Author

S. Paracchini

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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Cell Biology· 2 Evolutionary Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:genetic perturbation / CRISPR· 2 Organism:human· 2 Research Focus:cell-cell communication· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1 Assay:imaging· 1

Frequent Co-Authors

R. Diaz· 2 shared A. C. Riches· 1 shared A. Gardner· 1 shared A. Martinelli· 1 shared A. Tranchina· 1 shared B. Dong· 1 shared C. Bergamini· 1 shared C. Diquigiovanni· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersCell Biology

R. Diaz

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Kin selection as a modulator of human handedness: sex-specific, parental and parent-of-origin effects

B. Dong, S. Paracchini, A. Gardner

This study explores how kin selection influences human handedness, identifying sex-specific, parental, and parent-of-origin effects on handedness evolution.

bioRxiv · Aug 8, 2023Evolutionary Biology

KIAA0319 influences cilia length, cell migration and mechanical cell-substrate interaction

R. Diaz, N. M. Kronenberg, A. Martinelli, P. Liehm, A. C. Riches, M. C. Gather, S. Paracchini

This study investigates the role of KIAA0319 in cilia length, cell migration, and mechanical interactions using CRISPR-Cas9 knockout models and ERISM.

bioRxiv · Jan 8, 2021Cell Biology

In Troyer Syndrome Spartin loss induces Complex I impairments and alters pyruvate metabolism

C. Diquigiovanni, C. Bergamini, R. Diaz, I. Liparulo, L. Masin, F. Bianco, A. Tranchina, F. Buscherini, T. A. Wischmeijer, T. Pippucci, E. Scarano, D. M. Cordelli, R. Fato, J. M. Lucocq, M. Seri, , E. Bonora

This study shows that Spartin loss in Troyer syndrome causes Complex I impairments and metabolic changes, including altered pyruvate metabolism and increased glycolysis.

bioRxiv · Dec 6, 2018 · PreprintCell Biology