162 related articles for article (PubMed ID: 15670724)
1. Contrasting phenotypes in three patients with novel mutations in mitochondrial tRNA genes.
Anitori R; Manning K; Quan F; Weleber RG; Buist NR; Shoubridge EA; Kennaway NG
Mol Genet Metab; 2005 Feb; 84(2):176-88. PubMed ID: 15670724
[TBL] [Abstract][Full Text] [Related]
2. A novel heteroplasmic point mutation in the mitochondrial tRNA(Lys) gene in a sporadic case of mitochondrial encephalomyopathy: de novo mutation and no transmission to the offspring.
Houshmand M; Lindberg C; Moslemi AR; Oldfors A; Holme E
Hum Mutat; 1999; 13(3):203-9. PubMed ID: 10090475
[TBL] [Abstract][Full Text] [Related]
3. Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia.
Kornblum C; Zsurka G; Wiesner RJ; Schröder R; Kunz WS
Biosci Rep; 2008 Apr; 28(2):89-96. PubMed ID: 18384291
[TBL] [Abstract][Full Text] [Related]
4. Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
Moraes CT; Ciacci F; Bonilla E; Jansen C; Hirano M; Rao N; Lovelace RE; Rowland LP; Schon EA; DiMauro S
J Clin Invest; 1993 Dec; 92(6):2906-15. PubMed ID: 8254046
[TBL] [Abstract][Full Text] [Related]
5. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.
Ueki I; Koga Y; Povalko N; Akita Y; Nishioka J; Yatsuga S; Fukiyama R; Matsuishi T
Mitochondrion; 2006 Feb; 6(1):29-36. PubMed ID: 16337222
[TBL] [Abstract][Full Text] [Related]
6. Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.
Meulemans A; De Paepe B; De Bleecker J; Smet J; Lissens W; Van Coster R; De Meirleir L; Seneca S
Arch Neurol; 2007 Sep; 64(9):1339-43. PubMed ID: 17846276
[TBL] [Abstract][Full Text] [Related]
7. A novel heteroplasmic tRNA(Leu(CUN)) mtDNA point mutation associated with chronic progressive external ophthalmoplegia.
Cardaioli E; Da Pozzo P; Radi E; Dotti MT; Federico A
Biochem Biophys Res Commun; 2005 Feb; 327(3):675-8. PubMed ID: 15649400
[TBL] [Abstract][Full Text] [Related]
8. A tRNA suppressor mutation in human mitochondria.
El Meziane A; Lehtinen SK; Hance N; Nijtmans LG; Dunbar D; Holt IJ; Jacobs HT
Nat Genet; 1998 Apr; 18(4):350-3. PubMed ID: 9537417
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene.
Bidooki S; Jackson MJ; Johnson MA; Chrzanowska-Lightowlers ZM; Taylor RW; Venables G; Lightowlers RN; Turnbull DM; Bindoff LA
Neuromuscul Disord; 2004 Jul; 14(7):417-20. PubMed ID: 15210164
[TBL] [Abstract][Full Text] [Related]
11. A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss.
Cardaioli E; Da Pozzo P; Gallus GN; Malandrini A; Gambelli S; Gaudiano C; Malfatti E; Viscomi C; Zicari E; Berti G; Serni G; Dotti MT; Federico A
Neuromuscul Disord; 2007 Oct; 17(9-10):681-3. PubMed ID: 17614276
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNA(phe) gene.
Darin N; Kollberg G; Moslemi AR; Tulinius M; Holme E; Grönlund MA; Andersson S; Oldfors A
Neuromuscul Disord; 2006 Aug; 16(8):504-6. PubMed ID: 16806928
[TBL] [Abstract][Full Text] [Related]
13. Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome.
Ruppert V; Nolte D; Aschenbrenner T; Pankuweit S; Funck R; Maisch B
Biochem Biophys Res Commun; 2004 May; 318(2):535-43. PubMed ID: 15120634
[TBL] [Abstract][Full Text] [Related]
14. A novel mutation in the mitochondrial tRNA for tryptophan causing a late-onset mitochondrial encephalomyopathy.
Sanaker PS; Nakkestad HL; Downham E; Bindoff LA
Acta Neurol Scand; 2010 Feb; 121(2):109-13. PubMed ID: 19744136
[TBL] [Abstract][Full Text] [Related]
15. A mitochondrial tRNA anticodon swap associated with a muscle disease.
Moraes CT; Ciacci F; Bonilla E; Ionasescu V; Schon EA; DiMauro S
Nat Genet; 1993 Jul; 4(3):284-8. PubMed ID: 7689388
[TBL] [Abstract][Full Text] [Related]
16. A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathy.
Maeso E; Rueda A; Jiménez S; Del Hoyo P; Martín R; Cabello A; Mendoza LM; Arenas J; Campos Y
Neuromuscul Disord; 2007 May; 17(5):415-8. PubMed ID: 17363246
[TBL] [Abstract][Full Text] [Related]
17. The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations.
Marin-Garcia J; Goldenthal MJ; Ananthakrishnan R; Pierpont ME
J Card Fail; 2000 Dec; 6(4):321-9. PubMed ID: 11145757
[TBL] [Abstract][Full Text] [Related]
18. Novel mitochondrial tRNA Leu(CUN) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype.
Filosto M; Tonin P; Scarpelli M; Savio C; Greco F; Mancuso M; Vattemi G; Govoni V; Rizzuto N; Tupler R; Tomelleri G
Neuromuscul Disord; 2008 Mar; 18(3):204-9. PubMed ID: 18343111
[TBL] [Abstract][Full Text] [Related]
19. A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intolerance.
Mayr JA; Moslemi AR; Förster H; Kamper A; Idriceanu C; Muss W; Huemer M; Oldfors A; Sperl W
Neuromuscul Disord; 2006 Dec; 16(12):874-7. PubMed ID: 17056256
[TBL] [Abstract][Full Text] [Related]
20. A novel mitochondrial tRNA(Phe) mutation inhibiting anticodon stem formation associated with a muscle disease.
Kleinle S; Schneider V; Moosmann P; Brandner S; Krähenbühl S; Liechti-Gallati S
Biochem Biophys Res Commun; 1998 Jun; 247(1):112-5. PubMed ID: 9636664
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
