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Sfoglia per Autore  GAGLIARDI, STELLA

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Mostrati risultati da 1 a 20 di 37
Titolo Data di pubblicazione Autore(i) File
REGULATION OF SOD1 GENE EXPRESSION IN A CELLULAR MODEL OF NEURODEGENERATION 1-gen-2011 Milani, Pamela; Amadio, Marialaura; Gagliardi, Stella; Sardone, Valentina; Ghiroldi, Andrea; Cova, Emanuela; Pascale, ALESSIA ANGELA; Cereda, C.
POST-TRANSCRIPTIONAL REGULATION OF SOD1 mRNA LEVELS THROUGH THE 3’UTR BINDING TO ELAV PROTEINS 1-gen-2012 Milani, Pamela; Amadio, Marialaura; Dell’Orco, M.; Sardone, Valentina; Gagliardi, Stella; Pascale, ALESSIA ANGELA; Cereda, C.
SOD1 mRNA ARE SEQUENCES AS NOVEL TARGETS FOR ELAV-MEDIATED POST-TRANSCRIPTIONAL MODULATION: A NEW CLUE FOR ALS PATHOGENESIS? 1-gen-2012 Milani, Pamela; Amadio, Marialaura; Gagliardi, Stella; Pascale, ALESSIA ANGELA; Cereda, C.
Post-transcriptionalregulation of SOD1 gene expression by ELAV proteins. 1-gen-2012 Milani, Pamela; Amadio, Marialaura; Laforenza, Umberto; Dell’ Orco, M.; Sardone, Valentina; Gagliardi, Stella; Pascale, ALESSIA ANGELA; Cereda, C.
The role of the two 3'UTR transcripts and ELAV binding proteins in SOD1 mRNA regulation. 1-gen-2012 Sardone, Valentina; Milani, Pamela; Amadio, Marialaura; Pascale, ALESSIA ANGELA; Pansarasa, ORIETTA MARIA; Gagliardi, Stella; Cereda, C.
Posttranscriptional regulation of SOD1 gene expression under oxidative stress: Potential role of ELAV proteins in sporadic ALS 1-gen-2013 Milani, Pamela; Amadio, Marialaura; Laforenza, Umberto; Dell'Orco, Michela; Diamanti, Luca; Sardone, Valentina; Gagliardi, Stella; Govoni, Stefano; Ceroni, Mauro; Pascale, ALESSIA ANGELA; Cereda, C.
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 1-gen-2014 Fogh, Isabella; Ratti, Antonia; Gellera, Cinzia; Lin, Kuang; Tiloca, Cinzia; Moskvina, Valentina; Corrado, Lucia; Sorarù, Gianni; Cereda, Cristina; Corti, Stefania; Gentilini, Davide; Calini, Daniela; Castellotti, Barbara; Mazzini, Letizia; Querin, Giorgia; Gagliardi, Stella; Del bo, Roberto; Conforti, Francesca L.; Siciliano, Gabriele; Inghilleri, Maurizio; Saccà, Francesco; Bongioanni, Paolo; Penco, Silvana; Corbo, Massimo; Sorbi, Sandro; Filosto, Massimiliano; Ferlini, Alessandra; Di blasio, Anna M.; Signorini, Stefano; Shatunov, Aleksey; Jones, Ashley; Shaw, Pamela J.; Morrison, Karen E.; Farmer, Anne E.; Van damme, Philip; Robberecht, Wim; Chiò, Adriano; Traynor, Bryan J.; Sendtner, Michael; Melki, Judith; Meininger, Vincent; Hardiman, Orla; Andersen, Peter M.; Leigh, Nigel P.; Glass, Jonathan D.; Overste, Daniel; Diekstra, Frank P.; Veldink, Jan H.; Van es, Michael A.; Shaw, Christopher E.; Weale, Michael E.; Lewis, Cathryn M.; Williams, Julie; Brown, Robert H.; Landers, John E.; Ticozzi, Nicola; Ceroni, Mauro; Pegoraro, Elena; Comi, Giacomo P.; D'Alfonso, Sandra; Van den berg, Leonard H.; Taroni, Franco; Al-chalabi, Ammar; Powell, John; Silani, Vincenzo
Methodologies for the reliable analysis of amplicon-based NGS data managing allele drop-out artefacts 1-gen-2015 Zucca, Susanna; Villaraggia, M.; Gagliardi, Stella; Grieco, G.; Valente, MARIA LUISA; Cereda, C.; Magni, Paolo
GCConverter: a new tool for genomic coordinates conversion 1-gen-2015 Villaraggia, M.; Zucca, Susanna; Gagliardi, Stella; Grieco, G.; Valente, MARIA LUISA; Cereda, C.; Magni, Paolo
A methodology for the reliable analysis of amplicon-based NGS data 1-gen-2016 Zucca, Susanna; Valente, MARIA LUISA; Gagliardi, Stella; Grieco, G.; Garau, J.; Plumari, M.; Asaro, A.; Magni, Paolo; Cereda, C.
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis 1-gen-2016 Kenna, Kp; Van Doormaal, Pt; Dekker, Am; Ticozzi, N; Kenna, Bj; Diekstra, Fp; Van Rheenen, W; Van Eijk, Kr; Jones, Ar; Keagle, P; Shatunov, A; Sproviero, W; Smith, Bn; Van Es, Ma; Topp, Sd; Kenna, A; Miller, Jw; Fallini, C; Tiloca, C; Mclaughlin, Rl; Vance, C; Troakes, C; Colombrita, C; Mora, G; Calvo, A; Verde, F; Al sarraj, S; King, A; Calini, D; De Belleroche, J; Baas, F; Van Der Kooi, Aj; De Visser, M; Ten Asbroek, Al; Sapp, Pc; Mckenna yasek, D; Polak, M; Asress, S; Muñoz blanco, Jl; Strom, Tm; Meitinger, T; Morrison, Ke; Slagen, Consortium; Lauria, G; Williams, Kl; Leigh, Pn; Nicholson, Ga; Blair, Ip; Leblond, Cs; Dion, Pa; Rouleau, Ga; Pall, H; Shaw, Pj; Turner, Mr; Talbot, K; Taroni, F; Boylan, Kb; Van Blitterswijk, M; Rademakers, R; Esteban pérez, J; García redondo, A; Van Damme, P; Robberecht, W; Chio, A; Gellera, C; Drepper, C; Sendtner, M; Ratti, A; Glass, Jd; Mora, Js; Basak, Na; Hardiman, O; Ludolph, Ac; Andersen, Pm; Weishaupt, Jh; Brown Rh, Jr; Al chalabi, A; Silani, V; Shaw, Ce; Van Den Berg, Lh; Veldink, Jh; Landers, Je; D'Alfonso, S; Mazzini, L; Comi, Gp; Nullr, nullDel Bo; Ceroni, Mauro; Gagliardi, Stella; Querin, G; Bertolin, C; Pensato, V; Castellotti, B; Corti, S; Cereda, Cristina; Corrado, L; Sorarù, G.
Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management 1-gen-2016 Zucca, Susanna; Villaraggia, M.; Gagliardi, Stella; Grieco, G. S.; Valente, MARIA LUISA; Cereda, C.; Magni, Paolo
Pathological proteins are transported by extracellular vesicles of sporadic amyotrophic lateral sclerosis patients 1-gen-2018 Sproviero, Daisy; LA SALVIA, Sabrina; Giannini, Marta; Crippa, Valeria; Gagliardi, Stella; Bernuzzi, Stefano; Diamanti, Luca; Ceroni, Mauro; Pansarasa, Orietta; Poletti, Angelo; Cereda, Cristina
Curcumin and Novel Synthetic Analogs in Cell-Based Studies of Alzheimer's Disease 1-gen-2018 Gagliardi, S; Franco, V; Sorrentino, S; Zucca, S; Pandini, C; Rota, P; Bernuzzi, S; Costa, A; Sinforiani, E; Pansarasa, O; Cashman, Jr; Cereda, C.
Leukocite derived microvescicles as disease progression biomarkers in slow progressing amyotrophic lateral sclerosis. 1-gen-2019 Sproviero, D.; La Salvia, S.; Colombo, F.; Zucca, S.; Pansarasa, O.; Diamanti, L.; Costa, A.; Lova, Luca; Giannini, M.; Gagliardi, S.; Lauranzano, E.; Matteoli, M.; Ceroni, M.; Malaspina, A.; Cereda, Cristina
Nuclear Phospho-SOD1 Protects DNA from Oxidative Stress Damage in Amyotrophic Lateral Sclerosis 1-gen-2019 Bordoni, Matteo; Pansarasa, Orietta; Dell'Orco, Michela; Crippa, Valeria; Gagliardi, Stella; Sproviero, Daisy; Bernuzzi, Stefano; Diamanti, Luca; Ceroni, Mauro; Tedeschi, Gabriella; Poletti, Angelo; Cereda, Cristina
RNA-seq profiling in peripheral blood mononuclear cells of amyotrophic lateral sclerosis patients and controls 1-gen-2019 Zucca, Susanna; Gagliardi, Stella; Pandini, Cecilia; Diamanti, Luca; Bordoni, Matteo; Sproviero, Daisy; Arigoni, Maddalena; Olivero, Martina; Pansarasa, Orietta; Ceroni, Mauro; Calogero, Raffaele; Cereda, Cristina
Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2 1-gen-2019 De Mori, R.; Severino, M.; Mancardi, M. M.; Anello, D.; Tardivo, S.; Biagini, T.; Capra, V.; Casella, A.; Cereda, C.; Copeland, B. R.; Gagliardi, S.; Gamucci, A.; Ginevrino, M.; Illi, B.; Lorefice, E.; Musaev, D.; Stanley, V.; Micalizzi, A.; Gleeson, J. G.; Mazza, T.; Rossi, A.; Valente, E.
Alzheimer's, Parkinson's Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement 1-gen-2020 Garofalo, Maria; Pandini, Cecilia; Bordoni, Matteo; Pansarasa, Orietta; Rey, Federica; Costa, Alfredo; Minafra, Brigida; Diamanti, Luca; Zucca, Susanna; Carelli, Stephana; Cereda, Cristina; Gagliardi, Stella
Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2 1-gen-2021 Antonaci, Fabio; Ravaglia, Sabrina; Grieco, Gaetano S; Gagliardi, Stella; Cereda, Cristina; Costa, Alfredo
Mostrati risultati da 1 a 20 di 37
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