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Nature Communications|January 6, 2018
Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathyOlesia Ignatenko, Dmitri Chilov, Ilse Paetau, et al.Human Molecular Genetics|May 27, 2005
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndromePetri T Luoma, Ningguang Luo, Wolfgang N Löscher, et al.EMBO Molecular Medicine|January 20, 2021
Vegan diet in young children remodels metabolism and challenges the statuses of essential nutrientsTopi Hovinen, Liisa Korkalo, Riitta Freese, et al.Physiological Reports|July 4, 2019
Phenotypic effects of dietary stress in combination with a respiratory chain bypass in micePraveen K Dhandapani, Annina M Lyyski, Lars Paulin, et al.Nature Communications|September 14, 2024
Overactive mitochondrial DNA replication disrupts perinatal cardiac maturationJuan C Landoni, Semin Erkul, Tuomas Laalo, et al.Human Molecular Genetics|October 29, 2004
Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy numberHenna Tyynismaa, Hiroshi Sembongi, Monika Bokori-Brown, et al.Human Molecular Genetics|September 23, 2011
Thymidine kinase 2 mutations in autosomal recessive progressive external ophthalmoplegia with multiple mitochondrial DNA deletionsHenna Tyynismaa, Ren Sun, Sofia Ahola-Erkkilä, et al.Nature Communications|September 29, 2018
RNA modification landscape of the human mitochondrial tRNALys regulates protein synthesisUwe Richter, Molly E Evans, Wesley C Clark, et al.Nature Reviews. Disease Primers|October 25, 2016
Mitochondrial diseasesGráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, et al.EMBO Molecular Medicine|April 9, 2014
Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3Nahid A Khan, Mari Auranen, Ilse Paetau, et al.Pageof 16