BRINI, MARISA

BRINI, MARISA  

Dipartimento di Scienze del Farmaco - DSF  

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Risultati 1 - 20 di 149 (tempo di esecuzione: 0.021 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
14-3-3 epsilon: A protein partner for plasma-membrane Ca2+ pump isoform 4 and Na+/Ca2+ exchanger isoform 2 2005 BRINI, MARISARIZZUTO, ROSARIO + THE FEBS JOURNAL - -
[30] Photoprotein-mediated measurement of calcium ion concentration in mitochondria of living cellsMitochondrial Biogenesis and Genetics Part A 1995 RIZZUTO, ROSARIOBRINI, MARISAPOZZAN, TULLIO + METHODS IN ENZYMOLOGY - -
A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency. 1999 BRINI, MARISARIZZUTO, ROSARIO + NATURE MEDICINE - -
A calcium signalling defect in the pathogenesis of a mtDNA-inherited oxidative phosphorylation deficiency. 1999 BRINI, MARISARIZZUTO, ROSARIO + NATURE MEDICINE - -
A comparative functional analysis of plasma membrane Ca2+ pump isoforms in intact cells 2003 BRINI, MARISA + THE JOURNAL OF BIOLOGICAL CHEMISTRY - -
A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness 2007 BORTOLOZZI, MARIOBRINI, MARISAMAMMANO, FABIO + PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA - -
A new approach to cellular Ca2+ determination by the photoprotein aequorine 1993 Brini M.Rizzuto R. + GIORNALE ITALIANO DI CHIMICA CLINICA - -
A new split-GFP-based probe reveals DJ-1 translocation into the mitochondrial matrix to sustain ATP synthesis upon nutrient deprivation. 2015 CALI', TITOOTTOLINI, DENISSORIANO GARCIA - CUERVA, MARIA EUGENIABRINI, MARISA HUMAN MOLECULAR GENETICS - -
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 - -
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 - -
A SPLICS reporter reveals α-synuclein regulation of lysosome-mitochondria contacts which affects TFEB nuclear translocation 2024 Giamogante, FlaviaBarazzuol, LuciaMaiorca, FrancescaPoggio, ElenaCALI TITOBrini, Marisa + NATURE COMMUNICATIONS - -
A split-GFP tool reveals differences in the sub-mitochondrial distribution of wt and mutant alpha-synuclein 2019 Vicario M.Cieri D.Vallese F.Catoni C.Barazzuol L.Berto P.Grinzato A.Barbieri L.Brini M.Cali T. CELL DEATH & DISEASE - -
A study of the activity of the plasma membrane Na/Ca exchanger in the cellular enviroment 2002 BRINI, MARISAMANNI, SABRINA + ANNALS OF THE NEW YORK ACADEMY OF SCIENCES - -
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 - -
Alpha-synuclein aggregates activate calcium pump SERCA leading to calcium dysregulation 2018 ZHENG, JIANCALI', TITOBrini M + EMBO REPORTS - -
Alpha-synuclein at the intracellular and the extracellular side: functional and dysfunctional implications 2017 OTTOLINI, DENISCALI', TITOSZABO', ILDIKO'BRINI, MARISA BIOLOGICAL CHEMISTRY - -
An expanded palette of improved SPLICS reporters detects multiple organelle contacts in vitro and in vivo 2020 Vallese, FrancescaCatoni, CristinaCieri, DomenicoBarazzuol, LuciaGiamogante, FlaviaPinton, PaoloBrini, MarisaCalì, Tito + NATURE COMMUNICATIONS - -
Angiotensin II Promotes SARS-CoV-2 Infection via Upregulation of ACE2 in Human Bronchial Cells 2022 Caputo, IlariaCaroccia, BrasilinaFrasson, IlariaPoggio, ElenaMorpurgo, MargheritaSeccia, Teresa M.Calì, TitoBrini, MarisaRichter, Sara N.Rossi, Gian Paolo + INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES - -
ATP2B2 de novo variants as a cause of variable neurodevelopmental disorders that feature dystonia, ataxia, intellectual disability, behavioral symptoms, and seizures 2023 Poggio, ElenaBarazzuol, LuciaSalmaso, AndreaMilani, CelesteDeligiannopoulou, AdamantiaCALI TITOBrini, Marisa + GENETICS IN MEDICINE - -
Ca2+ handling at the mitochondria-ER contact sites in neurodegeneration 2021 Lim D.Cali T.Brini M. + CELL CALCIUM - -