298 related articles for article (PubMed ID: 21679777)
21. Effects of HSP27 downregulation on PDT resistance through PDT-induced autophagy in head and neck cancer cells.
Kim J; Lim H; Kim S; Cho H; Kim Y; Li X; Choi H; Kim O
Oncol Rep; 2016 Apr; 35(4):2237-45. PubMed ID: 26820233
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Generation of two isogenic human induced pluripotent stem cell lines from a 15 year-old female patient with MERRF syndrome and A8344G mutation of mitochondrial DNA.
Chou SJ; Ko YL; Yang YH; Yarmishyn AA; Wu YT; Chen CT; Lee HC; Wei YH; Chiou SH
Stem Cell Res; 2018 Jul; 30():201-205. PubMed ID: 29960149
[TBL] [Abstract][Full Text] [Related]
24. Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case.
Orcesi S; Gorni K; Termine C; Uggetti C; Veggiotti P; Carrara F; Zeviani M; Berardinelli A; Lanzi G
J Child Neurol; 2006 Jan; 21(1):79-82. PubMed ID: 16551460
[TBL] [Abstract][Full Text] [Related]
25. Mitochondrial diseases.
Nonaka I
Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):622-32. PubMed ID: 1392136
[TBL] [Abstract][Full Text] [Related]
26. A novel system for assigning the mode of inheritance in mitochondrial disorders using cybrids and rhodamine 6G.
Williams AJ; Murrell M; Brammah S; Minchenko J; Christodoulou J
Hum Mol Genet; 1999 Sep; 8(9):1691-7. PubMed ID: 10441332
[TBL] [Abstract][Full Text] [Related]
27. Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNA
Capristo M; Del Dotto V; Tropeano CV; Fiorini C; Caporali L; La Morgia C; Valentino ML; Montopoli M; Carelli V; Maresca A
Mol Med; 2022 Aug; 28(1):90. PubMed ID: 35922766
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by a multiplex molecular beacon based real-time fluorescence PCR.
Szuhai K; Ouweland J; Dirks R; Lemaître M; Truffert J; Janssen G; Tanke H; Holme E; Maassen J; Raap A
Nucleic Acids Res; 2001 Feb; 29(3):E13. PubMed ID: 11160915
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. [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]
33. [Molecular genetic analysis for myoclonus epilepsy associated with ragged-red fibers (MERRF)].
Tanno Y; Yoneda M; Tanaka K; Tsuji S
Nihon Rinsho; 1993 Sep; 51(9):2379-85. PubMed ID: 8411716
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Mitochondrial accumulation under oxidative stress is due to defects in autophagy.
Luo C; Li Y; Wang H; Feng Z; Li Y; Long J; Liu J
J Cell Biochem; 2013 Jan; 114(1):212-9. PubMed ID: 22903604
[TBL] [Abstract][Full Text] [Related]
36. Unusual presentations of patients with the mitochondrial MERRF mutation A8344G.
Wiedemann FR; Bartels C; Kirches E; Mawrin C; Wallesch CW
Clin Neurol Neurosurg; 2008 Sep; 110(8):859-63. PubMed ID: 18657354
[TBL] [Abstract][Full Text] [Related]
37. In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypes.
Masucci JP; Davidson M; Koga Y; Schon EA; King MP
Mol Cell Biol; 1995 May; 15(5):2872-81. PubMed ID: 7739567
[TBL] [Abstract][Full Text] [Related]
38. The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines.
Bornstein B; Mas JA; Fernández-Moreno MA; Campos Y; Martín MA; del Hoyo P; Rubio JC; Arenas J; Garesse R
Hum Mutat; 2002 Mar; 19(3):234-9. PubMed ID: 11857739
[TBL] [Abstract][Full Text] [Related]
39. Monocytes and vascular endothelial cells apoptosis. Role of p-HSP27.
Gawad A; Ptak-Belowska A; Brzozowski T; Pawlik WW
J Physiol Pharmacol; 2009 Dec; 60(4):55-61. PubMed ID: 20065497
[TBL] [Abstract][Full Text] [Related]
40. Detection of heat shock protein 27, 70, 90 expressions in primary parenchymatous organs of goats after transport stress by real-time PCR and ELISA.
Hu W; Fang M; Yang Y; Ye T; Liu B; Zheng W
Vet Med Sci; 2020 Nov; 6(4):788-795. PubMed ID: 32710597
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]