BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

239 related articles for article (PubMed ID: 15542384)

  • 1. Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiency.
    Meulemans A; Lissens W; Van Coster R; De Meirleir L; Smet J; Nassogne MC; Liebaers I; Seneca S
    Eur J Paediatr Neurol; 2004; 8(6):299-306. PubMed ID: 15542384
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency.
    Ugalde C; Janssen RJ; van den Heuvel LP; Smeitink JA; Nijtmans LG
    Hum Mol Genet; 2004 Mar; 13(6):659-67. PubMed ID: 14749350
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Progressive encephalopathy and complex I deficiency associated with mutations in MTND1.
    Moslemi AR; Darin N; Tulinius M; Wiklund LM; Holme E; Oldfors A
    Neuropediatrics; 2008 Feb; 39(1):24-8. PubMed ID: 18504678
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutations.
    Rubio-Gozalbo ME; Dijkman KP; van den Heuvel LP; Sengers RC; Wendel U; Smeitink JA
    Hum Mutat; 2000; 15(6):522-32. PubMed ID: 10862082
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma.
    Mayr JA; Meierhofer D; Zimmermann F; Feichtinger R; Kögler C; Ratschek M; Schmeller N; Sperl W; Kofler B
    Clin Cancer Res; 2008 Apr; 14(8):2270-5. PubMed ID: 18413815
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathy.
    Pereira C; Nogueira C; Barbot C; Tessa A; Soares C; Fattori F; Guimarães A; Santorelli FM; Vilarinho L
    Biochem Biophys Res Commun; 2007 Mar; 354(4):937-41. PubMed ID: 17266923
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease.
    Kirby DM; Boneh A; Chow CW; Ohtake A; Ryan MT; Thyagarajan D; Thorburn DR
    Ann Neurol; 2003 Oct; 54(4):473-8. PubMed ID: 14520659
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial complex I deficiency: from organelle dysfunction to clinical disease.
    Distelmaier F; Koopman WJ; van den Heuvel LP; Rodenburg RJ; Mayatepek E; Willems PH; Smeitink JA
    Brain; 2009 Apr; 132(Pt 4):833-42. PubMed ID: 19336460
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma.
    Gasparre G; Hervouet E; de Laplanche E; Demont J; Pennisi LF; Colombel M; Mège-Lechevallier F; Scoazec JY; Bonora E; Smeets R; Smeitink J; Lazar V; Lespinasse J; Giraud S; Godinot C; Romeo G; Simonnet H
    Hum Mol Genet; 2008 Apr; 17(7):986-95. PubMed ID: 18156159
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Secondary metabolic effects in complex I deficiency.
    Esteitie N; Hinttala R; Wibom R; Nilsson H; Hance N; Naess K; Teär-Fahnehjelm K; von Döbeln U; Majamaa K; Larsson NG
    Ann Neurol; 2005 Oct; 58(4):544-52. PubMed ID: 16044424
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Respiratory chain complex I deficiency.
    Triepels RH; Van Den Heuvel LP; Trijbels JM; Smeitink JA
    Am J Med Genet; 2001; 106(1):37-45. PubMed ID: 11579423
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiency.
    Hoefs SJ; Dieteren CE; Rodenburg RJ; Naess K; Bruhn H; Wibom R; Wagena E; Willems PH; Smeitink JA; Nijtmans LG; van den Heuvel LP
    Hum Mutat; 2009 Jul; 30(7):E728-36. PubMed ID: 19384974
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial cytopathies and neuromuscular disorders.
    Van Coster R; De Meirleir L
    Acta Neurol Belg; 2000 Sep; 100(3):156-61. PubMed ID: 11098288
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human mitochondrial complex I deficiency: investigating transcriptional responses by microarray.
    van der Westhuizen FH; van den Heuvel LP; Smeets R; Veltman JA; Pfundt R; van Kessel AG; Ursing BM; Smeitink JA
    Neuropediatrics; 2003 Feb; 34(1):14-22. PubMed ID: 12690563
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Adaptive selection of mitochondrial complex I subunits during primate radiation.
    Mishmar D; Ruiz-Pesini E; Mondragon-Palomino M; Procaccio V; Gaut B; Wallace DC
    Gene; 2006 Aug; 378():11-8. PubMed ID: 16828987
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogenic DNA mutations.
    Da Pozzo P; Cardaioli E; Radi E; Federico A
    Biochem Biophys Res Commun; 2004 Nov; 324(1):360-4. PubMed ID: 15465027
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Leigh disease with brainstem involvement in complex I deficiency due to assembly factor NDUFAF2 defect.
    Herzer M; Koch J; Prokisch H; Rodenburg R; Rauscher C; Radauer W; Forstner R; Pilz P; Rolinski B; Freisinger P; Mayr JA; Sperl W
    Neuropediatrics; 2010 Feb; 41(1):30-4. PubMed ID: 20571988
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy.
    Malfatti E; Bugiani M; Invernizzi F; de Souza CF; Farina L; Carrara F; Lamantea E; Antozzi C; Confalonieri P; Sanseverino MT; Giugliani R; Uziel G; Zeviani M
    Brain; 2007 Jul; 130(Pt 7):1894-904. PubMed ID: 17535832
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.