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249 related items for PubMed ID: 22879922

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  • 24. [Rare pathogenic nucleotide variants of mitochondrial DNA associated with Leber's hereditary optic neuropathy].
    Andreeva NA, Murakhovskaya YK, Krylova TD, Tsygankova PG, Sheremet NL.
    Vestn Oftalmol; 2023; 139(6):166-174. PubMed ID: 38235644
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  • 25. 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 29; 31(19):3299-3312. PubMed ID: 35567411
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  • 26. 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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  • 28. In silico model of mtDNA mutations effect on secondary and 3D structure of mitochondrial rRNA and tRNA in Leber's hereditary optic neuropathy.
    Rovcanin B, Jancic J, Samardzic J, Rovcanin M, Nikolic B, Ivancevic N, Novakovic I, Kostic V.
    Exp Eye Res; 2020 Dec 02; 201():108277. PubMed ID: 32991883
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  • 29. Frequency and spectrum of MT-TT variants associated with Leber's hereditary optic neuropathy in a Chinese cohort of subjects.
    Lyu Y, Xu M, Chen J, Ji Y, Guan MX, Zhang J.
    Mitochondrial DNA B Resour; 2019 Jul 12; 4(2):2266-2280. PubMed ID: 33365504
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  • 30. 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 19; 4(11):e7922. PubMed ID: 19936068
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  • 31. 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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  • 32. Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
    Jiang P, Liang M, Zhang C, Zhao X, He Q, Cui L, Liu X, Sun YH, Fu Q, Ji Y, Bai Y, Huang T, Guan MX.
    Hum Mol Genet; 2016 Aug 15; 25(16):3613-3625. PubMed ID: 27427386
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  • 33. 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 15; 21(1):201-208. PubMed ID: 31939618
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  • 34. Leber Hereditary Optic Neuropathy in Southwestern Ontario: A Growing List of Mutations.
    McDonald HM, Sadikovic B, Sheldon CA, Bursztyn LLCD.
    Can J Neurol Sci; 2023 Sep 15; 50(5):738-744. PubMed ID: 35892476
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  • 35. A simple oligonucleotide biochip capable of rapidly detecting known mitochondrial DNA mutations in Chinese patients with Leber's hereditary optic neuropathy (LHON).
    Du WD, Chen G, Cao HM, Jin QH, Liao RF, He XC, Chen DB, Huang SR, Zhao H, Lv YM, Tang HY, Tang XF, Wang YQ, Sun S, Zhao JL, Zhang XJ.
    Dis Markers; 2011 Sep 15; 30(4):181-90. PubMed ID: 21694444
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  • 36. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
    Chinnery PF, Brown DT, Andrews RM, Singh-Kler R, Riordan-Eva P, Lindley J, Applegarth DA, Turnbull DM, Howell N.
    Brain; 2001 Jan 15; 124(Pt 1):209-18. PubMed ID: 11133798
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  • 39. Identification and characterization of the novel point mutation m.3634A>G in the mitochondrial MT-ND1 gene associated with LHON syndrome.
    Carreño-Gago L, Gamez J, Cámara Y, Alvarez de la Campa E, Aller-Alvarez JS, Moncho D, Salvado M, Galan A, de la Cruz X, Pinós T, García-Arumí E.
    Biochim Biophys Acta Mol Basis Dis; 2017 Jan 15; 1863(1):182-187. PubMed ID: 27613247
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  • 40. Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.
    Yu D, Jia X, Zhang AM, Li S, Zou Y, Zhang Q, Yao YG.
    PLoS One; 2010 Oct 18; 5(10):e13426. PubMed ID: 20976138
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