Complex I Enzyme Activity试纸检测试剂盒(ab109720)

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ab109720 被引用在 24 文献中.

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  • Yao J  et al. Potentiation of brain mitochondrial function by S-equol and R/S-equol estrogen receptor ß-selective phytoSERM treatments. Brain Res 1514:128-41 (2013). Mouse . PubMed: 23428542
  • Hong Z  et al. Role of dynamin-related protein 1 (Drp1)-mediated mitochondrial fission in oxygen sensing and constriction of the ductus arteriosus. Circ Res 112:802-15 (2013). PubMed: 23334860
  • Bär F  et al. Mitochondrial Gene Polymorphisms That Protect Mice From Colitis. Gastroenterology N/A:N/A (2013). Mouse . PubMed: 23872498
  • Machado AM  et al. Helicobacter pylori infection affects mitochondrial function and DNA repair, thus, mediating genetic instability in gastric cells. Mech Ageing Dev N/A:N/A (2013). PubMed: 24012633
  • Ceusters JD  et al. Effect of different kinds of anoxia/reoxygenation on the mitochondrial function and the free radicals production of cultured primary equine skeletal myoblasts. Res Vet Sci 95:870-8 (2013). Functional Studies ; Horse . PubMed: 24099743
  • Bull VH  et al. Sorafenib-induced mitochondrial complex I inactivation and cell death in human neuroblastoma cells. J Proteome Res 11:1609-20 (2012). PubMed: 22268697
  • Claus C  et al. Involvement of p32 and microtubules in alteration of mitochondrial functions by rubella virus. J Virol 85:3881-92 (2011). PubMed: 21248045
  • Yao J  et al. Ovarian hormone loss induces bioenergetic deficits and mitochondrial ß-amyloid. Neurobiol Aging : (2011). Mouse . PubMed: 21514693
  • Valentin-Vega YA  et al. Mitochondrial dysfunction in ataxia telangiectasia. Blood : (2011). PubMed: 22144182
  • Fassone E  et al. FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy. Hum Mol Genet 19:4837-47 (2010). PubMed: 20858599
  • Calvo SE  et al. High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. Nat Genet 42:851-8 (2010). PubMed: 20818383
  • Calvo SE  et al. High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. Nat Genet 42:851-8 (2010). PubMed: 20818383
  • Pennington K  et al. Differential effects of wild-type and A53T mutant isoform of alpha-synuclein on the mitochondrial proteome of differentiated SH-SY5Y cells. J Proteome Res 9:2390-401 (2010). PubMed: 20334438
  • Fogal V  et al. Mitochondrial p32 protein is a critical regulator of tumor metabolism via maintenance of oxidative phosphorylation. Mol Cell Biol 30:1303-18 (2010). Human . PubMed: 20100866
  • Fogal V  et al. Mitochondrial p32 protein is a critical regulator of tumor metabolism via maintenance of oxidative phosphorylation. Mol Cell Biol 30:1303-18 (2010). Human . PubMed: 20100866
  • Hauben M  et al. Energy use efficiency is characterized by an epigenetic component that can be directed through artificial selection to increase yield. Proc Natl Acad Sci U S A 106:20109-14 (2009). PubMed: 19897729
  • Marusich MF  et al. Novel antibody-based strategies for the rapid diagnosis of mitochondrial disease and dysfunction. Int J Biochem Cell Biol 41:2081-8 (2009). PubMed: 19460456
  • Baughman JM  et al. A computational screen for regulators of oxidative phosphorylation implicates SLIRP in mitochondrial RNA homeostasis. PLoS Genet 5:e1000590 (2009). PubMed: 19680543
  • 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). PubMed: 19041632
  • Sugiana C  et al. Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease. Am J Hum Genet 83:468-78 (2008). PubMed: 18940309
  • Bannai S & Kasuga H Anti-inflammatory drug inhibition of transport of cystine and glutamate in cultured human fibroblasts. Biochem Pharmacol 34:1852-4 (1985). PubMed: 2860907

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