233 related articles for article (PubMed ID: 23304069)
1. Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy.
Bi R; Zhang AM; Jia X; Zhang Q; Yao YG
Mol Vis; 2012; 18():3087-94. PubMed ID: 23304069
[TBL] [Abstract][Full Text] [Related]
2. 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; 36(4):291-8. PubMed ID: 24417559
[TBL] [Abstract][Full Text] [Related]
3. mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population.
Jia X; Li S; Wang P; Guo X; Zhang Q
Biochem Biophys Res Commun; 2010 Dec; 403(2):237-41. PubMed ID: 21074518
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.
Zhang AM; Zou Y; Guo X; Jia X; Zhang Q; Yao YG
Biochem Biophys Res Commun; 2009 Aug; 386(2):392-5. PubMed ID: 19527690
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients.
Zhang AM; Jia X; Guo X; Zhang Q; Yao YG
J Transl Med; 2012 Mar; 10():43. PubMed ID: 22400981
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
Ji Y; Zhang AM; Jia X; Zhang YP; Xiao X; Li S; Guo X; Bandelt HJ; Zhang Q; Yao YG
Am J Hum Genet; 2008 Dec; 83(6):760-8. PubMed ID: 19026397
[TBL] [Abstract][Full Text] [Related]
9. 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; 5(10):e13426. PubMed ID: 20976138
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy.
Yu D; Jia X; Zhang AM; Guo X; Zhang YP; Zhang Q; Yao YG
Neurogenetics; 2010 Jul; 11(3):349-56. PubMed ID: 20232220
[TBL] [Abstract][Full Text] [Related]
12. [The analysis of mitochondrial DNA haplogroups and variants for Leber's hereditary optic neuropathy in Chinese families carrying the m.14484T >C mutation].
Meng X; Zhu J; Gao M; Zhang S; Zhao F; Zhang J; Liu X; Wei Q; Tong Y; Zhang M; Qu J; Guan M
Yi Chuan; 2014 Apr; 36(4):336-45. PubMed ID: 24846978
[TBL] [Abstract][Full Text] [Related]
13. Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy.
Li Y; Li J; Jia X; Xiao X; Li S; Guo X
PLoS One; 2017; 12(1):e0170090. PubMed ID: 28081242
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families.
Zhang J; Zhao F; Fu Q; Liang M; Tong Y; Liu X; Lin B; Mi H; Zhang M; Wei QP; Xue L; Jiang P; Zhou X; Mo JQ; Huang T; Qu J; Guan MX
Mitochondrion; 2013 Nov; 13(6):772-81. PubMed ID: 23665487
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Mutation profile of neurodegenerative mitochondriopathy - LHON in Southern India.
Gowri P; Sathish P; Mahesh Kumar S; Sundaresan P
Gene; 2022 Apr; 819():146202. PubMed ID: 35104579
[TBL] [Abstract][Full Text] [Related]
19. 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; 21(1):201-208. PubMed ID: 31939618
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation.
Piotrowska-Nowak A; Krawczyński MR; Kosior-Jarecka E; Ambroziak AM; Korwin M; Ołdak M; Tońska K; Bartnik E
Metab Brain Dis; 2020 Dec; 35(8):1317-1327. PubMed ID: 32740724
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]