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Journal Abstract Search

712 related items for PubMed ID: 26218905

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  • 2. 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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  • 3. Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy.
    Ji Y, Liang M, Zhang J, Zhu L, Zhang Z, Fu R, Liu X, Zhang M, Fu Q, Zhao F, Tong Y, Sun Y, Jiang P, Guan MX.
    Invest Ophthalmol Vis Sci; 2016 May 01; 57(6):2377-89. PubMed ID: 27177320
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  • 6. Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.
    Zhou X, Zhang H, Zhao F, Ji Y, Tong Y, Zhang J, Zhang Y, Yang L, Qian Y, Lu F, Qu J, Guan MX.
    Mol Genet Metab; 2010 Aug 01; 100(4):379-84. PubMed ID: 20627642
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  • 7. Mitochondrial tRNA variants in 811 Chinese probands with Leber's hereditary optic neuropathy.
    Ji Y, Zhang J, Liang M, Meng F, Zhang M, Mo JQ, Wang M, Guan MX.
    Mitochondrion; 2022 Jul 01; 65():56-66. PubMed ID: 35623556
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  • 9. 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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  • 11. 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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  • 12. 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 18; 21(1):201-208. PubMed ID: 31939618
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  • 14. 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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  • 16. Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation.
    Cai W, Fu Q, Zhou X, Qu J, Tong Y, Guan MX.
    J Genet Genomics; 2008 Nov 01; 35(11):649-55. PubMed ID: 19022198
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  • 17. The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
    Jiang P, Jin X, Peng Y, Wang M, Liu H, Liu X, Zhang Z, Ji Y, Zhang J, Liang M, Zhao F, Sun YH, Zhang M, Zhou X, Chen Y, Mo JQ, Huang T, Qu J, Guan MX.
    Hum Mol Genet; 2016 Feb 01; 25(3):584-96. PubMed ID: 26647310
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