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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 4
2006 1
2007 1
2009 1
2011 3
2012 4
2013 5
2014 5
2015 6
2016 3
2017 4
2018 8
2019 5
2020 4
2021 4
2022 4
2023 5
2024 2

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61 results

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Page 1
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: cappelli e. Front Genet. 2023 Jul 20;14:1209138. doi: 10.3389/fgene.2023.1209138. eCollection 2023. Front Genet. 2023. PMID: 37547463 Free PMC article.
Fanconi anemia: from DNA repair to metabolism.
Ravera S, Dufour C, Degan P, Cappelli E. Ravera S, et al. Among authors: cappelli e. Eur J Hum Genet. 2018 Apr;26(4):475-476. doi: 10.1038/s41431-017-0046-6. Epub 2018 Feb 2. Eur J Hum Genet. 2018. PMID: 29396564 Free PMC article. No abstract available.
Mitochondrial respiratory complex I defects in Fanconi anemia.
Cappelli E, Ravera S, Vaccaro D, Cuccarolo P, Bartolucci M, Panfoli I, Dufour C, Degan P. Cappelli E, et al. Trends Mol Med. 2013 Sep;19(9):513-4. doi: 10.1016/j.molmed.2013.07.008. Epub 2013 Aug 6. Trends Mol Med. 2013. PMID: 23932594 Review.
Impaired Mitochondrial Function and Marrow Failure in Patients Carrying a Variant of the SRSF4 Gene.
Miano M, Bertola N, Grossi A, Dell'Orso G, Regis S, Rusmini M, Uva P, Vozzi D, Fioredda F, Palmisani E, Lupia M, Lanciotti M, Grilli F, Corsolini F, Arcuri L, Giarratana MC, Ceccherini I, Dufour C, Cappelli E, Ravera S. Miano M, et al. Among authors: cappelli e. Int J Mol Sci. 2024 Feb 8;25(4):2083. doi: 10.3390/ijms25042083. Int J Mol Sci. 2024. PMID: 38396760 Free PMC article.
Defective FAS-Mediated Apoptosis and Immune Dysregulation in Gaucher Disease.
Miano M, Madeo A, Cappelli E, Lanza F, Lanza T, Stroppiano M, Terranova P, Venè R, Bleesing JJH, Di Rocco M. Miano M, et al. Among authors: cappelli e. J Allergy Clin Immunol Pract. 2020 Nov-Dec;8(10):3535-3542. doi: 10.1016/j.jaip.2020.06.065. Epub 2020 Jul 21. J Allergy Clin Immunol Pract. 2020. PMID: 32702516
Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: a comparison with Fanconi anemia.
Bottega R, Ravera S, Napolitano LMR, Chiappetta V, Zini N, Crescenzi B, Arniani S, Faleschini M, Cortone G, Faletra F, Medagli B, Sirchia F, Moretti M, de Lange J, Cappelli E, Mecucci C, Onesti S, Pisani FM, Savoia A. Bottega R, et al. Among authors: cappelli e. J Cell Physiol. 2021 Aug;236(8):5664-5675. doi: 10.1002/jcp.30265. Epub 2021 Jan 11. J Cell Physiol. 2021. PMID: 33432587 Free article.
61 results