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Journal Abstract Search

311 related items for PubMed ID: 35623556

  • 21. Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families.
    Zhou X, Wei Q, Yang L, Tong Y, Zhao F, Lu C, Qian Y, Sun Y, Lu F, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 03; 340(1):69-75. PubMed ID: 16364244
    [Abstract] [Full Text] [Related]

  • 22. Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.
    Qian Y, Zhou X, Hu Y, Tong Y, Li R, Lu F, Yang H, Mo JQ, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2005 Jul 01; 332(2):614-21. PubMed ID: 15896721
    [Abstract] [Full Text] [Related]

  • 23. Leber's Hereditary Optic Neuropathy is Associated with Compound Primary Mutations of Mitochondrial ND1 m.3635G > A and ND6 m.14502 T > C.
    Jin X, Wang L, Gong Y, Chen B, Wang Y, Chen T, Wei S.
    Ophthalmic Genet; 2015 Jul 01; 36(4):291-8. PubMed ID: 24417559
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  • 27. [Identification of mitochondrial DNA ND1 T3866C mutation in three ethnic Han Chinese families affected with Leber's hereditary optic neuropathy].
    Zhang S, Gao M, Zhang Z, Liu X, Guan M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr 01; 32(2):198-203. PubMed ID: 25863085
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  • 28. Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families.
    Zhou X, Qian Y, Zhang J, Tong Y, Jiang P, Liang M, Dai X, Zhou H, Zhao F, Ji Y, Mo JQ, Qu J, Guan MX.
    Invest Ophthalmol Vis Sci; 2012 Jul 09; 53(8):4586-94. PubMed ID: 22577081
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  • 29. Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families.
    Qu J, Wang Y, Tong Y, Zhou X, Zhao F, Yang L, Zhang S, Zhang J, West CE, Guan MX.
    Invest Ophthalmol Vis Sci; 2010 Oct 09; 51(10):4906-12. PubMed ID: 20435583
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  • 30. [The mitochondrial ND5 T12338C mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families].
    Ji YC, Liu XL, Zhao FX, Zhang JJ, Zhang Y, Zhou XT, Qu J, Guan MX.
    Yi Chuan; 2011 Apr 09; 33(4):322-8. PubMed ID: 21482521
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  • 31. Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy.
    Achilli A, Iommarini L, Olivieri A, Pala M, Hooshiar Kashani B, Reynier P, La Morgia C, Valentino ML, Liguori R, Pizza F, Barboni P, Sadun F, De Negri AM, Zeviani M, Dollfus H, Moulignier A, Ducos G, Orssaud C, Bonneau D, Procaccio V, Leo-Kottler B, Fauser S, Wissinger B, Amati-Bonneau P, Torroni A, Carelli V.
    PLoS One; 2012 Apr 09; 7(8):e42242. PubMed ID: 22879922
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  • 32. 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 09; 118(5):978-85. PubMed ID: 21131053
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  • 34. [The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families].
    Zhou HH, Dai XN, Lin B, Mi H, Liu XL, Zhao FX, Zhang JJ, Zhou XT, Sun YH, Wei QP, Qu J, Guan MX.
    Yi Chuan; 2012 Aug 09; 34(8):1031-42. PubMed ID: 22917908
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  • 35. Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation.
    Liang M, Guan M, Zhao F, Zhou X, Yuan M, Tong Y, Yang L, Wei QP, Sun YH, Lu F, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2009 Jun 05; 383(3):286-92. PubMed ID: 19324017
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  • 36. Mitochondrial tRNAThr 15891C>G mutation was not associated with Leber's hereditary optic neuropathy in Han Chinese patients.
    Jiang Z, Yu J, Xia B, Zhuo G.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Jun 05; 27(2):1564-6. PubMed ID: 25186221
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  • 37. Mitochondrial tRNA(Thr) A15951G mutation may not be associated with Leber's Hereditary Optic Neuropathy.
    Zhang X, Yu S, Tu Y, Huang W.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Jul 05; 27(4):2323-5. PubMed ID: 26000946
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  • 39. 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 05; 35(11):649-55. PubMed ID: 19022198
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  • 40. Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation.
    Zhang M, Zhou X, Li C, Zhao F, Zhang J, Yuan M, Sun YH, Wang J, Tong Y, Liang M, Yang L, Cai W, Wang L, Qu J, Guan MX.
    Mol Genet Metab; 2010 Nov 05; 101(2-3):192-9. PubMed ID: 20728388
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