Sfoglia per Autore
New pan-ALK inhibitor-resistant EML4::ALK mutations detected by liquid biopsy in lung cancer patients
2024 Villa, M; Malighetti, F; Sala, E; Sharma, G; Arosio, G; Gemelli, M; Manfroni, C; Fontana, D; Cordani, N; Meneveri, R; Zambon, A; Piazza, R; Pagni, F; Cortinovis, D; Mologni, L
Current Therapeutical Approaches Targeting Lipid Metabolism in NAFLD
2023 Vitulo, M; Gnodi, E; Rosini, G; Meneveri, R; Giovannoni, R; Barisani, D
Hematopoietic Stem Cell (HSC)-Independent Progenitors Are Susceptible to Mll-Af9-Induced Leukemic Transformation
2023 Barone, C; Orsenigo, R; Cazzola, A; D'Errico, E; Patelli, A; Quattrini, G; Vergani, B; Bombelli, S; De Marco, S; D'Orlando, C; Bianchi, C; Leone, B; Meneveri, R; Biondi, A; Cazzaniga, G; Rabbitts, T; Brunelli, S; Azzoni, E
Novel ALK mutations in EML4::ALK+ NSCLC resistant to TKIs identified by liquid biopsy
2022 Villa, M; Malighetti, F; Sharma, G; Arosio, G; Sala, E; Manfroni, C; Fontana, D; Cordani, N; Meneveri, R; Zambon, A; Piazza, R; Pagni, F; Cortinovis, D; Mologni, L
Interactions between Nanoparticles and Intestine
2022 Vitulo, M; Gnodi, E; Meneveri, R; Barisani, D
Celiac disease: From genetics to epigenetics
2022 Gnodi, E; Meneveri, R; Barisani, D
One Size Does Not Fit All: Heterogeneity in Developmental Hematopoiesis
2022 Barone, C; Orsenigo, R; Meneveri, R; Brunelli, S; Azzoni, E
Study protocol: understanding the pathophysiologic mechanisms underlying delirium in older people undergoing hip fracture surgery
2021 Gamberale, R; D'Orlando, C; Brunelli, S; Meneveri, R; Mazzola, P; Foti, G; Bellani, G; Zatti, G; Munegato, D; Volpato, S; Zurlo, A; Caruso, G; Andreano, A; Valsecchi, M; Bellelli, G
Gliadin, through the Activation of Innate Immunity, Triggers lncRNA NEAT1 Expression in Celiac Disease Duodenal Mucosa
2021 Gnodi, E; Mancuso, C; Elli, L; Ballarini, E; Meneveri, R; Beaulieu, J; Barisani, D
Prenatal Origin of Pediatric Leukemia: Lessons From Hematopoietic Development
2021 Cazzola, A; Cazzaniga, G; Biondi, A; Meneveri, R; Brunelli, S; Azzoni, E
Macrophages Guard Endothelial Lineage by Hindering Endothelial-to-Mesenchymal Transition: Implications for the Pathogenesis of Systemic Sclerosis
2019 Nicolosi, P; Tombetti, E; Giovenzana, A; Donè, E; Pulcinelli, E; Meneveri, R; Tirone, M; Maugeri, N; Rovere-Querini, P; Manfredi, A; Brunelli, S
Severe Heterotopic Ossification in the Skeletal Muscle and Endothelial Cells Recruitment to Chondrogenesis Are Enhanced by Monocyte/Macrophage Depletion
2019 Tirone, M; Giovenzana, A; Vallone, A; Zordan, P; Sormani, M; Nicolosi, P; Meneveri, R; Gigliotti, C; Spinelli, A; Bocciardi, R; Ravazzolo, R; Cifola, I; Brunelli, S
miRNA-regulated gene expression differs in celiac disease patients according to the age of presentation
2015 Buoli Comani, G; Panceri, R; Dinelli, M; Biondi, A; Mancuso, C; Meneveri, R; Barisani, D
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis
2014 Colangelo, V; Francois, S; Solda, G; Picco, R; Roma, F; Ginelli, E; Meneveri, R
miRNAs Affect the Expression of Innate and Adaptive Immunity Proteins in Celiac Disease
2014 Magni, S; BUOLI COMANI, G; Elli, L; Vanessi, S; Ballarini, E; Nicolini, G; Rusconi, M; Castoldi, M; Meneveri, R; Muckenthaler, M; Bardella, M; Barisani, D
Necdin Enhances Myoblasts Survival by Facilitating the Degradation of the Mediator of Apoptosis CCAR1/CARP1
2012 Francois, S; D'Orlando, C; Fatone, T; Touvier, T; Pessina, P; Meneveri, R; Brunelli, S
Necdin enhances muscle reconstitution of dystrophic muscle by vessel-associated progenitors, by promoting cell survival and myogenic differentiation
2012 Pessina, P; Conti, V; Tonlorenzi, R; Touvier, T; Meneveri, R; Cossu, G; Brunelli, S
Evolutionary history of linked D4Z4 and Beta satellite clusters at the FSHD locus (4q35)
2012 Giussani, M; Cardone, F; Bodega, B; Ginelli, E; Meneveri, R
Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns
2011 Cheli, S; Francois, S; Bodega, B; Ferrari, F; Tenedini, E; Roncaglia, E; Ferrari, S; Ginelli, E; Meneveri, R
Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation
2009 Bodega, B; Ramirez, G; Grasser, F; Cheli, S; Brunelli, S; Mora, M; Meneveri, R; Marozzi, A; Mueller, S; Battaglioli, E; Ginelli, E
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