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BMC Nephrology|July 3, 2014
Adenine phosphoribosyltransferase (APRT) deficiency: identification of a novel nonsense mutationRea Valaperta, Vittoria Rizzo, Fortunata Lombardi, et al.
Antioxidants (Basel, Switzerland)|January 21, 2023
Sphingolipids and Atherosclerosis: The Dual Role of Ceramide and Sphingosine-1-PhosphateMarco Piccoli, Federica Cirillo, Andrea Ghiroldi, et al.
Stem Cells International|September 14, 2018
GM1 Ganglioside Promotes Osteogenic Differentiation of Human Tendon Stem CellsSonia Bergante, Pasquale Creo, Marco Piccoli, et al.
International Journal of Molecular Sciences|June 10, 2022
Neu3 Sialidase Activates the RISK Cardioprotective Signaling Pathway during Ischemia and Reperfusion Injury (IRI)Marco Piccoli, Simona Coviello, Maria Elena Canali, et al.
International Journal of Molecular Sciences|December 9, 2023
Challenges in Brugada Syndrome Stratification: Investigating SCN5A Mutation Localization and Clinical PhenotypesAdriana Tarantino, Giuseppe Ciconte, Andrea Ghiroldi, et al.
Frontiers in Physiology|August 27, 2019
Sphingolipid Synthesis Inhibition by Myriocin Administration Enhances Lipid Consumption and Ameliorates Lipid Response to Myocardial Ischemia Reperfusion InjuryFabiola Bonezzi, Marco Piccoli, Michele Dei Cas, et al.
The Journal of Biological Chemistry|December 5, 2012
NEU3 sialidase is activated under hypoxia and protects skeletal muscle cells from apoptosis through the activation of the epidermal growth factor receptor signaling pathway and the hypoxia-inducible factor (HIF)-1αRaffaella Scaringi, Marco Piccoli, Nadia Papini, et al.
The Journal of Biological Chemistry|October 24, 2008
NEU3 sialidase strictly modulates GM3 levels in skeletal myoblasts C2C12 thus favoring their differentiation and protecting them from apoptosisLuigi Anastasia, Nadia Papini, Francesca Colazzo, et al.
Frontiers in Cell and Developmental Biology|December 2, 2020
HIF-1α Directly Controls WNT7A Expression During MyogenesisFederica Cirillo, Giulia Resmini, Elia Angelino, et al.
Frontiers in Physiology|June 14, 2019
Genotype/Phenotype Relationship in a Consanguineal Family With Brugada Syndrome Harboring the R1632C Missense Variant in the SCN5A GeneMichelle M Monasky, Emanuele Micaglio, Giuseppe Ciconte, et al.
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