ZONTA, FRANCESCO

ZONTA, FRANCESCO  

Dipartimento di Fisica e Astronomia "Galileo Galilei" - DFA  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
What is the length of a knot in a polymer? 2005 MARCONE, BORISORLANDINI, ENZOSTELLA, ATTILIOZONTA, FRANCESCO JOURNAL OF PHYSICS. A, MATHEMATICAL AND GENERAL - -
Size of knots in ring polymers 2007 MARCONE, BORISORLANDINI, ENZOSTELLA, ATTILIOZONTA, FRANCESCO PHYSICAL REVIEW E, STATISTICAL, NONLINEAR, AND SOFT MATTER PHYSICS - -
Slow topological time scale of knotted polymers 2008 ORLANDINI, ENZOSTELLA, ATTILIOZONTA, FRANCESCO + JOURNAL OF PHYSICS. A, MATHEMATICAL AND THEORETICAL - -
Topological Signatures of Globular Polymers 2011 BAIESI, MARCOORLANDINI, ENZOSTELLA, ATTILIOZONTA, FRANCESCO PHYSICAL REVIEW LETTERS - -
Permeation pathway of homomeric connexin 26 and connexin 30 channels investigated by molecular dynamics. 2012 ZONTA, FRANCESCOZANOTTI, GIUSEPPEMAMMANO, FABIO + JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS - -
Bioinformatic and mutational analysis of channelrhodopsin-2 cation conducting pathway. 2012 ZONTA, FRANCESCOFILIPPINI, FRANCESCOMONGILLO, MARCO + THE JOURNAL OF BIOLOGICAL CHEMISTRY - -
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 - -
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 - -
Molecular dynamics simulations highlight structural and functional alterations in deafness-related M34T mutation of connexin 26 2014 ZONTA, FRANCESCOBURATTO, DAMIANOCASSINI, CHIARABORTOLOZZI, MARIOMAMMANO, FABIO FRONTIERS IN PHYSIOLOGY - -
The p.Cys169Tyr variant of connexin 26 is not a polymorphism 2015 ZONTA, FRANCESCOBURATTO, DAMIANOCRISPINO, GIULIAMAMMANO, FABIO + HUMAN MOLECULAR GENETICS - -
Mitochondrial Thioredoxin System as a Modulator of Cyclophilin D Redox State 2016 FOLDA, ALESSANDRACITTA, ANNASCALCON, VALERIACALI', TITOZONTA, FRANCESCOSCUTARI, GUIDOBINDOLI, ALBERTORIGOBELLO, MARIA PIA SCIENTIFIC REPORTS - -
How local flexibility affects knot positioning in ring polymers 2016 ORLANDINI, ENZOBAIESI, MARCOZONTA, FRANCESCO MACROMOLECULES - -
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 - -
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 + - - -
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 - -
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 - -
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 Quantitative Assay for Ca2+ Uptake through Normal and Pathological Hemichannels 2022 Donati, ViolaPeres, ChiaraZonta, FrancescoMammano, Fabio + INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES - -