Publishing research using ab110271? Please let us know so that we can cite the reference in this datasheet.

ab110271 has been referenced in 27 publications.

  • Monteuuis G  et al. Non-canonical translation initiation in yeast generates a cryptic pool of mitochondrial proteins. Nucleic Acids Res 47:5777-5791 (2019). PubMed: 31216041
  • Su X  et al. Deregulating mitochondrial metabolite and ion transport has beneficial effects in yeast and human cellular models for NARP syndrome. Hum Mol Genet N/A:N/A (2019). PubMed: 31276579
  • de Taffin de Tilques M  et al. Overexpression of mitochondrial oxodicarboxylate carrier (ODC1) preserves oxidative phosphorylation in a yeast model of Barth syndrome. Dis Model Mech 10:439-450 (2017). WB . PubMed: 28188263
  • Kaniak-Golik A  et al. Activation of Dun1 in response to nuclear DNA instability accounts for the increase in mitochondrial point mutations in Rad27/FEN1 deficient S. cerevisiae. PLoS One 12:e0180153 (2017). WB ; Saccharomyces cerevisiae . PubMed: 28678842
  • Taylor NG  et al. The Assembly Factor Pet117 Couples Heme a Synthase Activity to Cytochrome Oxidase Assembly. J Biol Chem 292:1815-1825 (2017). PubMed: 27998984
  • Matsuhashi T  et al. Mitochonic Acid 5 (MA-5) Facilitates ATP Synthase Oligomerization and Cell Survival in Various Mitochondrial Diseases. EBioMedicine 20:27-38 (2017). PubMed: 28579242
  • Couvillion MT  et al. Synchronized mitochondrial and cytosolic translation programs. Nature 533:499-503 (2016). PubMed: 27225121
  • Swenson S  et al. Analysis of Oligomerization Properties of Heme a Synthase Provides Insights into Its Function in Eukaryotes. J Biol Chem 291:10411-25 (2016). PubMed: 26940873
  • 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
  • Wang X  et al. Dominant membrane uncoupling by mutant adenine nucleotide translocase in mitochondrial diseases. Hum Mol Genet 17:4036-44 (2008). PubMed: 18809618
  • 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
  • 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
  • Brandner K  et al. Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth Syndrome. Mol Biol Cell 16:5202-14 (2005). PubMed: 16135531
  • Horan S  et al. Analysis of COX2 mutants reveals cytochrome oxidase subassemblies in yeast. Biochem J 390:703-8 (2005). PubMed: 15921494
  • Hlavacek O  et al. The transcriptional activator HAP4 is a high copy suppressor of an oxa1 yeast mutation. Gene 354:53-7 (2005). PubMed: 15908145
  • Rinehart J  et al. Saccharomyces cerevisiae imports the cytosolic pathway for Gln-tRNA synthesis into the mitochondrion. Genes Dev 19:583-92 (2005). PubMed: 15706032
  • Chevtzoff C  et al. The yeast cAMP protein kinase Tpk3p is involved in the regulation of mitochondrial enzymatic content during growth. Biochim Biophys Acta 1706:117-25 (2005). PubMed: 15620372
  • Lemaire C  et al. A yeast mitochondrial membrane methyltransferase-like protein can compensate for oxa1 mutations. J Biol Chem 279:47464-72 (2004). PubMed: 15355998
  • Kissová I  et al. Uth1p is involved in the autophagic degradation of mitochondria. J Biol Chem 279:39068-74 (2004). PubMed: 15247238

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