168 related articles for article (PubMed ID: 9341162)
1. Pathophysiology of the MELAS 3243 transition mutation.
Flierl A; Reichmann H; Seibel P
J Biol Chem; 1997 Oct; 272(43):27189-96. PubMed ID: 9341162
[TBL] [Abstract][Full Text] [Related]
2. The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.
Chomyn A; Enriquez JA; Micol V; Fernandez-Silva P; Attardi G
J Biol Chem; 2000 Jun; 275(25):19198-209. PubMed ID: 10858457
[TBL] [Abstract][Full Text] [Related]
3. Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.
King MP; Koga Y; Davidson M; Schon EA
Mol Cell Biol; 1992 Feb; 12(2):480-90. PubMed ID: 1732728
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetes.
Li R; Guan MX
Mol Cell Biol; 2010 May; 30(9):2147-54. PubMed ID: 20194621
[TBL] [Abstract][Full Text] [Related]
6. Functional mitochondrial heterogeneity in heteroplasmic cells carrying the mitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes).
Bakker A; Barthélémy C; Frachon P; Chateau D; Sternberg D; Mazat JP; Lombès A
Pediatr Res; 2000 Aug; 48(2):143-50. PubMed ID: 10926287
[TBL] [Abstract][Full Text] [Related]
7. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.
Fabrizi GM; Cardaioli E; Grieco GS; Cavallaro T; Malandrini A; Manneschi L; Dotti MT; Federico A; Guazzi G
J Neurol Neurosurg Psychiatry; 1996 Jul; 61(1):47-51. PubMed ID: 8676159
[TBL] [Abstract][Full Text] [Related]
8. Isolated cytochrome c oxidase deficiency as a cause of MELAS.
Rossmanith W; Freilinger M; Roka J; Raffelsberger T; Moser-Thier K; Prayer D; Bernert G; Bittner RE
J Med Genet; 2008 Feb; 45(2):117-21. PubMed ID: 18245391
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.
Moraes CT; Ricci E; Bonilla E; DiMauro S; Schon EA
Am J Hum Genet; 1992 May; 50(5):934-49. PubMed ID: 1315123
[TBL] [Abstract][Full Text] [Related]
11. An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.
Ravn K; Wibrand F; Hansen FJ; Horn N; Rosenberg T; Schwartz M
Eur J Hum Genet; 2001 Oct; 9(10):805-9. PubMed ID: 11781695
[TBL] [Abstract][Full Text] [Related]
12. The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2.
Sasarman F; Antonicka H; Shoubridge EA
Hum Mol Genet; 2008 Dec; 17(23):3697-707. PubMed ID: 18753147
[TBL] [Abstract][Full Text] [Related]
13. The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.
Hammans SR; Sweeney MG; Hanna MG; Brockington M; Morgan-Hughes JA; Harding AE
Brain; 1995 Jun; 118 ( Pt 3)():721-34. PubMed ID: 7600089
[TBL] [Abstract][Full Text] [Related]
14. Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations.
James AM; Wei YH; Pang CY; Murphy MP
Biochem J; 1996 Sep; 318 ( Pt 2)(Pt 2):401-7. PubMed ID: 8809026
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS.
Koga Y; Davidson M; Schon EA; King MP
Nucleic Acids Res; 1993 Feb; 21(3):657-62. PubMed ID: 7680123
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNA(Leu(UUR)) gene.
Koga Y; Davidson M; Schon EA; King MP
Muscle Nerve Suppl; 1995; 3():S119-23. PubMed ID: 7603512
[TBL] [Abstract][Full Text] [Related]
19. Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).
Suzuki S; Hinokio Y; Hirai S; Onoda M; Matsumoto M; Ohtomo M; Kawasaki H; Satoh Y; Akai H; Abe K
Diabetologia; 1994 Aug; 37(8):818-25. PubMed ID: 7988784
[TBL] [Abstract][Full Text] [Related]
20. A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene.
Manfredi G; Schon EA; Moraes CT; Bonilla E; Berry GT; Sladky JT; DiMauro S
Neuromuscul Disord; 1995 Sep; 5(5):391-8. PubMed ID: 7496173
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
