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.
317 related articles for article (PubMed ID: 9150158)
1. 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]
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. 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]
6. The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity. Ghelli A; Porcelli AM; Zanna C; Vidoni S; Mattioli S; Barbieri A; Iommarini L; Pala M; Achilli A; Torroni A; Rugolo M; Carelli V PLoS One; 2009 Nov; 4(11):e7922. PubMed ID: 19936068 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy. Tharaphan P; Chuenkongkaew WL; Luangtrakool K; Sanpachudayan T; Suktitipat B; Suphavilai R; Srisawat C; Sura T; Lertrit P J Neuroophthalmol; 2006 Dec; 26(4):264-7. PubMed ID: 17204919 [TBL] [Abstract][Full Text] [Related]
9. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes. Hofmann S; Bezold R; Jaksch M; Obermaier-Kusser B; Mertens S; Kaufhold P; Rabl W; Hecker W; Gerbitz KD Genomics; 1997 Jan; 39(1):8-18. PubMed ID: 9027481 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. 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]
14. Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees. Howell N; Kubacka I; Halvorson S; Howell B; McCullough DA; Mackey D Genetics; 1995 May; 140(1):285-302. PubMed ID: 7635294 [TBL] [Abstract][Full Text] [Related]
15. Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background. Howell N; Herrnstadt C; Shults C; Mackey DA Am J Med Genet A; 2003 Jun; 119A(2):147-51. PubMed ID: 12749053 [TBL] [Abstract][Full Text] [Related]
16. Leber hereditary optic neuropathy: mitochondrial mutations and degeneration of the optic nerve. Howell N Vision Res; 1997 Dec; 37(24):3495-507. PubMed ID: 9425526 [TBL] [Abstract][Full Text] [Related]
17. Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians. Kalman B; Li S; Chatterjee D; O'Connor J; Voehl MR; Brown MD; Alder H Acta Neurol Scand; 1999 Jan; 99(1):16-25. PubMed ID: 9925234 [TBL] [Abstract][Full Text] [Related]
18. mtDNA haplogroup distribution in Chinese patients with Leber's hereditary optic neuropathy and G11778A mutation. Ji Y; Jia X; Zhang Q; Yao YG Biochem Biophys Res Commun; 2007 Dec; 364(2):238-42. PubMed ID: 17942074 [TBL] [Abstract][Full Text] [Related]
19. 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]