Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Granzotto M"'
Autor:
Alessandro Ventura, Sara Dal Bo, Elisa Piscianz, Tarcisio Not, Stefano Martelossi, Erica Valencic, Marilena Granzotto, Fortunato Ferrara, S Quaglia, Alberto Tommasini
Celiac disease (CD) is characterized by intolerance to gluten and high risk of developing autoimmune phenomena. Possible defects in immune tolerance could have a role in the pathogenesis of the disease. As regulatory T-cells (Tregs) are the main popu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54e66d9b677d869c006e44d9ceb19045
https://hdl.handle.net/11368/1854338
https://hdl.handle.net/11368/1854338
Summary The generation of regulatory T cells (Tregs) in vitro represents an attractive possibility to set up cellular therapies that could prevent and cure autoimmune disorders. Different methods have been proposed to generate Tregs in vitro and to e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f673d93ffb8aad05f3121194a33582e4
https://europepmc.org/articles/PMC2219374/
https://europepmc.org/articles/PMC2219374/
Autor:
Andrea D'Osualdo, Alessandro Ventura, Sergio Crovella, Hans R. Waterham, Lorenzo Calligaris, Marco Nevyjel, Alessandra Pontillo, Alberto Tommasini, Egidio Barbi, Marilena Granzotto
Publikováno v:
Pediatrics, 119(2), e523-e527. American Academy of Pediatrics
Mevalonate kinase deficiency is a rare inborn disorder of isoprenoid and sterol biosynthesis characterized by a recurrent autoinflammatory syndrome and, in most severe cases, psychomotor delay. Clinical manifestations can be very complex and, in some
Autor:
Egidio Barbi, Alberto Tommasini, Andrea Taddio, Erica Valencic, Alessandro Ventura, M. Andolina, Marilena Granzotto, Elena Faleschini, Loredana Lepore
This work studies IPEX (Immunodysregulation with Polyendocrinopathy and Enteropathy X-linked), a severe disorder of course in early childhood due to mutations in the FOXP3 gene (locus Xp11.23-q13.3) leading to failure in immune tolerance and his ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaf93436405d1828099141427433efd6
https://hdl.handle.net/11368/1702669
https://hdl.handle.net/11368/1702669
Autor:
Francesca Gombac, Marlenka Zerial, Valentina Leone, Alberto Tommasini, Loredana Lepore, Alessandro Ventura, Roberta Ciambra, Marilena Granzotto
Publikováno v:
Pediatric hematology and oncology. 22(2)
Chronic granulomatous disease (CGD) is a rare genetically determined immunodeficiency. Neutrophils from CGD patients show a defective killing of phagocytosed fungi and bacteria, due not only to an impairment in oxidative burst, but also to absence of
Autor:
Elisa Fabbro, S Quaglia, Massimo Maschio, Alessandro Ventura, Marilena Granzotto, Stefano Martelossi, Gianni Presani, Alberto Tommasini
Publikováno v:
World Journal of Gastroenterology. 13:6191
AIM: To investigate the function of monocytes in Crohn’s disease (CD) patients and to correlate this with disease-associated nucleotide-binding oligomerization domain-2 (NOD2) gene variants. METHODS: Monocytes from 47 consecutively referred CD pati