Zobrazeno 1 - 10
of 202
pro vyhledávání: '"Natascia, Tiso"'
Autor:
Raquel Brañas Casas, Alessandro Zuppardo, Giovanni Risato, Alberto Dinarello, Rudy Celeghin, Camilla Fontana, Eleonora Grelloni, Alexandru Ionut Gilea, Carlo Viscomi, Andrea Rasola, Luisa Dalla Valle, Tiziana Lodi, Enrico Baruffini, Nicola Facchinello, Francesco Argenton, Natascia Tiso
Publikováno v:
Cell Death and Disease, Vol 15, Iss 4, Pp 1-12 (2024)
Abstract The human mitochondrial DNA polymerase gamma is a holoenzyme, involved in mitochondrial DNA (mtDNA) replication and maintenance, composed of a catalytic subunit (POLG) and a dimeric accessory subunit (POLG2) conferring processivity. Mutation
Externí odkaz:
https://doaj.org/article/58a56ab3a25547089b9f2b151454fd8b
Autor:
Rudy Celeghin, Giovanni Risato, Giorgia Beffagna, Marco Cason, Maria Bueno Marinas, Mila Della Barbera, Nicola Facchinello, Alice Giuliodori, Raquel Brañas Casas, Micol Caichiolo, Andrea Vettori, Enrico Grisan, Stefania Rizzo, Luisa Dalla Valle, Francesco Argenton, Gaetano Thiene, Natascia Tiso, Kalliopi Pilichou, Cristina Basso
Publikováno v:
Cell Death Discovery, Vol 9, Iss 1, Pp 1-14 (2023)
Abstract Arrhythmogenic cardiomyopathy (AC) is an inherited disorder characterized by progressive loss of the ventricular myocardium causing life-threatening ventricular arrhythmias, syncope and sudden cardiac death in young and athletes. About 40% o
Externí odkaz:
https://doaj.org/article/19472e78aa4e4bbcaaac30f07520d4e5
Autor:
Giovanni Risato, Raquel Brañas Casas, Marco Cason, Maria Bueno Marinas, Serena Pinci, Monica De Gaspari, Silvia Visentin, Stefania Rizzo, Gaetano Thiene, Cristina Basso, Kalliopi Pilichou, Natascia Tiso, Rudy Celeghin
Publikováno v:
Cells, Vol 13, Iss 15, p 1264 (2024)
Arrhythmogenic cardiomyopathy (AC) is a hereditary cardiac disorder characterized by the gradual replacement of cardiomyocytes with fibrous and adipose tissue, leading to ventricular wall thinning, chamber dilation, arrhythmias, and sudden cardiac de
Externí odkaz:
https://doaj.org/article/ee3cf922c2ed4a989dfe6e3be29f26d0
Autor:
Marika Quadri, Natascia Tiso, Francesco Musmeci, Maria I. Morasso, Stephen R. Brooks, Luca Reggiani Bonetti, Rossana Panini, Roberta Lotti, Alessandra Marconi, Carlo Pincelli, Elisabetta Palazzo
Publikováno v:
Journal of Experimental & Clinical Cancer Research, Vol 42, Iss 1, Pp 1-19 (2023)
Abstract Background Cutaneous squamous cell carcinoma (cSCC) is the second most prevalent form of skin cancer, showing a rapid increasing incidence worldwide. Although most cSCC can be cured by surgery, a sizeable number of cases are diagnosed at adv
Externí odkaz:
https://doaj.org/article/13b666a0ba754bbcabd94f8530c27ae2
Autor:
Alberto Dinarello, Riccardo Massimiliano Betto, Linda Diamante, Annachiara Tesoriere, Rachele Ghirardo, Chiara Cioccarelli, Giacomo Meneghetti, Margherita Peron, Claudio Laquatra, Natascia Tiso, Graziano Martello, Francesco Argenton
Publikováno v:
Cell Death Discovery, Vol 9, Iss 1, Pp 1-12 (2023)
Abstract STAT3 and HIF1α are two fundamental transcription factors involved in many merging processes, like angiogenesis, metabolism, and cell differentiation. Notably, under pathological conditions, the two factors have been shown to interact genet
Externí odkaz:
https://doaj.org/article/80918e40eb454fe8b3e60f3d5b9e7c75
Autor:
Chiara Galber, Simone Fabbian, Cristina Gatto, Martina Grandi, Stefania Carissimi, Manuel Jesus Acosta, Gianluca Sgarbi, Natascia Tiso, Francesco Argenton, Giancarlo Solaini, Alessandra Baracca, Massimo Bellanda, Valentina Giorgio
Publikováno v:
Cell Death and Disease, Vol 14, Iss 1, Pp 1-19 (2023)
Abstract The mitochondrial protein IF1 binds to the catalytic domain of the ATP synthase and inhibits ATP hydrolysis in ischemic tissues. Moreover, IF1 is overexpressed in many tumors and has been shown to act as a pro-oncogenic protein, although its
Externí odkaz:
https://doaj.org/article/88067e01f93247babee88803fbde9796
Publikováno v:
Discover Oncology, Vol 13, Iss 1, Pp 1-16 (2022)
Abstract Recently, the zebrafish has been established as one of the most important model organisms for medical research. Several studies have proved that there is a high level of similarity between human and zebrafish genomes, which encourages the us
Externí odkaz:
https://doaj.org/article/ab98fe50bee346a6a4ada665baa52f10
Autor:
Luca Dalle Carbonare, Jessica Bertacco, Giulia Marchetto, Samuele Cheri, Michela Deiana, Arianna Minoia, Natascia Tiso, Monica Mottes, Maria Teresa Valenti
Publikováno v:
Stem Cell Research & Therapy, Vol 12, Iss 1, Pp 1-12 (2021)
Abstract Background Methylsulfonylmethane (MSM) is a nutraceutical compound which has been indicated to counteract osteoarthritis, a cartilage degenerative disorder. In addition, MSM has also been shown to increase osteoblast differentiation. So far,
Externí odkaz:
https://doaj.org/article/93c90b12a5684d2690c5cae79894753e
Autor:
Giovanni Risato, Rudy Celeghin, Raquel Brañas Casas, Alberto Dinarello, Alessandro Zuppardo, Andrea Vettori, Kalliopi Pilichou, Gaetano Thiene, Cristina Basso, Francesco Argenton, Silvia Visentin, Erich Cosmi, Natascia Tiso, Giorgia Beffagna
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Foetal Growth Restriction (FGR), previously known as Intrauterine Growth Restriction (IUGR), is an obstetrical condition due to placental insufficiency, affecting yearly about 30 million newborns worldwide. In this work, we aimed to identify and phar
Externí odkaz:
https://doaj.org/article/572cf07567404dd6bb3376e54cd51399
Autor:
Nicola Facchinello, Claudio Laquatra, Lisa Locatello, Giorgia Beffagna, Raquel Brañas Casas, Chiara Fornetto, Alberto Dinarello, Laura Martorano, Andrea Vettori, Giovanni Risato, Rudy Celeghin, Giacomo Meneghetti, Massimo Mattia Santoro, Agnes Delahodde, Francesco Vanzi, Andrea Rasola, Luisa Dalla Valle, Maria Berica Rasotto, Tiziana Lodi, Enrico Baruffini, Francesco Argenton, Natascia Tiso
Publikováno v:
Cell Death and Disease, Vol 12, Iss 1, Pp 1-18 (2021)
Abstract The DNA polymerase gamma (Polg) is a nuclear-encoded enzyme involved in DNA replication in animal mitochondria. In humans, mutations in the POLG gene underlie a set of mitochondrial diseases characterized by mitochondrial DNA (mtDNA) depleti
Externí odkaz:
https://doaj.org/article/e5b4a8a5e87b4483a23748afb74ea087