231 related articles for article (PubMed ID: 8111377)
21. Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.
Campos Y; Martin MA; Lorenzo G; Aparicio M; Cabello A; Arenas J
Muscle Nerve; 1996 Feb; 19(2):187-90. PubMed ID: 8559168
[TBL] [Abstract][Full Text] [Related]
22. An 80-year-old mitochondrial disease patient with A3243G tRNA(Leu(UUR)) gene presenting cardiac dysfunction as the main symptom.
Higashikata T; Koyama J; Shimada H; Yazaki M; Owa M; Ikeda S
Intern Med; 2001 May; 40(5):405-8. PubMed ID: 11393411
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA(Leu)(UUR) 3254C-to-G.
Kawarai T; Kawakami H; Kozuka K; Izumi Y; Matsuyama Z; Watanabe C; Kohriyama T; Nakamura S
Neurology; 1997 Aug; 49(2):598-600. PubMed ID: 9270605
[TBL] [Abstract][Full Text] [Related]
25. Mitochondrial genetic analysis in a Chinese family suffering from both mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes and diabetes.
Li W; Zhang W; Li F; Wang C
Int J Clin Exp Pathol; 2015; 8(6):7022-7. PubMed ID: 26261593
[TBL] [Abstract][Full Text] [Related]
26. A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes.
de Coo IF; Sistermans EA; de Wijs IJ; Catsman-Berrevoets C; Busch HF; Scholte HR; de Klerk JB; van Oost BA; Smeets HJ
Neurology; 1998 Jan; 50(1):293-5. PubMed ID: 9443499
[TBL] [Abstract][Full Text] [Related]
27. Organ distribution of mutant mitochondrial tRNA(leu(UUR)) gene in a MELAS patient.
Hamazaki S; Koshiba M; Sugiyama T
Acta Pathol Jpn; 1993 Apr; 43(4):187-91. PubMed ID: 8493868
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. [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]
30. MELAS phenotype associated with m.3302A>G mutation in mitochondrial tRNA(Leu(UUR)) gene.
Goto M; Komaki H; Saito T; Saito Y; Nakagawa E; Sugai K; Sasaki M; Nishino I; Goto Y
Brain Dev; 2014 Feb; 36(2):180-2. PubMed ID: 23582502
[TBL] [Abstract][Full Text] [Related]
31. Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene.
Kishimoto M; Hashiramoto M; Araki S; Ishida Y; Kazumi T; Kanda E; Kasuga M
Diabetologia; 1995 Feb; 38(2):193-200. PubMed ID: 7713314
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family.
Huang CC; Chen RS; Chen CM; Wang HS; Lee CC; Pang CY; Hsu HS; Lee HC; Wei YH
J Neurol Neurosurg Psychiatry; 1994 May; 57(5):586-9. PubMed ID: 8201329
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. 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]
36. 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]
37. Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) gene.
Shoffner JM; Bialer MG; Pavlakis SG; Lott M; Kaufman A; Dixon J; Teichberg S; Wallace DC
Neurology; 1995 Feb; 45(2):286-92. PubMed ID: 7854527
[TBL] [Abstract][Full Text] [Related]
38. Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients.
Börner GV; Zeviani M; Tiranti V; Carrara F; Hoffmann S; Gerbitz KD; Lochmüller H; Pongratz D; Klopstock T; Melberg A; Holme E; Pääbo S
Hum Mol Genet; 2000 Mar; 9(4):467-75. PubMed ID: 10699170
[TBL] [Abstract][Full Text] [Related]
39. Early onset cardiomyopathy associated with the mitochondrial tRNALeu((UUR)) 3271T>C MELAS mutation.
Brisca G; Fiorillo C; Nesti C; Trucco F; Derchi M; Andaloro A; Assereto S; Morcaldi G; Pedemonte M; Minetti C; Santorelli FM; Bruno C
Biochem Biophys Res Commun; 2015 Mar; 458(3):601-604. PubMed ID: 25680467
[TBL] [Abstract][Full Text] [Related]
40. Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.
Sternberg D; Chatzoglou E; Laforêt P; Fayet G; Jardel C; Blondy P; Fardeau M; Amselem S; Eymard B; Lombès A
Brain; 2001 May; 124(Pt 5):984-94. PubMed ID: 11335700
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
