483 related articles for article (PubMed ID: 15870203)
1. 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]
2. Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
Yasukawa T; Suzuki T; Ueda T; Ohta S; Watanabe K
J Biol Chem; 2000 Feb; 275(6):4251-7. PubMed ID: 10660592
[TBL] [Abstract][Full Text] [Related]
3. Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease.
Kirino Y; Yasukawa T; Ohta S; Akira S; Ishihara K; Watanabe K; Suzuki T
Proc Natl Acad Sci U S A; 2004 Oct; 101(42):15070-5. PubMed ID: 15477592
[TBL] [Abstract][Full Text] [Related]
4. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
Goto Y
Nihon Rinsho; 1993 Sep; 51(9):2373-8. PubMed ID: 8411715
[TBL] [Abstract][Full Text] [Related]
5. Reduction of mitochondrial tRNALeu(UUR) aminoacylation by some MELAS-associated mutations.
Hao R; Yao YN; Zheng YG; Xu MG; Wang ED
FEBS Lett; 2004 Dec; 578(1-2):135-9. PubMed ID: 15581630
[TBL] [Abstract][Full Text] [Related]
6. The pathogenic A3243G mutation in human mitochondrial tRNALeu(UUR) decreases the efficiency of aminoacylation.
Park H; Davidson E; King MP
Biochemistry; 2003 Feb; 42(4):958-64. PubMed ID: 12549915
[TBL] [Abstract][Full Text] [Related]
7. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
Thajeb P; Lee HC; Pang CY; Jeng CM; Huang SF; Wei YH
Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan; 63(1):71-6. PubMed ID: 10645055
[TBL] [Abstract][Full Text] [Related]
8. A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
Sato W; Hayasaka K; Shoji Y; Takahashi T; Takada G; Saito M; Fukawa O; Wachi E
Biochem Mol Biol Int; 1994 Aug; 33(6):1055-61. PubMed ID: 7804130
[TBL] [Abstract][Full Text] [Related]
9. Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect.
Kirino Y; Yasukawa T; Marjavaara SK; Jacobs HT; Holt IJ; Watanabe K; Suzuki T
Hum Mol Genet; 2006 Mar; 15(6):897-904. PubMed ID: 16446307
[TBL] [Abstract][Full Text] [Related]
10. [Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2].
Delgado-Sánchez R; Zárate-Moysen A; Monsalvo-Reyes A; Herrero MD; Ruiz-Pesini E; López-Pérez M; Montoya J; Montiel-Sosa JF
Rev Neurol; 2007 Jan 1-15; 44(1):18-22. PubMed ID: 17199225
[TBL] [Abstract][Full Text] [Related]
11. Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region.
Tsukuda K; Suzuki Y; Kameoka K; Osawa N; Goto Y; Katagiri H; Asano T; Yazaki Y; Oka Y
Diabet Med; 1997 Dec; 14(12):1032-7. PubMed ID: 9455930
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy.
Goto Y; Tojo M; Tohyama J; Horai S; Nonaka I
Ann Neurol; 1992 Jun; 31(6):672-5. PubMed ID: 1514779
[TBL] [Abstract][Full Text] [Related]
14. Quantitation of heteroplasmy of mitochondrial tRNA(Leu(UUR)) gene using PCR-SSCP.
Tanno Y; Yoneda M; Tanaka K; Tanaka H; Yamazaki M; Nishizawa M; Wakabayashi K; Ohama E; Tsuji S
Muscle Nerve; 1995 Dec; 18(12):1390-7. PubMed ID: 7477061
[TBL] [Abstract][Full Text] [Related]
15. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
Tokunaga M; Mita S; Sakuta R; Nonaka I; Araki S
Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581
[TBL] [Abstract][Full Text] [Related]
16. Accumulation of somatic nucleotide substitutions in mitochondrial DNA associated with the 3243 A-to-G tRNA(leu)(UUR) mutation in encephalomyopathy and cardiomyopathy.
Kovalenko SA; Tanaka M; Yoneda M; Iakovlev AF; Ozawa T
Biochem Biophys Res Commun; 1996 May; 222(2):201-7. PubMed ID: 8670183
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.
Du W; Li W; Chen G; Cao H; Tang H; Tang X; Jin Q; Sun Z; Zhao H; Zhou W; He S; Lv Y; Zhao J; Zhang X
Biosens Bioelectron; 2009 Apr; 24(8):2371-6. PubMed ID: 19155171
[TBL] [Abstract][Full Text] [Related]
19. Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation.
Yasukawa T; Suzuki T; Ishii N; Ueda T; Ohta S; Watanabe K
FEBS Lett; 2000 Feb; 467(2-3):175-8. PubMed ID: 10675533
[TBL] [Abstract][Full Text] [Related]
20. Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease.
Yasukawa T; Suzuki T; Ishii N; Ohta S; Watanabe K
EMBO J; 2001 Sep; 20(17):4794-802. PubMed ID: 11532943
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]