BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 11032337)

  • 21. Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene.
    Merante F; Tein I; Benson L; Robinson BH
    Am J Hum Genet; 1994 Sep; 55(3):437-46. PubMed ID: 8079988
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy.
    Loeffen J; Elpeleg O; Smeitink J; Smeets R; Stöckler-Ipsiroglu S; Mandel H; Sengers R; Trijbels F; van den Heuvel L
    Ann Neurol; 2001 Feb; 49(2):195-201. PubMed ID: 11220739
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mitochondrial complexes I, II, III, IV, and V in myocardial ischemia and autolysis.
    Rouslin W
    Am J Physiol; 1983 Jun; 244(6):H743-8. PubMed ID: 6305212
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The nuclear ABC1 gene is essential for the correct conformation and functioning of the cytochrome bc1 complex and the neighbouring complexes II and IV in the mitochondrial respiratory chain.
    Brasseur G; Tron G; Dujardin G; Slonimski PP; Brivet-Chevillotte P
    Eur J Biochem; 1997 May; 246(1):103-11. PubMed ID: 9210471
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Pathogenic mitochondrial DNA mutations in protein-coding genes.
    Wong LJ
    Muscle Nerve; 2007 Sep; 36(3):279-93. PubMed ID: 17503499
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography.
    van Den Bosch BJ; de Coo RF; Scholte HR; Nijland JG; van Den Bogaard R; de Visser M; de Die-Smulders CE; Smeets HJ
    Nucleic Acids Res; 2000 Oct; 28(20):E89. PubMed ID: 11024191
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Thyroid hormone regulates oxidative phosphorylation in the cerebral cortex and striatum of neonatal rats.
    Martinez B; del Hoyo P; Martin MA; Arenas J; Perez-Castillo A; Santos A
    J Neurochem; 2001 Sep; 78(5):1054-63. PubMed ID: 11553679
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
    Auré K; Fayet G; Leroy JP; Lacène E; Romero NB; Lombès A
    Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mitochondrial cardiomyopathy.
    Ozawa T
    Herz; 1994 Apr; 19(2):105-18, 125. PubMed ID: 8194831
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy.
    Andreu AL; Bruno C; Shanske S; Shtilbans A; Hirano M; Krishna S; Hayward L; Systrom DS; Brown RH; DiMauro S
    Neurology; 1998 Nov; 51(5):1444-7. PubMed ID: 9818877
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.
    Sternberg D; Chatzoglou E; Laforêt P; Fayet G; Jardel C; Blondy P; Fardeau M; Amselem S; Eymard B; Lombès A
    Brain; 2001 May; 124(Pt 5):984-94. PubMed ID: 11335700
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mechanism of somatic mitochondrial DNA mutations associated with age and diseases.
    Ozawa T
    Biochim Biophys Acta; 1995 May; 1271(1):177-89. PubMed ID: 7599206
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C > T mutation.
    Campos Y; García A; Eiris J; Fuster M; Rubio JC; Martín MA; del Hoyo P; Pintos E; Castro-Gago M; Arenas J
    J Inherit Metab Dis; 2001 Nov; 24(6):685-7. PubMed ID: 11768589
    [No Abstract]   [Full Text] [Related]  

  • 34. Genotype and phenotype of severe mitochondrial cardiomyopathy: a recipient of heart transplantation and the genetic control.
    Ozawa T; Katsumata K; Hayakawa M; Tanaka M; Sugiyama S; Tanaka T; Itoyama S; Nunoda S; Sekiguchi M
    Biochem Biophys Res Commun; 1995 Feb; 207(2):613-20. PubMed ID: 7864851
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Retrospective, multicentric study of 180 children with cytochrome C oxidase deficiency.
    Böhm M; Pronicka E; Karczmarewicz E; Pronicki M; Piekutowska-Abramczuk D; Sykut-Cegielska J; Mierzewska H; Hansikova H; Vesela K; Tesarova M; Houstkova H; Houstek J; Zeman J
    Pediatr Res; 2006 Jan; 59(1):21-6. PubMed ID: 16326995
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Optic neuropathy, cardiomyopathy, cognitive disability in patients with a homozygous mutation in the nuclear MTO1 and a mitochondrial MT-TF variant.
    Charif M; Titah SM; Roubertie A; Desquiret-Dumas V; Gueguen N; Meunier I; Leid J; Massal F; Zanlonghi X; Mercier J; Raynaud de Mauverger E; Procaccio V; Mousson de Camaret B; Lenaers G; Hamel CP
    Am J Med Genet A; 2015 Oct; 167A(10):2366-74. PubMed ID: 26061759
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Co-existence of high levels of a cytochrome b mutation and of a tandem 200 bp duplication in the D-loop of muscle human mitochondrial DNA.
    Bouzidi MF; Poyau A; Godinot C
    Hum Mol Genet; 1998 Mar; 7(3):385-91. PubMed ID: 9466994
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel nonsense mutation (Q352X) in the mitochondrial cytochrome b gene associated with a combined deficiency of complexes I and III.
    Lamantea E; Carrara F; Mariotti C; Morandi L; Tiranti V; Zeviani M
    Neuromuscul Disord; 2002 Jan; 12(1):49-52. PubMed ID: 11731284
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Efficient and specific amplification of identified partial duplications of human mitochondrial DNA by long PCR.
    Fromenty B; Manfredi G; Sadlock J; Zhang L; King MP; Schon EA
    Biochim Biophys Acta; 1996 Sep; 1308(3):222-30. PubMed ID: 8809114
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Molecular pathology of mitochondrial disorders].
    Müller-Höcker J
    Verh Dtsch Ges Pathol; 1994; 78():48-93. PubMed ID: 7534019
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.