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ab110240 has been referenced in 28 publications.

  • Rouzier C  et al. NDUFS6 related Leigh syndrome: a case report and review of the literature. J Hum Genet N/A:N/A (2019). PubMed: 30948790
  • Zhou C  et al. Oncogenic HSP60 regulates mitochondrial oxidative phosphorylation to support Erk1/2 activation during pancreatic cancer cell growth. Cell Death Dis 9:161 (2018). WB . PubMed: 29415987
  • Kremer LS  et al. Genetic diagnosis of Mendelian disorders via RNA sequencing. Nat Commun 8:15824 (2017). WB ; Human . PubMed: 28604674
  • Kim JH  et al. GRIM-19 Restricts HCV Replication by Attenuating Intracellular Lipid Accumulation. Front Microbiol 8:576 (2017). WB . PubMed: 28443075
  • Srinivasan S  et al. Disruption of cytochrome c oxidase function induces the Warburg effect and metabolic reprogramming. Oncogene 35:1585-95 (2016). PubMed: 26148236
  • Phillips J  et al. Development of passive CLARITY and immunofluorescent labelling of multiple proteins in human cerebellum: understanding mechanisms of neurodegeneration in mitochondrial disease. Sci Rep 6:26013 (2016). PubMed: 27181107
  • Peyta L  et al. Reduced cardiolipin content decreases respiratory chain capacities and increases ATP synthesis yield in the human HepaRG cells. Biochim Biophys Acta 1857:443-53 (2016). PubMed: 26768115
  • Grünewald A  et al. Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons. Ann Neurol 79:366-78 (2016). PubMed: 26605748
  • Chrysostomou A  et al. Investigating complex I deficiency in Purkinje cells and synapses in patients with mitochondrial disease. Neuropathol Appl Neurobiol 42:477-92 (2016). PubMed: 26337858
  • Yue X  et al. GRIM-19 inhibition induced autophagy through activation of ERK and HIF-1a not STAT3 in Hela cells. Tumour Biol 37:9789-96 (2016). PubMed: 26810068
  • Peng M  et al. Inhibiting cytosolic translation and autophagy improves health in mitochondrial disease. Hum Mol Genet 24:4829-47 (2015). WB . PubMed: 26041819
  • Fang H  et al. Exercise intolerance and developmental delay associated with a novel mitochondrial ND5 mutation. Sci Rep 5:10480 (2015). WB ; Human . PubMed: 26014388
  • Guarani V  et al. TIMMDC1/C3orf1 functions as a membrane-embedded mitochondrial complex I assembly factor through association with the MCIA complex. Mol Cell Biol 34:847-61 (2014). PubMed: 24344204
  • Yarham JW  et al. Defective i6A37 modification of mitochondrial and cytosolic tRNAs results from pathogenic mutations in TRIT1 and its substrate tRNA. PLoS Genet 10:e1004424 (2014). WB ; Human . PubMed: 24901367
  • Pienaar IS  et al. Mitochondrial abnormality associates with type-specific neuronal loss and cell morphology changes in the pedunculopontine nucleus in Parkinson disease. Am J Pathol 183:1826-40 (2013). Human . PubMed: 24099985
  • Sheftel AD  et al. The human mitochondrial ISCA1, ISCA2, and IBA57 proteins are required for [4Fe-4S] protein maturation. Mol Biol Cell 23:1157-66 (2012). WB ; Human . PubMed: 22323289
  • Gerards M  et al. Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene. Brain 134:210-9 (2011). PubMed: 20929961
  • Sheftel AD  et al. Human ind1, an iron-sulfur cluster assembly factor for respiratory complex I. Mol Cell Biol 29:6059-73 (2009). WB ; Human . PubMed: 19752196
  • Leshinsky-Silver E  et al. NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement. Mol Genet Metab 97:185-9 (2009). PubMed: 19364667
  • Yahata N  et al. Nicotinamide mononucleotide adenylyltransferase expression in mitochondrial matrix delays Wallerian degeneration. J Neurosci 29:6276-84 (2009). WB ; Mouse . PubMed: 19439605
  • Potluri P  et al. A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease. Mol Genet Metab 96:189-95 (2009). WB ; Mouse . PubMed: 19185523
  • Minai L  et al. Mitochondrial respiratory chain complex assembly and function during human fetal development. Mol Genet Metab 94:120-6 (2008). PubMed: 18249146
  • Lebon S  et al. A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome. Mol Genet Metab 92:104-8 (2007). PubMed: 17604671
  • Li Y  et al. An assembled complex IV maintains the stability and activity of complex I in mammalian mitochondria. J Biol Chem 282:17557-62 (2007). PubMed: 17452320
  • Mehrabian Z  et al. The IFN-beta and retinoic acid-induced cell death regulator GRIM-19 is upregulated during focal cerebral ischemia. J Interferon Cytokine Res 27:383-92 (2007). PubMed: 17523870
  • Vogel RO  et al. Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunits. J Biol Chem 282:7582-90 (2007). PubMed: 17209039
  • Deng JH  et al. Nuclear suppression of mitochondrial defects in cells without the ND6 subunit. Mol Cell Biol 26:1077-86 (2006). PubMed: 16428459
  • Ogilvie I  et al. A molecular chaperone for mitochondrial complex I assembly is mutated in a progressive encephalopathy. J Clin Invest 115:2784-92 (2005). PubMed: 16200211

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