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Identification of a novel heterozygous guanosine monophosphate reductase (GMPR) variant in a patient with a late-onset disorder of mitochondrial DNA maintenance.
Sommerville EW, Dalla Rosa I, Rosenberg MM, Bruni F, Thompson K, Rocha M, Blakely EL, He L, Falkous G, Schaefer AM, Yu-Wai-Man P, Chinnery PF, Hedstrom L, Spinazzola A, Taylor RW, Gorman GS. Sommerville EW, et al. Among authors: bruni f. Clin Genet. 2020 Feb;97(2):276-286. doi: 10.1111/cge.13652. Epub 2019 Nov 14. Clin Genet. 2020. PMID: 31600844 Free PMC article.
Defective i6A37 modification of mitochondrial and cytosolic tRNAs results from pathogenic mutations in TRIT1 and its substrate tRNA.
Yarham JW, Lamichhane TN, Pyle A, Mattijssen S, Baruffini E, Bruni F, Donnini C, Vassilev A, He L, Blakely EL, Griffin H, Santibanez-Koref M, Bindoff LA, Ferrero I, Chinnery PF, McFarland R, Maraia RJ, Taylor RW. Yarham JW, et al. Among authors: bruni f. PLoS Genet. 2014 Jun 5;10(6):e1004424. doi: 10.1371/journal.pgen.1004424. eCollection 2014 Jun. PLoS Genet. 2014. PMID: 24901367 Free PMC article.
Human mitochondrial nucleases.
Bruni F, Lightowlers RN, Chrzanowska-Lightowlers ZM. Bruni F, et al. FEBS J. 2017 Jun;284(12):1767-1777. doi: 10.1111/febs.13981. Epub 2017 Feb 1. FEBS J. 2017. PMID: 27926991 Free PMC article. Review.
Clinical, biochemical, and genetic features associated with VARS2-related mitochondrial disease.
Bruni F, Di Meo I, Bellacchio E, Webb BD, McFarland R, Chrzanowska-Lightowlers ZMA, He L, Skorupa E, Moroni I, Ardissone A, Walczak A, Tyynismaa H, Isohanni P, Mandel H, Prokisch H, Haack T, Bonnen PE, Enrico B, Pronicka E, Ghezzi D, Taylor RW, Diodato D. Bruni F, et al. Hum Mutat. 2018 Apr;39(4):563-578. doi: 10.1002/humu.23398. Epub 2018 Feb 7. Hum Mutat. 2018. PMID: 29314548 Free PMC article.
Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23).
Zagnoli-Vieira G, Bruni F, Thompson K, He L, Walker S, de Brouwer APM, Taylor RW, Niyazov D, Caldecott KW. Zagnoli-Vieira G, et al. Among authors: bruni f. Neurol Genet. 2018 Aug 1;4(4):e262. doi: 10.1212/NXG.0000000000000262. eCollection 2018 Aug. Neurol Genet. 2018. PMID: 30109272 Free PMC article.
Biallelic Mutations in MTPAP Associated with a Lethal Encephalopathy.
Van Eyck L, Bruni F, Ronan A, Briggs TA, Roscioli T, Rice GI, Vassallo G, Rodero MP, He L, Taylor RW, Livingston JH, Chrzanowska-Lightowlers ZMA, Crow YJ. Van Eyck L, et al. Among authors: bruni f. Neuropediatrics. 2020 Jun;51(3):178-184. doi: 10.1055/s-0039-3400979. Epub 2019 Nov 28. Neuropediatrics. 2020. PMID: 31779033
The mystery of mitochondrial RNases.
Bruni F, Gramegna P, Lightowlers RN, Chrzanowska-Lightowlers ZM. Bruni F, et al. Biochem Soc Trans. 2012 Aug;40(4):865-9. doi: 10.1042/BST20120022. Biochem Soc Trans. 2012. PMID: 22817749 Review.
A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression.
Wilson WC, Hornig-Do HT, Bruni F, Chang JH, Jourdain AA, Martinou JC, Falkenberg M, Spåhr H, Larsson NG, Lewis RJ, Hewitt L, Baslé A, Cross HE, Tong L, Lebel RR, Crosby AH, Chrzanowska-Lightowlers ZM, Lightowlers RN. Wilson WC, et al. Among authors: bruni f. Hum Mol Genet. 2014 Dec 1;23(23):6345-55. doi: 10.1093/hmg/ddu352. Epub 2014 Jul 9. Hum Mol Genet. 2014. PMID: 25008111 Free PMC article.
Mutations in glycyl-tRNA synthetase impair mitochondrial metabolism in neurons.
Boczonadi V, Meyer K, Gonczarowska-Jorge H, Griffin H, Roos A, Bartsakoulia M, Bansagi B, Ricci G, Palinkas F, Zahedi RP, Bruni F, Kaspar B, Lochmüller H, Boycott KM, Müller JS, Horvath R. Boczonadi V, et al. Among authors: bruni f. Hum Mol Genet. 2018 Jun 15;27(12):2187-2204. doi: 10.1093/hmg/ddy127. Hum Mol Genet. 2018. PMID: 29648643 Free PMC article.
371 results