186 related articles for article (PubMed ID: 24199594)
1. Treatment of human cells derived from MERRF syndrome by peptide-mediated mitochondrial delivery.
Chang JC; Liu KH; Chuang CS; Su HL; Wei YH; Kuo SJ; Liu CS
Cytotherapy; 2013 Dec; 15(12):1580-96. PubMed ID: 24199594
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Parkin-mediated mitophagy and autophagy flux disruption in cellular models of MERRF syndrome.
Villanueva-Paz M; Povea-Cabello S; Villalón-García I; Álvarez-Córdoba M; Suárez-Rivero JM; Talaverón-Rey M; Jackson S; Falcón-Moya R; Rodríguez-Moreno A; Sánchez-Alcázar JA
Biochim Biophys Acta Mol Basis Dis; 2020 Jun; 1866(6):165726. PubMed ID: 32061767
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Upregulation of matrix metalloproteinase 1 and disruption of mitochondrial network in skin fibroblasts of patients with MERRF syndrome.
Ma YS; Chen YC; Lu CY; Liu CY; Wei YH
Ann N Y Acad Sci; 2005 May; 1042():55-63. PubMed ID: 15965045
[TBL] [Abstract][Full Text] [Related]
6. Delivering healthy mitochondria for the therapy of mitochondrial diseases and beyond.
Liu CS; Chang JC; Kuo SJ; Liu KH; Lin TT; Cheng WL; Chuang SF
Int J Biochem Cell Biol; 2014 Aug; 53():141-6. PubMed ID: 24842105
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Mitochondrial DNA mutation-elicited oxidative stress, oxidative damage, and altered gene expression in cultured cells of patients with MERRF syndrome.
Wu SB; Ma YS; Wu YT; Chen YC; Wei YH
Mol Neurobiol; 2010 Jun; 41(2-3):256-66. PubMed ID: 20411357
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Recovery of MERRF fibroblasts and cybrids pathophysiology by coenzyme Q10.
De la Mata M; Garrido-Maraver J; Cotán D; Cordero MD; Oropesa-Ávila M; Izquierdo LG; De Miguel M; Lorite JB; Infante ER; Ybot P; Jackson S; Sánchez-Alcázar JA
Neurotherapeutics; 2012 Apr; 9(2):446-63. PubMed ID: 22354625
[TBL] [Abstract][Full Text] [Related]
11. Impaired ROS Scavenging System in Human Induced Pluripotent Stem Cells Generated from Patients with MERRF Syndrome.
Chou SJ; Tseng WL; Chen CT; Lai YF; Chien CS; Chang YL; Lee HC; Wei YH; Chiou SH
Sci Rep; 2016 Mar; 6():23661. PubMed ID: 27025901
[TBL] [Abstract][Full Text] [Related]
12. The Bacterial Protein CNF1 as a Potential Therapeutic Strategy against Mitochondrial Diseases: A Pilot Study.
Fabbri A; Travaglione S; Maroccia Z; Guidotti M; Pierri CL; Primiano G; Servidei S; Loizzo S; Fiorentini C
Int J Mol Sci; 2018 Jun; 19(7):. PubMed ID: 29933571
[TBL] [Abstract][Full Text] [Related]
13. Disruption of the human COQ5-containing protein complex is associated with diminished coenzyme Q10 levels under two different conditions of mitochondrial energy deficiency.
Yen HC; Liu YC; Kan CC; Wei HJ; Lee SH; Wei YH; Feng YH; Chen CW; Huang CC
Biochim Biophys Acta; 2016 Sep; 1860(9):1864-76. PubMed ID: 27155576
[TBL] [Abstract][Full Text] [Related]
14. Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers.
Chomyn A; Lai ST; Shakeley R; Bresolin N; Scarlato G; Attardi G
Am J Hum Genet; 1994 Jun; 54(6):966-74. PubMed ID: 8198140
[TBL] [Abstract][Full Text] [Related]
15. Role of taurine in the pathologies of MELAS and MERRF.
Schaffer SW; Jong CJ; Ito T; Azuma J
Amino Acids; 2014 Jan; 46(1):47-56. PubMed ID: 23179085
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Mitochondrial Transfer from Wharton's Jelly Mesenchymal Stem Cell to MERRF Cybrid Reduces Oxidative Stress and Improves Mitochondrial Bioenergetics.
Chuang YC; Liou CW; Chen SD; Wang PW; Chuang JH; Tiao MM; Hsu TY; Lin HY; Lin TK
Oxid Med Cell Longev; 2017; 2017():5691215. PubMed ID: 28607632
[TBL] [Abstract][Full Text] [Related]
18. A novel mitochondrial tRNAPhe mutation causes MERRF syndrome.
Mancuso M; Filosto M; Mootha VK; Rocchi A; Pistolesi S; Murri L; DiMauro S; Siciliano G
Neurology; 2004 Jun; 62(11):2119-21. PubMed ID: 15184630
[TBL] [Abstract][Full Text] [Related]
19. MERRF-like phenotype associated with a rare mitochondrial trnaile mutation (m.4284 G>A).
Hahn A; Schänzer A; Neubauer BA; Gizewski E; Ahting U; Rolinski B
Neuropediatrics; 2011 Aug; 42(4):148-51. PubMed ID: 21766266
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
