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

Year Number of Results
1981 1
2010 1
2012 1
2013 4
2014 6
2015 6
2016 6
2017 7
2018 5
2019 6
2020 7
2021 6
2022 1
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50 results
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Page 1
NURR1 Impairment in Multiple Sclerosis.
Montarolo F, Martire S, Perga S, Bertolotto A. Montarolo F, et al. Among authors: martire s. Int J Mol Sci. 2019 Sep 30;20(19):4858. doi: 10.3390/ijms20194858. Int J Mol Sci. 2019. PMID: 31574937 Free PMC article. Review.
Poly(ADP-ribosylated) proteins in β-amyloid peptide-stimulated microglial cells.
Correani V, Martire S, Mignogna G, Caruso LB, Tempera I, Giorgi A, Grieco M, Mosca L, Schininà ME, Maras B, d'Erme M. Correani V, et al. Among authors: martire s. Biochem Pharmacol. 2019 Sep;167:50-57. doi: 10.1016/j.bcp.2018.10.026. Epub 2018 Nov 9. Biochem Pharmacol. 2019. PMID: 30414941
Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility.
Zuccalà M, Barizzone N, Boggio E, Gigliotti L, Sorosina M, Basagni C, Bordoni R, Clarelli F, Anand S, Mangano E, Vecchio D, Corsetti E, Martire S, Perga S, Ferrante D, Gajofatto A, Ivashynka A, Solaro C, Cantello R, Martinelli V, Comi G, Filippi M, Esposito F, Leone M, De Bellis G, Dianzani U, Martinelli-Boneschi F, D'Alfonso S. Zuccalà M, et al. Among authors: martire s. J Genet Genomics. 2021 Jun 20;48(6):497-507. doi: 10.1016/j.jgg.2021.03.017. Epub 2021 May 25. J Genet Genomics. 2021. PMID: 34353742
NURR1 deficiency is associated to ADHD-like phenotypes in mice.
Montarolo F, Martire S, Perga S, Spadaro M, Brescia I, Allegra S, De Francia S, Bertolotto A. Montarolo F, et al. Among authors: martire s. Transl Psychiatry. 2019 Aug 27;9(1):207. doi: 10.1038/s41398-019-0544-0. Transl Psychiatry. 2019. PMID: 31455763 Free PMC article.
50 results