BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 21609548)

  • 1. [Screening of mitochondrial deoxyribonucleic acid 3271T > C, 8356T > C, 9176T > C/G and 13513G > A mutations in mitochondrial encephalomyopathies].
    Xu JB; Ma YN; Pan H; Zheng XF; Zhang Y; Wang ST; Bu DF; Qi Y
    Zhonghua Yi Xue Za Zhi; 2011 Apr; 91(14):969-72. PubMed ID: 21609548
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes / myoclonus epilepsy with ragged-red fibers /Leigh overlap syndrome caused by mitochondrial DNA 8344A>G mutation].
    Hou Y; Zhao XT; Xie ZY; Yuan Y; Wang ZX
    Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Oct; 52(5):851-855. PubMed ID: 33047718
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Point mutations of muscle mitochondrial DNA from patients with mitochondrial encephalomyopathies.
    Song D; Zhang Y; Shi J; Lü Q; Chen J; Zhang H; Zhang W; Wang H; Cai Q
    Chin Med J (Engl); 2001 Dec; 114(12):1273-5. PubMed ID: 11793851
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Screening of common mitochondrial mutations in Chinese patients with mitochondrial encephalomyopathies.
    Qi Y; Zhang Y; Wang Z; Yang Y; Yuan Y; Niu S; Pei P; Wang S; Ma Y; Bu D; Zou L; Fang F; Xiao J; Sun F; Zhang Y; Wu Y; Wang S; Xiong H; Wu X
    Mitochondrion; 2007; 7(1-2):147-50. PubMed ID: 17276742
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.
    Campos Y; Garcia-Silva T; Barrionuevo CR; Cabello A; Muley R; Arenas J
    Pediatr Neurol; 1995 Jul; 13(1):69-72. PubMed ID: 7575854
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Mitochondrial DNA mutation analysis in 97 Chinese patients with mitochondrial cephalomyopathy].
    Wang ZX; Luan XH; Zhang Y; Yang YL; Qi Y; Bu DF; Yuan Y
    Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3254-6. PubMed ID: 19159548
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Screening of common point-mutations and discovery of new T14727C change in mitochondrial genome of Vietnamese encephalomyopathy patients.
    Truong HT; Nguyen VA; Nguyen LV; Pham VA; Phan TN
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016; 27(1):441-8. PubMed ID: 24708131
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Screening for mitochondrial DNA (mtDNA) point mutations using nonradioactive single strand conformation polymorphism (SSCP) analysis.
    Jaksch M; Gerbitz KD; Kilger C
    Clin Biochem; 1995 Oct; 28(5):503-9. PubMed ID: 8582049
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies.
    Jean-Francois MJ; Lertrit P; Berkovic SF; Crimmins D; Morris J; Marzuki S; Byrne E
    Aust N Z J Med; 1994 Apr; 24(2):188-93. PubMed ID: 8042948
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy.
    Houshmand M; Larsson NG; Holme E; Oldfors A; Tulinius MH; Andersen O
    Biochim Biophys Acta; 1994 Apr; 1226(1):49-55. PubMed ID: 8155739
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan.
    Pang CY; Huang CC; Yen MY; Wang EK; Kao KP; Chen SS; Wei YH
    J Formos Med Assoc; 1999 May; 98(5):326-34. PubMed ID: 10420700
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation].
    Zhang Y; Wang ZX; Niu SL; Xu YF; Pei P; Yuan Y; Yang YL; Qi Y
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb; 27(1):77-80. PubMed ID: 15782498
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The study of point mutation of muscular mitochondrial DNA from patients with mitochondrial encephalomyopathies].
    Song D; Zhang Y; Shi J
    Zhonghua Yi Xue Za Zhi; 2001 Jun; 81(11):659-61. PubMed ID: 11798943
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Defects of mitochondrial DNA.
    Zeviani M; Antozzi C
    Brain Pathol; 1992 Apr; 2(2):121-32. PubMed ID: 1341953
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinical characterization of diabetes mellitus in the families with mitochondrial encephalomyopathies].
    Suzuki S
    Nihon Rinsho; 1994 Oct; 52(10):2606-10. PubMed ID: 7527090
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies.
    Huang CC; Kuo HC; Chu CC; Liou CW; Ma YS; Wei YH
    J Biomed Sci; 2002; 9(6 Pt 1):527-33. PubMed ID: 12372990
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The 8,344 mutation in mitochondrial DNA: a comparison between the proportion of mutant DNA and clinico-pathologic findings.
    Ozawa M; Goto Y; Sakuta R; Tanno Y; Tsuji S; Nonaka I
    Neuromuscul Disord; 1995 Nov; 5(6):483-8. PubMed ID: 8580730
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Childhood mitochondrial encephalomyopathies: clinical course, diagnosis, neuroimaging findings, mtDNA mutations and outcome in six children.
    Lu J; Huang Y
    Ital J Pediatr; 2013 Sep; 39():60. PubMed ID: 24069936
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.