Publishing research using ab109881? Please let us know so that we can cite the reference in this datasheet.

ab109881 has been referenced in 16 publications.

  • Crombie DE  et al. Friedreich's ataxia induced pluripotent stem cell-derived cardiomyocytes display electrophysiological abnormalities and calcium handling deficiency. Aging (Albany NY) 9:1440-1452 (2017). PubMed: 28562313
  • Chapdelaine P  et al. Development of an AAV9 coding for a 3XFLAG-TALEfrat#8-VP64 able to increase in vivo the human frataxin in YG8R mice. Gene Ther 23:606-14 (2016). Human . PubMed: 27082765
  • Wedding IM  et al. Friedreich ataxia in Norway - an epidemiological, molecular and clinical study. Orphanet J Rare Dis 10:108 (2015). Human . PubMed: 26338206
  • Deutsch EC  et al. Usefulness of frataxin immunoassays for the diagnosis of Friedreich ataxia. J Neurol Neurosurg Psychiatry N/A:N/A (2014). Human . PubMed: 24463479
  • Sandi C  et al. Generation and characterisation of Friedreich ataxia YG8R mouse fibroblast and neural stem cell models. PLoS One 9:e89488 (2014). PubMed: 24586819
  • Bird MJ  et al. Functional characterization of Friedreich ataxia iPS-derived neuronal progenitors and their integration in the adult brain. PLoS One 9:e101718 (2014). PubMed: 25000412
  • Sahdeo S  et al. Dyclonine rescues frataxin deficiency in animal models and buccal cells of patients with Friedreich's ataxia. Hum Mol Genet N/A:N/A (2014). PubMed: 25113747
  • Li L  et al. Pharmacological screening using an FXN-EGFP cellular genomic reporter assay for the therapy of Friedreich ataxia. PLoS One 8:e55940 (2013). Mouse . PubMed: 23418481
  • Plasterer HL  et al. Development of frataxin gene expression measures for the evaluation of experimental treatments in Friedreich's ataxia. PLoS One 8:e63958 (2013). Human . PubMed: 23691127
  • Lufino MM  et al. A GAA repeat expansion reporter model of Friedreich's ataxia recapitulates the genomic context and allows rapid screening of therapeutic compounds. Hum Mol Genet N/A:N/A (2013). Human . PubMed: 23943791
  • Selak MA  et al. Blood cells from Friedreich ataxia patients harbor frataxin deficiency without a loss of mitochondrial function. Mitochondrion 11:342-50 (2011). Human . PubMed: 21147271
  • Kemp K  et al. Mesenchymal stem cells restore frataxin expression and increase hydrogen peroxide scavenging enzymes in friedreich ataxia fibroblasts. PLoS One 6:e26098 (2011). Human . PubMed: 22016819
  • Saccà F  et al. Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit. Mov Disord : (2010). PubMed: 21069859
  • Deutsch EC  et al. A rapid, noninvasive immunoassay for frataxin: utility in assessment of Friedreich ataxia. Mol Genet Metab 101:238-45 (2010). Human . PubMed: 20675166
  • Willis JH  et al. Isolated deficiencies of OXPHOS complexes I and IV are identified accurately and quickly by simple enzyme activity immunocapture assays. Biochim Biophys Acta 1787:533-8 (2009). Human . PubMed: 19041632
  • Willis JH  et al. Lateral-flow immunoassay for the frataxin protein in Friedreich's ataxia patients and carriers. Mol Genet Metab 94:491-7 (2008). Human . PubMed: 18485778


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