Alexandru Ionut Gilea - Search Results

Year	Number of Results
2020	1
2021	1
2023	3
2024	3

1

Zebrafish polg2 knock-out recapitulates human POLG-disorders; implications for drug treatment.

Brañas Casas R, Zuppardo A, Risato G, Dinarello A, Celeghin R, Fontana C, Grelloni E, Gilea AI, Viscomi C, Rasola A, Dalla Valle L, Lodi T, Baruffini E, Facchinello N, Argenton F, Tiso N. Brañas Casas R, et al. Among authors: gilea ai. Cell Death Dis. 2024 Apr 20;15(4):281. doi: 10.1038/s41419-024-06622-9. Cell Death Dis. 2024. PMID: 38643274 Free PMC article.

2

The Saccharomyces cerevisiae mitochondrial DNA polymerase and its contribution to the knowledge about human POLG-related disorders.

Gilea AI, Magistrati M, Notaroberto I, Tiso N, Dallabona C, Baruffini E. Gilea AI, et al. IUBMB Life. 2023 Dec;75(12):983-1002. doi: 10.1002/iub.2770. Epub 2023 Jul 20. IUBMB Life. 2023. PMID: 37470284 Review.

3

Modopathies Caused by Mutations in Genes Encoding for Mitochondrial RNA Modifying Enzymes: Molecular Mechanisms and Yeast Disease Models.

Magistrati M, Gilea AI, Ceccatelli Berti C, Baruffini E, Dallabona C. Magistrati M, et al. Among authors: gilea ai. Int J Mol Sci. 2023 Jan 22;24(3):2178. doi: 10.3390/ijms24032178. Int J Mol Sci. 2023. PMID: 36768505 Free PMC article. Review.

4

Saccharomyces cerevisiae as a Tool for Studying Mutations in Nuclear Genes Involved in Diseases Caused by Mitochondrial DNA Instability.

Gilea AI, Ceccatelli Berti C, Magistrati M, di Punzio G, Goffrini P, Baruffini E, Dallabona C. Gilea AI, et al. Genes (Basel). 2021 Nov 24;12(12):1866. doi: 10.3390/genes12121866. Genes (Basel). 2021. PMID: 34946817 Free PMC article. Review.

5

Drug Drop Test: How to Quickly Identify Potential Therapeutic Compounds for Mitochondrial Diseases Using Yeast Saccharomyces cerevisiae.

Magistrati M, Gilea AI, Gerra MC, Baruffini E, Dallabona C. Magistrati M, et al. Among authors: gilea ai. Int J Mol Sci. 2023 Jun 27;24(13):10696. doi: 10.3390/ijms241310696. Int J Mol Sci. 2023. PMID: 37445873 Free PMC article. Review.

6

Severe mitochondrial encephalomyopathy caused by de novo variants in OPA1 gene.

Di Nottia M, Rizza T, Baruffini E, Nesti C, Torraco A, Diodato D, Martinelli D, Dal Canto F, Gilea AI, Zoccola M, Siri B, Dionisi-Vici C, Bertini E, Santorelli FM, Goffrini P, Carrozzo R. Di Nottia M, et al. Among authors: gilea ai. Front Genet. 2024 Aug 20;15:1437959. doi: 10.3389/fgene.2024.1437959. eCollection 2024. Front Genet. 2024. PMID: 39233737 Free PMC article.

7

Functional characterization of archaic-specific variants in mitonuclear genes: insights from comparative analysis in S. cerevisiae.

Aneli S, Ceccatelli Berti C, Gilea AI, Birolo G, Mutti G, Pavesi A, Baruffini E, Goffrini P, Capelli C. Aneli S, et al. Among authors: gilea ai. Hum Mol Genet. 2024 Jun 21;33(13):1152-1163. doi: 10.1093/hmg/ddae057. Hum Mol Genet. 2024. PMID: 38558123

8

Exploring Yeast as a Study Model of Pantothenate Kinase-Associated Neurodegeneration and for the Identification of Therapeutic Compounds.

Ceccatelli Berti C, Gilea AI, De Gregorio MA, Goffrini P. Ceccatelli Berti C, et al. Among authors: gilea ai. Int J Mol Sci. 2020 Dec 30;22(1):293. doi: 10.3390/ijms22010293. Int J Mol Sci. 2020. PMID: 33396642 Free PMC article.

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