CCP1/YKR066C Literature Guide Help

Other names published for CCP1: YKR066C

CCP1 - Regulation of (24)

ReferenceOther Genes Addressed
Baumann K, et al.  (2011) The impact of oxygen on the transcriptome of recombinant S. cerevisiae and P. pastoris - a comparative analysis. BMC Genomics 12(1):218
Ferreira TC, et al.  (2011) Cell density-dependent linoleic acid toxicity to Saccharomyces cerevisiae. FEMS Yeast Res 11(5):408-17
Kumar A, et al.  (2011) Converging evidence of mitochondrial dysfunction in a yeast model of homocysteine metabolism imbalance. J Biol Chem 286(24):21779-95
Shuster A, et al.  (2011) Microbial alcohol-conferred hemolysis is a late response to alcohol stress. FEMS Yeast Res 11(4):315-23
Otero JM, et al.  (2010) Whole genome sequencing of Saccharomyces cerevisiae: from genotype to phenotype for improved metabolic engineering applications. BMC Genomics 11():723
Goldberg AA, et al.  (2009) Effect of calorie restriction on the metabolic history of chronologically aging yeast. Exp Gerontol 44(9):555-71
von Plehwe U, et al.  (2009) The Hsp70 homolog Ssb is essential for glucose sensing via the SNF1 kinase network. Genes Dev 23(17):2102-15
Puig S, et al.  (2008) Cooperation of two mRNA-binding proteins drives metabolic adaptation to iron deficiency. Cell Metab 7(6):555-64
Rojas M, et al.  (2008) Genomewide expression profiling of cryptolepine-induced toxicity in Saccharomyces cerevisiae. Antimicrob Agents Chemother 52(11):3844-50
Molin M, et al.  (2007) Ionizing radiation induces a Yap1-dependent peroxide stress response in yeast. Free Radic Biol Med 43(1):136-44
Rautio JJ, et al.  (2007) Monitoring yeast physiology during very high gravity wort fermentations by frequent analysis of gene expression. Yeast 24(9):741-60
Aragon AD, et al.  (2006) Release of extraction-resistant mRNA in stationary phase Saccharomyces cerevisiae produces a massive increase in transcript abundance in response to stress. Genome Biol 7(2):R9
He XJ and Fassler JS  (2005) Identification of novel Yap1p and Skn7p binding sites involved in the oxidative stress response of Saccharomyces cerevisiae. Mol Microbiol 58(5):1454-67
Puig S, et al.  (2005) Coordinated remodeling of cellular metabolism during iron deficiency through targeted mRNA degradation. Cell 120(1):99-110
Branco MR, et al.  (2004) Decrease of H2O2 plasma membrane permeability during adaptation to H2O2 in Saccharomyces cerevisiae. J Biol Chem 279(8):6501-6
Kwon M, et al.  (2003) Oxidative stresses elevate the expression of cytochrome c peroxidase in Saccharomyces cerevisiae. Biochim Biophys Acta 1623(1):1-5
Esser K, et al.  (2002) A novel two-step mechanism for removal of a mitochondrial signal sequence involves the mAAA complex and the putative rhomboid protease Pcp1. J Mol Biol 323(5):835-43
Marc P, et al.  (2002) Genome-wide analysis of mRNAs targeted to yeast mitochondria. EMBO Rep 3(2):159-64
Vido K, et al.  (2001) A proteome analysis of the cadmium response in Saccharomyces cerevisiae. J Biol Chem 276(11):8469-74
Lee J, et al.  (1999) Yap1 and Skn7 control two specialized oxidative stress response regulons in yeast. J Biol Chem 274(23):16040-6
Kuo MH and Grayhack E  (1994) A library of yeast genomic MCM1 binding sites contains genes involved in cell cycle control, cell wall and membrane structure, and metabolism. Mol Cell Biol 14(1):348-59
Ho PS, et al.  (1984) Kinetics and energetics of intramolecular electron transfer in yeast cytochrome c peroxidase. Biochemistry 23(18):4122-8
Djavadi-Ohaniance L, et al.  (1978) Identification of enzymically inactive apocytochrome c peroxidase in anaerobically grown Saccharomyces cerevisiae. J Biol Chem 253(12):4402-7
Kang CH, et al.  (1977) Steady state kinetics and binding of eukaryotic cytochromes c with yeast cytochrome c peroxidase. J Biol Chem 252(3):919-26