BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 9511882)

  • 1. Recent developments in the molecular genetics of mitochondrial disorders.
    Graeber MB; Müller U
    J Neurol Sci; 1998 Jan; 153(2):251-63. PubMed ID: 9511882
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The expanding clinical spectrum of mitochondrial diseases.
    De Vivo DC
    Brain Dev; 1993; 15(1):1-22. PubMed ID: 8338207
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial biogenesis: pharmacological approaches.
    Valero T
    Curr Pharm Des; 2014; 20(35):5507-9. PubMed ID: 24606795
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. [Eye diseases in mitochondrial encephalomyopathies].
    Mojon D
    Ther Umsch; 2001 Jan; 58(1):49-55. PubMed ID: 11217487
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Movement disorders in mitochondrial diseases.
    Tranchant C; Anheim M
    Rev Neurol (Paris); 2016; 172(8-9):524-529. PubMed ID: 27476418
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial DNA alterations and genetic diseases: a review.
    Lestienne P; Bataillé N
    Biomed Pharmacother; 1994; 48(5-6):199-214. PubMed ID: 7999980
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation.
    Isashiki Y; Nakagawa M; Ohba N; Kamimura K; Sakoda Y; Higuchi I; Izumo S; Osame M
    Acta Ophthalmol Scand; 1998 Feb; 76(1):6-13. PubMed ID: 9541428
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human mitochondrial diseases: answering questions and questioning answers.
    Howell N
    Int Rev Cytol; 1999; 186():49-116. PubMed ID: 9770297
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Analysis of common mitochondrial DNA mutations by allele-specific oligonucleotide and Southern blot hybridization.
    Tang S; Halberg MC; Floyd KC; Wang J
    Methods Mol Biol; 2012; 837():259-79. PubMed ID: 22215554
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 99mTc-HMPAO brain single photon emission computerized tomography in mitochondrial encephalomyopathies.
    Yen TC; Yeh SH
    Zhonghua Yi Xue Za Zhi (Taipei); 1995 Nov; 56(5):287-91. PubMed ID: 8605641
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial Retinopathies.
    Zeviani M; Carelli V
    Int J Mol Sci; 2021 Dec; 23(1):. PubMed ID: 35008635
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Accurate detection and quantitation of heteroplasmic mitochondrial point mutations by pyrosequencing.
    White HE; Durston VJ; Seller A; Fratter C; Harvey JF; Cross NC
    Genet Test; 2005; 9(3):190-9. PubMed ID: 16225398
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.