729 related articles for article (PubMed ID: 10645055)
21. 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]
22. [Identification of an ideal noninvasive method to detect A3243G gene mutation in MELAS syndrome].
Ma YN; Fang F; Yang YL; Zhang Y; Wang ST; Xu YF; Pei P; Yuan Y; Bu DF; Qi Y
Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3250-3. PubMed ID: 19159547
[TBL] [Abstract][Full Text] [Related]
23. Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese family.
Lu J; Wang D; Li R; Li W; Ji J; Zhao J; Ye W; Yang L; Qian Y; Zhu Y; Guan MX
Biochem Biophys Res Commun; 2006 Sep; 348(1):115-9. PubMed ID: 16876129
[TBL] [Abstract][Full Text] [Related]
24. Mitochondrial tRNALeu(UUR) mutation in a patient with steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis.
Löwik MM; Hol FA; Steenbergen EJ; Wetzels JF; van den Heuvel LP
Nephrol Dial Transplant; 2005 Feb; 20(2):336-41. PubMed ID: 15585516
[TBL] [Abstract][Full Text] [Related]
25. [Mitochondrial encephalomyopathy associated with parkinsonism and a point mutation in the mitochondrial tRNA(Leu)(UUR)) gene].
Hara K; Yamamoto M; Anegawa T; Sakuta R; Nakamura M
Rinsho Shinkeigaku; 1994 Apr; 34(4):361-5. PubMed ID: 8026131
[TBL] [Abstract][Full Text] [Related]
26. [Comparison of clinical pictures of mitochondrial encephalomyopathy with tRNA(Leu(UUR)) mutation in 3243 with that in 3254].
Mitsuoka T; Kawarai T; Watanabe C; Katayama S; Nakamura S
No To Shinkei; 1998 Dec; 50(12):1089-92. PubMed ID: 9989353
[TBL] [Abstract][Full Text] [Related]
27. Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation.
Okhuijsen-Kroes EJ; Trijbels JM; Sengers RC; Mariman E; van den Heuvel LP; Wendel U; Koch G; Smeitink JA
Neuropediatrics; 2001 Aug; 32(4):183-90. PubMed ID: 11571698
[TBL] [Abstract][Full Text] [Related]
28. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
Nakamura M; Yabe I; Sudo A; Hosoki K; Yaguchi H; Saitoh S; Sasaki H
J Med Genet; 2010 Oct; 47(10):659-64. PubMed ID: 20610441
[TBL] [Abstract][Full Text] [Related]
29. Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes.
Kawakami Y; Sakuta R; Hashimoto K; Fujino O; Fujita T; Hida M; Horai S; Goto Y; Nonaka I
Ann Neurol; 1994 Mar; 35(3):370-3. PubMed ID: 8122892
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome.
Li JY; Hsieh RH; Peng NJ; Lai PH; Lee CF; Lo YK; Wei YH
J Formos Med Assoc; 2007 Jul; 106(7):528-36. PubMed ID: 17660142
[TBL] [Abstract][Full Text] [Related]
32. [Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) with chronic renal failure: report of mother-child cases].
Ihara M; Tanaka H; Yashiro M; Nishimura Y
Rinsho Shinkeigaku; 1996 Sep; 36(9):1069-73. PubMed ID: 8976130
[TBL] [Abstract][Full Text] [Related]
33. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.
Melone MA; Tessa A; Petrini S; Lus G; Sampaolo S; di Fede G; Santorelli FM; Cotrufo R
Arch Neurol; 2004 Feb; 61(2):269-72. PubMed ID: 14967777
[TBL] [Abstract][Full Text] [Related]
34. Mitochondrial DNA and RNA processing in MELAS.
Kaufmann P; Koga Y; Shanske S; Hirano M; DiMauro S; King MP; Schon EA
Ann Neurol; 1996 Aug; 40(2):172-80. PubMed ID: 8773598
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. 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]
38. [Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA].
Coelho-Miranda L; Playan A; Artuch R; Vilaseca MA; Colomer J; Briones P; Coll-Cantí J; Conill J; Sans A; López de Munain A; Solano A; Alcaine MJ; Montoya J; Pineda M
Rev Neurol; 2000 Nov 1-15; 31(9):804-11. PubMed ID: 11127079
[TBL] [Abstract][Full Text] [Related]
39. Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation.
Degoul F; Diry M; Pou-Serradell A; Lloreta J; Marsac C
Ann Neurol; 1994 Mar; 35(3):365-70. PubMed ID: 8122891
[TBL] [Abstract][Full Text] [Related]
40. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.
Liu CS; Cheng WL; Lee CF; Ma YS; Lin CY; Huang CC; Wei YH
Acta Neurol Scand; 2006 May; 113(5):334-41. PubMed ID: 16629770
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
