331 related articles for article (PubMed ID: 34311469)
1. Assocation Between Leber's Hereditary Optic Neuropathy and MT-ND1 3460G>A Mutation-Induced Alterations in Mitochondrial Function, Apoptosis, and Mitophagy.
Zhang J; Ji Y; Chen J; Xu M; Wang G; Ci X; Lin B; Mo JQ; Zhou X; Guan MX
Invest Ophthalmol Vis Sci; 2021 Jul; 62(9):38. PubMed ID: 34311469
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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; 57(6):2377-89. PubMed ID: 27177320
[TBL] [Abstract][Full Text] [Related]
6. Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations.
Jin X; Zhang J; Yi Q; Meng F; Yu J; Ji Y; Mo JQ; Tong Y; Jiang P; Guan MX
Invest Ophthalmol Vis Sci; 2021 Jun; 62(7):22. PubMed ID: 34156427
[TBL] [Abstract][Full Text] [Related]
7. 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; 28(9):1515-1529. PubMed ID: 30597069
[TBL] [Abstract][Full Text] [Related]
8. 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; 295(38):13224-13238. PubMed ID: 32723871
[TBL] [Abstract][Full Text] [Related]
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; 25(16):3613-3625. PubMed ID: 27427386
[TBL] [Abstract][Full Text] [Related]
10. Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON).
Peron C; Mauceri R; Cabassi T; Segnali A; Maresca A; Iannielli A; Rizzo A; Sciacca FL; Broccoli V; Carelli V; Tiranti V
Stem Cell Res; 2020 Oct; 48():101939. PubMed ID: 32771908
[TBL] [Abstract][Full Text] [Related]
11. Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families.
Zhang J; Jiang P; Jin X; Liu X; Zhang M; Xie S; Gao M; Zhang S; Sun YH; Zhu J; Ji Y; Wei QP; Tong Y; Guan MX
Mitochondrion; 2014 Sep; 18():18-26. PubMed ID: 25194554
[TBL] [Abstract][Full Text] [Related]
12. Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.
Khan NA; Govindaraj P; Soumittra N; Sharma S; Srilekha S; Ambika S; Vanniarajan A; Meena AK; Uppin MS; Sundaram C; Bindu PS; Gayathri N; Taly AB; Thangaraj K
Invest Ophthalmol Vis Sci; 2017 Aug; 58(10):3923-3930. PubMed ID: 28768321
[TBL] [Abstract][Full Text] [Related]
13. 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; 53(8):4586-94. PubMed ID: 22577081
[TBL] [Abstract][Full Text] [Related]
14. Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy.
Jiang P; Liang M; Zhang J; Gao Y; He Z; Yu H; Zhao F; Ji Y; Liu X; Zhang M; Fu Q; Tong Y; Sun Y; Zhou X; Huang T; Qu J; Guan MX
Invest Ophthalmol Vis Sci; 2015 Jul; 56(8):4778-88. PubMed ID: 26218905
[TBL] [Abstract][Full Text] [Related]
15. m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.
Kodroń A; Krawczyński MR; Tońska K; Bartnik E
J Clin Pathol; 2014 Jul; 67(7):639-41. PubMed ID: 24747208
[TBL] [Abstract][Full Text] [Related]
16. 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; 25(3):584-96. PubMed ID: 26647310
[TBL] [Abstract][Full Text] [Related]
17. 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; 55(3):1321-31. PubMed ID: 24398099
[TBL] [Abstract][Full Text] [Related]
18. Generation of an induced pluripotent stem cell line from a patient with leber's hereditary optic neuropathy carrying a homoplasmic m.3635G > A mutation in the mitochondrial ND1 gene.
Ji D; Su X; Hu C; Zhang Z; Wang M; Zou W; Shen L; Liu Y; Liang C; Du Y; Liang D; Cao Y
Stem Cell Res; 2022 Aug; 63():102858. PubMed ID: 35905669
[TBL] [Abstract][Full Text] [Related]
19. 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; 1863(1):182-187. PubMed ID: 27613247
[TBL] [Abstract][Full Text] [Related]
20. 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; 201():108277. PubMed ID: 32991883
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
