BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 25972744)

  • 1. Screening of mitochondrial mutations and insertion-deletion polymorphism in gestational diabetes mellitus in the Asian Indian population.
    Khan IA; Shaik NA; Pasupuleti N; Chava S; Jahan P; Hasan Q; Rao P
    Saudi J Biol Sci; 2015 May; 22(3):243-8. PubMed ID: 25972744
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Screening of mitochondrial mutations in Saudi women diagnosed with gestational diabetes mellitus: A non-replicative case-control study.
    Alharbi KK; Alsaikhan AS; Alshammary AF; Al-Hakeem MM; Ali Khan I
    Saudi J Biol Sci; 2022 Jan; 29(1):360-365. PubMed ID: 35002430
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. High prevalence of the COII/tRNA(Lys) intergenic 9-bp deletion in mitochondrial DNA of Taiwanese patients with MELAS or MERRF syndrome.
    Liu CS; Cheng WL; Chen YY; Ma YS; Pang CY; Wei YH
    Ann N Y Acad Sci; 2005 May; 1042():82-7. PubMed ID: 15965049
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Infantile encephalopathy associated with the MELAS A3243G mutation. Case report].
    Guevara-Campos J; Gonzalez-Guevara L; Parada Y; Urbáez-Cano J
    Invest Clin; 2007 Jun; 48(2):243-8. PubMed ID: 17598646
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autopsied case with MERRF/MELAS overlap syndrome accompanied by stroke-like episodes localized to the precentral gyrus.
    Miyahara H; Matsumoto S; Mokuno K; Dei R; Akagi A; Mimuro M; Iwasaki Y; Yoshida M
    Neuropathology; 2019 Jun; 39(3):212-217. PubMed ID: 30972844
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Histochemical and molecular genetic study of MELAS and MERRF in Korean patients.
    Kim DS; Jung DS; Park KH; Kim IJ; Kim CM; Lee WH; Rho SK
    J Korean Med Sci; 2002 Feb; 17(1):103-12. PubMed ID: 11850598
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Development of a DNA biochip for detection of known mtDNA mutations associated with MELAS and MERRF syndromes.].
    Chen G; Li W; DU WD; Cao HM; Tang HY; Tang XF; Sun ZW; Zhao H; Jin QH; Zhao JL; Zhang XJ
    Yi Chuan; 2008 Oct; 30(10):1279-86. PubMed ID: 18930887
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations.
    James AM; Wei YH; Pang CY; Murphy MP
    Biochem J; 1996 Sep; 318 ( Pt 2)(Pt 2):401-7. PubMed ID: 8809026
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990-2001.
    Marotta R; Chin J; Quigley A; Katsabanis S; Kapsa R; Byrne E; Collins S
    Intern Med J; 2004; 34(1-2):10-9. PubMed ID: 14748908
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation.
    Yasukawa T; Suzuki T; Ishii N; Ueda T; Ohta S; Watanabe K
    FEBS Lett; 2000 Feb; 467(2-3):175-8. PubMed ID: 10675533
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome.
    Vastagh I; Gál A; Reményi V; Semjén J; Lukács T; Valikovics A; Molnár MJ
    Ideggyogy Sz; 2011 Nov; 64(11-12):399-403. PubMed ID: 22611618
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Search for differences in post-transcriptional modification patterns of mitochondrial DNA-encoded wild-type and mutant human tRNALys and tRNALeu(UUR).
    Helm M; Florentz C; Chomyn A; Attardi G
    Nucleic Acids Res; 1999 Feb; 27(3):756-63. PubMed ID: 9889270
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.
    Chomyn A; Enriquez JA; Micol V; Fernandez-Silva P; Attardi G
    J Biol Chem; 2000 Jun; 275(25):19198-209. PubMed ID: 10858457
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.