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Transcriptomic and metabolomic changes might predict frailty in SAMP8 mice.
Dacomo L, La Vitola P, Brunelli L, Messa L, Micotti E, Artioli L, Sinopoli E, Cecutti G, Leva S, Gagliardi S, Pansarasa O, Carelli S, Guaita A, Pastorelli R, Forloni G, Cereda C, Balducci C. Dacomo L, et al. Among authors: gagliardi s. Aging Cell. 2024 Oct;23(10):e14263. doi: 10.1111/acel.14263. Epub 2024 Jul 3. Aging Cell. 2024. PMID: 38961613 Free PMC article.
SOD1 mRNA expression in sporadic amyotrophic lateral sclerosis.
Gagliardi S, Cova E, Davin A, Guareschi S, Abel K, Alvisi E, Laforenza U, Ghidoni R, Cashman JR, Ceroni M, Cereda C. Gagliardi S, et al. Neurobiol Dis. 2010 Aug;39(2):198-203. doi: 10.1016/j.nbd.2010.04.008. Epub 2010 Apr 23. Neurobiol Dis. 2010. PMID: 20399857
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum.
Ticozzi N, Tiloca C, Calini D, Gagliardi S, Altieri A, Colombrita C, Cereda C, Ratti A, Pezzoli G, Borroni B, Goldwurm S, Padovani A, Silani V. Ticozzi N, et al. Among authors: gagliardi s. Neurobiol Aging. 2014 Apr;35(4):936.e13-7. doi: 10.1016/j.neurobiolaging.2013.09.037. Epub 2013 Oct 2. Neurobiol Aging. 2014. PMID: 24169076
Legius Syndrome: two novel mutations in the SPRED1 gene.
Bianchi M, Saletti V, Micheli R, Esposito S, Molinaro A, Gagliardi S, Orcesi S, Cereda C. Bianchi M, et al. Among authors: gagliardi s. Hum Genome Var. 2015 Dec 3;2:15051. doi: 10.1038/hgv.2015.51. eCollection 2015. Hum Genome Var. 2015. PMID: 27081556 Free PMC article.
238 results