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 *

238 related articles for article (PubMed ID: 28607632)

  • 1. 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]  

  • 2. Mitochondrial transfer from Wharton's jelly-derived mesenchymal stem cells to mitochondria-defective cells recaptures impaired mitochondrial function.
    Lin HY; Liou CW; Chen SD; Hsu TY; Chuang JH; Wang PW; Huang ST; Tiao MM; Chen JB; Lin TK; Chuang YC
    Mitochondrion; 2015 May; 22():31-44. PubMed ID: 25746175
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial Transfer of Wharton's Jelly Mesenchymal Stem Cells Eliminates Mutation Burden and Rescues Mitochondrial Bioenergetics in Rotenone-Stressed MELAS Fibroblasts.
    Lin TK; Chen SD; Chuang YC; Lan MY; Chuang JH; Wang PW; Hsu TY; Wang FS; Tsai MH; Huang ST; Wang XW; Tsai PC; Lin HY; Liou CW
    Oxid Med Cell Longev; 2019; 2019():9537504. PubMed ID: 31249652
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial impairment and synaptic dysfunction are associated with neurological defects in iPSCs-derived cortical neurons of MERRF patients.
    Wu YT; Tay HY; Yang JT; Liao HH; Ma YS; Wei YH
    J Biomed Sci; 2023 Aug; 30(1):70. PubMed ID: 37605213
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 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. 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]  

  • 13. 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]  

  • 14. Miro1 improves the exogenous engraftment efficiency and therapeutic potential of mitochondria transfer using Wharton's jelly mesenchymal stem cells.
    Lin YH; Lin KL; Wang XW; Lee JJ; Wang FS; Wang PW; Lan MY; Liou CW; Lin TK
    Mitochondrion; 2024 May; 76():101856. PubMed ID: 38408618
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Distal weakness with respiratory insufficiency caused by the m.8344A > G "MERRF" mutation.
    Blakely EL; Alston CL; Lecky B; Chakrabarti B; Falkous G; Turnbull DM; Taylor RW; Gorman GS
    Neuromuscul Disord; 2014 Jun; 24(6):533-6. PubMed ID: 24792523
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of new variants in MTRNR1 and MTRNR2 genes using whole mitochondrial genome sequencing in a Taiwanese family with MERRF (myoclonic epilepsy with ragged-red fibers) syndrome.
    Wu YT; Huang SC; Shiao YM; Syu WC; Wei YH; Hsu YC
    Hear Res; 2023 Oct; 438():108876. PubMed ID: 37683310
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. A xeno-free culture method that enhances Wharton's jelly mesenchymal stromal cell culture efficiency over traditional animal serum-supplemented cultures.
    Julavijitphong S; Wichitwiengrat S; Tirawanchai N; Ruangvutilert P; Vantanasiri C; Phermthai T
    Cytotherapy; 2014 May; 16(5):683-91. PubMed ID: 24119645
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutation: data from the German mitoNET registry.
    Altmann J; Büchner B; Nadaj-Pakleza A; Schäfer J; Jackson S; Lehmann D; Deschauer M; Kopajtich R; Lautenschläger R; Kuhn KA; Karle K; Schöls L; Schulz JB; Weis J; Prokisch H; Kornblum C; Claeys KG; Klopstock T
    J Neurol; 2016 May; 263(5):961-972. PubMed ID: 26995359
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.