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OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases.
Sturm G, Karan KR, Monzel AS, Santhanam B, Taivassalo T, Bris C, Ware SA, Cross M, Towheed A, Higgins-Chen A, McManus MJ, Cardenas A, Lin J, Epel ES, Rahman S, Vissing J, Grassi B, Levine M, Horvath S, Haller RG, Lenaers G, Wallace DC, St-Onge MP, Tavazoie S, Procaccio V, Kaufman BA, Seifert EL, Hirano M, Picard M. Sturm G, et al. Among authors: hirano m. Commun Biol. 2023 Jan 12;6(1):22. doi: 10.1038/s42003-022-04303-x. Commun Biol. 2023. PMID: 36635485 Free PMC article.
Mitochondrial diseases.
Vu TH, Hirano M, DiMauro S. Vu TH, et al. Among authors: hirano m. Neurol Clin. 2002 Aug;20(3):809-39, vii-viii. doi: 10.1016/s0733-8619(01)00017-2. Neurol Clin. 2002. PMID: 12432831 Review.
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease.
Duncan AJ, Bitner-Glindzicz M, Meunier B, Costello H, Hargreaves IP, López LC, Hirano M, Quinzii CM, Sadowski MI, Hardy J, Singleton A, Clayton PT, Rahman S. Duncan AJ, et al. Among authors: hirano m. Am J Hum Genet. 2009 May;84(5):558-66. doi: 10.1016/j.ajhg.2009.03.018. Epub 2009 Apr 16. Am J Hum Genet. 2009. PMID: 19375058 Free PMC article.
Pathogenesis and treatment of mitochondrial disorders.
DiMauro S, Hirano M. DiMauro S, et al. Among authors: hirano m. Adv Exp Med Biol. 2009;652:139-70. doi: 10.1007/978-90-481-2813-6_10. Adv Exp Med Biol. 2009. PMID: 20225024 Free PMC article. Review.
Therapeutic prospects for mitochondrial disease.
Schon EA, DiMauro S, Hirano M, Gilkerson RW. Schon EA, et al. Among authors: hirano m. Trends Mol Med. 2010 Jun;16(6):268-76. doi: 10.1016/j.molmed.2010.04.007. Trends Mol Med. 2010. PMID: 20556877 Free PMC article. Review.
2,262 results