| Q34348944 | "Sleeping beauty": quiescence in Saccharomyces cerevisiae |
| Q39937236 | A growth rate-limiting process in the last growth phase of the yeast life cycle involves RPB4, a subunit of RNA polymerase II. |
| Q35310848 | A high ratio of G1 to G0 phase cells and an accumulation of G1 phase cells before S phase progression after injurious stimuli in the proximal tubule |
| Q40656654 | A portion of RNA polymerase II molecules has a component essential for stress responses and stress survival |
| Q35617502 | A stationary-phase gene in Saccharomyces cerevisiae is a member of a novel, highly conserved gene family. |
| Q77761336 | ALG gene expression and cell cycle progression |
| Q27935845 | AZF1 is a glucose-dependent positive regulator of CLN3 transcription in Saccharomyces cerevisiae |
| Q37406087 | Adaptation of topoisomerase I paralogs to nuclear and mitochondrial DNA. |
| Q42093343 | Chromatin structure of the Saccharomyces cerevisiae DNA topoisomerase I promoter in different growth phases |
| Q36842182 | Cloning of a cDNA encoding DNA topoisomerase I in Daucus carota and expression analysis in relation to cell proliferation |
| Q40656523 | DNA topoisomerase I controls the kinetics of promoter activation and DNA topology in Saccharomyces cerevisiae |
| Q36424250 | DNA topoisomerase I is essential in Drosophila melanogaster |
| Q42508509 | DNA topoisomerase I is involved in both repression and activation of transcription |
| Q40884550 | Degradation of DNA topoisomerase I by a novel trypsin-like serine protease in proliferating human T lymphocytes |
| Q37698156 | Differentiated cytoplasmic granule formation in quiescent and non-quiescent cells upon chronological aging |
| Q33874440 | Dynamic reorganization of metabolic enzymes into intracellular bodies |
| Q39504318 | Eukaryotic translation initiation factor 4E-dependent translation is not essential for survival of starved yeast cells |
| Q33877872 | Expression variability of co-regulated genes differentiates Saccharomyces cerevisiae strains |
| Q24561963 | General requirement for RNA polymerase II holoenzymes in vivo |
| Q47791769 | Genetic tests of the role of Abf1p in driving transcription of the yeast TATA box bindng protein-encoding gene, SPT15. |
| Q33207493 | Genomic analysis of stationary-phase and exit in Saccharomyces cerevisiae: gene expression and identification of novel essential genes. |
| Q28776472 | Global control of histone modification by the anaphase-promoting complex |
| Q73666167 | Glucose starvation induces a drastic reduction in the rates of both transcription and degradation of mRNA in yeast |
| Q33722431 | Growth-independent regulation of CLN3 mRNA levels by nutrients in Saccharomyces cerevisiae |
| Q27937757 | Integrity of the Saccharomyces cerevisiae Rpn11 protein is critical for formation of proteasome storage granules (PSG) and survival in stationary phase |
| Q48328653 | Interference of a speB 5' untranslated region partial deletion with mRNA degradation in Streptococcus pyogenes. |
| Q56765006 | Investigating the biological functions of DNA topoisomerases in eukaryotic cells |
| Q36118209 | Isolation of quiescent and nonquiescent cells from yeast stationary-phase cultures |
| Q52660779 | Large-scale profiling of noncoding RNA function in yeast. |
| Q41913134 | Mat formation in Saccharomyces cerevisiae requires nutrient and pH gradients. |
| Q39528206 | Molecular genetic dissection of TAF25, an essential yeast gene encoding a subunit shared by TFIID and SAGA multiprotein transcription factors |
| Q78088472 | Monitoring dynamics of gene expression in yeast during stationary phase |
| Q24548535 | Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae |
| Q39576156 | Mutations in RNA polymerase II and elongation factor SII severely reduce mRNA levels in Saccharomyces cerevisiae |
| Q36017040 | Production of medium-chain volatile flavour esters in Pichia pastoris whole-cell biocatalysts with extracellular expression of Saccharomyces cerevisiae acyl-CoA:ethanol O-acyltransferase Eht1 or Eeb1. |
| Q42166737 | Proteasome disassembly and downregulation is correlated with viability during stationary phase |
| Q35975291 | Protein synthesis in long-term stationary-phase cultures of Saccharomyces cerevisiae |
| Q39455811 | Quantitative proteomic comparison of stationary/G0 phase cells and tetrads in budding yeast |
| Q33737849 | Quiescent fibroblasts exhibit high metabolic activity. |
| Q38827679 | RNA Polymerase Collision versus DNA Structural Distortion: Twists and Turns Can Cause Break Failure |
| Q39575463 | Rapamycin induces the G0 program of transcriptional repression in yeast by interfering with the TOR signaling pathway |
| Q33992641 | Regulation of gene expression by glucose in Saccharomyces cerevisiae: a role for ADA2 and ADA3/NGG1. |
| Q34522253 | Release of extraction-resistant mRNA in stationary phase Saccharomyces cerevisiae produces a massive increase in transcript abundance in response to stress |
| Q39568713 | Rpb4, a subunit of RNA polymerase II, enables the enzyme to transcribe at temperature extremes in vitro |
| Q27939602 | Rpb4p, a subunit of RNA polymerase II, mediates mRNA export during stress |
| Q27934751 | Rpb7 can interact with RNA polymerase II and support transcription during some stresses independently of Rpb4 |
| Q72993312 | Saccharomyces cerevisiae colony growth and ageing: biphasic growth accompanied by changes in gene expression |
| Q37531957 | Separation of the transcriptional coactivator and antirepression functions of transcription factor IIA |
| Q42606445 | Starved Saccharomyces cerevisiae cells have the capacity to support internal initiation of translation |
| Q37059288 | Stationary phase in the yeast Saccharomyces cerevisiae |
| Q36023733 | Staying alive: metabolic adaptations to quiescence |
| Q27933345 | The RNA polymerase II subunit Rpb4p mediates decay of a specific class of mRNAs |
| Q34613348 | The Ras/PKA signaling pathway of Saccharomyces cerevisiae exhibits a functional interaction with the Sin4p complex of the RNA polymerase II holoenzyme |
| Q27937902 | The Rpb7p subunit of yeast RNA polymerase II plays roles in the two major cytoplasmic mRNA decay mechanisms. |
| Q33700559 | The SR protein B52/SRp55 is required for DNA topoisomerase I recruitment to chromatin, mRNA release and transcription shutdown. |
| Q40723856 | The genetics of aging in the yeast Saccharomyces cerevisiae |
| Q35861844 | The histone deacetylase Hos2 forms an Hsp42-dependent cytoplasmic granule in quiescent yeast cells |
| Q38114535 | The normalcy of dormancy: common themes in microbial quiescence |
| Q27932113 | The rye mutants identify a role for Ssn/Srb proteins of the RNA polymerase II holoenzyme during stationary phase entry in Saccharomyces cerevisiae |
| Q36724522 | The topoisomerase I gene from Ustilago maydis: sequence, disruption and mutant phenotype |
| Q28170377 | The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase |
| Q36558770 | Topoisomerase I involvement in illegitimate recombination in Saccharomyces cerevisiae |
| Q36662169 | Transcription elongation in the human c-myc gene is governed by overall transcription initiation levels in Xenopus oocytes |
| Q35097810 | Transcriptional Regulation in Yeast during Diauxic Shift and Stationary Phase |
| Q33513760 | Validation of reference genes for quantitative expression analysis by real-time RT-PCR in Saccharomyces cerevisiae |
| Q27933749 | Widespread reorganization of metabolic enzymes into reversible assemblies upon nutrient starvation. |
| Q40694313 | Yeast Saccharomyces cerevisiae as a model system to study the cytotoxic activity of the antitumor drug camptothecin |
| Q77652532 | yTAFII61 has a general role in RNA polymerase II transcription and is required by Gcn4p to recruit the SAGA coactivator complex |