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.
101 related articles for article (PubMed ID: 22037425)
1. Hypersensitivity of A8344G MERRF mutated cybrid cells to staurosporine-induced cell death is mediated by calcium-dependent activation of calpains. Rommelaere G; Michel S; Malaisse J; Charlier S; Arnould T; Renard P Int J Biochem Cell Biol; 2012 Jan; 44(1):139-49. PubMed ID: 22037425 [TBL] [Abstract][Full Text] [Related]
2. The protective roles of phosphorylated heat shock protein 27 in human cells harboring myoclonus epilepsy with ragged-red fibers A8344G mtDNA mutation. Chen HF; Chen CY; Lin TH; Huang ZW; Chi TH; Ma YS; Wu SB; Wei YH; Hsieh M FEBS J; 2012 Aug; 279(16):2987-3001. PubMed ID: 22742457 [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 heat shock protein 27 expression and altered autophagy in human cells harboring A8344G mitochondrial DNA mutation. Chen CY; Chen HF; Gi SJ; Chi TH; Cheng CK; Hsu CF; Ma YS; Wei YH; Liu CS; Hsieh M Mitochondrion; 2011 Sep; 11(5):739-49. PubMed ID: 21679777 [TBL] [Abstract][Full Text] [Related]
5. Fibrous dysplasia in a child with mitochondrial A8344G mutation. Chen ST; Fan PC; Hwu WL; Wu MH J Child Neurol; 2008 Dec; 23(12):1447-50. PubMed ID: 18772492 [TBL] [Abstract][Full Text] [Related]
6. Mitochondrial DNA mutation and depletion increase the susceptibility of human cells to apoptosis. Liu CY; Lee CF; Hong CH; Wei YH Ann N Y Acad Sci; 2004 Apr; 1011():133-45. PubMed ID: 15126291 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Loss of mutant mitochondrial DNA harboring the MELAS A3243G mutation in human cybrid cells after cell-cell fusion with normal tissue-derived fibroblast cells. Yano T; Tanaka M; Fukuda N; Ueda T; Nagase H Int J Mol Med; 2010 Jan; 25(1):153-8. PubMed ID: 19956914 [TBL] [Abstract][Full Text] [Related]
9. Functional recovery of human cells harbouring the mitochondrial DNA mutation MERRF A8344G via peptide-mediated mitochondrial delivery. Chang JC; Liu KH; Li YC; Kou SJ; Wei YH; Chuang CS; Hsieh M; Liu CS Neurosignals; 2013; 21(3-4):160-73. PubMed ID: 23006856 [TBL] [Abstract][Full Text] [Related]
10. Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells. Kolesnikova OA; Entelis NS; Jacquin-Becker C; Goltzene F; Chrzanowska-Lightowlers ZM; Lightowlers RN; Martin RP; Tarassov I Hum Mol Genet; 2004 Oct; 13(20):2519-34. PubMed ID: 15317755 [TBL] [Abstract][Full Text] [Related]
11. Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres ('MERRF') at position 8344 nt. Antonická H; Floryk D; Klement P; Stratilová L; Hermanská J; Houstková H; Kalous M; Drahota Z; Zeman J; Houstek J Biochem J; 1999 Sep; 342 Pt 3(Pt 3):537-44. PubMed ID: 10477264 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. mtDNA mutations confer cellular sensitivity to oxidant stress that is partially rescued by calcium depletion and cyclosporin A. Wong A; Cortopassi G Biochem Biophys Res Commun; 1997 Oct; 239(1):139-45. PubMed ID: 9345284 [TBL] [Abstract][Full Text] [Related]
16. 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]
18. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype. Melone MA; Tessa A; Petrini S; Lus G; Sampaolo S; di Fede G; Santorelli FM; Cotrufo R Arch Neurol; 2004 Feb; 61(2):269-72. PubMed ID: 14967777 [TBL] [Abstract][Full Text] [Related]
19. [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]
20. [Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome]. Stratilová L; Zeman J; Houst'ková H; Hansíková H; Konrádová V; Hůlková H; Elleder M; Růzicka E; Tyl D; Hrubá E; Houstĕk J Cas Lek Cesk; 1999 Jun; 138(13):401-5. PubMed ID: 10566210 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]