BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

235 related articles for article (PubMed ID: 15969653)

  • 1. Effects of nitric oxide donors on cybrids harbouring the mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) A3243G mitochondrial DNA mutation.
    Sandhu JK; Sodja C; McRae K; Li Y; Rippstein P; Wei YH; Lach B; Lee F; Bucurescu S; Harper ME; Sikorska M
    Biochem J; 2005 Oct; 391(Pt 2):191-202. PubMed ID: 15969653
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy.
    Hsieh RH; Li JY; Pang CY; Wei YH
    J Biomed Sci; 2001; 8(4):328-35. PubMed ID: 11455195
    [TBL] [Abstract][Full Text] [Related]  

  • 3. MELAS mitochondrial DNA mutation A3243G reduces glutamate transport in cybrids cell lines.
    DiFrancesco JC; Cooper JM; Lam A; Hart PE; Tremolizzo L; Ferrarese C; Schapira AH
    Exp Neurol; 2008 Jul; 212(1):152-6. PubMed ID: 18455161
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pioglitazone and Deoxyribonucleoside Combination Treatment Increases Mitochondrial Respiratory Capacity in m.3243A>G MELAS Cybrid Cells.
    Burgin HJ; Lopez Sanchez MIG; Smith CM; Trounce IA; McKenzie M
    Int J Mol Sci; 2020 Mar; 21(6):. PubMed ID: 32244971
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Enhanced oxidative damage in human cells harboring A3243G mutation of mitochondrial DNA: implication of oxidative stress in the pathogenesis of mitochondrial diabetes.
    Pang CY; Lee HC; Wei YH
    Diabetes Res Clin Pract; 2001 Dec; 54 Suppl 2():S45-56. PubMed ID: 11733109
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Secondary coenzyme Q10 deficiency triggers mitochondria degradation by mitophagy in MELAS fibroblasts.
    Cotán D; Cordero MD; Garrido-Maraver J; Oropesa-Ávila M; Rodríguez-Hernández A; Gómez Izquierdo L; De la Mata M; De Miguel M; Lorite JB; Infante ER; Jackson S; Navas P; Sánchez-Alcázar JA
    FASEB J; 2011 Aug; 25(8):2669-87. PubMed ID: 21551238
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M; Mita S; Sakuta R; Nonaka I; Araki S
    Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome.
    Li JY; Hsieh RH; Peng NJ; Lai PH; Lee CF; Lo YK; Wei YH
    J Formos Med Assoc; 2007 Jul; 106(7):528-36. PubMed ID: 17660142
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Effect of humanin on decreased ATP levels of human lymphocytes harboring A3243G mutant mitochondrial DNA.
    Kariya S; Hirano M; Furiya Y; Ueno S
    Neuropeptides; 2005 Apr; 39(2):97-101. PubMed ID: 15752543
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Impaired Cellular Bioenergetics Causes Mitochondrial Calcium Handling Defects in MT-ND5 Mutant Cybrids.
    McKenzie M; Duchen MR
    PLoS One; 2016; 11(4):e0154371. PubMed ID: 27110715
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nitric oxide-mediated chondrocyte cell death requires the generation of additional reactive oxygen species.
    Del Carlo M; Loeser RF
    Arthritis Rheum; 2002 Feb; 46(2):394-403. PubMed ID: 11840442
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELAS.
    Desquiret-Dumas V; Gueguen N; Barth M; Chevrollier A; Hancock S; Wallace DC; Amati-Bonneau P; Henrion D; Bonneau D; Reynier P; Procaccio V
    Biochim Biophys Acta; 2012 Jun; 1822(6):1019-29. PubMed ID: 22306605
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report.
    Hoptasz M; Szczuciński A; Losy J
    Neurol Neurochir Pol; 2014; 48(2):150-3. PubMed ID: 24821643
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical features of MELAS and its relation with A3243G gene point mutation.
    Zhang J; Guo J; Fang W; Jun Q; Shi K
    Int J Clin Exp Pathol; 2015; 8(10):13411-5. PubMed ID: 26722549
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
    Thajeb P; Lee HC; Pang CY; Jeng CM; Huang SF; Wei YH
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan; 63(1):71-6. PubMed ID: 10645055
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T; Hirose S; Goto Y; Naitou E; Mitsudome A
    Pediatr Neurol; 2006 Mar; 34(3):235-8. PubMed ID: 16504796
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M; Mita S; Murakami T; Kumamoto T; Uchino M; Nonaka I; Ando M
    Ann Neurol; 1994 Apr; 35(4):413-9. PubMed ID: 8154867
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2].
    Delgado-Sánchez R; Zárate-Moysen A; Monsalvo-Reyes A; Herrero MD; Ruiz-Pesini E; López-Pérez M; Montoya J; Montiel-Sosa JF
    Rev Neurol; 2007 Jan 1-15; 44(1):18-22. PubMed ID: 17199225
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNA(Leu(UUR)) gene.
    Koga Y; Davidson M; Schon EA; King MP
    Muscle Nerve Suppl; 1995; 3():S119-23. PubMed ID: 7603512
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y
    Nihon Rinsho; 1993 Sep; 51(9):2373-8. PubMed ID: 8411715
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.