101 related articles for article (PubMed ID: 15052619)
1. Attenuation of free radical production and paracrystalline inclusions by creatine supplementation in a patient with a novel cytochrome b mutation.
Tarnopolsky MA; Simon DK; Roy BD; Chorneyko K; Lowther SA; Johns DR; Sandhu JK; Li Y; Sikorska M
Muscle Nerve; 2004 Apr; 29(4):537-47. PubMed ID: 15052619
[TBL] [Abstract][Full Text] [Related]
2. Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy.
Jeppesen TD; Schwartz M; Olsen DB; Wibrand F; Krag T; Dunø M; Hauerslev S; Vissing J
Brain; 2006 Dec; 129(Pt 12):3402-12. PubMed ID: 16815877
[TBL] [Abstract][Full Text] [Related]
3. A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance.
Dumoulin R; Sagnol I; Ferlin T; Bozon D; Stepien G; Mousson B
Mol Cell Probes; 1996 Oct; 10(5):389-91. PubMed ID: 8910895
[TBL] [Abstract][Full Text] [Related]
4. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
Auré K; Fayet G; Leroy JP; Lacène E; Romero NB; Lombès A
Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
[TBL] [Abstract][Full Text] [Related]
5. Clinical manifestation and a new ISCU mutation in iron-sulphur cluster deficiency myopathy.
Kollberg G; Tulinius M; Melberg A; Darin N; Andersen O; Holmgren D; Oldfors A; Holme E
Brain; 2009 Aug; 132(Pt 8):2170-9. PubMed ID: 19567699
[TBL] [Abstract][Full Text] [Related]
6. Evidence of ROS generation by mitochondria in cells with impaired electron transport chain and mitochondrial DNA damage.
Indo HP; Davidson M; Yen HC; Suenaga S; Tomita K; Nishii T; Higuchi M; Koga Y; Ozawa T; Majima HJ
Mitochondrion; 2007; 7(1-2):106-18. PubMed ID: 17307400
[TBL] [Abstract][Full Text] [Related]
7. Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivo.
Chinnery PF; Taylor DJ; Brown DT; Manners D; Styles P; Lodi R
Ann Neurol; 2000 Mar; 47(3):381-4. PubMed ID: 10716261
[TBL] [Abstract][Full Text] [Related]
8. Identification of ataxia-associated mtDNA mutations (m.4052T>C and m.9035T>C) and evaluation of their pathogenicity in transmitochondrial cybrids.
Sikorska M; Sandhu JK; Simon DK; Pathiraja V; Sodja C; Li Y; Ribecco-Lutkiewicz M; Lanthier P; Borowy-Borowski H; Upton A; Raha S; Pulst SM; Tarnopolsky MA
Muscle Nerve; 2009 Sep; 40(3):381-94. PubMed ID: 19626676
[TBL] [Abstract][Full Text] [Related]
9. Functional diagnostics in mitochondrial diseases.
Siciliano G; Volpi L; Piazza S; Ricci G; Mancuso M; Murri L
Biosci Rep; 2007 Jun; 27(1-3):53-67. PubMed ID: 17492503
[TBL] [Abstract][Full Text] [Related]
10. Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.
Bonora E; Porcelli AM; Gasparre G; Biondi A; Ghelli A; Carelli V; Baracca A; Tallini G; Martinuzzi A; Lenaz G; Rugolo M; Romeo G
Cancer Res; 2006 Jun; 66(12):6087-96. PubMed ID: 16778181
[TBL] [Abstract][Full Text] [Related]
11. Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.
Lalani SR; Vladutiu GD; Plunkett K; Lotze TE; Adesina AM; Scaglia F
Arch Neurol; 2005 Feb; 62(2):317-20. PubMed ID: 15710863
[TBL] [Abstract][Full Text] [Related]
12. Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome.
Götz A; Isohanni P; Pihko H; Paetau A; Herva R; Saarenpää-Heikkilä O; Valanne L; Marjavaara S; Suomalainen A
Brain; 2008 Nov; 131(Pt 11):2841-50. PubMed ID: 18819985
[TBL] [Abstract][Full Text] [Related]
13. Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) gene.
van den Bosch BJ; de Coo IF; Hendrickx AT; Busch HF; de Jong G; Scholte HR; Smeets HJ
Neuromuscul Disord; 2004 Oct; 14(10):683-8. PubMed ID: 15351426
[TBL] [Abstract][Full Text] [Related]
14. Enhanced generation of mitochondrial reactive oxygen species in cybrids containing 4977-bp mitochondrial DNA deletion.
Jou MJ; Peng TI; Wu HY; Wei YH
Ann N Y Acad Sci; 2005 May; 1042():221-8. PubMed ID: 15965066
[TBL] [Abstract][Full Text] [Related]
15. The deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriers.
Haut S; de Villemeur TB; Brivet M; Guiochon-Mantel A; Boutron A; Rustin P; Legrand A; Slama A
Eur J Hum Genet; 2004 Mar; 12(3):220-4. PubMed ID: 14735157
[TBL] [Abstract][Full Text] [Related]
16. Respiratory function decline and DNA mutation in mitochondria, oxidative stress and altered gene expression during aging.
Wei YH; Wu SB; Ma YS; Lee HC
Chang Gung Med J; 2009; 32(2):113-32. PubMed ID: 19403001
[TBL] [Abstract][Full Text] [Related]
17. Enhanced ROS production and antioxidant defenses in cybrids harbouring mutations in mtDNA.
Vives-Bauza C; Gonzalo R; Manfredi G; Garcia-Arumi E; Andreu AL
Neurosci Lett; 2006 Jan; 391(3):136-41. PubMed ID: 16165271
[TBL] [Abstract][Full Text] [Related]
18. Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions.
Molnar M; Schröder JM
Acta Neuropathol; 1998 Jul; 96(1):41-51. PubMed ID: 9678512
[TBL] [Abstract][Full Text] [Related]
19. Late-onset mitochondrial myopathy with dystrophic changes due to a G7497A mutation in the mitochondrial tRNA(Ser(UCN)) gene.
Müller T; Deschauer M; Neudecker S; Zierz S
Acta Neuropathol; 2005 Oct; 110(4):426-30. PubMed ID: 16133542
[TBL] [Abstract][Full Text] [Related]
20. [Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy].
Zhang XA; Wu HC; Zhang BF; Yu W; Fan QS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):18-21. PubMed ID: 15696472
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]