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

Year Number of Results
1990 1
1991 1
1992 1
2003 1
2004 1
2006 2
2007 1
2010 1
2014 1
2015 1
2017 2
2018 6
2019 4
2020 8
2021 4
2022 2
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32 results
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Page 1
The epigenetic implication in coronavirus infection and therapy.
Atlante S, Mongelli A, Barbi V, Martelli F, Farsetti A, Gaetano C. Atlante S, et al. Among authors: mongelli a. Clin Epigenetics. 2020 Oct 21;12(1):156. doi: 10.1186/s13148-020-00946-x. Clin Epigenetics. 2020. PMID: 33087172 Free PMC article. Review.
Digenic inheritance of STUB1 variants and TBP polyglutamine expansions explains the incomplete penetrance of SCA17 and SCA48.
Magri S, Nanetti L, Gellera C, Sarto E, Rizzo E, Mongelli A, Ricci B, Fancellu R, Sambati L, Cortelli P, Brusco A, Bruzzone MG, Mariotti C, Di Bella D, Taroni F. Magri S, et al. Among authors: mongelli a. Genet Med. 2022 Jan;24(1):29-40. doi: 10.1016/j.gim.2021.08.003. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906452 Free article.
Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1.
Quatrana A, Morini E, Tiano F, Vancheri C, Panarello L, Romano S, Marcotulli C, Casali C, Mariotti C, Mongelli A, Fichera M, Rufini A, Condò I, Novelli G, Testi R, Amati F, Malisan F. Quatrana A, et al. Among authors: mongelli a. Hum Mol Genet. 2022 Jan 7:ddac005. doi: 10.1093/hmg/ddac005. Online ahead of print. Hum Mol Genet. 2022. PMID: 35015850
32 results