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 *

275 related articles for article (PubMed ID: 11735375)

  • 1. The expanding spectrum of nuclear gene mutations in mitochondrial disorders.
    Zeviani M
    Semin Cell Dev Biol; 2001 Dec; 12(6):407-16. PubMed ID: 11735375
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial disorders.
    Zeviani M; Klopstock T
    Curr Opin Neurol; 2001 Oct; 14(5):553-60. PubMed ID: 11562565
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nuclear genes in mitochondrial disorders.
    Zeviani M; Spinazzola A; Carelli V
    Curr Opin Genet Dev; 2003 Jun; 13(3):262-70. PubMed ID: 12787788
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular genetic and clinical aspects of mitochondrial disorders in childhood.
    Moslemi AR; Darin N
    Mitochondrion; 2007 Jul; 7(4):241-52. PubMed ID: 17376748
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. [Diseases of the human mitochondrial oxidative phosphorylation system].
    Ruiz-Pesini E; López-Gallardo E; Dahmani Y; Herrero MD; Solano A; Díez-Sánchez C; López-Pérez M; Montoya J
    Rev Neurol; 2006 Oct 1-15; 43(7):416-24. PubMed ID: 17006861
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial diseases--an expanding spectrum of disorders and affected genes.
    von Kleist-Retzow JC; Schauseil-Zipf U; Michalk DV; Kunz WS
    Exp Physiol; 2003 Jan; 88(1):155-66. PubMed ID: 12525864
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mouse models for mitochondrial disease.
    Wallace DC
    Am J Med Genet; 2001; 106(1):71-93. PubMed ID: 11579427
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Mitochondrial disorders.
    Zeviani M; Carelli V
    Curr Opin Neurol; 2007 Oct; 20(5):564-71. PubMed ID: 17885446
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders.
    Cohen BH; Naviaux RK
    Methods; 2010 Aug; 51(4):364-73. PubMed ID: 20558295
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Infantile-onset disorders of mitochondrial replication and protein synthesis.
    Nogueira C; Carrozzo R; Vilarinho L; Santorelli FM
    J Child Neurol; 2011 Jul; 26(7):866-75. PubMed ID: 21572058
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. 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]  

  • 16. Molecular analysis of oxidative phosphorylation diseases for detection of mitochondrial DNA mutations.
    Shoffner JM
    Curr Protoc Hum Genet; 2001 May; Chapter 9():Unit 9.9. PubMed ID: 18428320
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial defects in neurodegenerative disease.
    Wallace DC
    Ment Retard Dev Disabil Res Rev; 2001; 7(3):158-66. PubMed ID: 11553931
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.
    Gómez-Durán A; Pacheu-Grau D; López-Gallardo E; Díez-Sánchez C; Montoya J; López-Pérez MJ; Ruiz-Pesini E
    Hum Mol Genet; 2010 Sep; 19(17):3343-53. PubMed ID: 20566709
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An introduction: oxidative phosphorylation diseases.
    Shoffner JM
    Semin Neurol; 2001 Sep; 21(3):237-50. PubMed ID: 11641814
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.