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.


PUBMED FOR HANDHELDS

Journal Abstract Search


132 related items for PubMed ID: 24476000

  • 1. Effects of carbonic anhydrase-related protein VIII on human cells harbouring an A8344G mitochondrial DNA mutation.
    Wang TK, Cheng CK, Chi TH, Ma YS, Wu SB, Wei YH, Hsieh M.
    Biochem J; 2014 Apr 01; 459(1):149-60. PubMed ID: 24476000
    [Abstract] [Full Text] [Related]

  • 2. 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 01; 11(5):739-49. PubMed ID: 21679777
    [Abstract] [Full Text] [Related]

  • 3. Promoter analysis and transcriptional regulation of human carbonic anhydrase VIII gene in a MERRF disease cell model.
    Lo CM, Ma YS, Wei YH, Hsieh BYT, Hsieh M.
    Arch Biochem Biophys; 2018 Mar 01; 641():50-61. PubMed ID: 29407793
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. 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 01; 9(2):446-63. PubMed ID: 22354625
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. 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 01; 41(2-3):256-66. PubMed ID: 20411357
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. 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 01; 21(1):79-82. PubMed ID: 16551460
    [Abstract] [Full Text] [Related]

  • 20. ATOH1/RFX1/RFX3 transcription factors facilitate the differentiation and characterisation of inner ear hair cell-like cells from patient-specific induced pluripotent stem cells harbouring A8344G mutation of mitochondrial DNA.
    Chen YC, Tsai CL, Wei YH, Wu YT, Hsu WT, Lin HC, Hsu YC.
    Cell Death Dis; 2018 Apr 01; 9(4):437. PubMed ID: 29740017
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 7.