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Premature ageing in mice expressing defective mitochondrial DNA polymerase.
Trifunovic A, Wredenberg A, Falkenberg M, Spelbrink JN, Rovio AT, Bruder CE, Bohlooly-Y M, Gidlöf S, Oldfors A, Wibom R, Törnell J, Jacobs HT, Larsson NG. Trifunovic A, et al. Nature. 2004 May 27;429(6990):417-23. doi: 10.1038/nature02517. Nature. 2004. PMID: 15164064
Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.
Oldfors A, Larsson NG, Holme E, Tulinius M, Kadenbach B, Droste M. Oldfors A, et al. J Neurol Sci. 1992 Jul;110(1-2):169-77. doi: 10.1016/0022-510x(92)90025-g. J Neurol Sci. 1992. PMID: 1324295
Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.
Larsson NG, Tulinius MH, Holme E, Oldfors A, Andersen O, Wahlström J, Aasly J. Larsson NG, et al. Am J Hum Genet. 1992 Dec;51(6):1201-12. Am J Hum Genet. 1992. PMID: 1463006 Free PMC article.
Mitochondrial DNA deletions in muscle fibers in inclusion body myositis.
Oldfors A, Moslemi AR, Fyhr IM, Holme E, Larsson NG, Lindberg C. Oldfors A, et al. J Neuropathol Exp Neurol. 1995 Jul;54(4):581-7. doi: 10.1097/00005072-199507000-00012. J Neuropathol Exp Neurol. 1995. PMID: 7602331
Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletions.
Tulinius MH, Oldfors A, Holme E, Larsson NG, Houshmand M, Fahleson P, Sigström L, Kristiansson B. Tulinius MH, et al. Eur J Pediatr. 1995 Jan;154(1):35-42. doi: 10.1007/BF01972970. Eur J Pediatr. 1995. PMID: 7895754
Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion.
Larsson NG, Oldfors A, Holme E, Clayton DA. Larsson NG, et al. Biochem Biophys Res Commun. 1994 May 16;200(3):1374-81. doi: 10.1006/bbrc.1994.1603. Biochem Biophys Res Commun. 1994. PMID: 8185589
Mitochondrial DNA deletions in inclusion body myositis.
Oldfors A, Larsson NG, Lindberg C, Holme E. Oldfors A, et al. Brain. 1993 Apr;116 ( Pt 2):325-36. doi: 10.1093/brain/116.2.325. Brain. 1993. PMID: 8384916
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