These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 9798744)

  • 1. MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring.
    Chinnery PF; Howell N; Lightowlers RN; Turnbull DM
    Brain; 1998 Oct; 121 ( Pt 10)():1889-94. PubMed ID: 9798744
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes.
    Chinnery PF; Howell N; Lightowlers RN; Turnbull DM
    Brain; 1997 Oct; 120 ( Pt 10)():1713-21. PubMed ID: 9365365
    [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. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.
    Fabrizi GM; Cardaioli E; Grieco GS; Cavallaro T; Malandrini A; Manneschi L; Dotti MT; Federico A; Guazzi G
    J Neurol Neurosurg Psychiatry; 1996 Jul; 61(1):47-51. PubMed ID: 8676159
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.
    Campos Y; Martin MA; Lorenzo G; Aparicio M; Cabello A; Arenas J
    Muscle Nerve; 1996 Feb; 19(2):187-90. PubMed ID: 8559168
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.
    Zeviani M; Muntoni F; Savarese N; Serra G; Tiranti V; Carrara F; Mariotti C; DiDonato S
    Eur J Hum Genet; 1993; 1(1):80-7. PubMed ID: 8069654
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. 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]  

  • 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. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.
    Liu CS; Cheng WL; Lee CF; Ma YS; Lin CY; Huang CC; Wei YH
    Acta Neurol Scand; 2006 May; 113(5):334-41. PubMed ID: 16629770
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Inheritance and expression of mitochondrial DNA point mutations.
    Holme E; Tulinius MH; Larsson NG; Oldfors A
    Biochim Biophys Acta; 1995 May; 1271(1):249-52. PubMed ID: 7599216
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation.
    Mongini T; Doriguzzi C; Chiadò-Piat L; Silvestri G; Servidei S; Palmucci L
    Clin Neuropathol; 2002; 21(2):72-6. PubMed ID: 12005255
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of A3243G point mutation in mitochondrial DNA from 10 cases of MELAS.
    Wang Z; Liu S; Yang Y; Yuan Y; Wu L; Qi Y; Chen Q
    Chin Med J (Engl); 2002 Jul; 115(7):995-7. PubMed ID: 12150728
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical features of A3243G mitochondrial tRNA mutation.
    Chae JH; Hwang H; Lim BC; Cheong HI; Hwang YS; Kim KJ
    Brain Dev; 2004 Oct; 26(7):459-62. PubMed ID: 15351082
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial diseases.
    Nonaka I
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):622-32. PubMed ID: 1392136
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Classical MERRF phenotype associated with mitochondrial tRNA(Leu) (m.3243A>G) mutation.
    Brackmann F; Abicht A; Ahting U; Schröder R; Trollmann R
    Eur J Pediatr; 2012 May; 171(5):859-62. PubMed ID: 22270878
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cerebral lactic acidosis correlates with neurological impairment in MELAS.
    Kaufmann P; Shungu DC; Sano MC; Jhung S; Engelstad K; Mitsis E; Mao X; Shanske S; Hirano M; DiMauro S; De Vivo DC
    Neurology; 2004 Apr; 62(8):1297-302. PubMed ID: 15111665
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.