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A self-repair history: compensatory effect of a de novo variant on the FANCA c.2778+83C>G splicing mutation.
Persico I, Fontana G, Faleschini M, Zanchetta ME, Ammeti D, Cappelli E, Corsolini F, Mosa C, Guarina A, Bogliolo M, Surrallés J, Dufour C, Farruggia P, Savoia A, Bottega R. Persico I, et al. Among authors: zanchetta me. Front Genet. 2023 Jul 20;14:1209138. doi: 10.3389/fgene.2023.1209138. eCollection 2023. Front Genet. 2023. PMID: 37547463 Free PMC article.
The dual action of glioma-derived exosomes on neuronal activity: synchronization and disruption of synchrony.
Spelat R, Jihua N, Sánchez Triviño CA, Pifferi S, Pozzi D, Manzati M, Mortal S, Schiavo I, Spada F, Zanchetta ME, Ius T, Manini I, Rolle IG, Parisse P, Millán AP, Bianconi G, Cesca F, Giugliano M, Menini A, Cesselli D, Skrap M, Torre V. Spelat R, et al. Among authors: zanchetta me. Cell Death Dis. 2022 Aug 13;13(8):705. doi: 10.1038/s41419-022-05144-6. Cell Death Dis. 2022. PMID: 35963860 Free PMC article.
A unique missense mutation in the RING domain impairs MID1 E3 ubiquitin ligase activity and localisation and is associated with uncommon Opitz Syndrome-like signs.
Mascaro M, D'Ambrosio L, Lazzari E, Almoguera B, Swafiri ST, Zanchetta ME, Meroni G. Mascaro M, et al. Among authors: zanchetta me. Biochim Biophys Acta Mol Basis Dis. 2024 Apr;1870(4):167126. doi: 10.1016/j.bbadis.2024.167126. Epub 2024 Mar 18. Biochim Biophys Acta Mol Basis Dis. 2024. PMID: 38508475 Free article. No abstract available.