These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
641 related articles for article (PubMed ID: 19656491)
1. Random point mutations with major effects on protein-coding genes are the driving force behind premature aging in mtDNA mutator mice. Edgar D; Shabalina I; Camara Y; Wredenberg A; Calvaruso MA; Nijtmans L; Nedergaard J; Cannon B; Larsson NG; Trifunovic A Cell Metab; 2009 Aug; 10(2):131-8. PubMed ID: 19656491 [TBL] [Abstract][Full Text] [Related]
2. DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice. Vermulst M; Wanagat J; Kujoth GC; Bielas JH; Rabinovitch PS; Prolla TA; Loeb LA Nat Genet; 2008 Apr; 40(4):392-4. PubMed ID: 18311139 [TBL] [Abstract][Full Text] [Related]
3. Somatic mtDNA mutations and aging--facts and fancies. Kukat A; Trifunovic A Exp Gerontol; 2009; 44(1-2):101-5. PubMed ID: 18585880 [TBL] [Abstract][Full Text] [Related]
4. Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production. Trifunovic A; Hansson A; Wredenberg A; Rovio AT; Dufour E; Khvorostov I; Spelbrink JN; Wibom R; Jacobs HT; Larsson NG Proc Natl Acad Sci U S A; 2005 Dec; 102(50):17993-8. PubMed ID: 16332961 [TBL] [Abstract][Full Text] [Related]
5. Does premature aging of the mtDNA mutator mouse prove that mtDNA mutations are involved in natural aging? Khrapko K; Kraytsberg Y; de Grey AD; Vijg J; Schon EA Aging Cell; 2006 Jun; 5(3):279-82. PubMed ID: 16842501 [TBL] [Abstract][Full Text] [Related]
6. The mtDNA mutator mouse: Dissecting mitochondrial involvement in aging. Edgar D; Trifunovic A Aging (Albany NY); 2009 Dec; 1(12):1028-32. PubMed ID: 20157586 [TBL] [Abstract][Full Text] [Related]
7. 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 Nature; 2004 May; 429(6990):417-23. PubMed ID: 15164064 [TBL] [Abstract][Full Text] [Related]
8. A new mechanism for mtDNA pathogenesis: impairment of post-transcriptional maturation leads to severe depletion of mitochondrial tRNASer(UCN) caused by T7512C and G7497A point mutations. Möllers M; Maniura-Weber K; Kiseljakovic E; Bust M; Hayrapetyan A; Jaksch M; Helm M; Wiesner RJ; von Kleist-Retzow JC Nucleic Acids Res; 2005; 33(17):5647-58. PubMed ID: 16199753 [TBL] [Abstract][Full Text] [Related]
9. Estimation of the mtDNA mutation rate in aging mice by proteome analysis and mathematical modeling. Mao L; Zabel C; Wacker MA; Nebrich G; Sagi D; Schrade P; Bachmann S; Kowald A; Klose J Exp Gerontol; 2006 Jan; 41(1):11-24. PubMed ID: 16307857 [TBL] [Abstract][Full Text] [Related]
10. Restoration of mitochondrial function in cells with complex I deficiency. Bai Y; Park JS; Deng JH; Li Y; Hu P Ann N Y Acad Sci; 2005 May; 1042():25-35. PubMed ID: 15965042 [TBL] [Abstract][Full Text] [Related]
11. Somatic mtDNA mutations cause progressive hearing loss in the mouse. Niu X; Trifunovic A; Larsson NG; Canlon B Exp Cell Res; 2007 Nov; 313(18):3924-34. PubMed ID: 17662273 [TBL] [Abstract][Full Text] [Related]
13. Mitochondrial dysfunction as a cause of ageing. Trifunovic A; Larsson NG J Intern Med; 2008 Feb; 263(2):167-78. PubMed ID: 18226094 [TBL] [Abstract][Full Text] [Related]
14. Respiratory function decline and DNA mutation in mitochondria, oxidative stress and altered gene expression during aging. Wei YH; Wu SB; Ma YS; Lee HC Chang Gung Med J; 2009; 32(2):113-32. PubMed ID: 19403001 [TBL] [Abstract][Full Text] [Related]
15. Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunction. Raha S; Merante F; Shoubridge E; Myint AT; Tein I; Benson L; Johns T; Robinson BH Hum Mutat; 1999; 13(3):245-54. PubMed ID: 10090480 [TBL] [Abstract][Full Text] [Related]
16. Point mutations are causing progeroid phenotypes in the mtDNA mutator mouse. Edgar D; Larsson NG; Trifunovic A Cell Metab; 2010 Jan; 11(1):1. PubMed ID: 20005181 [No Abstract] [Full Text] [Related]
17. Random mtDNA deletions and functional consequence in aged human skeletal muscle. Chabi B; Mousson de Camaret B; Chevrollier A; Boisgard S; Stepien G Biochem Biophys Res Commun; 2005 Jul; 332(2):542-9. PubMed ID: 15896715 [TBL] [Abstract][Full Text] [Related]
18. False positive results of mitochondrial DNA depletion/deletion due to single nucleotide substitutions causing appearance of additional PvuII restriction sites. Weglewska-Jurkiewicz A; Jakóbkiewicz-Banecka J; Pronicka E; Wegrzyn G Diagn Mol Pathol; 2007 Jun; 16(2):116-20. PubMed ID: 17525683 [TBL] [Abstract][Full Text] [Related]
19. Mosaic Deficiency in Mitochondrial Oxidative Metabolism Promotes Cardiac Arrhythmia during Aging. Baris OR; Ederer S; Neuhaus JF; von Kleist-Retzow JC; Wunderlich CM; Pal M; Wunderlich FT; Peeva V; Zsurka G; Kunz WS; Hickethier T; Bunck AC; Stöckigt F; Schrickel JW; Wiesner RJ Cell Metab; 2015 May; 21(5):667-77. PubMed ID: 25955204 [TBL] [Abstract][Full Text] [Related]
20. Leydig cell steroidogenesis unexpectedly escapes mitochondrial dysfunction in prematurely aging mice. Shabalina IG; Landreh L; Edgar D; Hou M; Gibanova N; Atanassova N; Petrovic N; Hultenby K; Söder O; Nedergaard J; Svechnikov K FASEB J; 2015 Aug; 29(8):3274-86. PubMed ID: 25900807 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]