| Q24682174 | A novel human Ada2 homologue functions with Gcn5 or Brg1 to coactivate transcription |
| Q34425440 | ATM, a central controller of cellular responses to DNA damage. |
| Q33771767 | ATM: a mediator of multiple responses to genotoxic stress |
| Q28201456 | ATM: genome stability, neuronal development, and cancer cross paths |
| Q24548503 | Acetylation of histones and transcription-related factors |
| Q30308769 | Adenovirus E1A requires the yeast SAGA histone acetyltransferase complex and associates with SAGA components Gcn5 and Tra1. |
| Q33908306 | An ATPase/helicase complex is an essential cofactor for oncogenic transformation by c-Myc |
| Q27934769 | Analysis of Spt7 function in the Saccharomyces cerevisiae SAGA coactivator complex. |
| Q27936978 | Applicability of tandem affinity purification MudPIT to pathway proteomics in yeast |
| Q52348613 | Architecture of the Saccharomyces cerevisiae NuA4/TIP60 complex. |
| Q24537695 | BAF53 forms distinct nuclear complexes and functions as a critical c-Myc-interacting nuclear cofactor for oncogenic transformation |
| Q33293626 | C-terminal processing of yeast Spt7 occurs in the absence of functional SAGA complex |
| Q46632622 | Characterization of Ire1 in the yeast Yarrowia lipolytica reveals an important role for the Sls1 nucleotide exchange factor in unfolded protein response regulation |
| Q24309909 | Chk1 is a histone H3 threonine 11 kinase that regulates DNA damage-induced transcriptional repression |
| Q46751466 | Chromatin Regulation by the NuA4 Acetyltransferase Complex Is Mediated by Essential Interactions Between Enhancer of Polycomb (Epl1) and Esa1. |
| Q33899619 | Chromatin regulation and sumoylation in the inhibition of Ras-induced vulval development in Caenorhabditis elegans |
| Q34194492 | Chromatin remodeling enzymes: who's on first? |
| Q34064159 | Chromatin-remodeling complexes involved in gene activation by the glucocorticoid receptor |
| Q41910227 | Cliques and duplication-divergence network growth. |
| Q27937089 | Cluster analysis of mass spectrometry data reveals a novel component of SAGA |
| Q34281088 | Components of the SAGA histone acetyltransferase complex are required for repressed transcription of ARG1 in rich medium |
| Q26777171 | Composition of the SAGA complex in plants and its role in controlling gene expression in response to abiotic stresses |
| Q41559771 | Cryo-EM structure of the SAGA and NuA4 coactivator subunit Tra1 at 3.7 angstrom resolution |
| Q27936344 | Distinct mutations in yeast TAF(II)25 differentially affect the composition of TFIID and SAGA complexes as well as global gene expression patterns. |
| Q34478777 | Distinct regulatory mechanisms of eukaryotic transcriptional activation by SAGA and TFIID |
| Q39958860 | Distribution of acetylated histones resulting from Gal4-VP16 recruitment of SAGA and NuA4 complexes |
| Q42141775 | Domains of Tra1 important for activator recruitment and transcription coactivator functions of SAGA and NuA4 complexes. |
| Q44419402 | E-proteins directly regulate expression of activation-induced deaminase in mature B cells |
| Q27931128 | Eaf1 is the platform for NuA4 molecular assembly that evolutionarily links chromatin acetylation to ATP-dependent exchange of histone H2A variants |
| Q39956356 | Ethylnitrosourea-induced thymus-defective mutants identify roles of KIAA1440, TRRAP, and SKIV2L2 in teleost organ development |
| Q91604833 | Formation of a structurally-stable conformation by the intrinsically disordered MYC:TRRAP complex |
| Q28198743 | Function and regulation of the transcription factors of the Myc/Max/Mad network |
| Q34183768 | Function of the c-Myc oncoprotein in chromatin remodeling and transcription. |
| Q38238829 | Functions of SAGA in development and disease |
| Q33680840 | Gene activation by histone and factor acetyltransferases |
| Q34643704 | Genetic and bioinformatic analysis of 41C and the 2R heterochromatin of Drosophila melanogaster: a window on the heterochromatin-euchromatin junction |
| Q36076885 | Genetic evidence links the ASTRA protein chaperone component Tti2 to the SAGA transcription factor Tra1. |
| Q40315335 | Genome-wide analysis of gene expression regulated by the HAT cofactor Trrap in conditional knockout cells |
| Q27939759 | H2B ubiquitin protease Ubp8 and Sgf11 constitute a discrete functional module within the Saccharomyces cerevisiae SAGA complex. |
| Q40619789 | HAT cofactor Trrap regulates the mitotic checkpoint by modulation of Mad1 and Mad2 expression |
| Q28240437 | HATs and HDACs: from structure, function and regulation to novel strategies for therapy and prevention |
| Q24554353 | Helix-loop-helix proteins: regulators of transcription in eucaryotic organisms |
| Q33959141 | Histone acetyltransferase complexes can mediate transcriptional activation by the major glucocorticoid receptor activation domain |
| Q24291710 | Human STAGA complex is a chromatin-acetylating transcription coactivator that interacts with pre-mRNA splicing and DNA damage-binding factors in vivo |
| Q22010008 | Identification of TATA-binding protein-free TAFII-containing complex subunits suggests a role in nucleosome acetylation and signal transduction |
| Q38357478 | Improving the thermodynamic stability of the leucine zipper of max increases the stability of its b-HLH-LZ:E-box complex |
| Q37553936 | Insights into SAGA function during gene expression |
| Q28593423 | Loss of Gcn5 acetyltransferase activity leads to neural tube closure defects and exencephaly in mouse embryos |
| Q34206662 | Loss of nonsense mediated decay suppresses mutations in Saccharomyces cerevisiae TRA1 |
| Q33690584 | MYC interacts with the human STAGA coactivator complex via multivalent contacts with the GCN5 and TRRAP subunits. |
| Q36908401 | MYST opportunities for growth control: yeast genes illuminate human cancer gene functions |
| Q33818846 | Mass spectrometry. From genomics to proteomics |
| Q36578696 | Mechanism of transcriptional activation by the Myc oncoproteins |
| Q22122454 | Multi-protein complexes in eukaryotic gene transcription |
| Q30443104 | Multi-tasking on chromatin with the SAGA coactivator complexes |
| Q42045741 | Multiple faces of the SAGA complex |
| Q27931945 | Multiple links between the NuA4 histone acetyltransferase complex and epigenetic control of transcription. |
| Q34374051 | N-terminal domain of nuclear IL-1α shows structural similarity to the C-terminal domain of Snf1 and binds to the HAT/core module of the SAGA complex. |
| Q54473745 | New insights into the SAGA complex from studies of the Tra1 subunit in budding and fission yeast. |
| Q34519966 | Nipped-A, the Tra1/TRRAP subunit of the Drosophila SAGA and Tip60 complexes, has multiple roles in Notch signaling during wing development |
| Q37629627 | NuA4 and SWR1-C: two chromatin-modifying complexes with overlapping functions and components |
| Q34662254 | Orchestration of chromatin-based processes: mind the TRRAP. |
| Q27933247 | Reconstitution of the mammalian PI3K/PTEN/Akt pathway in yeast |
| Q35080744 | Regulation of cyclin D2 gene expression by the Myc/Max/Mad network: Myc-dependent TRRAP recruitment and histone acetylation at the cyclin D2 promoter. |
| Q33807801 | Regulation of p53 in response to DNA damage |
| Q33645251 | Replication-induced protein synthesis and its importance to proteomics |
| Q33775005 | Role of covalent modifications of histones in regulating gene expression |
| Q42552805 | SAGA function in tissue-specific gene expression |
| Q27936016 | SALSA, a variant of yeast SAGA, contains truncated Spt7, which correlates with activated transcription |
| Q26795760 | SGF29 and Sry pathway in hepatocarcinogenesis |
| Q58099442 | Share and share alike: the role of Tra1 from the SAGA and NuA4 coactivator complexes |
| Q27938611 | Spt3 plays opposite roles in filamentous growth in Saccharomyces cerevisiae and Candida albicans and is required for C. albicans virulence. |
| Q24810339 | Stimulation of Myc transactivation by the TATA binding protein in promoter-reporter assays |
| Q45889376 | Structure of the transcription activator target Tra1 within the chromatin modifying complex SAGA. |
| Q41580909 | Structure/function analysis of the phosphatidylinositol-3-kinase domain of yeast tra1. |
| Q26824496 | Substrate recognition and function of the R2TP complex in response to cellular stress |
| Q27937843 | Sus1, a functional component of the SAGA histone acetylase complex and the nuclear pore-associated mRNA export machinery |
| Q27932073 | Systematic genetic array analysis links the Saccharomyces cerevisiae SAGA/SLIK and NuA4 component Tra1 to multiple cellular processes |
| Q52162403 | TAC, a TBP-sans-TAFs complex containing the unprocessed TFIIAalphabeta precursor and the TFIIAgamma subunit |
| Q28566674 | TIP49, but not TRRAP, modulates c-Myc and E2F1 dependent apoptosis |
| Q22008654 | The 400 kDa subunit of the PCAF histone acetylase complex belongs to the ATM superfamily |
| Q27931014 | The ADA complex is a distinct histone acetyltransferase complex in Saccharomyces cerevisiae |
| Q24601182 | The ATM-related domain of TRRAP is required for histone acetyltransferase recruitment and Myc-dependent oncogenesis |
| Q55036334 | The ATRs, ATMs, and TORs are giant HEAT repeat proteins. |
| Q27937771 | The C-terminal residues of Saccharomyces cerevisiae Mec1 are required for its localization, stability, and function |
| Q28513184 | The PCAF acetylase complex as a potential tumor suppressor |
| Q33632328 | The PIK-related kinases intercept conventional signaling pathways |
| Q52329552 | The Pseudokinase Domain of Saccharomyces cerevisiae Tra1 Is Required for Nuclear Localization and Incorporation into the SAGA and NuA4 Complexes. |
| Q30438554 | The SAGA continues: expanding the cellular role of a transcriptional co-activator complex |
| Q43845830 | The SANT domain of Ada2 is required for normal acetylation of histones by the yeast SAGA complex |
| Q34769706 | The Spt-Ada-Gcn5 Acetyltransferase (SAGA) complex in Aspergillus nidulans |
| Q51417803 | The bromodomain-containing protein Ibd1 links multiple chromatin-related protein complexes to highly expressed genes in Tetrahymena thermophila. |
| Q38027720 | The chromatin code of fungal secondary metabolite gene clusters |
| Q33296914 | The complement of protein kinases of the microsporidium Encephalitozoon cuniculi in relation to those of Saccharomyces cerevisiae and Schizosaccharomyces pombe |
| Q34205129 | The diverse functions of histone acetyltransferase complexes. |
| Q35666251 | The diverse superfamily of lysine acetyltransferases and their roles in leukemia and other diseases |
| Q24554343 | The essential cofactor TRRAP recruits the histone acetyltransferase hGCN5 to c-Myc |
| Q38411598 | The essential gene wda encodes a WD40 repeat subunit of Drosophila SAGA required for histone H3 acetylation |
| Q24554357 | The human TFIID components TAF(II)135 and TAF(II)20 and the yeast SAGA components ADA1 and TAF(II)68 heterodimerize to form histone-like pairs |
| Q27931766 | The mRNA export machinery requires the novel Sac3p-Thp1p complex to dock at the nucleoplasmic entrance of the nuclear pores |
| Q34555987 | The myc oncogene: MarvelouslY Complex |
| Q27934606 | The novel SLIK histone acetyltransferase complex functions in the yeast retrograde response pathway. |
| Q27930726 | The something about silencing protein, Sas3, is the catalytic subunit of NuA3, a yTAF(II)30-containing HAT complex that interacts with the Spt16 subunit of the yeast CP (Cdc68/Pob3)-FACT complex |
| Q27935520 | The yeast NuA4 and Drosophila MSL complexes contain homologous subunits important for transcription regulation |
| Q27932063 | Three yeast proteins related to the human candidate tumor suppressor p33(ING1) are associated with histone acetyltransferase activities. |
| Q33460851 | Tra1 as a screening target for transcriptional activation domain discovery |
| Q33923344 | Tra1 has specific regulatory roles, rather than global functions, within the SAGA co-activator complex |
| Q27933975 | Transcriptional activation via sequential histone H2B ubiquitylation and deubiquitylation, mediated by SAGA-associated Ubp8. |
| Q35078088 | Transcriptional adaptor and histone acetyltransferase proteins in Arabidopsis and their interactions with CBF1, a transcriptional activator involved in cold-regulated gene expression |
| Q35542072 | Transcriptional regulation in Saccharomyces cerevisiae: transcription factor regulation and function, mechanisms of initiation, and roles of activators and coactivators. |
| Q33853240 | Transformation/transcription domain-associated protein (TRRAP)-mediated regulation of Wee1 |
| Q34930387 | Two Drosophila Ada2 Homologues Function in Different Multiprotein Complexes |
| Q34462842 | Two different Drosophila ADA2 homologues are present in distinct GCN5 histone acetyltransferase-containing complexes |
| Q27935097 | Yng1p modulates the activity of Sas3p as a component of the yeast NuA3 Hhistone acetyltransferase complex |
| Q35560399 | mTOR as a Positive Regulator of Tumor Cell Responses to Hypoxia |
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