LOMARTIRE, ANNAROSA
LOMARTIRE, ANNAROSA
NEUROSCIENZE "RITA LEVI MONTALCINI"
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
2018-01-01 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
2021-01-01 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.
Beta-catenin triggers nuclear factor kB - dependent up-regulation of hepatocyte inducible nitric oxide synthase
2008-01-01 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.
Cytoplasmic accumulation of TDP-43 in circulating lymphomonocytes of ALS patients with and without TARDBP mutations
2011-01-01 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.
Deregulated Sphingolipid Metabolism and Membrane Organization in Neurodegenerative Disorders
2010-01-01 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.
Dysfunctions in N_CAM and unexpected accumulation of PSA_NCAM in brain of Autosomal dominant adult onset leukodystrophy (ADLD)
2009-01-01 Buccinnà B; De Marco G; Piccinini M; Lupino E; Lomartire A; Ramondetti C; Grifoni S; Giordana MT; Rinaudo MT
Effects of intracellular calcium accumulation on proteins encoded by the major genes underlying amyotrophic lateral sclerosis
2022-01-01 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.
Expression of NOX2 protein in neutrophils of patients with ALS
2015-01-01 De Marco G, Lomartire A, Casale F, Marrali G, Cammarosano S, Ilardi A, Canosa A, Moglia C, Calvo A, Rinaudo MT, Chiò A
In CD28-costimulated human naïve CD4(+) T cells, I-κB kinase controls the expression of cell cycle regulatory proteins via interleukin-2-independent mechanisms
2010-01-01 Lupino E; Buccinnà B; Ramondetti C; Lomartire A; De Marco G; Ricotti E; Tovo PA; Rinaudo MT; Piccinini M
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.
2011-01-01 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.
Litium chloride, a wnt/beta-catenin mimicking signal, as a long-lasting proliferating stimulus for cultured rat hepatocytes
2006-01-01 Compagnone A.; Bandino A.; Lomartire A.; Bravoco V.; Cravanzola C.; Valfrè di Bonzo L.; Parola M.; Colombatto S.
Monocytes of patients with Amyotrophic Lateral Sclerosis linked to gene mutations display altered TDP-43 subcellular distribution
2017-01-01 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
Novel dysfunctions at the origin of hypomyelination, a feature of Niemann Pick type A
2011-01-01 Buccinnà B; Lomartire A; Ramondetti C; De Marco G; Rinaudo MT; Lupino E; Piccinini M
NOX2 in the hSOD1G93A Transgenic Swine: a preliminary overview
2015-01-01 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
Reduced cellular Ca(2+) availability enhances TDP-43 cleavage by apoptotic caspases.
2014-01-01 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
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
2009-01-01 De Marco G; Piccinini M; Lupino E; Lomartire A; Buccinnà B; Ramondetti C; Grifoni S; Giordana MT; Rinaudo MT
The heterozygous deletion c.1509_1510delAG in exon 14 of FUS causes an aggressive childhood-onset ALS with cognitive impairment
2021-01-01 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.
The molecular basis of the hypomyelination characterizing the brains of sphingomyelinase-deficient mice, an animal model of Niemann-Pick disease type A
2009-01-01 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
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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 | |
| 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. | |
| 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 | |
| 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 | |
| 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. | |
| 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. | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 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. | |
| 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 |