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
Exploring the genetic variability of the PRNP gene at codons 127, 142, 146, 154, 211, 222, and 240 in goats farmed in the Lombardy Region, Italy
2024 C. Ferrari, C. Punturiero, R. Milanesi, A. Delledonne, A. Bagnato, M.G. Strillacci
Mt-ND5 DNA variability in wildcats living in Central Italy Protected Areas
2024 M. Maini, C. Polce, R. Milanesi, S. Comazzi, R. Cazzolla Gatti, M. Longeri
Copy number variant scan in more than four thousand Holstein cows bred in Lombardy, Italy
2024 A. Delledonne, C. Punturiero, C. Ferrari, F. Bernini, R. Milanesi, A. Bagnato, M.G. Strillacci
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
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
A novel de novo HCN2 loss‐of‐function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet
2023 J.C. Difrancesco, F. Ragona, C. Murano, A. Frosio, D. Melgari, A. Binda, S. Calamaio, R. Prevostini, M. Mauri, L. Canafoglia, B. Castellotti, G. Messina, C. Gellera, R. Previtali, P. Veggiotti, R. Milanesi, A. Barbuti, R. Solazzi, E. Freri, T. Granata, I. Rivolta
Genomic approach to manage genetic variability in dairy farms
2023 C. Punturiero, R. Milanesi, F. Bernini, A. Delledonne, A. Bagnato, M.G. Strillacci
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
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
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. Pecchiari, A. Barbuti, M. Baruscotti, A. Bucchi
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
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
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 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 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