BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

242 related articles for article (PubMed ID: 1370535)

  • 41. 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]  

  • 42. Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromes.
    Zupanc ML; Moraes CT; Shanske S; Langman CB; Ciafaloni E; DiMauro S
    Ann Neurol; 1991 Jun; 29(6):680-3. PubMed ID: 1892371
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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]  

  • 44. Increased mitochondrial processing intermediates associated with three tRNA(Leu(UUR)) gene mutations.
    Koga A; Koga Y; Akita Y; Fukiyama R; Ueki I; Yatsuga S; Matsuishi T
    Neuromuscul Disord; 2003 Mar; 13(3):259-62. PubMed ID: 12609508
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. 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]  

  • 47. Mitochondrial encephalomyopathy associated with a novel mutation in the mitochondrial tRNA(leu)(UUR) gene (A3243T).
    Shaag A; Saada A; Steinberg A; Navon P; Elpeleg ON
    Biochem Biophys Res Commun; 1997 Apr; 233(3):637-9. PubMed ID: 9168904
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Acute pancreatitis in an infant with lactic acidosis and a mutation at nucleotide 3243 in the mitochondrial DNA tRNALeu(UUR) gene.
    Kishnani PS; Van Hove JL; Shoffner JS; Kaufman A; Bossen EH; Kahler SG
    Eur J Pediatr; 1996 Oct; 155(10):898-903. PubMed ID: 8891562
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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]  

  • 50. MELAS syndrome with mitochondrial tRNA(Leu)(UUR) mutation: correlation of clinical state, nerve conduction, and muscle 31P magnetic resonance spectroscopy during treatment with nicotinamide and riboflavin.
    Penn AM; Lee JW; Thuillier P; Wagner M; Maclure KM; Menard MR; Hall LD; Kennaway NG
    Neurology; 1992 Nov; 42(11):2147-52. PubMed ID: 1436526
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. MELAS without ragged red fibers or lactic acidosis diagnosed by mitochondrial DNA testing.
    Ujike H; Wakagi T; Kohira I; Kuroda S; Otsuki S; Sato T
    Jpn J Psychiatry Neurol; 1993 Sep; 47(3):637-41. PubMed ID: 8301880
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tanaka M; Ino H; Ohno K; Ohbayashi T; Ikebe S; Sano T; Ichiki T; Kobayashi M; Wada Y; Ozawa T
    Biochem Biophys Res Commun; 1991 Jan; 174(2):861-8. PubMed ID: 1899574
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. 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]  

  • 56. 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]  

  • 57. 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]  

  • 58. [A case of mitochondrial encephalomyopathy--Mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS)].
    Ihara Y; Namba R; Demiya M; Matsumoto T; Shirabe T
    Rinsho Shinkeigaku; 1987 Aug; 27(8):969-75. PubMed ID: 3690923
    [No Abstract]   [Full Text] [Related]  

  • 59. [Mitochondrial encephalomyopathy--MERRF and MELAS are clinicopathologically distinctive entities].
    Tanaka K; Nishizawa M; Miyatake T; Takeda S; Ohama E
    Rinsho Shinkeigaku; 1987 Nov; 27(11):1468-73. PubMed ID: 3129227
    [No Abstract]   [Full Text] [Related]  

  • 60. [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]  

    [Previous]   [Next]    [New Search]
    of 13.