ZONTA, FRANCESCO

ZONTA, FRANCESCO  

Dipartimento di Fisica e Astronomia "Galileo Galilei" - DFA  

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Risultati 1 - 20 di 25 (tempo di esecuzione: 0.049 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Connexin hemichannel blockade by abEC1.1 disrupts glioblastoma progression, suppresses invasiveness, and reduces hyperexcitability in preclinical models 2025 Donati, ViolaPersano, LucaPanarelli, MariateresaCalistri, AriannaZonta, FrancescoMammano, Fabio + CELL COMMUNICATION AND SIGNALING - -
A fully human IgG1 antibody targeting connexin 32 extracellular domain blocks CMTX1 hemichannel dysfunction in an in vitro model 2024 Donati, ViolaPanarelli, MariateresaCalistri, AriannaFornaini, Maria VittoriaZonta, FrancescoMammano, Fabio + CELL COMMUNICATION AND SIGNALING - -
Molecular Dynamics Simulation of Permeation Through Connexin Channels 2024 Zonta F.Mammano F. + - METHODS IN MOLECULAR BIOLOGY Connexin Hemichannels: Methods and Protocols
RAGE engagement by SARS-CoV-2 enables monocyte infection and underlies COVID-19 severity 2023 Angioni, RobertaSánchez-Rodríguez, RicardoMunari, FabioBertoldi, NicoleZonta, FrancescoCattelan, Anna MariaMolon, BarbaraViola, Antonella + CELL REPORTS MEDICINE - -
A Quantitative Assay for Ca2+ Uptake through Normal and Pathological Hemichannels 2022 Donati, ViolaPeres, ChiaraZonta, FrancescoMammano, Fabio + INTERNATIONAL JOURNAL OF MOLECULAR 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 - -
Cx32 hemichannel opening by cytosolic Ca2+is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease 2018 CARRER, ANDREALEPARULO, ALESSANDROCrispino, GiuliaCiubotaru, Catalin DacianMarin, OrianoZonta, FrancescoBortolozzi, Mario HUMAN MOLECULAR GENETICS - -
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 - -
Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease 2017 Carrer, AndreaLeparulo, AlessandroCrispino, GiuliaCiubotaru, Catalin DacianMarin, OrianoZonta, Francesco + HUMAN MOLECULAR GENETICS ONLINE - -
Design and Characterization of a Human Monoclonal Antibody that Modulates Mutant Connexin 26 Hemichannels Implicated in Deafness and Skin Disorders 2017 CARRER, ANDREAZONTA, FRANCESCOCERIANI, FEDERICOBURATTO, DAMIANOCRISPINO, GIULIAZORZI, VERONICAZIRALDO, GAIABRUNO, FRANCESCAMAMMANO, FABIO + FRONTIERS IN MOLECULAR NEUROSCIENCE - -
Fully human antibody specifically inhibiting connexin 26 2017 MAMMANO FabioZONTA Francesco + - - -
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 - -
How local flexibility affects knot positioning in ring polymers 2016 ORLANDINI, ENZOBAIESI, MARCOZONTA, FRANCESCO MACROMOLECULES - -
Mitochondrial Thioredoxin System as a Modulator of Cyclophilin D Redox State 2016 FOLDA, ALESSANDRACITTA, ANNASCALCON, VALERIACALI', TITOZONTA, FRANCESCOSCUTARI, GUIDOBINDOLI, ALBERTORIGOBELLO, MARIA PIA SCIENTIFIC REPORTS - -
Hemichannels; from the molecule to the function 2015 Francesco ZontaMario BortolozziFabio Mammano + - FRONTIERS RESEARCH TOPICS Hemichannels; from the molecule to the function
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 2015 ZONTA, FRANCESCOBURATTO, DAMIANOCRISPINO, GIULIAMAMMANO, FABIO + HUMAN MOLECULAR GENETICS - -
Molecular dynamics simulations highlight structural and functional alterations in deafness-related M34T mutation of connexin 26 2014 ZONTA, FRANCESCOBURATTO, DAMIANOCASSINI, CHIARAMAMMANO, FABIO + FRONTIERS IN PHYSIOLOGY - -
Role of gamma carboxylated Glu47 in connexin 26 hemichannel regulation by extracellular Ca2+: Insight from a local quantum chemistry study 2014 ZONTA, FRANCESCOMAMMANO, FABIOTORSELLO, MAUROFORTUNATI, NICOLAORIAN, LAURAPOLIMENO, ANTONINO BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS - -
The 3.5 ångström X−ray structure of the human connexin26 gap junction channel is unlikely that of a fully open channel 2013 ZONTA, FRANCESCOBORTOLOZZI, MARIOMAMMANO, FABIO + CELL COMMUNICATION AND SIGNALING - -
Bioinformatic and mutational analysis of channelrhodopsin-2 cation conducting pathway. 2012 ZONTA, FRANCESCOFILIPPINI, FRANCESCOMONGILLO, MARCO + THE JOURNAL OF BIOLOGICAL CHEMISTRY - -