554 related articles for article (PubMed ID: 20566709)
1. Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.
Gómez-Durán A; Pacheu-Grau D; López-Gallardo E; Díez-Sánchez C; Montoya J; López-Pérez MJ; Ruiz-Pesini E
Hum Mol Genet; 2010 Sep; 19(17):3343-53. PubMed ID: 20566709
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial medicine--molecular pathology of defective oxidative phosphorylation.
Fosslien E
Ann Clin Lab Sci; 2001 Jan; 31(1):25-67. PubMed ID: 11314862
[TBL] [Abstract][Full Text] [Related]
3. The mitochondrial genome in human adaptive radiation and disease: on the road to therapeutics and performance enhancement.
Wallace DC
Gene; 2005 Jul; 354():169-80. PubMed ID: 16024186
[TBL] [Abstract][Full Text] [Related]
4. Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy.
Gómez-Durán A; Pacheu-Grau D; Martínez-Romero I; López-Gallardo E; López-Pérez MJ; Montoya J; Ruiz-Pesini E
Biochim Biophys Acta; 2012 Aug; 1822(8):1216-22. PubMed ID: 22561905
[TBL] [Abstract][Full Text] [Related]
5. Mechanisms of mitochondrial diseases.
Ylikallio E; Suomalainen A
Ann Med; 2012 Feb; 44(1):41-59. PubMed ID: 21806499
[TBL] [Abstract][Full Text] [Related]
6. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.
Kellar-Wood H; Robertson N; Govan GG; Compston DA; Harding AE
Ann Neurol; 1994 Jul; 36(1):109-12. PubMed ID: 8024249
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
Abu-Amero KK; Bosley TM
Invest Ophthalmol Vis Sci; 2006 Oct; 47(10):4211-20. PubMed ID: 17003408
[TBL] [Abstract][Full Text] [Related]
9. [Diseases of the human mitochondrial oxidative phosphorylation system].
Ruiz-Pesini E; López-Gallardo E; Dahmani Y; Herrero MD; Solano A; Díez-Sánchez C; López-Pérez M; Montoya J
Rev Neurol; 2006 Oct 1-15; 43(7):416-24. PubMed ID: 17006861
[TBL] [Abstract][Full Text] [Related]
10. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
Mao YJ; Qu J; Guan MX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):45-9. PubMed ID: 18247303
[TBL] [Abstract][Full Text] [Related]
11. The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines.
Bornstein B; Mas JA; Fernández-Moreno MA; Campos Y; Martín MA; del Hoyo P; Rubio JC; Arenas J; Garesse R
Hum Mutat; 2002 Mar; 19(3):234-9. PubMed ID: 11857739
[TBL] [Abstract][Full Text] [Related]
12. The transmission of OXPHOS disease and methods to prevent this.
Jacobs LJ; de Wert G; Geraedts JP; de Coo IF; Smeets HJ
Hum Reprod Update; 2006; 12(2):119-36. PubMed ID: 16199488
[TBL] [Abstract][Full Text] [Related]
13. The pathophysiology of mitochondrial biogenesis: towards four decades of mitochondrial DNA research.
Fernández-Moreno MA; Bornstein B; Petit N; Garesse R
Mol Genet Metab; 2000 Nov; 71(3):481-95. PubMed ID: 11073716
[TBL] [Abstract][Full Text] [Related]
14. Cybrid models of mtDNA disease and transmission, from cells to mice.
Trounce IA; Pinkert CA
Curr Top Dev Biol; 2007; 77():157-83. PubMed ID: 17222703
[TBL] [Abstract][Full Text] [Related]
15. [Mitochondrial syndrome].
Kozłowska I; Rózański J; Ciechanowski K
Pol Merkur Lekarski; 2004 Oct; 17(100):395-8. PubMed ID: 15690713
[TBL] [Abstract][Full Text] [Related]
16. Hereditary optic neuropathies share a common mitochondrial coupling defect.
Chevrollier A; Guillet V; Loiseau D; Gueguen N; de Crescenzo MA; Verny C; Ferre M; Dollfus H; Odent S; Milea D; Goizet C; Amati-Bonneau P; Procaccio V; Bonneau D; Reynier P
Ann Neurol; 2008 Jun; 63(6):794-8. PubMed ID: 18496845
[TBL] [Abstract][Full Text] [Related]
17. Tissue-specific differences in mitochondrial activity and biogenesis.
Fernández-Vizarra E; Enríquez JA; Pérez-Martos A; Montoya J; Fernández-Silva P
Mitochondrion; 2011 Jan; 11(1):207-13. PubMed ID: 20933104
[TBL] [Abstract][Full Text] [Related]
18. Molecular genetic and clinical aspects of mitochondrial disorders in childhood.
Moslemi AR; Darin N
Mitochondrion; 2007 Jul; 7(4):241-52. PubMed ID: 17376748
[TBL] [Abstract][Full Text] [Related]
19. Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J.
Moilanen JS; Finnila S; Majamaa K
Mol Biol Evol; 2003 Dec; 20(12):2132-42. PubMed ID: 12949126
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial DNA mutations in Cuban optic and peripheral neuropathy.
Johns DR; Neufeld MJ; Hedges TR
J Neuroophthalmol; 1994 Sep; 14(3):135-40. PubMed ID: 7804416
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
