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Titolo Data di pubblicazione Autore(i) File
Litium chloride, a wnt/beta-catenin mimicking signal, as a long-lasting proliferating stimulus for cultured rat hepatocytes 2006 Compagnone A.; Bandino A.; Lomartire A.; Bravoco V.; Cravanzola C.; Valfrè di Bonzo L.; Parola M.; Colombatto S.
Beta-catenin triggers nuclear factor kB - dependent up-regulation of hepatocyte inducible nitric oxide synthase 2008 Bandino A; Compagnone A; Bravoco V; Cravanzola C; Lomartire A; Novo E; Cannito S; Valfrè di Bonzo L; Zamara E; Autelli R; Parola M; Colombatto S.
The expression pattern of TAR DNA-binding protein 43 (TDP-43) in peripheral blood mononuclear cells (PBMC) in individuals affected by amyotrophific lateral sclerosis (ALS) and their healthy relatives 2009 De Marco G; Piccinini M; Lupino E; Lomartire A; Buccinnà B; Ramondetti C; Grifoni S; Giordana MT; Rinaudo MT
The molecular basis of the hypomyelination characterizing the brains of sphingomyelinase-deficient mice, an animal model of Niemann-Pick disease type A 2009 Buccinnà B; Piccinini M; Prinetti A; Scandroglio F; Prioni S; Valsecchi M; Lupino E; Ramondetti C; De Marco G; Lomartire A; Giordana M T; Sonnino S; Rinaudo M T
Dysfunctions in N_CAM and unexpected accumulation of PSA_NCAM in brain of Autosomal dominant adult onset leukodystrophy (ADLD) 2009 Buccinnà B; De Marco G; Piccinini M; Lupino E; Lomartire A; Ramondetti C; Grifoni S; Giordana MT; Rinaudo MT
In CD28-costimulated human naïve CD4(+) T cells, I-κB kinase controls the expression of cell cycle regulatory proteins via interleukin-2-independent mechanisms 2010 Lupino E; Buccinnà B; Ramondetti C; Lomartire A; De Marco G; Ricotti E; Tovo PA; Rinaudo MT; Piccinini M
Deregulated Sphingolipid Metabolism and Membrane Organization in Neurodegenerative Disorders 2010 Piccinini Marco; Scandroglio Federica; Prioni Simona; Buccinnà Barbara; Loberto Nicoletta; Aureli Massimo; Chigorno Vanna; Lupino Elisa; Demarco Giovanni; Lomartire Annarosa; Rinaudo Maria Teresa; Sonnino Sandro; Prinetti Alessandro.
Increased cytoplasmic mislocalization of TAR DNA binding protein 43 (TDP-43) in circulating lymphomonocytes of ALS patients recapitulates the major dysfunction featuring motor neurons in the disease. 2011 De Marco G; Lupino E; Grifoni S; Calvo A; Moglia C; Buccinnà B; Ramondetti C; Lomartire A; Piccinini M; Rinaudo MT;Giordana MT; Chiò A.
Novel dysfunctions at the origin of hypomyelination, a feature of Niemann Pick type A 2011 Buccinnà B; Lomartire A; Ramondetti C; De Marco G; Rinaudo MT; Lupino E; Piccinini M
Cytoplasmic accumulation of TDP-43 in circulating lymphomonocytes of ALS patients with and without TARDBP mutations 2011 De Marco G; Lupino E; Calvo A; Moglia C; Buccinnà B; Grifoni S; Ramondetti C; Lomartire A; Rinaudo MT; Piccinini M; Giordana MT; Chiò A.
Reduced cellular Ca(2+) availability enhances TDP-43 cleavage by apoptotic caspases. 2014 G. De Marco; A. Lomartire; G. Mandili; E. Lupino; B. Buccinnà; C. Ramondetti; C. Moglia; F. Novelli; M. Piccinini; M. Mostert; MT Rinaudo; A. Chiò; A. Calvo
Expression of NOX2 protein in neutrophils of patients with ALS 2015 De Marco G, Lomartire A, Casale F, Marrali G, Cammarosano S, Ilardi A, Canosa A, Moglia C, Calvo A, Rinaudo MT, Chiò A
NOX2 in the hSOD1G93A Transgenic Swine: a preliminary overview 2015 Casale F, De Marco G, Lomartire A, Marrali G, Salamone P, Fuda G, Berrone E, Crociara P, Chieppa MN, Corona C, Casalone C, Calvo A, Chiò A
Monocytes of patients with Amyotrophic Lateral Sclerosis linked to gene mutations display altered TDP-43 subcellular distribution 2017 De Marco, Giovanni; Lomartire, Annarosa; Calvo, Andrea; Risso, Alessandra; De Luca, Elisa; Mostert, Michael; Mandrioli, Jessica; Caponnetto, Claudia; Borghero, Giuseppe; Manera, Umberto; Canosa, Antonio; Moglia, Cristina; Restagno, Gabriella; Fini, Nicola; Tarella, Corrado; Giordana, Maria Teresa; Rinaudo, Maria Teresa; Chiò, Adriano
A novel p.Ser108LeufsTer15 SOD1 mutation leading to the formation of a premature stop codon in an apparently sporadic ALS patient: insights into the underlying pathomechanisms 2018 Canosa A.; De Marco G.; Lomartire A.; Rinaudo M.T.; Di Cunto F.; Turco E.; Barberis M.; Brunetti M.; Casale F.; Moglia C.; Calvo A.; Marklund S.L.; Andersen P.M.; Mora G.; Chio A.
A novel splice site FUS mutation in a familial ALS case: effects on protein expression 2021 Canosa A.; Lomartire A.; De Marco G.; Grassano M.; Brunetti M.; Manera U.; Vasta R.; Salamone P.; Fuda G.; Sbaiz L.; Gallone S.; Moglia C.; Calvo A.; Chio A.
The heterozygous deletion c.1509_1510delAG in exon 14 of FUS causes an aggressive childhood-onset ALS with cognitive impairment 2021 Lanteri P.; Meola I.; Canosa A.; De Marco G.; Lomartire A.; Rinaudo M.T.; Albamonte E.; Sansone V.A.; Lunetta C.; Manera U.; Vasta R.; Moglia C.; Calvo A.; Origone P.; Chio A.; Mandich P.
Effects of intracellular calcium accumulation on proteins encoded by the major genes underlying amyotrophic lateral sclerosis 2022 De Marco G.; Lomartire A.; Manera U.; Canosa A.; Grassano M.; Casale F.; Fuda G.; Salamone P.; Rinaudo M.T.; Colombatto S.; Moglia C.; Chio A.; Calvo A.
Mostrati risultati da 1 a 18 di 18
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