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 *

204 related articles for article (PubMed ID: 15342361)

  • 1. Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines.
    Beretta S; Mattavelli L; Sala G; Tremolizzo L; Schapira AH; Martinuzzi A; Carelli V; Ferrarese C
    Brain; 2004 Oct; 127(Pt 10):2183-92. PubMed ID: 15342361
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybrids.
    Baracca A; Solaini G; Sgarbi G; Lenaz G; Baruzzi A; Schapira AH; Martinuzzi A; Carelli V
    Arch Neurol; 2005 May; 62(5):730-6. PubMed ID: 15883259
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Antioxidants partially restore glutamate transport defect in leber hereditary optic neuropathy cybrids.
    Sala G; Trombin F; Beretta S; Tremolizzo L; Presutto P; Montopoli M; Fantin M; Martinuzzi A; Carelli V; Ferrarese C
    J Neurosci Res; 2008 Nov; 86(15):3331-7. PubMed ID: 18615737
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial mitochondrial complex I inhibition induces oxidative damage and perturbs glutamate transport in primary retinal cultures. Relevance to Leber Hereditary Optic Neuropathy (LHON).
    Beretta S; Wood JP; Derham B; Sala G; Tremolizzo L; Ferrarese C; Osborne NN
    Neurobiol Dis; 2006 Nov; 24(2):308-17. PubMed ID: 16959493
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration.
    Carelli V; Rugolo M; Sgarbi G; Ghelli A; Zanna C; Baracca A; Lenaz G; Napoli E; Martinuzzi A; Solaini G
    Biochim Biophys Acta; 2004 Jul; 1658(1-2):172-9. PubMed ID: 15282189
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells.
    Wong A; Cavelier L; Collins-Schramm HE; Seldin MF; McGrogan M; Savontaus ML; Cortopassi GA
    Hum Mol Genet; 2002 Feb; 11(4):431-8. PubMed ID: 11854175
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical characterization and mitochondrial DNA sequence variations in Leber hereditary optic neuropathy.
    Kumar M; Kaur P; Kumar M; Saxena R; Sharma P; Dada R
    Mol Vis; 2012; 18():2687-99. PubMed ID: 23170061
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation.
    Wang J; Ji Y; Ai C; Chen JR; Gan D; Zhang J; Mo JQ; Guan MX
    J Biomed Sci; 2023 Aug; 30(1):63. PubMed ID: 37537557
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy.
    Carelli V; Vergani L; Bernazzi B; Zampieron C; Bucchi L; Valentino M; Rengo C; Torroni A; Martinuzzi A
    Biochim Biophys Acta; 2002 Oct; 1588(1):7-14. PubMed ID: 12379308
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy.
    Kumar M; Tanwar M; Saxena R; Sharma P; Dada R
    Mol Vis; 2010 Apr; 16():782-92. PubMed ID: 20454697
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium.
    Ghelli A; Zanna C; Porcelli AM; Schapira AH; Martinuzzi A; Carelli V; Rugolo M
    J Biol Chem; 2003 Feb; 278(6):4145-50. PubMed ID: 12446713
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy.
    Floreani M; Napoli E; Martinuzzi A; Pantano G; De Riva V; Trevisan R; Bisetto E; Valente L; Carelli V; Dabbeni-Sala F
    FEBS J; 2005 Mar; 272(5):1124-35. PubMed ID: 15720387
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The G11778A LHON mutation does not enhance ethambutol cytotoxicity in a cybrid model.
    Pommer R; Schoeler S; Mawrin C; Szibor R; Kirches E
    Clin Neuropathol; 2008; 27(6):414-23. PubMed ID: 19130740
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Leber's hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagy.
    Liang M; Ji Y; Zhang L; Wang X; Hu C; Zhang J; Zhu Y; Mo JQ; Guan MX
    Hum Mol Genet; 2022 Sep; 31(19):3299-3312. PubMed ID: 35567411
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity.
    Ghelli A; Porcelli AM; Zanna C; Vidoni S; Mattioli S; Barbieri A; Iommarini L; Pala M; Achilli A; Torroni A; Rugolo M; Carelli V
    PLoS One; 2009 Nov; 4(11):e7922. PubMed ID: 19936068
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis.
    Danielson SR; Wong A; Carelli V; Martinuzzi A; Schapira AH; Cortopassi GA
    J Biol Chem; 2002 Feb; 277(8):5810-5. PubMed ID: 11741983
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Involvement of endoplasmic reticulum stress in rotenone-induced leber hereditary optic neuropathy model and the discovery of new therapeutic agents.
    Aoyama Y; Inagaki S; Aoshima K; Iwata Y; Nakamura S; Hara H; Shimazawa M
    J Pharmacol Sci; 2021 Oct; 147(2):200-207. PubMed ID: 34384568
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Leber Hereditary Optic Neuropathy-Light at the End of the Tunnel?
    Kim US; Jurkute N; Yu-Wai-Man P
    Asia Pac J Ophthalmol (Phila); 2018; 7(4):242-245. PubMed ID: 30008192
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Leber's hereditary optic neuropathy (LHON)-associated ND5 12338T > C mutation altered the assembly and function of complex I, apoptosis and mitophagy.
    Zhang J; Ji Y; Lu Y; Fu R; Xu M; Liu X; Guan MX
    Hum Mol Genet; 2018 Jun; 27(11):1999-2011. PubMed ID: 29579248
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A review of the molecular mechanism of development of Leber hereditary optic neuropathy].
    Nakamura M
    Nippon Ganka Gakkai Zasshi; 2005 Apr; 109(4):189-96. PubMed ID: 15859148
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.