| P50 | author | Rana P. Singh | Q39274526 |
| P2093 | author name string | Krishnamurthy Natarajan | |
| | Ishani Sinha | |
| | Rahul Siddharthan | |
| | Anushikha Thakur | |
| | Sonal Sawhney | |
| | Malika Saint | |
| | Rashmi Dahiya | |
| P2860 | cites work | Selective anchoring of TFIID to nucleosomes by trimethylation of histone H3 lysine 4 | Q24294553 |
| | In vivo functional analysis of the histone 3-like TAF9 and a TAF9-related factor, TAF9L | Q24306731 |
| | Distinct modes of gene regulation by a cell-specific transcriptional activator | Q24316297 |
| | Function of TAF(II)-containing complex without TBP in transcription by RNA polymerase II | Q24320008 |
| | Core promoter binding by histone-like TAF complexes | Q24322695 |
| | TFIID and Spt-Ada-Gcn5-acetyltransferase functions probed by genome-wide synthetic genetic array analysis using a Saccharomyces cerevisiae taf9-ts allele | Q24545962 |
| | Significance analysis of microarrays applied to the ionizing radiation response | Q24606608 |
| | Activator Gcn4 employs multiple segments of Med15/Gal11, including the KIX domain, to recruit mediator to target genes in vivo | Q24646051 |
| | A multiplicity of coactivators is required by Gcn4p at individual promoters in vivo | Q24684851 |
| | Bayesian analysis of gene expression levels: statistical quantification of relative mRNA level across multiple strains or treatments | Q24803156 |
| | Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method | Q25938999 |
| | Structure and function of a human TAFII250 double bromodomain module | Q27622657 |
| | The Acidic Transcription Activator Gcn4 Binds the Mediator Subunit Gal11/Med15 Using a Simple Protein Interface Forming a Fuzzy Complex | Q27676397 |
| | TFIID TAF6-TAF9 Complex Formation Involves the HEAT Repeat-containing C-terminal Domain of TAF6 and Is Modulated by TAF5 Protein | Q27681162 |
| | Structural similarity between TAFs and the heterotetrameric core of the histone octamer | Q27732598 |
| | A new mathematical model for relative quantification in real-time RT-PCR | Q27860781 |
| | Transcriptional regulatory networks in Saccharomyces cerevisiae | Q27860846 |
| | Use of a genetically introduced cross-linker to identify interaction sites of acidic activators within native transcription factor IID and SAGA. | Q27929763 |
| | The histone H3-like TAF is broadly required for transcription in yeast | Q27930236 |
| | Distinct classes of yeast promoters revealed by differential TAF recruitment | Q27931136 |
| | Proteomics of the eukaryotic transcription machinery: identification of proteins associated with components of yeast TFIID by multidimensional mass spectrometry | Q27931371 |
| | An array of coactivators is required for optimal recruitment of TATA binding protein and RNA polymerase II by promoter-bound Gcn4p | Q27932320 |
| | A protein complex of translational regulators of GCN4 mRNA is the guanine nucleotide-exchange factor for translation initiation factor 2 in yeast | Q27933536 |
| | Recruitment of HAT complexes by direct activator interactions with the ATM-related Tra1 subunit | Q27933602 |
| | Transcriptional regulatory code of a eukaryotic genome | Q27933887 |
| | Isolation and characterization of TAF25, an essential yeast gene that encodes an RNA polymerase II-specific TATA-binding protein-associated factor | Q27935508 |
| | Simultaneous recruitment of coactivators by Gcn4p stimulates multiple steps of transcription in vivo | Q27935555 |
| | Transcriptional activation by Gcn4p involves independent interactions with the SWI/SNF complex and the SRB/mediator | Q27936339 |
| | A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation | Q27936635 |
| | Yeast TFIID serves as a coactivator for Rap1p by direct protein-protein interaction | Q27938360 |
| | A yeast taf17 mutant requires the Swi6 transcriptional activator for viability and shows defects in cell cycle-regulated transcription | Q27938450 |
| | A triad of subunits from the Gal11/tail domain of Srb mediator is an in vivo target of transcriptional activator Gcn4p | Q27938961 |
| | Interdependent recruitment of SAGA and Srb mediator by transcriptional activator Gcn4p | Q27939381 |
| | Systematic analysis of essential yeast TAFs in genome-wide transcription and preinitiation complex assembly | Q27939428 |
| | TAF-Containing and TAF-independent forms of transcriptionally active TBP in vivo. | Q27939707 |
| | SAGA is an essential in vivo target of the yeast acidic activator Gal4p | Q28345347 |
| | Transformation of yeast by lithium acetate/single-stranded carrier DNA/polyethylene glycol method | Q29547550 |
| | Transcriptional profiling shows that Gcn4p is a master regulator of gene expression during amino acid starvation in yeast | Q29614487 |
| | Binding of TBP to promoters in vivo is stimulated by activators and requires Pol II holoenzyme | Q29614681 |
| | Progression through the RNA polymerase II CTD cycle | Q29614782 |
| | Preparation of high molecular weight RNA | Q29614859 |
| | Histone acetyltransferase complexes: one size doesn't fit all | Q29620006 |
| | The Gcn4p activation domain interacts specifically in vitro with RNA polymerase II holoenzyme, TFIID, and the Adap-Gcn5p coactivator complex | Q33772811 |
| | Gcn4p, a master regulator of gene expression, is controlled at multiple levels by diverse signals of starvation and stress | Q33905702 |
| | Genome-wide structure and organization of eukaryotic pre-initiation complexes | Q34248195 |
| | The general transcription machinery and general cofactors | Q34549899 |
| | Full and partial genome-wide assembly and disassembly of the yeast transcription machinery in response to heat shock | Q35004993 |
| | Interaction between the N-terminal domain of the 230-kDa subunit and the TATA box-binding subunit of TFIID negatively regulates TATA-box binding | Q35180776 |
| | The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAFII60 of Drosophila | Q35196382 |
| | Transcriptional regulation in Saccharomyces cerevisiae: transcription factor regulation and function, mechanisms of initiation, and roles of activators and coactivators. | Q35542072 |
| | H3K4me3 interactions with TAF3 regulate preinitiation complex assembly and selective gene activation | Q36657584 |
| | Transcriptional activation in an improved whole-cell extract from Saccharomyces cerevisiae | Q36731857 |
| | How eukaryotic genes are transcribed | Q37514183 |
| | Insights into SAGA function during gene expression | Q37553936 |
| | A synthetic HIS4 regulatory element confers general amino acid control on the cytochrome c gene (CYC1) of yeast | Q37675227 |
| | Changes in genomewide occupancy of core transcriptional regulators during heat stress | Q37695539 |
| | ATAC-king the complexity of SAGA during evolution | Q37994551 |
| | Redundant roles for the TFIID and SAGA complexes in global transcription | Q38311191 |
| | Structural and functional analysis of yeast putative adaptors. Evidence for an adaptor complex in vivo | Q38361167 |
| | Genome-wide localization analysis of a complete set of Tafs reveals a specific effect of the taf1 mutation on Taf2 occupancy and provides indirect evidence for different TFIID conformations at different promoters | Q39843802 |
| | Autonomous function of the amino-terminal inhibitory domain of TAF1 in transcriptional regulation | Q40736935 |
| | A comprehensive genomic binding map of gene and chromatin regulatory proteins in Saccharomyces | Q41957756 |
| | Sequential Recruitment of SAGA and TFIID in a Genomic Response to DNA Damage in Saccharomyces cerevisiae | Q41999510 |
| | Domains of Tra1 important for activator recruitment and transcription coactivator functions of SAGA and NuA4 complexes. | Q42141775 |
| | Increased recruitment of TATA-binding protein to the promoter by transcriptional activation domains in vivo | Q42492288 |
| | Dissection of coactivator requirement at RNR3 reveals unexpected contributions from TFIID and SAGA. | Q43125554 |
| | Activator-specific recruitment of TFIID and regulation of ribosomal protein genes in yeast | Q43975761 |
| | Screening the yeast "disruptome" for mutants affecting resistance to the immunosuppressive drug, mycophenolic acid | Q43997248 |
| | Structural insight into the recognition of the H3K4me3 mark by the TFIID subunit TAF3. | Q46444527 |
| | A genome-wide housekeeping role for TFIID and a highly regulated stress-related role for SAGA in Saccharomyces cerevisiae | Q48017973 |
| | A movie of RNA polymerase II transcription | Q48424870 |
| | Gcn5 promotes acetylation, eviction, and methylation of nucleosomes in transcribed coding regions. | Q53577981 |
| | H2B Ubiquitylation Acts as a Barrier to Ctk1 Nucleosomal Recruitment Prior to Removal by Ubp8 within a SAGA-Related Complex | Q54998786 |
| | Histone-like TAFs are essential for transcription in vivo | Q77652527 |
| | yTAFII61 has a general role in RNA polymerase II transcription and is required by Gcn4p to recruit the SAGA coactivator complex | Q77652532 |
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cell biology | Q7141 |
| | Histone acetyltransferase TRA1 YHR099W | Q27547700 |
| | SAGA histone acetyltransferase complex subunit SPT7 YBR081C | Q27552944 |
| P304 | page(s) | 1547-1563 | |
| P577 | publication date | 2014-02-18 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | The TAF9 C-terminal conserved region domain is required for SAGA and TFIID promoter occupancy to promote transcriptional activation | |
| P478 | volume | 34 | |