MILANESI, RAFFAELLA
MILANESI, RAFFAELLA
Dipartimento di Medicina Veterinaria e Scienze Animali
A caveolin-binding motif in the N-terminus of HCN4 controls channel properties
2008 A. Barbuti, R. Milanesi, N. Mazzocchi, D. Di Francesco
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
A gain-of-function mutation in the cardiac pacemaker HCN4 channel increasing cAMP sensitivity is associated with familial Inappropriate Sinus Tachycardia
2017 M. Baruscotti, A. Bucchi, R. Milanesi, M. Paina, A. Barbuti, T. Gnecchi Ruscone, E. Bianco, L. Vitali Serdoz, R. Cappato, D. Difrancesco
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
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
Allele drop-out cases in screening of HCM associated ALMS1 gene variant in Italian Sphynx cats
2022 M. Longeri, M.E. Turba, P. Ferrari, R. Milanesi, F. Gentilini
An LQTS6 MiRP1 mutation suppresses pacemaker current and is associated with sinus bradycardia
2013 P.A. Nawathe, Y. Kryukova, R.V. Oren, R. Milanesi, C.E. Clancy, J.T. Lu, A.J. Moss, D. Difrancesco, R.B. Robinson
Animal Bio Arkivi: establishment of a phenotype and tissue repository for farm animals and pets at the University of Milan
2021 M.L.E. Longeri, L. Zaniboni, M.C.S. Cozzi, R. Milanesi, A. Bagnato
Coexistence of seizure episodes and symptomatic sinoatrial arrest occurring in two sisters suggests an underlying cardioneuronal channelopathy
2013 G.P. Carboni, J.C. Difrancesco, R. Milanesi, M. Baruscotti
Copy number variants in four Italian turkey breeds
2021 M.G. Strillacci, S.P. Marelli, R. Milanesi, L. Zaniboni, C. Punturiero, S. Cerolini
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
Embryonic stem cell-derived CD166+ precursors develop into fully functional sinoatrial-like cells
2013 A. Scavone, D. Capilupo, N. Mazzocchi, A. Crespi, S. Zoia, G. Campostrini, A. Bucchi, R. Milanesi, M. Baruscotti, S. Benedetti, S. Antonini, G. Messina, D. DiFrancesco, A. Barbuti
Familial sinus bradycardia associated with a mutation in the cardiac pacemaker channel
2006 R. Milanesi, M. Baruscotti, T. Gnecchi Ruscone, D. Difrancesco
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
HCN-related channelopathies
2010 M. Baruscotti, G. Bottelli, R. Milanesi, J.C. DiFrancesco, D. DiFrancesco
HCN1 and HCN4: the competition for the same channel
2003 A. Barbuti, C. Altomare, M. Riolfo, C. Brioschi, B. Terragni, A. Tognati, R. Milanesi, C. Viscomi, M. Baruscotti, D. Di Francesco
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
Heteromeric HCN1-HCN4 channels: a comparison with native pacemaker channels from the rabbit sinoatrial node
2003 C. Altomare, B. Terragni, C. Brioschi, R. Milanesi, C. Pagliuca, C. Viscomi, A. Moroni, M. Baruscotti, D. DiFrancesco
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