Sfoglia per Scienze biologiche
A mouse model for creatine transporter deficiency reveals early onset cognitive impairment and neuropathology associated with brain aging
2016 Baroncelli, Laura; Molinaro, Angelo; Cacciante, Francesco; Alessandrì, Maria Grazia; Napoli, Debora; Putignano, Elena; Tola, Jonida; Leuzzi, Vincenzo; Cioni, Giovanni; Pizzorusso, Tommaso
Mössbauer studies of frataxin role in iron-sulfur cluster assembly and dysfunction-related disease
2012 Garcia-Serres, R.; Clémancey, M.; Oddou, J. -L.; Pastore, A; Lesuisse, E.; Latour, J. -M.
Multi-site investigation of gut microbiota in CDKL5 deficiency disorder mouse models : Targeting dysbiosis to improve neurological outcomes
2025 Damiani, F.; Giuliano, M. G.; Cornuti, S.; Putignano, E.; Tognozzi, A.; Suckow, V.; Kalscheuer, V. M.; Pizzorusso, T.; Tognini, P.
Multi-Target Protective Effects of β-Caryophyllene (BCP) at the Intersection of Neuroinflammation and Neurodegeneration
2025 Ricardi, Caterina; Mazzierli, Anna; Guglielmo, Stefano; Origlia, Nicola; Gado, Francesca; Manera, Clementina; Chiellini, Grazia; Polini, Beatrice
Multilevel investigation of Tau pathology: from the cytoplasm to the nucleus
2019 Siano, Giacomo
MULTIMODAL ACTIVATION AND REGULATION OF NEURONAL MECHANOSENSITIVE CATION CHANNELS
2008 Pellegrino, M; Barsanti, C; Pellegrini, Monica
Multiple domains of TonEBP cooperate to stimulate transcription in response to hypertonicity
2003 Do Lee, S; Colla, Emanuela; Sheen, Mr; Na, Ky; Kwon, Hm
Multiple sequence alignment based on structural properties
2010 Ozer, B.; Gezici, Gizem; Meydan, C.; Sezerman, U.
Multiscale morphology of organic semiconductor thin films controls the adhesion and viability of human neural cells
2010 Tonazzini, Ilaria; Bystrenova, E; Chelli, B; Greco, P; Stoliar, P; Calò, A; Lazar, A; Borgatti, F; Dangelo, P; Martini, C; Biscarini, F.
Muscular dystrophy in adult and aged anti-NGF transgenic mice resembles an inclusion body myopathy
2000 Capsoni, Simona; Ruberti, F; Di Daniel, E; Cattaneo, Antonino
Mutant Exon1 Huntingtin Aggregation is Regulated by T3 Phosphorylation-Induced Structural Changes and Crosstalk between T3 Phosphorylation and Acetylation at K6
2017 Chiki, Anass; Deguire Sean, M.; Ruggeri Francesco, S.; Sanfelice, Domenico; Ansaloni, Annalisa; Wang, Zhe-Ming; Cendrowska, Urszula; Burai, Ritwik; Vieweg, Sophie; Pastore, Annalisa; Dietler, Giovanni; Lashuel Hilal, A
The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma
2019 Wagener, R.; Seufert, J.; Raimondi, F.; Bens, S.; Kleinheinz, K.; Nagel, I.; Ller, J. A.; Thiele, H.; Hubschmann, D.; Kohler, C. W.; Nurnberg, P.; Au-Yeung, R.; Burkhardt, B.; Horn, H.; Leoncini, L.; Jaffe, E. S.; Ott, G.; Rymkiewicz, G.; Schlesner, M.; Russell, R. B.; Klapper, W.; Siebert, R.
Mutations in Bcl9 and Pygo genes cause congenital heart defects by tissue-specific perturbation of Wnt/β-catenin signaling
2018 Cantu, C.; Felker, A.; Zimmerli, D.; Prummel, K. D.; Cabello, E. M.; Chiavacci, E.; Mendez-Acevedo, K. M.; Kirchgeorg, L.; Burger, S.; Ripoll, J.; Valenta, T.; Hausmann, G.; Vilain, N.; Aguet, M.; Burger, A.; Panakova, D.; Basler, K.; Mosimann, C.
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28
2010 Di Bella, Daniela; Lazzaro, Federico; Brusco, Alfredo; Plumari, Massimo; Battaglia, Giorgio; Pastore, A; Finardi, Adele; Cagnoli, Claudia; Tempia, Filippo; Frontali, Marina; Veneziano, Liana; Sacco, Tiziana; Boda, Enrica; Brussino, Alessandro; Bonn, Florian; Castellotti, Barbara; Baratta, Silvia; Mariotti, Caterina; Gellera, Cinzia; Fracasso, Valentina; Magri, Stefania; Langer, Thomas; Plevani, Paolo; Di Donato, Stefano; Muzi-Falconi, Marco; Taroni, Franco; RI Tempia Filippo/A-5883-2012 Muzi-Falconi Marco/A-6035-2012 Di Donato, Stefano/B-9717-2012
Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergetics
2014 De Rocco, Daniela; Cerqua, Cristina; Goffrini, Paola; Russo, Giovanna; Pastore, Annalisa; Meloni, Francesca; Nicchia, Elena; Moraes, Carlos T.; Pecci, Alessandro; Salviati, Leonardo; Savoia, Anna
MUTEINS OF HNGF, THERAPEUTIC USES AND PHARMACEUTICAL COMPOSITIONS
2006 Capsoni, Simona; Cattaneo, Antonino; Covaceuszach, S.
MYH9 related disease: a novel missense Ala95Asp mutation of the MYH9 gene
2009 De Rocco, D.; Heller, P. G.; Girotto, G.; Pastore, Annalisa; Glembotsky, A. C.; Marta, R. F.; Bozzi, V.; Pecci, Alessandro; Molinas, F. C.; Savoia, A.
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype
2010 Pecci, Alessandro; Panza, Emanuele; De Rocco, Daniela; Pujol-Moix, Nuria; Girotto, Giorgia; Podda, Luigi; Paparo, Carmelo; Bozzi, Valeria; Pastore, A; Balduini Carlo, L.; Seri, Marco; Savoia, Anna; RI panza emanuele/G-9083-2011 Pecci, Alessandro/E-9288-2012
MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations
2013 De Rocco, D.; Zieger, B.; Platokouki, H.; Heller, P. G.; Pastore, A.; Bottega, R.; Noris, P.; Barozzi, S.; Glembotsky, A.; Pergantou, H.; Balduini, C.; Savoia, A.; Pecci, A.
Nanoscale protein diffusion by STED-based pair correlation analysis
2014 Bianchini, Paolo; Cardarelli, Francesco; Di Luca, Mariagrazia; Diaspro, Alberto; Bizzarri, Ranieri
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