A. Ghiroldi

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Novel SCN5A p.V1429M Variant Segregation in a Family with Brugada Syndrome

C. Pappone, G. Vicedomini, E. Locati, 2020, International journal of molecular sciences.

SCN5A Nonsense Mutation and NF1 Frameshift Mutation in a Family With Brugada Syndrome and Neurofibromatosis

V. Santinelli, C. Pappone, G. Vicedomini, 2019, Front. Genet..

Novel SCN5A p.W697X Nonsense Mutation Segregation in a Family with Brugada Syndrome

C. Pappone, G. Vicedomini, E. Locati, 2019, International journal of molecular sciences.

Role of Sialidase Neu3 and Ganglioside GM3 in cardiac fibroblasts activation.

C. Pappone, L. Menicanti, M. Aureli, 2020, The Biochemical journal.

Clinical Considerations for a Family with Dilated Cardiomyopathy, Sudden Cardiac Death, and a Novel TTN Frameshift Mutation

C. Pappone, E. Locati, M. Piccoli, 2021, International journal of molecular sciences.

Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths

C. Pappone, S. Benedetti, G. Casari, 2021, International journal of molecular sciences.

Brugada syndrome genetics is associated with phenotype severity

E. Petretto, V. Santinelli, C. Pappone, 2020, European heart journal.

Human Sarcopenic Myoblasts Can Be Rescued by Pharmacological Reactivation of HIF-1α

C. Pappone, B. Canciani, Simona Coviello, 2022, International journal of molecular sciences.

HIF-1α Directly Controls WNT7A Expression During Myogenesis

C. Pappone, A. Graziani, Michele Ferrara, 2020, Frontiers in Cell and Developmental Biology.

Activation of the hypoxia‐inducible factor 1a promotes myogenesis through the noncanonical Wnt pathway, leading to hypertrophic myotubes

S. Bergante, M. Piccoli, F. Cirillo, 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

NEU3 sialidase role in activating HIF-1α in response to chronic hypoxia in cyanotic congenital heart patients.

F. Pluchinotta, A. Varrica, A. Giamberti, 2017, International journal of cardiology.

Neu3 Sialidase Activates the RISK Cardioprotective Signaling Pathway during Ischemia and Reperfusion Injury (IRI)

C. Pappone, Simona Coviello, M. Piccoli, 2022, International journal of molecular sciences.

Isolation and Characterization of 2 New Human Rotator Cuff and Long Head of Biceps Tendon Cells Possessing Stem Cell–Like Self-Renewal and Multipotential Differentiation Capacity

S. Bergante, P. Randelli, M. Piccoli, 2013, The American journal of sports medicine.

G93A SOD1 alters cell cycle in a cellular model of Amyotrophic Lateral Sclerosis.

G. Mazzini, C. Cereda, A. Davin, 2010, Cellular signalling.

Altered Intracellular Localization of SOD1 in Leukocytes from Patients with Sporadic Amyotrophic Lateral Sclerosis

G. Mazzini, O. Pansarasa, C. Cereda, 2013, PloS one.

NEU3 Sialidase Protein Interactors in the Plasma Membrane and in the Endosomes*

C. Gelfi, E. Torretta, M. Piccoli, 2016, The Journal of Biological Chemistry.

2β-3,4-Unsaturated sialic acid derivatives: Synthesis optimization, and biological evaluation as Newcastle disease virus hemagglutinin-neuraminidase inhibitors.

M. Piccoli, F. Cirillo, P. La Rocca, 2020, Bioorganic & medicinal chemistry.

Cell-Based Therapies for Cardiac Regeneration: A Comprehensive Review of Past and Ongoing Strategies

C. Pappone, M. Piccoli, F. Cirillo, 2018, International journal of molecular sciences.

Regenerating the human heart: direct reprogramming strategies and their current limitations

C. Pappone, M. Piccoli, G. Ciconte, 2017, Basic Research in Cardiology.

Adenine phosphoribosyltransferase (APRT) deficiency: identification of a novel nonsense mutation

R. Valaperta, F. Lombardi, M. Piccoli, 2014, BMC Nephrology.

Sphingolipids and Atherosclerosis: The Dual Role of Ceramide and Sphingosine-1-Phosphate

C. Pappone, Simona Coviello, M. Piccoli, 2023, Antioxidants.

The antithetic role of ceramide and sphingosine‐1‐phosphate in cardiac dysfunction

C. Pappone, M. Piccoli, F. Cirillo, 2021, Journal of cellular physiology.

GM1 Ganglioside Promotes Osteogenic Differentiation of Human Tendon Stem Cells

C. Pappone, S. Bergante, P. Randelli, 2018, Stem cells international.

Calcium in Brugada Syndrome: Questions for Future Research

C. Pappone, M. Piccoli, M. Monasky, 2018, Front. Physiol..

Genotype/Phenotype Relationship in a Consanguineal Family With Brugada Syndrome Harboring the R1632C Missense Variant in the SCN5A Gene

V. Santinelli, C. Pappone, G. Vicedomini, 2019, Front. Physiol..

Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants.

V. Santinelli, C. Pappone, G. Vicedomini, 2019, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Reversine: A Synthetic Purine with a Dual Activity as a Cell Dedifferentiating Agent and a Selective Anticancer Drug.

C. Pappone, M. Piccoli, F. Cirillo, 2019, Current medicinal chemistry.

Genotype–Phenotype Correlation in a Family with Brugada Syndrome Harboring the Novel p.Gln371* Nonsense Variant in the SCN5A Gene

C. Pappone, G. Vicedomini, E. Locati, 2019, International journal of molecular sciences.

Ambient Intelligence-from vision to reality

A. Ghiroldi, A. Ghiroldi, 2003 .

Analysis of the intramolecular 1,7-lactone of N-acetylneuraminic acid using HPLC–MS: relationship between detection and stability

C. Pappone, M. Piccoli, F. Cirillo, 2023, Glycoconjugate Journal.

Design, Synthesis, and Antiviral Evaluation of Sialic Acid Derivatives as Inhibitors of Newcastle Disease Virus Hemagglutinin-Neuraminidase: A Translational Study on Human Parainfluenza Viruses

C. Pappone, M. Piccoli, F. Cirillo, 2023, ACS infectious diseases.

Alterations of the Sialylation Machinery in Brugada Syndrome

C. Pappone, G. Vicedomini, E. Locati, 2022, International journal of molecular sciences.

Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

I. Rivolta, I. Polsinelli, S. Ricagno, 2023, International journal of molecular sciences.

A new GLUT‐1 mutation in a family with glucose transporter 1 deficiency syndrome

F. Pierelli, G. Grieco, C. Casali, 2012, Movement disorders : official journal of the Movement Disorder Society.

Challenges in Brugada Syndrome Stratification: Investigating SCN5A Mutation Localization and Clinical Phenotypes

V. Santinelli, G. Vicedomini, M. Piccoli, 2023, International journal of molecular sciences.

Gangliosides as a potential new class of stem cell markers: the case of GD1a in human bone marrow mesenchymal stem cells[S]

S. Bergante, A. Ibatici, C. Gelfi, 2014, Journal of Lipid Research.