BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

431 related articles for article (PubMed ID: 21074512)

  • 1. Genetic insights into OXPHOS defect and its role in cancer.
    Chandra D; Singh KK
    Biochim Biophys Acta; 2011 Jun; 1807(6):620-5. PubMed ID: 21074512
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial regulation of epigenetics and its role in human diseases.
    Minocherhomji S; Tollefsbol TO; Singh KK
    Epigenetics; 2012 Apr; 7(4):326-34. PubMed ID: 22419065
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial DNA mutations and breast tumorigenesis.
    Yadav N; Chandra D
    Biochim Biophys Acta; 2013 Dec; 1836(2):336-44. PubMed ID: 24140413
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Significance of Mitochondria DNA Mutations in Diseases.
    Zhu Z; Wang X
    Adv Exp Med Biol; 2017; 1038():219-230. PubMed ID: 29178079
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial DNA mutations in disease and aging.
    Wallace DC
    Environ Mol Mutagen; 2010 Jun; 51(5):440-50. PubMed ID: 20544884
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial disorders due to nuclear OXPHOS gene defects.
    Ugalde C; Morán M; Blázquez A; Arenas J; Martín MA
    Adv Exp Med Biol; 2009; 652():85-116. PubMed ID: 20225021
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The mitochondrial genome in human adaptive radiation and disease: on the road to therapeutics and performance enhancement.
    Wallace DC
    Gene; 2005 Jul; 354():169-80. PubMed ID: 16024186
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial determinants of cancer health disparities.
    Choudhury AR; Singh KK
    Semin Cancer Biol; 2017 Dec; 47():125-146. PubMed ID: 28487205
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial DNA copy number in human disease: the more the better?
    Filograna R; Mennuni M; Alsina D; Larsson NG
    FEBS Lett; 2021 Apr; 595(8):976-1002. PubMed ID: 33314045
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human mitochondrial DNA: roles of inherited and somatic mutations.
    Schon EA; DiMauro S; Hirano M
    Nat Rev Genet; 2012 Dec; 13(12):878-90. PubMed ID: 23154810
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial DNA and disease.
    Greaves LC; Reeve AK; Taylor RW; Turnbull DM
    J Pathol; 2012 Jan; 226(2):274-86. PubMed ID: 21989606
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies.
    Gardeitchik T; Mohamed M; Ruzzenente B; Karall D; Guerrero-Castillo S; Dalloyaux D; van den Brand M; van Kraaij S; van Asbeck E; Assouline Z; Rio M; de Lonlay P; Scholl-Buergi S; Wolthuis DFGJ; Hoischen A; Rodenburg RJ; Sperl W; Urban Z; Brandt U; Mayr JA; Wong S; de Brouwer APM; Nijtmans L; Munnich A; Rötig A; Wevers RA; Metodiev MD; Morava E
    Am J Hum Genet; 2018 Apr; 102(4):685-695. PubMed ID: 29576219
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondria and Cancer.
    Zong WX; Rabinowitz JD; White E
    Mol Cell; 2016 Mar; 61(5):667-676. PubMed ID: 26942671
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mechanisms of mitochondrial diseases.
    Ylikallio E; Suomalainen A
    Ann Med; 2012 Feb; 44(1):41-59. PubMed ID: 21806499
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The striatum is highly susceptible to mitochondrial oxidative phosphorylation dysfunctions.
    Pickrell AM; Fukui H; Wang X; Pinto M; Moraes CT
    J Neurosci; 2011 Jul; 31(27):9895-904. PubMed ID: 21734281
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The transmission of OXPHOS disease and methods to prevent this.
    Jacobs LJ; de Wert G; Geraedts JP; de Coo IF; Smeets HJ
    Hum Reprod Update; 2006; 12(2):119-36. PubMed ID: 16199488
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An In Vitro Approach to Study Mitochondrial Dysfunction: A Cybrid Model.
    Cavaliere A; Marchet S; Di Meo I; Tiranti V
    J Vis Exp; 2022 Mar; (181):. PubMed ID: 35343952
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Histochemical methods for the diagnosis of mitochondrial diseases.
    De Paepe B; De Bleecker JL; Van Coster R
    Curr Protoc Hum Genet; 2009 Oct; Chapter 19():Unit19.2. PubMed ID: 19806589
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Assaying the probabilities of obtaining maternally inherited heteroplasmy as the basis for modeling OXPHOS diseases in animals.
    Bass MG; Sokolova VA; Kustova ME; Grachyova EV; Kidgotko OV; Sorokin AV; Vasilyev VB
    Biochim Biophys Acta; 2006; 1757(5-6):679-85. PubMed ID: 16829232
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Mitochondrial DNA: properties and applications].
    Atig RK; Hsouna S; Beraud-Colomb E; Abdelhak S
    Arch Inst Pasteur Tunis; 2009; 86(1-4):3-14. PubMed ID: 20707216
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.