Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Stefania Masneri"'
Autor:
Vera Radici, Cinzia Giagulli, Eugenia Accorsi Buttini, Mirko Farina, Nicola Polverelli, Duilio Brugnoni, Marco Chiarini, Anna Galvagni, Camillo Almici, Emilio Ferrari, Andrea Bianchetti, Stefania Masneri, Alessandro Leoni, Federica Re, Simona Bernardi, Michele Malagola, Alessandro Re, Arnaldo Caruso, Domenico Russo
Publikováno v:
Frontiers in Transplantation, Vol 2 (2023)
BackgroundThe COVID-19 pandemic has had a significant impact on the management and care of onco-hematological patients, particularly those with lymphoproliferative disorders who are at higher risk for COVID-19 associated bacterial and fungal superinf
Externí odkaz:
https://doaj.org/article/d0165fccbf9a414894d27b2ef0caf53b
Autor:
Micaela Fredi, Nicola Bizzaro, Margherita Zen, Chiara Baldini, Ilaria Cavazzana, Roberto Giacomelli, Valeria Riccieri, Marco Fornaro, Franco Franceschini, Roberto Gerli, Anna Ghirardello, Paola Migliorini, Maurizio Benucci, Maria Infantino, Mariangela Manfredi, Elena Bartoloni, Antonella Fioravanti, Amelia Rigon, Silvia Piantoni, Onelia Bistoni, Francesca Bellisai, Carlo Perricone, Giacomo Cafaro, Danilo Villalta, Stefania Masneri, Paola Parronchi, Boaz Palterer, Stefania Del Rosso, Fabiana Topini, Manuela Sebastiano, Emirena Garrafa, Sara Cheleschi, Maria-Romana Bacarelli, Marilina Tampoia, Daniele Cammelli, Luisa Arcarese, Patrizia Rovere Querini, Valentina Canti
Publikováno v:
RMD Open, Vol 9, Iss 3 (2023)
Objective Assessment of circulating autoantibodies represents one of the earliest diagnostic procedures in patients with suspected connective tissue disease (CTD), providing important information for disease diagnosis, identification and prediction o
Externí odkaz:
https://doaj.org/article/0027a7e5276442cc9e1f550a552e4b22
Autor:
Eltahir Ali, Rosalba Monica Ferraro, Adele Guglielmi, Gaetana Lanzi, Stefania Masneri, Giovanna Piovani, Elena Laura Mazzoldi, Lidia Pollara, Enza Maria Valente, Patrizia Accorsi, Lucio Giordano, Silvia Clara Giliani
Publikováno v:
Stem Cell Research, Vol 54, Iss , Pp 102430- (2021)
We have developed Joubert syndrome (JS)-derived induced pluripotent stem cell (iPSC) lines from dermal fibroblasts biopsied from a female patient harbouring novel compound heterozygous mutations in CC2D2A gene. The newly established iPSC lines provid
Externí odkaz:
https://doaj.org/article/148541f6e03e45fb8c8053574f7d14b5
Autor:
Silvia Piantoni, Francesca Regola, Stefania Masneri, Michele Merletti, Torsten Lowin, Paolo Airò, Angela Tincani, Franco Franceschini, Laura Andreoli, Georg Pongratz
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Background: Patients with systemic lupus erythematosus (SLE) show increased serum levels of tumor necrosis factor (TNF)/TNF receptor (R) superfamily member, e.g. BAFF (B lymphocyte stimulator). Belimumab, a monoclonal antibody against soluble BAFF, i
Externí odkaz:
https://doaj.org/article/a3820d5e7a8f427ea9c50a3b3ff310c5
Autor:
Eltahir Ali, Rosalba Monica Ferraro, Gaetana Lanzi, Stefania Masneri, Giovanna Piovani, Elena Laura Mazzoldi, Valentina Serpieri, Enza Maria Valente, Lucio Giordano, Silvia Clara Giliani
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102007- (2020)
We have generated new disease-specific induced pluripotent stem cell (iPSC) lines from skin fibroblasts obtained from a female patient with Joubert syndrome (JS) caused by compound heterozygous mutations in C5orf42 gene. The generated iPSCs offer an
Externí odkaz:
https://doaj.org/article/da4be61c1074473f8586f23e7a3cf5d1
Autor:
Maria Orietta Borghi, Asmaa Beltagy, Emirena Garrafa, Daniele Curreli, Germana Cecchini, Caterina Bodio, Claudia Grossi, Simonetta Blengino, Angela Tincani, Franco Franceschini, Laura Andreoli, Maria Grazia Lazzaroni, Silvia Piantoni, Stefania Masneri, Francesca Crisafulli, Duilio Brugnoni, Maria Lorenza Muiesan, Massimo Salvetti, Gianfranco Parati, Erminio Torresani, Michael Mahler, Francesca Heilbron, Francesca Pregnolato, Martino Pengo, Francesco Tedesco, Nicola Pozzi, Pier Luigi Meroni
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
BackgroundCritically ill patients with coronavirus disease 2019 (COVID-19) have a profound hypercoagulable state and often develop coagulopathy which leads to organ failure and death. Because of a prolonged activated partial-thromboplastin time (aPTT
Externí odkaz:
https://doaj.org/article/5b099cdbcb0444d7a098a9fdc716fc5b
Autor:
Gaetana Lanzi, Rosalba Monica Ferraro, Stefania Masneri, Giovanna Piovani, Chiara Barisani, Cristina Sobacchi, Anna Villa, Paolo Vezzoni, Silvia Giliani
Publikováno v:
Stem Cell Research, Vol 42, Iss , Pp - (2020)
Autosomal recessive osteopetrosis (ARO) is a rare inherited disorder leading to increased bone density with impairment in bone resorption. Among the genes responsible for ARO, the TCIRG1 gene, coding for the a3 subunit of the osteoclast proton pump,
Externí odkaz:
https://doaj.org/article/75dc4a791c1a4a38a302ed744b9da98d
Autor:
Rosalba Monica Ferraro, Stefania Masneri, Gaetana Lanzi, Chiara Barisani, Giovanna Piovani, Giulia Savio, Marco Cattalini, Jessica Galli, Cristina Cereda, Marco Muzi-Falconi, Simona Orcesi, Elisa Fazzi, Silvia Giliani
Publikováno v:
Stem Cell Research, Vol 41, Iss , Pp - (2019)
We report the generation of three isogenic iPSC clones (UNIBSi007-A, UNIBSi007-B, and UNIBSi007-C) obtained from fibroblasts of a patient with Aicardi Goutières Syndrome (AGS) carrying a homozygous mutation in RNaseH2B. Cells were transduced using a
Externí odkaz:
https://doaj.org/article/7936818511614171a15fb7a38b451c33
Autor:
Stefania Masneri, Gaetana Lanzi, Rosalba Monica Ferraro, Chiara Barisani, Giovanna Piovani, Giulia Savio, Marco Cattalini, Jessica Galli, Cristina Cereda, Marco Muzi-Falconi, Simona Orcesi, Elisa Fazzi, Silvia Giliani
Publikováno v:
Stem Cell Research, Vol 41, Iss , Pp - (2019)
Aicardi-Goutières syndrome (AGS) is an early-onset monogenic encephalopathy characterized by intracranial calcification, leukodystrophy and cerebrospinal fluid lymphocytosis. To date, seven genes have been related to AGS. Among these, IFIH1 encodes
Externí odkaz:
https://doaj.org/article/24d0bbdd0d5949659e0707045183fb4b
Autor:
Rosalba Monica Ferraro, Gaetana Lanzi, Stefania Masneri, Chiara Barisani, Giovanna Piovani, Giulia Savio, Marco Cattalini, Jessica Galli, Cristina Cereda, Marco Muzi-Falconi, Simona Orcesi, Elisa Fazzi, Silvia Giliani
Publikováno v:
Stem Cell Research, Vol 41, Iss , Pp - (2019)
Fibroblasts from a patient with Aicardi Goutières Syndrome (AGS) carrying a compound heterozygous mutation in TREX1, were reprogrammed into induced pluripotent stem cells (iPSCs) to establish isogenic clonal stem cell lines: UNIBSi006-A, UNIBSi006-B
Externí odkaz:
https://doaj.org/article/d6b8ae0253ba47c18733a9552c0bdedf