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Human wild-type and D76N β2-microglobulin variants are significant proteotoxic and metabolic stressors for transgenic C. elegans.
Raimondi S, Faravelli G, Nocerino P, Mondani V, Baruffaldi A, Marchese L, Mimmi MC, Canetti D, Verona G, Caterino M, Ruoppolo M, Mangione PP, Bellotti V, Lavatelli F, Giorgetti S. Raimondi S, et al. Among authors: ruoppolo m. FASEB Bioadv. 2023 Oct 25;5(11):484-505. doi: 10.1096/fba.2023-00073. eCollection 2023 Nov. FASEB Bioadv. 2023. PMID: 37936921 Free PMC article.
Metabolic rewiring and autophagy inhibition correct lysosomal storage disease in mucopolysaccharidosis IIIB.
Scarcella M, Scerra G, Ciampa M, Caterino M, Costanzo M, Rinaldi L, Feliciello A, Anzilotti S, Fiorentino C, Renna M, Ruoppolo M, Pavone LM, D'Agostino M, De Pasquale V. Scarcella M, et al. Among authors: ruoppolo m. iScience. 2024 Jan 29;27(3):108959. doi: 10.1016/j.isci.2024.108959. eCollection 2024 Mar 15. iScience. 2024. PMID: 38361619 Free PMC article.
Sex-Gender-Based Differences in Metabolic Diseases.
Campesi I, Ruoppolo M, Franconi F, Caterino M, Costanzo M. Campesi I, et al. Among authors: ruoppolo m. Handb Exp Pharmacol. 2023;282:241-257. doi: 10.1007/164_2023_683. Handb Exp Pharmacol. 2023. PMID: 37528324
Lipidomic alterations in human saliva from cystic fibrosis patients.
Caterino M, Fedele R, Carnovale V, Castaldo A, Gelzo M, Iacotucci P, Ruoppolo M, Castaldo G. Caterino M, et al. Among authors: ruoppolo m. Sci Rep. 2023 Jan 12;13(1):600. doi: 10.1038/s41598-022-24429-6. Sci Rep. 2023. PMID: 36635275 Free PMC article.
Metabolomic fingerprinting of renal disease progression in Bardet-Biedl syndrome reveals mitochondrial dysfunction in kidney tubular cells.
Marchese E, Caterino M, Viggiano D, Cevenini A, Tolone S, Docimo L, Di Iorio V, Del Vecchio Blanco F, Fedele R, Simonelli F, Perna A, Nigro V, Capasso G, Ruoppolo M, Zacchia M. Marchese E, et al. Among authors: ruoppolo m. iScience. 2022 Sep 27;25(11):105230. doi: 10.1016/j.isci.2022.105230. eCollection 2022 Nov 18. iScience. 2022. PMID: 36281451 Free PMC article.
Contribution of Genetic Test to Early Diagnosis of Methylenetetrahydrofolate Reductase (MTHFR) Deficiency: The Experience of a Reference Center in Southern Italy.
Barretta F, Uomo F, Fecarotta S, Albano L, Crisci D, Verde A, Fisco MG, Gallo G, Dottore Stagna D, Pricolo MR, Alagia M, Terrone G, Rossi A, Parenti G, Ruoppolo M, Mazzaccara C, Frisso G. Barretta F, et al. Among authors: ruoppolo m. Genes (Basel). 2023 Apr 26;14(5):980. doi: 10.3390/genes14050980. Genes (Basel). 2023. PMID: 37239340 Free PMC article.
163 results