228 related articles for article (PubMed ID: 8680405)
1. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations.
Brown MD; Torroni A; Reckord CL; Wallace DC
Hum Mutat; 1995; 6(4):311-25. PubMed ID: 8680405
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
Brown MD; Voljavec AS; Lott MT; Torroni A; Yang CC; Wallace DC
Genetics; 1992 Jan; 130(1):163-73. PubMed ID: 1732158
[TBL] [Abstract][Full Text] [Related]
3. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.
Brown MD; Sun F; Wallace DC
Am J Hum Genet; 1997 Feb; 60(2):381-7. PubMed ID: 9012411
[TBL] [Abstract][Full Text] [Related]
4. No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON.
Gerbitz KD; Paprotta A; Obermaier-Kusser B; Rietschel M; Zerres K
FEBS Lett; 1992 Dec; 314(3):251-5. PubMed ID: 1361456
[TBL] [Abstract][Full Text] [Related]
5. Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy.
Mashima Y; Yamada K; Wakakura M; Kigasawa K; Kudoh J; Shimizu N; Oguchi Y
Curr Eye Res; 1998 Apr; 17(4):403-8. PubMed ID: 9561832
[TBL] [Abstract][Full Text] [Related]
6. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
Pénisson-Besnier I; Moreau C; Jacques C; Roger JC; Dubas F; Reynier P
Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
[TBL] [Abstract][Full Text] [Related]
7. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
Leo-Kottler B; Christ-Adler M; Baumann B; Zrenner E; Wissinger B
Ger J Ophthalmol; 1996 Jul; 5(4):233-40. PubMed ID: 8854108
[TBL] [Abstract][Full Text] [Related]
8. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.
Torroni A; Petrozzi M; D'Urbano L; Sellitto D; Zeviani M; Carrara F; Carducci C; Leuzzi V; Carelli V; Barboni P; De Negri A; Scozzari R
Am J Hum Genet; 1997 May; 60(5):1107-21. PubMed ID: 9150158
[TBL] [Abstract][Full Text] [Related]
9. Leber's hereditary optic neuropathy mitochondrial DNA mutations in familial multiple sclerosis.
Mojon DS; Fujihara K; Hirano M; Miller C; Lincoff NS; Jacobs LD; Greenberg SJ
Graefes Arch Clin Exp Ophthalmol; 1999 Apr; 237(4):348-50. PubMed ID: 10208269
[TBL] [Abstract][Full Text] [Related]
10. Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population.
Dogulu CF; Kansu T; Seyrantepe V; Ozguc M; Topaloglu H; Johns DR
Eye (Lond); 2001 Apr; 15(Pt 2):183-8. PubMed ID: 11339587
[TBL] [Abstract][Full Text] [Related]
11. 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; 124(Pt 1):209-18. PubMed ID: 11133798
[TBL] [Abstract][Full Text] [Related]
12. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.
Brown MD; Starikovskaya E; Derbeneva O; Hosseini S; Allen JC; Mikhailovskaya IE; Sukernik RI; Wallace DC
Hum Genet; 2002 Feb; 110(2):130-8. PubMed ID: 11935318
[TBL] [Abstract][Full Text] [Related]
13. mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy.
Lamminen T; Huoponen K; Sistonen P; Juvonen V; Lahermo P; Aula P; Nikoskelainen E; Savontaus ML
Eur J Hum Genet; 1997; 5(5):271-9. PubMed ID: 9412783
[TBL] [Abstract][Full Text] [Related]
14. Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy.
Matsumoto M; Hayasaka S; Kadoi C; Hotta Y; Fujiki K; Fujimaki T; Takeda M; Ishida N; Endo S; Kanai A
Ophthalmic Genet; 1999 Sep; 20(3):153-60. PubMed ID: 10520236
[TBL] [Abstract][Full Text] [Related]
15. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis.
Mojon DS; Herbert J; Sadiq SA; Miller JR; Madonna M; Hirano M
Ophthalmologica; 1999; 213(3):171-5. PubMed ID: 10202290
[TBL] [Abstract][Full Text] [Related]
16. Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.
Brown MD; Voljavec AS; Lott MT; MacDonald I; Wallace DC
FASEB J; 1992 Jul; 6(10):2791-9. PubMed ID: 1634041
[TBL] [Abstract][Full Text] [Related]
17. Exclusive homoplasmic 11778 mutation in mitochondrial DNA of Chinese patients with Leber's hereditary optic neuropathy.
Yen MY; Lee HC; Wang AG; Chang WL; Liu JH; Wei YH
Jpn J Ophthalmol; 1999; 43(3):196-200. PubMed ID: 10413253
[TBL] [Abstract][Full Text] [Related]
18. Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy.
Jacobi FK; Leo-Kottler B; Mittelviefhaus K; Zrenner E; Meyer J; Pusch CM; Wissinger B
Invest Ophthalmol Vis Sci; 2001 May; 42(6):1208-14. PubMed ID: 11328729
[TBL] [Abstract][Full Text] [Related]
19. Mutation screening of mitochondrial DNA as well as OPA1 and OPA3 in a Chinese cohort with suspected hereditary optic atrophy.
Chen J; Xu K; Zhang X; Jiang F; Liu L; Dong B; Ren Y; Li Y
Invest Ophthalmol Vis Sci; 2014 Sep; 55(10):6987-95. PubMed ID: 25205859
[TBL] [Abstract][Full Text] [Related]
20. Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families.
Brown MD; Zhadanov S; Allen JC; Hosseini S; Newman NJ; Atamonov VV; Mikhailovskaya IE; Sukernik RI; Wallace DC
Hum Genet; 2001 Jul; 109(1):33-9. PubMed ID: 11479733
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
