Author

Emilia Turco

University of Turin

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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Cancer Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Alessandro BrussinoiD· 1 shared Alessandro SarcinellaiD· 1 shared Alessia LamolinaraiD· 1 shared Alfredo BruscoiD· 1 shared Andrea Scavuzzo· 1 shared Anna Maria PorcelliiD· 1 shared Barbara BellettiiD· 1 shared Brendan James BattersbyiD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Alessandro BrussinoORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

p140Cap enhances breast cancer chemosensitivity by limiting an ABCC1-enriched stem-like compartment via β-Catenin inhibition

Andrea Scavuzzo, Matteo Poncina, Alessia Lamolinara, Alessandro Sarcinella, Mahdis Jahanbin, Maria Grazia Filippone, Laura Bottoni, Francesco Antonio Tucci, Yaron Vinik, Sima Lev, Manuela Iezzi, Ugo Ala, Daniela Taverna, Francesca Orso, Barbara Belletti, , Vincenzo Salemme

This study shows p140Cap improves chemotherapy response in breast cancer by reducing stem-like cells and enhancing drug retention through β-Catenin inhibition.

bioRxiv · Aug 18, 2026 · PreprintCancer Biology

Mice harboring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity.

Cecilia Mancini, Eriola Hoxha, Luisa Iommarini, Alessandro Brussino, Uwe Richter, Francesca Montarolo, Claudia Cagnoli, Roberta Parolisi, Diana Iulia Gondor Morosini, Valentina Nicolò, Francesca Maltecca, Luísa Muratori, Giulia Ronchi, Stefano Geuna, Francesca Arnaboldi, , Filippo Tempia

This study creates a new mouse model with a patient-derived SCA28 mutation and shows it leads to late-onset ataxia and mitochondrial dysfunction.

Neurobiology of Disease · Oct 30, 2018Peer-reviewedGenetics