appear down-ex
Externí odkaz:
https://doaj.org/article/2f0e247638be48e4b793dfa7bc67e293
Autor:
Maurizio Miano, Daniela Guardo, Alice Grossi, Elena Palmisani, Francesca Fioredda, Paola Terranova, Enrico Cappelli, Michela Lupia, Monica Traverso, Gianluca Dell’Orso, Fabio Corsolini, Andrea Beccaria, Marina Lanciotti, Isabella Ceccherini, Carlo Dufour
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundEvans syndrome (ES) is a rare disorder classically defined as the simultaneous or sequential presence of autoimmune haemolytic anaemia and immune thrombocytopenia, but it has also been described as the presence of at least two autoimmune cy
Externí odkaz:
https://doaj.org/article/6c959308b41d4cab9b865c7c7100a1b3
Autor:
Nadia Bertola, Silvia Bruno, Cristina Capanni, Marta Columbaro, Andrea Nicola Mazzarello, Fabio Corsolini, Stefano Regis, Paolo Degan, Enrico Cappelli, Silvia Ravera
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 7, p 6557 (2023)
Fanconi anemia (FA) is a rare genetic disorder characterized by bone marrow failure and aplastic anemia. So far, 23 genes are involved in this pathology, and their mutations lead to a defect in DNA repair. In recent years, it has been observed that F
Externí odkaz:
https://doaj.org/article/9f730fbb260f498091cdac9cd0291ae7
Autor:
Philippe Fernandes, Benoit Miotto, Claude Saint-Ruf, Maha Said, Viviana Barra, Viola Nähse, Silvia Ravera, Enrico Cappelli, Valeria Naim
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-16 (2021)
Fernandes et al. discover a connection between the mitochondrial stress response and genomic stability. They find that transcription of common fragile site (CFS) genes is induced by mitochondrial stress, whereas a regulator of CFS stability, FANCD2,
Externí odkaz:
https://doaj.org/article/e0f19b4840814983bdab55f7127e98cd
Publikováno v:
Cells, Vol 11, Iss 15, p 2353 (2022)
Fanconi Anaemia (FA) is a rare recessive genetic disorder characterized by a defective DNA repair mechanism. Although aplastic anaemia is the principal clinical sign in FA, patients develop a head and neck squamous cell carcinoma (HNSCC) with a frequ
Externí odkaz:
https://doaj.org/article/c930d7e490d048c98aac460bde535942
Autor:
Enrico Cappelli, Paolo Degan, Silvia Bruno, Filomena Pierri, Maurizio Miano, Federica Raggi, Piero Farruggia, Cristina Mecucci, Barbara Crescenzi, Valeria Naim, Carlo Dufour, Silvia Ravera
Publikováno v:
Redox Biology, Vol 36, Iss , Pp 101618- (2020)
Fanconi Anemia (FA) is a disease characterized by bone marrow (BM) failure and aplastic anemia. In addition to a defective DNA repair system, other mechanisms are involved in its pathogenesis, such as defective mitochondrial metabolism, accumulation
Externí odkaz:
https://doaj.org/article/f2836c13ebfe443caacce39fedf1df81