Zobrazeno 1 - 10
of 608
pro vyhledávání: '"Raffaele, Badolato"'
Autor:
Lorenzo Loffredo, Annarosa Soresina, Bianca Laura Cinicola, Martina Capponi, Francesca Salvatori, Simona Bartimoccia, Vittorio Picchio, Maurizio Forte, Caterina Caputi, Roberto Poscia, Vincenzo Leuzzi, Alberto Spalice, Pasquale Pignatelli, Raffaele Badolato, Marzia Duse, Francesco Violi, Roberto Carnevale, Anna Maria Zicari, Ilaria Maria Palumbo, Arianna Magna, Alessia Fallarino, Arianna Pannunzio, Enrico Maggio, Chiara Bagnato, Vittoria Cammisotto, Valentina Castellani
Publikováno v:
Redox Biology, Vol 77, Iss , Pp 103347- (2024)
Background: Subjects with mutations in the Ataxia-Telangiectasia mutated (ATM) gene encoding for ATM kinase have a greater predisposition to develop atherosclerosis, but the mechanism behind this phenomenon is not yet understood. NADPH oxidase type 2
Externí odkaz:
https://doaj.org/article/311ff2b2e19f46d58a4930364cc07b47
Autor:
Vassilios Lougaris, Federico Le Piane, Caterina Cancrini, Francesca Conti, Alberto Tommasini, Raffaele Badolato, Antonino Trizzino, Marco Zecca, Antonio De Rosa, Federica Barzaghi, Claudio Pignata
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-11 (2024)
Abstract Activated phosphoinositide 3-kinase (PI3Kδ) Syndrome (APDS) is an inborn error of immunity (IEI) with a variable clinical presentation, characterized by infection susceptibility and immune dysregulation that may overlaps with other Primary
Externí odkaz:
https://doaj.org/article/c3a720bfdd824b72a325d875a42d7813
Autor:
Emilia Cirillo, Antonietta Tarallo, Elisabetta Toriello, Annamaria Carissimo, Giuliana Giardino, Antonio De Rosa, Carla Damiano, Annarosa Soresina, Raffaele Badolato, Rosa Maria Dellepiane, Lucia A. Baselli, Maria Carrabba, Giovanna Fabio, Patrizia Bertolini, Davide Montin, Francesca Conti, Roberta Romano, Elisa Pozzi, Giulio Ferrero, Roberta Roncarati, Manuela Ferracin, Alfredo Brusco, Giancarlo Parenti, Claudio Pignata
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionAtaxia telangiectasia (AT) is a rare disorder characterized by neurodegeneration, combined immunodeficiency, a predisposition to malignancies, and high clinical variability. Profiling of microRNAs (miRNAs) may offer insights into the unde
Externí odkaz:
https://doaj.org/article/fcaa1e5e99644d8590fe1280ba7fae17
Autor:
Sergio Ghirardo, Nicola Ullmann, Alessandro Zago, Michele Ghezzi, Marta Minute, Barbara Madini, Enza D’Auria, Cecilia Basile, Francesca Castelletti, Federica Chironi, Agata Capodiferro, Beatrice Andrenacci, Francesco Maria Risso, Salvatore Aversa, Laura Dotta, Antonella Coretti, Anna Chiara Vittucci, Raffaele Badolato, Alessandro Amaddeo, Egidio Barbi, Renato Cutrera
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-9 (2024)
Abstract Background The coronavirus 2019 (COVID-19) related containment measures led to the disruption of all virus distribution. Bronchiolitis-related hospitalizations shrank during 2020–2021, rebounding to pre-pandemic numbers the following year.
Externí odkaz:
https://doaj.org/article/7d807d7e5054430888b0f67be4dca304
Autor:
Claudia Asperti, Daniele Canarutto, Simona Porcellini, Francesca Sanvito, Francesca Cecere, Valentina Vavassori, Samuele Ferrari, Elisabetta Rovelli, Luisa Albano, Aurelien Jacob, Lucia Sergi Sergi, Elisa Montaldo, Francesca Ferrua, Luis Ignacio González-Granado, Vassilios Lougaris, Raffaele Badolato, Andrea Finocchi, Anna Villa, Marina Radrizzani, Luigi Naldini
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 30, Iss , Pp 546-557 (2023)
Hyper-IgM1 is a rare X-linked combined immunodeficiency caused by mutations in the CD40 ligand (CD40LG) gene with a median survival of 25 years, potentially treatable with in situ CD4+ T cell gene editing with Cas9 and a one-size-fits-most corrective
Externí odkaz:
https://doaj.org/article/95bf4664548f487685bff24201e74568
Autor:
Giulia Sbrini, Zaira Tomasoni, Maria Rosa Cutrì, Alba Pilotta, Chiara Mingotti, Raffaele Badolato, Luca La Via, Alessandro Barbon, Federica Bono, Chiara Fiorentini
Publikováno v:
Stem Cell Research, Vol 74, Iss , Pp 103293- (2024)
We have established Noonan syndrome (NS)-derived induced pluripotent stem cell (iPSC) lines derived from peripheral blood mononuclear cells (PBMCs) of a family cohort carrying the heterozygous PTPN11 c.188 A > G (p.Y63C) mutation. The new iPSC lines
Externí odkaz:
https://doaj.org/article/aee40349e31e43ecb048ec38c4a60166
Autor:
Samuele Roncareggi, Katia Girardi, Francesca Fioredda, Lucia Pedace, Luca Arcuri, Raffaele Badolato, Sonia Bonanomi, Erika Borlenghi, Emilia Cirillo, Tiziana Coliva, Filippo Consonni, Francesca Conti, Piero Farruggia, Eleonora Gambineri, Fabiola Guerra, Gaia Mancuso, Antonio Marzollo, Riccardo Masetti, Concetta Micalizzi, Daniela Onofrillo, Claudio Pignata, Valeria Santini, Francesca Vendemini, Andrea Biondi, Francesco Saettini
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100057- (2023)
Externí odkaz:
https://doaj.org/article/52010328d3e042c2842062ff7b1de744
Autor:
Melania Degli Antoni, Verena Crosato, Francesca Pennati, Andrea Borghesi, Graziella Cristini, Roberto Allegri, Susanna Capone, Alberto Bergamasco, Annarosa Soresina, Raffaele Badolato, Roberto Maroldi, Eugenia Quiros-Roldan, Alberto Matteelli, Francesco Castelli, Emanuele Focà
Publikováno v:
Tomography, Vol 9, Iss 3, Pp 894-900 (2023)
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency characterized by marked reduction in serum immunoglobulins and early-onset infections. Coronavirus Disease-2019 (COVID-19) pneumonia in immunocompromised patients presents clinical and r
Externí odkaz:
https://doaj.org/article/f4b3f8e1cc0a4d1da891b5b112e3731d
Autor:
Maria Carrabba, Rosa Maria Dellepiane, Manuela Cortesi, Lucia Augusta Baselli, Annarosa Soresina, Emilia Cirillo, Giuliana Giardino, Francesca Conti, Laura Dotta, Andrea Finocchi, Caterina Cancrini, Cinzia Milito, Lucia Pacillo, Bianca Laura Cinicola, Fausto Cossu, Rita Consolini, Davide Montin, Isabella Quinti, Andrea Pession, Giovanna Fabio, Claudio Pignata, Maria Cristina Pietrogrande, Raffaele Badolato
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 19, Iss 1, Pp 1-12 (2023)
Abstract Job’s syndrome, or autosomal dominant hyperimmunoglobulin E syndrome (AD-HIES, STAT3-Dominant Negative), is a rare inborn error of immunity (IEI) with multi-organ involvement and long-life post-infective damage. Longitudinal registries are
Externí odkaz:
https://doaj.org/article/e562c8d325804325ab0a1eb01d5a36b2
Publikováno v:
HemaSphere, Vol 7, p e684700a (2023)
Externí odkaz:
https://doaj.org/article/894818817ad6499ebefa6ef0e98eafaf