These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 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].
    PĂ©nisson-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]
    of 12.