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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 7599205)

  • 1. Modelling the effects of age-related mtDNA mutation accumulation; complex I deficiency, superoxide and cell death.
    Cortopassi G; Wang E
    Biochim Biophys Acta; 1995 May; 1271(1):171-6. PubMed ID: 7599205
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Accumulation of deletions and point mutations in mitochondrial genome in degenerative diseases.
    Tanaka M; Kovalenko SA; Gong JS; Borgeld HJ; Katsumata K; Hayakawa M; Yoneda M; Ozawa T
    Ann N Y Acad Sci; 1996 Jun; 786():102-11. PubMed ID: 8687011
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.
    Morgan-Hughes JA; Sweeney MG; Cooper JM; Hammans SR; Brockington M; Schapira AH; Harding AE; Clark JB
    Biochim Biophys Acta; 1995 May; 1271(1):135-40. PubMed ID: 7599199
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial DNA mutations and oxidative damage in aging and diseases: an emerging paradigm of gerontology and medicine.
    Wei YH
    Proc Natl Sci Counc Repub China B; 1998 Apr; 22(2):55-67. PubMed ID: 9615468
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Quantification of tRNA3243(Leu) point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcription.
    Suomalainen A; Majander A; Pihko H; Peltonen L; Syvänen AC
    Hum Mol Genet; 1993 May; 2(5):525-34. PubMed ID: 8518790
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Metabolic interventions against complex I deficiency in MELAS syndrome.
    Majamaa K; Rusanen H; Remes A; Hassinen IE
    Mol Cell Biochem; 1997 Sep; 174(1-2):291-6. PubMed ID: 9309702
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Human mitochondrial complex I dysfunction.
    Cooper JM; Mann VM; Krige D; Schapira AH
    Biochim Biophys Acta; 1992 Jul; 1101(2):198-203. PubMed ID: 1633185
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial DNA mutations and aging.
    Krishnan KJ; Greaves LC; Reeve AK; Turnbull DM
    Ann N Y Acad Sci; 2007 Apr; 1100():227-40. PubMed ID: 17460184
    [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. 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]  

  • 11. Animal models for mitochondrial disease.
    Wallace DC
    Methods Mol Biol; 2002; 197():3-54. PubMed ID: 12013805
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency.
    Chol M; Lebon S; Bénit P; Chretien D; de Lonlay P; Goldenberg A; Odent S; Hertz-Pannier L; Vincent-Delorme C; Cormier-Daire V; Rustin P; Rötig A; Munnich A
    J Med Genet; 2003 Mar; 40(3):188-91. PubMed ID: 12624137
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial DNA in Parkinson's disease.
    Schapira AH
    Adv Neurol; 1999; 80():233-7. PubMed ID: 10410727
    [No Abstract]   [Full Text] [Related]  

  • 15. Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase.
    Pitkanen S; Robinson BH
    J Clin Invest; 1996 Jul; 98(2):345-51. PubMed ID: 8755643
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Targeted elimination of mutant mitochondrial DNA in MELAS-iPSCs by mitoTALENs.
    Yang Y; Wu H; Kang X; Liang Y; Lan T; Li T; Tan T; Peng J; Zhang Q; An G; Liu Y; Yu Q; Ma Z; Lian Y; Soh BS; Chen Q; Liu P; Chen Y; Sun X; Li R; Zhen X; Liu P; Yu Y; Li X; Fan Y
    Protein Cell; 2018 Mar; 9(3):283-297. PubMed ID: 29318513
    [TBL] [Abstract][Full Text] [Related]  

  • 17. LHON/MELAS overlap syndrome associated with a mitochondrial MTND1 gene mutation.
    Blakely EL; de Silva R; King A; Schwarzer V; Harrower T; Dawidek G; Turnbull DM; Taylor RW
    Eur J Hum Genet; 2005 May; 13(5):623-7. PubMed ID: 15657614
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Mitochondrial gene mutation].
    Shin WS; Toyo-oka T
    Nihon Rinsho; 2000 Jan; 58(1):129-33. PubMed ID: 10885300
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Somatic mitochondrial DNA mutations do not increase neuronal vulnerability to MPTP in young POLG mutator mice.
    Dai Y; Clark J; Zheng K; Kujoth GC; Prolla TA; Simon DK
    Neurotoxicol Teratol; 2014; 46():62-7. PubMed ID: 25450660
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association between mitochondrial DNA 4,977 bp deletion and NAD(P)H:quinone oxidoreductase 1 C609T polymorphism in human breast tissues.
    Tseng LM; Yin PH; Tsai YF; Chi CW; Wu CW; Lee LM; Lee HC
    Oncol Rep; 2009 May; 21(5):1169-74. PubMed ID: 19360290
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.