Author

P. Barassi

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Pharmacology & Toxicology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:host-pathogen & immune response· 1 Assay:metabolomics· 1 Organism:mouse· 1 Assay:proteomics· 1 Organism:rat· 1

Frequent Co-Authors

A. Zaza· 2 shared M. Ferrandi· 2 shared A. Luraghi· 1 shared A. S. Maione· 1 shared C. Florindi· 1 shared C. Maniezzi· 1 shared C. Ronchi· 1 shared E. Sacco· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersPhysiology

A. Zaza

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Early consequences of the phospholamban mutation PLN-R14del+/- in a transgenic mouse model

C. Maniezzi, M. Eskandr, C. Florindi, M. Ferrandi, P. Barassi, E. Sacco, V. Pasquale, A. S. Maione, G. Pompilio, V. Oliveira Nunes Teixeira, R. A. de Boer, H. H. W. Sillje, F. Lodola, A. Zaza

This study examines Ca2+ dynamics and energy metabolism in a transgenic mouse model of the PLN-R14del mutation before cardiomyopathy onset, finding altered mitochondrial function and ER-stress activation.

bioRxiv · Apr 5, 2023Physiology

Istaroxime metabolite PST3093 selectively stimulates SERCA2a and reverses disease-induced changes in cardiac function

M. Arici, M. Ferrandi, P. Barassi, S.-C. Hsu, E. Torre, A. Luraghi, C. Ronchi, G.-J. Chang, F. Peri, P. Ferrari, G. Bianchi, M. Rocchetti, A. Zaza

This paper investigates PST3093, a metabolite of istaroxime, showing it selectively stimulates SERCA2a and improves cardiac function in a rat model of diabetic cardiomyopathy.

bioRxiv · Aug 17, 2021Pharmacology & Toxicology