Zobrazeno 1 - 10
of 119
pro vyhledávání: '"Silvia Brunelli"'
Autor:
Cristina Rodríguez, Filipa Timóteo-Ferreira, Gabriella Minchiotti, Silvia Brunelli, Ombretta Guardiola
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
Skeletal muscle regeneration relies on the intricate interplay of various cell populations within the muscle niche—an environment crucial for regulating the behavior of muscle stem cells (MuSCs) and ensuring postnatal tissue maintenance and regener
Externí odkaz:
https://doaj.org/article/ce5cb5c49514490d9b7a10629cac9eaa
Autor:
Emanuele Azzoni, Cristiana Barone, Roberto Orsenigo, Anna Cazzola, Arianna Patelli, Matthew Nicholls, Mario Mauri, Silvia Bombelli, Giulia Quattrini, Alison Domingues, Deborah D’aliberti, Silvia Spinelli, Alessandro Muratore, Elisabetta D’errico, Cristina D’orlando, Roberto Perego, Raffaella Meneveri, Marella De Bruijn, Alessandro Fantin, Silvia Brunelli, Rocco Piazza
Publikováno v:
HemaSphere, Vol 7, p e62813b2 (2023)
Externí odkaz:
https://doaj.org/article/f1587bbba91446af91e884fec9304982
Autor:
Giulio Cossu, Rossana Tonlorenzi, Silvia Brunelli, Maurilio Sampaolesi, Graziella Messina, Emanuele Azzoni, Sara Benedetti, Stefano Biressi, Chiara Bonfanti, Laricia Bragg, Jordi Camps, Ornella Cappellari, Marco Cassano, Fabio Ciceri, Marcello Coletta, Diego Covarello, Stefania Crippa, M. Gabriella Cusella-De Angelis, Luciana De Angelis, Arianna Dellavalle, Jordi Diaz-Manera, Daniela Galli, Francesco Galli, Cesare Gargioli, Mattia F. M. Gerli, Giorgia Giacomazzi, Beatriz G. Galvez, Hidetoshi Hoshiya, Maria Guttinger, Anna Innocenzi, M. Giulia Minasi, Laura Perani, Stefano C Previtali, Mattia Quattrocelli, Martina Ragazzi, Urmas Roostalu, Giuliana Rossi, Raffaella Scardigli, Dario Sirabella, Francesco Saverio Tedesco, Yvan Torrente, Gonzalo Ugarte
Publikováno v:
Frontiers in Genetics, Vol 13 (2023)
In 2002 we published an article describing a population of vessel-associated progenitors that we termed mesoangioblasts (MABs). During the past decade evidence had accumulated that during muscle development and regeneration things may be more complex
Externí odkaz:
https://doaj.org/article/1f35883d296649508fec2319ea20c37c
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Externí odkaz:
https://doaj.org/article/a78eeb4195f54ac9aa11d56ec7a66952
Autor:
Anna Cazzola, Giovanni Cazzaniga, Andrea Biondi, Raffaella Meneveri, Silvia Brunelli, Emanuele Azzoni
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2021)
Several lines of evidence suggest that childhood leukemia, the most common cancer in young age, originates during in utero development. However, our knowledge of the cellular origin of this large and heterogeneous group of malignancies is still incom
Externí odkaz:
https://doaj.org/article/5e0652beb8bf4157a1b211c69dceb6b9
Publikováno v:
Cells, Vol 11, Iss 6, p 1061 (2022)
Our knowledge of the complexity of the developing hematopoietic system has dramatically expanded over the course of the last few decades. We now know that, while hematopoietic stem cells (HSCs) firmly reside at the top of the adult hematopoietic hier
Externí odkaz:
https://doaj.org/article/96ffecd12b0a4e4cbae8b51e24cbbd3b
Autor:
Mario Tirone, Anna Giovenzana, Arianna Vallone, Paola Zordan, Martina Sormani, Pier Andrea Nicolosi, Raffaela Meneveri, Carmen Rosaria Gigliotti, Antonello E. Spinelli, Renata Bocciardi, Roberto Ravazzolo, Ingrid Cifola, Silvia Brunelli
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Altered macrophage infiltration upon tissue damage results in inadequate healing due to inappropriate remodeling and stem cell recruitment and differentiation. We investigated in vivo whether cells of endothelial origin phenotypically change upon het
Externí odkaz:
https://doaj.org/article/bc87664b4c78408ba5e1420adb821323
Publikováno v:
Biomedicines, Vol 8, Iss 12, p 611 (2020)
Heterotopic ossification is defined as an aberrant formation of bone in extraskeletal soft tissue, for which both genetic and acquired conditions are known. This pathologic process may occur in many different sites such as the skin, subcutaneous tiss
Externí odkaz:
https://doaj.org/article/d12de57e916b40b88250867975068d96
Autor:
Serena Cappato, Laura Tonachini, Francesca Giacopelli, Mario Tirone, Luis J. V. Galietta, Martina Sormani, Anna Giovenzana, Antonello E. Spinelli, Barbara Canciani, Silvia Brunelli, Roberto Ravazzolo, Renata Bocciardi
Publikováno v:
Disease Models & Mechanisms, Vol 9, Iss 6, Pp 685-696 (2016)
The ACVR1 gene encodes a type I receptor of bone morphogenetic proteins (BMPs). Activating mutations in ACVR1 are responsible for fibrodysplasia ossificans progressiva (FOP), a rare disease characterized by congenital toe malformation and progressive
Externí odkaz:
https://doaj.org/article/bc8881ef03a44f499df1f39179097a51
Publikováno v:
Stem Cells International, Vol 2016 (2016)
Externí odkaz:
https://doaj.org/article/5c1c6b6eff634340bdca8ec9f14dc31f