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Year Number of Results
2004 1
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2009 1
2010 1
2011 2
2012 1
2014 1
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2016 2
2017 3
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2019 3
2020 4
2021 3
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26 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: perga 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.
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: perga 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: perga s. Transl Psychiatry. 2019 Aug 27;9(1):207. doi: 10.1038/s41398-019-0544-0. Transl Psychiatry. 2019. PMID: 31455763 Free PMC article.
Nurr1 reduction influences the onset of chronic EAE in mice.
Montarolo F, Perga S, Martire S, Bertolotto A. Montarolo F, et al. Among authors: perga s. Inflamm Res. 2015 Nov;64(11):841-4. doi: 10.1007/s00011-015-0871-4. Epub 2015 Sep 4. Inflamm Res. 2015. PMID: 26337347
26 results