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Cardiovascular Research|April 8, 2022
Maturation of hiPSC-derived cardiomyocytes promotes adult alternative splicing of SCN5A and reveals changes in sodium current associated with cardiac arrhythmiaGiulia Campostrini, Georgios Kosmidis, Dorien Ward-van Oostwaard, et al.
Neurobiology of Disease|June 25, 2018
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitabilityMattia Bonzanni, Jacopo C DiFrancesco, Raffaella Milanesi, et al.
Frontiers in Molecular Neuroscience|August 22, 2018
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal ExcitabilityGiulia Campostrini, Jacopo C DiFrancesco, Barbara Castellotti, et al.
Frontiers in Bioscience (Landmark Edition)|December 29, 2015
Higher cardiogenic potential of iPSCs derived from cardiac versus skin stromal cellsViviana Meraviglia, Jianyan Wen, Luca Piacentini, et al.
Nature Communications|May 15, 2023
RagD auto-activating mutations impair MiT/TFE activity in kidney tubulopathy and cardiomyopathy syndromeIrene Sambri, Marco Ferniani, Giulia Campostrini, et al.
Science (New York, N.Y.)|May 18, 2023
Interplay between calcium and sarcomeres directs cardiomyocyte maturation during regenerationPhong D Nguyen, Iris Gooijers, Giulia Campostrini, et al.
Cardiovascular Research|September 11, 2019
Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytesPatrizia Benzoni, Giulia Campostrini, Sara Landi, et al.
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