European Mind & Metabolism Association

D'Addario C

Most relevant works on (epi)genetics: 14

Dynorphin/KOP and nociceptin/NOP gene expression and epigenetic changes by cocaine in rat striatum and nucleus accumbens.

Caputi FF, Di Benedetto M, Carretta D, Bastias del Carmen Candia S, D'Addario C, Cavina C, Candeletti S, Romualdi P. Prog Neuropsychopharmacol Biol Psychiatry. 2014 Mar 3;49:36-46. doi: 10.1016/j.pnpbp.2013.10.016. Epub 2013 Nov 1.

Epigenetic control of skin differentiation genes by phytocannabinoids.

Pucci M, Rapino C, Di Francesco A, Dainese E, D'Addario C, Maccarrone M. Br J Pharmacol. 2013 Oct;170(3):581-91. doi: 10.1111/bph.12309.

Involvement of 5-lipoxygenase in Alzheimer's disease: a role for DNA methylation.

Di Francesco A, Arosio B, Gussago C, Dainese E, Mari D, D'Addario C, Maccarrone M. J Alzheimers Dis. 2013;37(1):3-8. doi: 10.3233/JAD-130506.

Epigenetic mechanisms and endocannabinoid signalling.

D'Addario C, Di Francesco A, Pucci M, Finazzi Agrò A, Maccarrone M. FEBS J. 2013 May;280(9):1905-17. doi: 10.1111/febs.12125. Epub 2013 Feb 11. Review.

Epigenetic modulation of BDNF gene in patients with major depressive disorder.

D'Addario C, Dell'Osso B, Galimberti D, Palazzo MC, Benatti B, Di Francesco A, Scarpini E, Altamura AC, Maccarrone M. Biol Psychiatry. 2013 Jan 15;73(2):e6-7. doi: 10.1016/j.biopsych.2012.07.009. Epub 2012 Aug 14. No abstract available.

Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degeneration.

Galimberti D, D'Addario C, Dell'osso B, Fenoglio C, Marcone A, Cerami C, Cappa SF, Palazzo MC, Arosio B, Mari D, Maccarrone M, Bresolin N, Altamura AC, Scarpini E. Neurol Sci. 2013 Jun;34(6):899-903. doi: 10.1007/s10072-012-1151-5. Epub 2012 Jul 14.

Epigenetic regulation of fatty acid amide hydrolase in Alzheimer disease.

D'Addario C, Di Francesco A, Arosio B, Gussago C, Dell'Osso B, Bari M, Galimberti D, Scarpini E, Altamura AC, Mari D, Maccarrone M. PLoS One. 2012;7(6):e39186. doi: 10.1371/journal.pone.0039186. Epub 2012 Jun 12.

Ethanol induces epigenetic modulation of prodynorphin and pronociceptin gene expression in the rat amygdala complex.

D'Addario C, Caputi FF, Ekström TJ, Di Benedetto M, Maccarrone M, Romualdi P, Candeletti S. J Mol Neurosci. 2013 Feb;49(2):312-9. doi: 10.1007/s12031-012-9829-y. Epub 2012 Jun 10.

Selective DNA methylation of BDNF promoter in bipolar disorder: differences among patients with BDI and BDII.

D'Addario C, Dell'Osso B, Palazzo MC, Benatti B, Lietti L, Cattaneo E, Galimberti D, Fenoglio C, Cortini F, Scarpini E, Arosio B, Di Francesco A, Di Benedetto M, Romualdi P, Candeletti S, Mari D, Bergamaschini L, Bresolin N, Maccarrone M, Altamura AC. Neuropsychopharmacology. 2012 Jun;37(7):1647-55. doi: 10.1038/npp.2012.10. Epub 2012 Feb 22.

Pin1 contribution to Alzheimer's disease: transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's disease.

Arosio B, Bulbarelli A, Bastias Candia S, Lonati E, Mastronardi L, Romualdi P, Candeletti S, Gussago C, Galimberti D, Scarpini E, Dell'Osso B, Altamura C, MacCarrone M, Bergamaschini L, D'Addario C, Mari D. Neurodegener Dis. 2012;10(1-4):207-11. doi: 10.1159/000333799. Epub 2012 Jan 17.

Ethanol and acetaldehyde exposure induces specific epigenetic modifications in the prodynorphin gene promoter in a human neuroblastoma cell line.

D'Addario C, Johansson S, Candeletti S, Romualdi P, Ögren SO, Terenius L, Ekström TJ. FASEB J. 2011 Mar;25(3):1069-75. doi: 10.1096/fj.10-168534. Epub 2010 Nov 24.

The role of 5-HT(1A) receptors in learning and memory.

Ogren SO, Eriksson TM, Elvander-Tottie E, D'Addario C, Ekström JC, Svenningsson P, Meister B, Kehr J, Stiedl O. Behav Brain Res. 2008 Dec 16;195(1):54-77. doi: 10.1016/j.bbr.2008.02.023. Epub 2008 Feb 20. Review.

Linkage disequilibrium, haplotype and association studies of a chromosome 4 GABA receptor gene cluster: candidate gene variants for addictions.

Drgon T, D'Addario C, Uhl GR. Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):854-60.

Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome.

Maruo Y, D'Addario C, Mori A, Iwai M, Takahashi H, Sato H, Takeuchi Y. Hum Genet. 2004 Nov;115(6):525-6. Epub 2004 Sep 17.

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