Sfoglia per Rivista  BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE

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Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts 1-gen-2021 Chiarelli, Nicola; Zoppi, Nicoletta; Ritelli, Marco; Venturini, Marina; Capitanio, Daniele; Gelfi, Cecilia; Colombi, Marina
Cerebrospinal fluid from frontotemporal dementia patients is toxic to neurons 1-gen-2021 Spalloni, A.; Caioli, S.; Bonomi, E.; Zona, C.; Buratti, E.; Alberici, A.; Borroni, B.; Longone, P.
Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts 1-gen-2024 Chiarelli, N.; Cinquina, V.; Martini, P.; Bertini, V.; Zoppi, N.; Venturini, M.; Ritelli, M.; Colombi, M.
Dermal fibroblast-to-myofibroblast transition sustained by αvβ3 integrin-ILK-Snail1/Slug signaling is a common feature for hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders 1-gen-2018 Zoppi, Nicoletta; Chiarelli, Nicola; Binetti, Silvia; Ritelli, Marco; Colombi, Marina
The effects of frataxin silencing in HeLa cells are rescued by the expression of human mitochondrial ferritin. 1-gen-2008 Zanella, Isabella; Derosas, M; Corrado, M; Cocco, E; Cavadini, P; Biasiotto, Giorgio; Poli, M; Verardi, R; Arosio, Paolo
Gene expression analysis identifies two distinct molecular clusters of idiopatic epiretinal membranes 1-gen-2020 Coltrini, Daniela; Belleri, Mirella; Gambicorti, Elena; Romano, Davide; Morescalchi, Francesco; Manu, Krishna Chandran Adwaid; Calza, Stefano; Semeraro, Francesco; Presta, Marco
Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A>G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagy 1-gen-2020 Micale, L.; Morlino, S.; Biagini, T.; Carbone, A.; Fusco, C.; Ritelli, M.; Giambra, V.; Zoppi, N.; Nardella, G.; Notarangelo, A.; Schirizzi, A.; Mazzoccoli, G.; Grammatico, P.; Wade, E. M.; Mazza, T.; Colombi, M.; Castori, M.
Novel potential oncogenic and druggable mutations of FGFRs recur in the kinase domain across cancer types 1-gen-2022 Grillo, E.; Ravelli, C.; Corsini, M.; Gaudenzi, C.; Zammataro, L.; Mitola, S.
Optimising the clinical strategy for autoimmune liver diseases: Principles of value-based medicine 1-gen-2018 Carbone, M; Cristoferi, L; Cortesi, Pa; Rota, M; Ciaccio, A; Okolicsanyi, S; Gemma, M; Scalone, L; Cesana, G; Fabris, L; Colledan, M; Fagiuoli, S; Ideo, G; Belli, Ls; Munari, Lm; Mantovani, L; Strazzabosco, M
Point mutated Caveolin-3 form (P104L) impairs myoblast differentiation via Akt and p38 signalling reduction, leading to an immature cell signature 1-gen-2011 Elena, Stoppani; Rossi, Stefania; Elisabetta, Meacci; Fabio, Penna; Paola, Costelli; Bellucci, Arianna; Fiorella, Faggi; Maiolo, Daniele; Monti, Eugenio; Fanzani, Alessandro
Signal transduction and epigenetic mechanisms in the control of microglia activation during neuroinflammation 1-gen-2016 Kaminska, B; COELHO DA MOTA, Mariana; Pizzi, Marina
Vitreous from idiopathic epiretinal membrane patients induces glial-to-mesenchymal transition in Müller cells 1-gen-2021 Krishna Chandran, A. M.; Coltrini, D.; Belleri, M.; Rezzola, S.; Gambicorti, E.; Romano, D.; Morescalchi, F.; Calza, S.; Semeraro, F.; Presta, M.
Zebrafish (Danio rerio) embryo as a platform for the identification of novel angiogenesis inhibitors of retinal vascular diseases 1-gen-2016 Rezzola, Sara; Paganini, Giuseppe; Semeraro, Francesco; Presta, Marco; Tobia, Chiara
Zebrafish disease models in hematology: Highlights on biological and translational impact 1-gen-2019 Zizioli, D.; Mione, M.; Varinelli, M.; Malagola, M.; Bernardi, S.; Alghisi, E.; Borsani, G.; Finazzi, D.; Monti, E.; Presta, M.; Russo, D.
Mostrati risultati da 1 a 14 di 14
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