Anti-COX5A抗体[6E9B12D5] (ab110262)

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ab110262 被引用在 31 文献中.

  • Pérez-Pérez R  et al. COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation. Cell Rep 16:2387-98 (2016). WB . PubMed: 27545886
  • Davoudi M  et al. Complex I function and supercomplex formation are preserved in liver mitochondria despite progressive complex III deficiency. PLoS One 9:e86767 (2014). WB ; Mouse . PubMed: 24466228
  • Huang R  et al. Megakaryocytic Differentiation of K562 Cells Induced by PMA Reduced the Activity of Respiratory Chain Complex IV. PLoS One 9:e96246 (2014). PubMed: 24817082
  • Szklarczyk R  et al. A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia. Hum Mol Genet 22:656-67 (2013). Human . PubMed: 23125284
  • van Bon BW  et al. CEP89 is required for mitochondrial metabolism and neuronal function in man and fly. Hum Mol Genet 22:3138-51 (2013). PubMed: 23575228
  • Chen WL  et al. The role of cytochrome c oxidase subunit Va in non-small cell lung carcinoma cells: association with migration, invasion and prediction of distant metastasis. BMC Cancer 12:273 (2012). WB, IHC-P ; Human . PubMed: 22748147
  • Atkinson A  et al. Mzm1 influences a labile pool of mitochondrial zinc important for respiratory function. J Biol Chem 285:19450-9 (2010). PubMed: 20404342
  • Di Bella D  et al. Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. Nat Genet 42:313-21 (2010). PubMed: 20208537
  • Puchta O  et al. DMR1 (CCM1/YGR150C) of Saccharomyces cerevisiae encodes an RNA-binding protein from the pentatricopeptide repeat family required for the maintenance of the mitochondrial 15S ribosomal RNA. Genetics 184:959-73 (2010). PubMed: 20124025
  • Ilkow CS  et al. The rubella virus capsid protein inhibits mitochondrial import. J Virol 84:119-30 (2010). PubMed: 19846524
  • Bestwick M  et al. The role of Coa2 in hemylation of yeast Cox1 revealed by its genetic interaction with Cox10. Mol Cell Biol 30:172-85 (2010). PubMed: 19841065
  • Kucharczyk R  et al. Biochemical consequences in yeast of the human mitochondrial DNA 8993T>C mutation in the ATPase6 gene found in NARP/MILS patients. Biochim Biophys Acta 1793:817-24 (2009). PubMed: 19269308
  • Annibaldi A  et al. Role of the sub-cellular localization of RasGAP fragment N2 for its ability to sensitize cancer cells to genotoxin-induced apoptosis. Exp Cell Res 315:2081-91 (2009). PubMed: 19328779
  • Chu CH  et al. Activation of insulin-like growth factor II receptor induces mitochondrial-dependent apoptosis through G(alpha)q and downstream calcineurin signaling in myocardial cells. Endocrinology 150:2723-31 (2009). PubMed: 19095737
  • Samper E  et al. Increase in mitochondrial biogenesis, oxidative stress, and glycolysis in murine lymphomas. Free Radic Biol Med 46:387-96 (2009). PubMed: 19038329
  • Sohal RS  et al. Age-related decrease in expression of mitochondrial DNA encoded subunits of cytochrome c oxidase in Drosophila melanogaster. Mech Ageing Dev 129:558-61 (2008). PubMed: 18538373
  • Kitamura H  et al. Genome-wide identification and characterization of transcripts translationally regulated by bacterial lipopolysaccharide in macrophage-like J774.1 cells. Physiol Genomics 33:121-32 (2008). PubMed: 18230670
  • Wang X  et al. Dominant membrane uncoupling by mutant adenine nucleotide translocase in mitochondrial diseases. Hum Mol Genet 17:4036-44 (2008). PubMed: 18809618
  • Uddin M  et al. Molecular evolution of the cytochrome c oxidase subunit 5A gene in primates. BMC Evol Biol 8:8 (2008). PubMed: 18197981
  • Bonawitz ND  et al. Reduced TOR signaling extends chronological life span via increased respiration and upregulation of mitochondrial gene expression. Cell Metab 5:265-77 (2007). PubMed: 17403371
  • Rak M  et al. Yeast cells lacking the mitochondrial gene encoding the ATP synthase subunit 6 exhibit a selective loss of complex IV and unusual mitochondrial morphology. J Biol Chem 282:10853-64 (2007). PubMed: 17261589
  • Nouet C  et al. Rmd9p controls the processing/stability of mitochondrial mRNAs and its overexpression compensates for a partial deficiency of oxa1p in Saccharomyces cerevisiae. Genetics 175:1105-15 (2007). PubMed: 17194787
  • Kirchman PA & Botta G Copper supplementation increases yeast life span under conditions requiring respiratory metabolism. Mech Ageing Dev 128:187-95 (2007). PubMed: 17129597
  • Janssen GM  et al. The A3243G tRNALeu(UUR) mutation induces mitochondrial dysfunction and variable disease expression without dominant negative acting translational defects in complex IV subunits at UUR codons. Hum Mol Genet 16:2472-81 (2007). PubMed: 17656376
  • Baden KN  et al. Early developmental pathology due to cytochrome c oxidase deficiency is revealed by a new zebrafish model. J Biol Chem 282:34839-49 (2007). PubMed: 17761683
  • Benard G  et al. Physiological diversity of mitochondrial oxidative phosphorylation. Am J Physiol Cell Physiol 291:C1172-82 (2006). PubMed: 16807301
  • Genter MB  et al. Comparison of mouse hepatic mitochondrial versus microsomal cytochromes P450 following TCDD treatment. Biochem Biophys Res Commun 342:1375-81 (2006). PubMed: 16516144
  • Cui XS  et al. Gene expression of cox5a, 5b, or 6b1 and their roles in preimplantation mouse embryos. Biol Reprod 74:601-10 (2006). PubMed: 16291927
  • Krause-Buchholz U  et al. YIL042c and YOR090c encode the kinase and phosphatase of the Saccharomyces cerevisiae pyruvate dehydrogenase complex. FEBS Lett 580:2553-60 (2006). PubMed: 16643908
  • Stiburek L  et al. Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1. Biochem J 392:625-32 (2005). PubMed: 16083427
  • Persichini T  et al. Mitochondrial type I nitric oxide synthase physically interacts with cytochrome c oxidase. Neurosci Lett 384:254-9 (2005). PubMed: 15923083

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