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Journal Abstract Search

392 related items for PubMed ID: 19936068

  • 21. Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy.
    Dawod PGA, Jancic J, Marjanovic A, Brankovic M, Jankovic M, Samardzic J, Potkonjak D, Djuric V, Mesaros S, Novakovic I, Abdel Motaleb FI, Kostic VS, Nikolic D.
    Genes (Basel); 2020 Sep 02; 11(9):. PubMed ID: 32887465
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  • 22. Whole mitochondrial genome analysis in South Indian patients with Leber's hereditary optic neuropathy.
    Saikia BB, Dubey SK, Shanmugam MK, Sundaresan P.
    Mitochondrion; 2017 Sep 02; 36():21-28. PubMed ID: 27989883
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  • 24. Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy.
    Caporali L, Iommarini L, La Morgia C, Olivieri A, Achilli A, Maresca A, Valentino ML, Capristo M, Tagliavini F, Del Dotto V, Zanna C, Liguori R, Barboni P, Carbonelli M, Cocetta V, Montopoli M, Martinuzzi A, Cenacchi G, De Michele G, Testa F, Nesti A, Simonelli F, Porcelli AM, Torroni A, Carelli V.
    PLoS Genet; 2018 Feb 02; 14(2):e1007210. PubMed ID: 29444077
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  • 25. Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.
    Ji Y, Zhang J, Yu J, Wang Y, Lu Y, Liang M, Li Q, Jin X, Wei Y, Meng F, Gao Y, Cang X, Tong Y, Liu X, Zhang M, Jiang P, Zhu T, Mo JQ, Huang T, Jiang P, Guan MX.
    Hum Mol Genet; 2019 May 01; 28(9):1515-1529. PubMed ID: 30597069
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  • 26. Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease.
    Pello R, Martín MA, Carelli V, Nijtmans LG, Achilli A, Pala M, Torroni A, Gómez-Durán A, Ruiz-Pesini E, Martinuzzi A, Smeitink JA, Arenas J, Ugalde C.
    Hum Mol Genet; 2008 Dec 15; 17(24):4001-11. PubMed ID: 18806273
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  • 27. Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy.
    Ji Y, Zhang J, Lu Y, Yi Q, Chen M, Xie S, Mao X, Xiao Y, Meng F, Zhang M, Yang R, Guan MX.
    J Biol Chem; 2020 Sep 18; 295(38):13224-13238. PubMed ID: 32723871
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  • 30. 'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation.
    Lodi R, Montagna P, Cortelli P, Iotti S, Cevoli S, Carelli V, Barbiroli B.
    Brain; 2000 Sep 18; 123 ( Pt 9)():1896-902. PubMed ID: 10960053
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  • 31. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
    Liang M, Jiang P, Li F, Zhang J, Ji Y, He Y, Xu M, Zhu J, Meng X, Zhao F, Tong Y, Liu X, Sun Y, Zhou X, Mo JQ, Qu J, Guan MX.
    Invest Ophthalmol Vis Sci; 2014 Mar 06; 55(3):1321-31. PubMed ID: 24398099
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  • 32. Mitochondrial tRNAAla 5601C>T variant may affect the clinical expression of the LHON‑related ND4 11778G>A mutation in a family.
    Ding Y, Ye YF, Li MY, Xia BH, Leng JH.
    Mol Med Rep; 2020 Jan 06; 21(1):201-208. PubMed ID: 31939618
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  • 33. 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 30; 16():782-92. PubMed ID: 20454697
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  • 38. Leber's hereditary optic neuropathy: a multifactorial disease.
    Yen MY, Wang AG, Wei YH.
    Prog Retin Eye Res; 2006 Jul 30; 25(4):381-96. PubMed ID: 16829155
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  • 39. Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.
    Liu XL, Zhou X, Zhou J, Zhao F, Zhang J, Li C, Ji Y, Zhang Y, Wei QP, Sun YH, Yang L, Lin B, Yuan Y, Li Y, Qu J, Guan MX.
    Ophthalmology; 2011 May 30; 118(5):978-85. PubMed ID: 21131053
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