BARBUTI, ANDREA FRANCESCO
BARBUTI, ANDREA FRANCESCO
Dipartimento di Bioscienze
Caveolin-3 and Caveolin-1 Interaction Decreases Channel Dysfunction Due to Caveolin-3 Mutations
2024 P. Benzoni, E. Gazzerro, C. Fiorillo, S. Baratto, C. Bartolucci, S. Severi, R. Milanesi, M. Lippi, M. Langione, C. Murano, C. Meoni, V. Popolizio, A. Cospito, M. Baruscotti, A. Bucchi, A. Barbuti
PITX2 gain-of-function mutation associated with atrial fibrillation alters mitochondrial activity in human iPSC atrial-like cardiomyocytes
2023 P. Benzoni, L. Da Dalt, N. Elia, V. Popolizio, A. Cospito, F. Giannetti, P. Dell'Era, M.S. Olesen, A. Bucchi, M. Baruscotti, G.D. Norata, A. Barbuti
Lack of the transcription factor Nfix causes tachycardia in mice sinus node and rats neonatal cardiomyocytes
2023 S. Landi, F. Giannetti, P. Benzoni, G. Campostrini, G. Rossi, C. Piantoni, G. Bertoli, C. Bonfanti, L. Carnevali, A. Bucchi, M. Baruscotti, G. Careccia, G. Messina, A. Barbuti
Modeling incomplete penetrance in arrhythmogenic cardiomyopathy by human induced pluripotent stem cell derived cardiomyocytes
2023 M. De Bortoli, V. Meraviglia, K. Mackova, L.S. Frommelt, E. König, J. Rainer, C. Volani, P. Benzoni, M. Schlittler, G. Cattelan, B.M. Motta, C. Volpato, W. Rauhe, A. Barbuti, S. Zacchigna, P.P. Pramstaller, A. Rossini
Liraglutide preserves CD34+ stem cells from dysfunction Induced by high glucose exposure
2022 A. Sforza, V. Vigorelli, E. Rurali, G.L. Perrucci, E. Gambini, M. Arici, A. Metallo, R. Rinaldi, P. Fiorina, A. Barbuti, A. Raucci, E. Sacco, M. Rocchetti, G. Pompilio, S. Genovese, M.C. Vinci
Chinese natural compound decreases pacemaking of rabbit cardiac sinoatrial cells by targeting second messenger regulation of f-channels
2022 C. Piantoni, M. Paina, D. Molla, S. Liu, G. Bertoli, H. Jiang, Y. Wang, Y. Wang, Y. Wang, D. Difrancesco, A. Barbuti, A. Bucchi, M. Baruscotti
A detailed characterization of the hyperpolarization-activated "funny" current (If) in human-induced pluripotent stem cell (iPSC)-derived cardiomyocytes with pacemaker activity
2021 F. Giannetti, P. Benzoni, G. Campostrini, R. Milanesi, A. Bucchi, M. Baruscotti, P. Dell'Era, A. Rossini, A. Barbuti
Dual role of miR-1 in the development and function of sinoatrial cells
2021 P. Benzoni, L. Nava, F. Giannetti, G. Guerini, A. Gualdoni, C. Bazzini, R. Milanesi, A. Bucchi, M. Baruscotti, A. Barbuti
f/HCN channels : From a tiny current controlling cardiac pacemaking to a pleiotropic current all over the body
2021 A. Bucchi, M. Baruscotti, A. Barbuti
PCSK9 deficiency rewires heart metabolism and drives heart failure with preserved ejection fraction
2021 L. Da Dalt, L. Castiglioni, A. Baragetti, M. Audano, M. Svecla, F. Bonacina, S. Pedretti, P. Uboldi, P. Benzoni, F. Giannetti, A. Barbuti, F. Pellegatta, S. Indino, E. Donetti, L. Sironi, N. Mitro, A.L. Catapano, G.D. Norata
Age-related changes in cardiac autonomic modulation and heart rate variability in mice
2021 C. Piantoni, L. Carnevali, D. Molla, A. Barbuti, D. DiFrancesco, A. Bucchi, M. Baruscotti
The funny current: Even funnier than 40 years ago. Uncanonical expression and roles of {HCN}/f channels all over the body
2021 P. Benzoni, G. Bertoli, F. Giannetti, C. Piantoni, R. Milanesi, M.M. Pecchiari, A.F. Barbuti, M. Baruscotti, A. Bucchi
Optical investigation of action potential and calcium handling maturation of hiPSC-cardiomyocytes on biomimetic substrates
2019 J.M. Pioner, L. Santini, C. Palandri, D. Martella, F. Lupi, M. Langione, S. Querceto, B. Grandinetti, V. Balducci, P. Benzoni, S. Landi, A. Barbuti, F.F. Lupi, L. Boarino, L. Sartiani, C. Tesi, D.L. Mack, M. Regnier, E. Cerbai, C. Parmeggiani, C. Poggesi, C. Ferrantini, R. Coppini
Human iPSC modeling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes
2019 P. Benzoni, G. Campostrini, S. Landi, V. Bertini, E. Marchina, M. Iascone, G. Ahlberg, M.S. Olesen, E. Crescini, C. Mora, G. Bisleri, C. Muneretto, R. Ronca, M. Presta, P.L. Poliani, G. Piovani, R. Verardi, E.D. Pasquale, A. Consiglio, A. Raya, E. Torre, A.M. Lodrini, R. Milanesi, M. Rocchetti, M. Baruscotti, D. Difrancesco, M. Memo, A. Barbuti, P. Dell'Era
Functional Characterization of a Novel Scn5a Mutation Associated With the Brugada Syndrome
2019 A. Frosio, D. Molla, G. Bertoli, C. Bazzini, R. Milanesi, F. Gennaro, A.F. Barbuti, A. Bucchi, L. Moretti, P. Marchese, D. DI FRANCESCO, M. Baruscotti
Generation of the induced human pluripotent stem cell lines CSSi009-A from a patient with a GNB5 pathogenic variant, and CSSi010-A from a CRISPR/Cas9 engineered GNB5 knock-out human cell line
2019 N. Malerba, P. Benzoni, G.M. Squeo, R. Milanesi, F. Giannetti, L.G. Sadleir, G. Poke, B. Augello, A.I. Croce, A. Barbuti, G. Merla
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability
2018 G. Campostrini, J.C. Difrancesco, B. Castellotti, R. Milanesi, T. Gnecchi-Ruscone, M. Bonzanni, A. Bucchi, M. Baruscotti, C. Ferrarese, S. Franceschetti, L. Canafoglia, F. Ragona, E. Freri, A. Labate, A. Gambardella, C. Costa, C. Gellera, T. Granata, A. Barbuti, D. Di Francesco
Preferential myofibroblast differentiation of cardiac mesenchymal progenitor cells in the presence of atrial fibrillation
2018 E. Gambini, G.L. Perrucci, B. Beatrice, G. Spaltro, G. Campostrini, M.C. Lionetti, A. Pilozzi, F. Martinelli, F. Andrea, D. Difrancesco, A. Barbuti, G. Pompilio
HCN1 mutation spectrum : From neonatal epileptic encephalopathy to benign generalized epilepsy and beyond
2018 C. Marini, A. Porro, A. Rastetter, C. Dalle, I. Rivolta, D. Bauer, R. Oegema, C. Nava, E. Parrini, D. Mei, C. Mercer, R. Dhamija, C. Chambers, C. Coubes, J. Thevenon, P. Kuentz, S. Julia, L. Pasquier, C. Dubourg, W. Carre, A. Rosati, F. Melani, T. Pisano, M. Giardino, A.M. Innes, Y. Alembik, S. Scheidecker, M. Santos, S. Figueiroa, C. Garrido, C. Fusco, D. Frattini, C. Spagnoli, A. Binda, T. Granata, F. Ragona, E. Freri, S. Franceschetti, L. Canafoglia, B. Castellotti, C. Gellera, R. Milanesi, M.M. Mancardi, D.R. Clark, F. Kok, K.L. Helbig, S. Ichikawa, L. Sadler, J. Neupauerova, P. Lassuthova, K. Sterbova, A. Laridon, E. Brilstra, B. Koeleman, J.R. Lemke, F. Zara, P. Striano, J. Soblet, G. Smits, N. Deconinck, A. Barbuti, D. Difrancesco, E. Leguern, R. Guerrini, B. Santoro, K. Hamacher, G. Thiel, A. Moroni, J.C. Difrancesco, C. Depienne
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability
2018 M. Bonzanni, J.C. Difrancesco, R. Milanesi, G. Campostrini, B. Castellotti, A. Bucchi, M. Baruscotti, C. Ferrarese, S. Franceschetti, L. Canafoglia, F. Ragona, E. Freri, A. Labate, A. Gambardella, C. Costa, I. Rivolta, C. Gellera, T. Granata, A. Barbuti, D. Di Francesco