BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

223 related articles for article (PubMed ID: 7477061)

  • 1. 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]  

  • 2. 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]  

  • 3. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
    Ma L; Wang H; Chen J; Jin W; Liu L; Ban B; Shen J; Hua Z; Chai J
    Chin Med J (Engl); 2000 Feb; 113(2):111-6. PubMed ID: 11775531
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rapid quantification of the heteroplasmy of mutant mitochondrial DNAs in Leber's hereditary optic neuropathy using the Invader technology.
    Mashima Y; Nagano M; Funayama T; Zhang Q; Egashira T; Kudho J; Shimizu N; Oguchi Y
    Clin Biochem; 2004 Apr; 37(4):268-76. PubMed ID: 15003728
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [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]  

  • 7. Sequencing and quantitative assessment of mutant and wild-type mitochondrial DNA in paraffin sections from cases of MELAS.
    Love S; Nicoll JA; Kinrade E
    J Pathol; 1993 May; 170(1):9-14. PubMed ID: 8326463
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.
    Goto Y; Nonaka I; Horai S
    Nature; 1990 Dec; 348(6302):651-3. PubMed ID: 2102678
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.
    Ueki I; Koga Y; Povalko N; Akita Y; Nishioka J; Yatsuga S; Fukiyama R; Matsuishi T
    Mitochondrion; 2006 Feb; 6(1):29-36. PubMed ID: 16337222
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
    Seibel P; Flierl A; Kottlors M; Reichmann H
    Biochem Biophys Res Commun; 1994 Apr; 200(2):938-42. PubMed ID: 8179630
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial DNA 3243A>G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia.
    Munakata K; Iwamoto K; Bundo M; Kato T
    Biol Psychiatry; 2005 Mar; 57(5):525-32. PubMed ID: 15737668
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases.
    Mkaouar-Rebai E; Tlili A; Masmoudi S; Belguith N; Charfeddine I; Mnif M; Triki C; Fakhfakh F
    Biochem Biophys Res Commun; 2007 Apr; 355(4):1031-7. PubMed ID: 17336924
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.