Sfoglia per Autore

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Mostrati risultati da 1 a 20 di 39
Titolo Data di pubblicazione Autore(i) Rivista Serie Titolo libro
SOD1 in ALS: Taking Stock in Pathogenic Mechanisms and the Role of Glial and Muscle Cells 2022 Peggion, CaterinaScalcon, ValeriaMassimino, Maria LinaLopreiato, RaffaeleRigobello, Maria PiaBertoli, Alessandro + ANTIOXIDANTS - -
Large-scale sequencing and comparative analysis of oenological Saccharomyces cerevisiae strains supported by nanopore refinement of key genomes 2021 De Pascale F.Bianca F.De Bernardini N.Lopreiato R.Treu L.Campanaro S. + FOOD MICROBIOLOGY - -
Regulation of endoplasmic reticulum–mitochondria tethering and Ca2+ fluxes by TDP-43 via GSK3β 2021 Peggion C.Massimino M. L.Lia F.Lopreiato R.Cagnin S.Calì T.Bertoli A. + INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES - -
Nucleolin Rescues TDP-43 Toxicity in Yeast and Human Cell Models 2021 Peggion C.Massimino M. L.Maldi A.Sartori G.Bertoli A.Lopreiato R. + FRONTIERS IN CELLULAR NEUROSCIENCE - -
The E3 ubiquitin-protein ligase MDM2 is a novel interactor of the von Hippel-Lindau tumor suppressor 2020 Falconieri, AntonellaMinervini, GiovanniBortolotto, RaissaPiovesan, DamianoLopreiato, RaffaeleSartori, GeppoPennuto, MariaTosatto, Silvio C E SCIENTIFIC REPORTS - -
A V1143F mutation in the neuronal-enriched isoform 2 of the PMCA pump is linked with ataxia 2018 Vicario, MattiaVallese, FrancescaGRINZATO, ALESSANDROCieri, DomenicoBerto, PaolaFrizzarin, MartinaLopreiato, RaffaeleZonta, FrancescoFerro, StefaniaSandre, MicheleMarin, OrianoRuzzene, MariaZanotti, GiuseppeBrini, MarisaCalì, TitoCarafoli, Ernesto + NEUROBIOLOGY OF DISEASE - -
A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defect 2017 Vicario, MattiaCalì, TitoCieri, DomenicoVallese, FrancescaBortolotto, RaissaLopreiato, RaffaeleZonta, FrancescoZanotti, GiuseppeBrini, MarisaCarafoli, Ernesto + BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE - -
Novel interactions of the von Hippel-Lindau (pVHL) tumor suppressor with the CDKN1 family of cell cycle inhibitors 2017 MINERVINI, GIOVANNILOPREIATO, RAFFAELEBORTOLOTTO, RAISSAFALCONIERI, ANTONELLASARTORI, GEPPOTOSATTO, SILVIO SCIENTIFIC REPORTS - -
The ataxia related G1107D mutation of the plasma membrane Ca2+ ATPase isoform 3 affects its interplay with calmodulin and the autoinhibition process. 2017 CALI', TITOFRIZZARIN, MARTINAZONTA, FRANCESCOBERTIPAGLIA, ILENIARUZZENE, MARIADAMIANO, NUNZIOMARIN, ORIANOZANOTTI, GIUSEPPEBRINI, MARISALOPREIATO, RAFFAELECARAFOLI, ERNESTO + BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE - -
Generation and validation of novel adeno-associated viral vectors for the analysis of Ca2+ homeostasis in motor neurons 2017 Norante, Rosa PiaMassimino, Maria LinaLORENZON, PAOLODe Mario, AgnesePeggion, CaterinaVICARIO, MATTIAAlbiero, MattiaSorgato, Maria CatiaLopreiato, RaffaeleBertoli, Alessandro SCIENTIFIC REPORTS - -
Carotid plaque detection improves the predictve value of CHA2DS2-VASc score in patients with non-valvular atrial fibrilation: The ARAPACIS Study 2017 Basili S.Loffredo L.Farcomeni A.Corazza G. R.Mozzini C.Spagnuolo V.Mule G.Barbagallo M.Pisano M.Signorelli S.Sacerdoti D.Iuliano L.Pacelli A.Cilli M.Bertazzoni G.Zanoli L.Fidone F.Maio R.Spagnuolo V.Desideri G.Mezzetti M.Gresele P.Puccetti L.Bertolotti M.Mussi C.Fabris F.Treleani M.De Zaiacomo F.Manica A.Sechi L. A.Miceli E.Serra M. G.Antonaci S.Ventrella F.Salvati F.Scozzari F.Muiesan M. L.De Vincentis A.Cosio P.Bracco C.Sparagna A.Musumeci M.Delfino M.Melis G.Scordo A.Cheli P.Stanghellini V.Mancuso G.Cozzolino D.Galasso D.Mazzei F.Fattorini A.Lopreiato F.Parente F.Ageno W.Vicario T.Bianchi P. I.Bracco G.Marra A. M.Miceli G.Pretti V.Vidili G.Vitale F. + INTERNATIONAL JOURNAL OF CARDIOLOGY - -
Spontaneous shaker rat mutant - A new model for X-linked tremor/ataxia 2016 CALI', TITOLOPREIATO, RAFFAELEFRIZZARIN, MARTINABRINI, MARISACARAFOLI, ERNESTO + DISEASE MODELS & MECHANISMS - -
Heterologous Expression in Yeast of Human Ornithine Carriers ORNT1 and ORNT2 and of ORNT1 Alleles Implicated in HHH Syndrome in Humans 2016 DOIMO, MARALOPREIATO, RAFFAELEBASSO, VALENTINABORTOLOTTO, RAISSATREVISSON, EVASALVIATI, LEONARDO + JIMD REPORTS - -
A novel mutation in isoform 3 of the plasma membrane Ca2+ pump impairs cellular Ca2+ homeostasis in a patient with cerebellar ataxia and laminin subunit 1α mutations. 2015 CALI', TITOLOPREIATO, RAFFAELEFRIZZARIN, MARTINAZANOTTI, GIUSEPPEBRINI, MARISACARAFOLI, ERNESTO + THE JOURNAL OF BIOLOGICAL CHEMISTRY - -
Heterologous Expression in Yeast of Human Ornithine Carriers ORNT1 and ORNT2 and of ORNT1 Alleles Implicated in HHH Syndrome in Humans 2015 Doimo, MaraLopreiato, RaffaeleBortolotto, RaissaTrevisson, EvaSalviati, Leonardo + JIMD REPORTS - -
The Plasma Membrane Calcium Pump: New Ways to Look at an Old Enzyme 2014 LOPREIATO, RAFFAELEGIACOMELLO, MARTACARAFOLI, ERNESTO THE JOURNAL OF BIOLOGICAL CHEMISTRY - -
The neuro-cardiac interaction defines an extracellular microdomain required for neurotrophic signaling 2014 Sandre MMARIN, ORIANOLOPREIATO, RAFFAELEMONGILLO, MARCO + CARDIOVASCULAR RESEARCH - -
Structural basis of the neuro-cardiac interaction and its involvement in NGF signaling 2013 Sandre M.MARIN, ORIANOLOPREIATO, RAFFAELEMONGILLO, MARCO + - - Summer School on Cardiovascular Sciences
Huntington's disease, Calcium and Mitochondria. 2011 GIACOMELLO MLOPREIATO, RAFFAELE + BIOFACTORS - -
Mutations in PMCA2 and hereditary deafness: a molecular analysis of the pump defect. 2011 GIACOMELLO, MARTADE MARIO, AGNESELOPREIATO, RAFFAELEBRINI, MARISA + CELL CALCIUM - -
Mostrati risultati da 1 a 20 di 39
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