MILANESI, RAFFAELLA
MILANESI, RAFFAELLA
Dipartimento di Medicina Veterinaria e Scienze Animali
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
Antibiotic treatments and somatic cell count as phenotype to map QTL for mastitis susceptibility in Holstein cattle breed
2023 M. Giuseppina Strillacci, C. Punturiero, R. Milanesi, F. Bernini, T. Mason, A. Bagnato
Assessing major genes allele frequencies and the genetic diversity of the native Aosta cattle female population
2023 F. Bernini, C. Punturiero, M. Vevey, V. Blanchet, R. Milanesi, A. Delledonne, A. Bagnato, M.G. Strillacci
HCM-ASSOCIATED ALMS1 VARIANT: ALLELE DROP-OUT AND FREQUENCY IN ITALIAN SPHYNX CATS
2023 M.E. Turba, P. Ferrari, R. Milanesi, F. Gentilini, M. Longeri
Genomic approach to manage genetic variability in dairy farms
2023 C. Punturiero, R. Milanesi, F. Bernini, A. Delledonne, A. Bagnato, M.G. Strillacci
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
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
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
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
Copy number variants in four Italian turkey breeds
2021 M.G. Strillacci, S.P. Marelli, R. Milanesi, L. Zaniboni, C. Punturiero, S. Cerolini
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
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
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
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
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
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
The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability
2017 G. Campostrini, M. Bonzanni, A. Lissoni, C. Bazzini, R. Milanesi, E. Vezzoli, M. Francolini, M. Baruscotti, A. Bucchi, I. Rivolta, M. Fantini, S. Severi, R. Cappato, L. Crotti, P.J. Schwartz, D. Di Francesco, A. Barbuti
RICERCA DI MUTAZIONI NEL CANALE PACEMAKER HCN4 IN PAZIENTI AFFETTI DA DISTURBI DEL RITMO CARDIACO
2015 R. Milanesi