361 related articles for article (PubMed ID: 11553931)
21. Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs.
Suzuki T; Nagao A; Suzuki T
Wiley Interdiscip Rev RNA; 2011; 2(3):376-86. PubMed ID: 21957023
[TBL] [Abstract][Full Text] [Related]
22. Oxidative stress, mitochondrial dysfunction and cellular stress response in Friedreich's ataxia.
Calabrese V; Lodi R; Tonon C; D'Agata V; Sapienza M; Scapagnini G; Mangiameli A; Pennisi G; Stella AM; Butterfield DA
J Neurol Sci; 2005 Jun; 233(1-2):145-62. PubMed ID: 15896810
[TBL] [Abstract][Full Text] [Related]
23. mtDNA mutations confer cellular sensitivity to oxidant stress that is partially rescued by calcium depletion and cyclosporin A.
Wong A; Cortopassi G
Biochem Biophys Res Commun; 1997 Oct; 239(1):139-45. PubMed ID: 9345284
[TBL] [Abstract][Full Text] [Related]
24. Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders.
Mimaki M; Hatakeyama H; Ichiyama T; Isumi H; Furukawa S; Akasaka M; Kamei A; Komaki H; Nishino I; Nonaka I; Goto Y
Mitochondrion; 2009 Apr; 9(2):115-22. PubMed ID: 19460299
[TBL] [Abstract][Full Text] [Related]
25. Mitochondrial DNA mutations in human disease.
Greaves LC; Taylor RW
IUBMB Life; 2006 Mar; 58(3):143-51. PubMed ID: 16766381
[TBL] [Abstract][Full Text] [Related]
26. Clinical implications of mitochondrial disease.
Muravchick S
Adv Drug Deliv Rev; 2008; 60(13-14):1553-60. PubMed ID: 18647627
[TBL] [Abstract][Full Text] [Related]
27. Genotype-phenotype correlation of maternally inherited disorders due to mutations in mitochondrial DNA.
Thajeb P; Dai D; Chiang MF; Shyu WC
Taiwan J Obstet Gynecol; 2006 Sep; 45(3):201-7. PubMed ID: 17175464
[TBL] [Abstract][Full Text] [Related]
28. Headache and mitochondrial disorders.
Rosen N
Headache; 2008 May; 48(5):733-4. PubMed ID: 18471127
[TBL] [Abstract][Full Text] [Related]
29. Mitochondrial DNA mutations: an overview of clinical and molecular aspects.
Craigen WJ
Methods Mol Biol; 2012; 837():3-15. PubMed ID: 22215537
[TBL] [Abstract][Full Text] [Related]
30. Molecular research technologies in mitochondrial diseases: the microarray approach.
Crimi M; O'Hearn SF; Wallace DC; Comi GP
IUBMB Life; 2005 Dec; 57(12):811-8. PubMed ID: 16393784
[TBL] [Abstract][Full Text] [Related]
31. Mitochondria and degenerative disorders.
Orth M; Schapira AH
Am J Med Genet; 2001; 106(1):27-36. PubMed ID: 11579422
[TBL] [Abstract][Full Text] [Related]
32. 20 years of human mtDNA pathologic point mutations: carefully reading the pathogenicity criteria.
Montoya J; López-Gallardo E; Díez-Sánchez C; López-Pérez MJ; Ruiz-Pesini E
Biochim Biophys Acta; 2009 May; 1787(5):476-83. PubMed ID: 18840399
[TBL] [Abstract][Full Text] [Related]
33. [Mitochondrial disorders: a classification for the 21st century].
Andreu AL; Gonzalo-Sanz R
Neurologia; 2004; 19(1):15-22. PubMed ID: 14762729
[TBL] [Abstract][Full Text] [Related]
34. Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease.
Kirino Y; Goto Y; Campos Y; Arenas J; Suzuki T
Proc Natl Acad Sci U S A; 2005 May; 102(20):7127-32. PubMed ID: 15870203
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Maternal inheritance and the evaluation of oxidative phosphorylation diseases.
Shoffner JM
Lancet; 1996 Nov; 348(9037):1283-8. PubMed ID: 8909383
[TBL] [Abstract][Full Text] [Related]
37. Mitochondrial DNA medicine.
DiMauro S
Biosci Rep; 2007 Jun; 27(1-3):5-9. PubMed ID: 17484047
[TBL] [Abstract][Full Text] [Related]
38. Mitochondrial DNA mutations in human disease.
DiMauro S; Schon EA
Am J Med Genet; 2001; 106(1):18-26. PubMed ID: 11579421
[TBL] [Abstract][Full Text] [Related]
39. [The mitochondrial genome and human mitochondrial diseases].
Sukernik RI; Derbeneva OA; Starikovskaia EB; Volod'ko NV; Mikhaĭlovskaia IE; Bychkov IIu; Lott M; Brown M; Wallace D
Genetika; 2002 Feb; 38(2):161-70. PubMed ID: 11898607
[TBL] [Abstract][Full Text] [Related]
40. Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation.
Finsterer J
Acta Neurol Scand; 2007 Jul; 116(1):1-14. PubMed ID: 17587249
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
