R. Milanesi

发表

Localization of Pacemaker Channels in Lipid Rafts Regulates Channel Kinetics

D. DiFrancesco, A. Barbuti, B. Gravante, 2004, Circulation research.

The genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunction

A. Bucchi, M. Baruscotti, R. Milanesi, 2015, Journal of Interventional Cardiac Electrophysiology.

The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability

S. Severi, R. Cappato, M. Francolini, 2017, Cardiovascular research.

Embryonic Stem Cell–Derived CD166+ Precursors Develop Into Fully Functional Sinoatrial-Like Cells

S. Benedetti, S. Antonini, D. DiFrancesco, 2013, Circulation research.

Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes

M. Memo, A. Consiglio, Á. Raya, 2019, Cardiovascular research.

Properties of ivabradine‐induced block of HCN1 and HCN4 pacemaker channels

D. DiFrancesco, A. Bucchi, M. Baruscotti, 2006, The Journal of physiology.

HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature

B. Castellotti, C. Gellera, S. Franceschetti, 2019, Epilepsy Research.

Recessive Loss-of-Function Mutation in the Pacemaker HCN2 Channel Causing Increased Neuronal Excitability in a Patient with Idiopathic Generalized Epilepsy

S. Franceschetti, D. DiFrancesco, C. Ferrarese, 2011, The Journal of Neuroscience.

A detailed characterization of the hyperpolarization-activated “funny” current (If) in human-induced pluripotent stem cell (iPSC)–derived cardiomyocytes with pacemaker activity

A. Rossini, P. Benzoni, P. Dell’Era, 2021, Pflügers Archiv - European Journal of Physiology.

Interaction of the Pacemaker Channel HCN1 with Filamin A*

D. DiFrancesco, C. Viscomi, A. Barbuti, 2004, Journal of Biological Chemistry.

A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability

B. Castellotti, T. Gnecchi-Ruscone, C. Gellera, 2018, Front. Mol. Neurosci..

The “Funny” Pacemaker Current

D. DiFrancesco, A. Bucchi, Georgia Bottelli, 2009 .

Familial sinus bradycardia associated with a mutation in the cardiac pacemaker channel.

Tomaso Gnecchi-Ruscone, Dario DiFrancesco, Mirko Baruscotti, 2006, The New England journal of medicine.

HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond

K. Hamacher, C. Mercer, P. Striano, 2018, Brain : a journal of neurology.

Copy Number Variants in Four Italian Turkey Breeds

S. Marelli, R. Milanesi, S. Cerolini, 2021, Animals : an open access journal from MDPI.

The funny current: Even funnier than 40 years ago. Uncanonical expression and roles of HCN/f channels all over the body.

P. Benzoni, M. Pecchiari, A. Bucchi, 2021, Progress in biophysics and molecular biology.

A gain-of-function mutation in the cardiac pacemaker HCN4 channel increasing cAMP sensitivity is associated with familial Inappropriate Sinus Tachycardia

R. Cappato, T. Gnecchi-Ruscone, D. DiFrancesco, 2017, European heart journal.

A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability

B. Castellotti, C. Gellera, S. Franceschetti, 2018, Neurobiology of Disease.

HCN-related channelopathies

Dario DiFrancesco, Mirko Baruscotti, D. DiFrancesco, 2010, Pflügers Archiv - European Journal of Physiology.

An LQTS6 MiRP1 Mutation Suppresses Pacemaker Current and is Associated with Sinus Bradycardia

Yelena Kryukova, Arthur J Moss, Colleen E Clancy, 2013, Journal of cardiovascular electrophysiology.

MiRP 1 Mutation Suppresses Pacemaker Current and is Associated with Sinus Bradycardia

Ronit V. Oren, A. Moss, R. Robinson, 2013 .

Heteromeric HCN1–HCN4 Channels: A Comparison with Native Pacemaker Channels from the Rabbit Sinoatrial Node

D. DiFrancesco, C. Viscomi, A. Moroni, 2003, The Journal of physiology.

HCM-associated ALMS1 variant: Allele drop-out and frequency in Italian Sphynx cats.

M. Turba, R. Milanesi, M. Longeri, 2023, Animal genetics.

Genomic approach to manage genetic variability in dairy farms

Francesca Bernini, R. Milanesi, A. Bagnato, 2023, Italian Journal of Animal Science.

A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability

B. Castellotti, C. Gellera, S. Franceschetti, 2018, Neurobiology of Disease.

Dual role of miR-1 in the development and function of sinoatrial cells.

P. Benzoni, A. Bucchi, M. Baruscotti, 2021, Journal of molecular and cellular cardiology.

Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of I f and I CaL in patient-derived cardiomyocytes

E. Crescini, A. Consiglio, P. Benzoni, 2019 .

Antibiotic treatments and somatic cell count as phenotype to map QTL for mastitis susceptibility in Holstein cattle breed

Francesca Bernini, R. Milanesi, A. Bagnato, 2023, Italian Journal of Animal Science.

Assessing major genes allele frequencies and the genetic diversity of the native Aosta cattle female population

R. Milanesi, A. Bagnato, M. Strillacci, 2023, Italian Journal of Animal Science.

Caveolin-3 and Caveolin-1 Interaction Decreases Channel Dysfunction Due to Caveolin-3 Mutations

P. Benzoni, S. Baratto, A. Bucchi, 2024, International Journal of Molecular Sciences.