| Q48906137 | A copper-responsive promoter replacement system to investigate gene functions in Trichoderma reesei: a case study in characterizing SAGA genes |
| Q24682174 | A novel human Ada2 homologue functions with Gcn5 or Brg1 to coactivate transcription |
| Q28571312 | A role for Gcn5 in cardiomyocyte differentiation of rat mesenchymal stem cells |
| Q28363091 | A specific lysine in c-Jun is required for transcriptional repression by E1A and is acetylated by p300 |
| Q37994551 | ATAC-king the complexity of SAGA during evolution |
| Q47858497 | Absence of Gcn5 HAT activity defines a novel state in the opening of chromatin at the PHO5 promoter in yeast |
| Q24548503 | Acetylation of histones and transcription-related factors |
| Q44747129 | Acetylation of histones associated with the p21WAF1/CIP1 gene by butyrate is not sufficient for p21WAF1/CIP1 gene transcription in human colorectal adenocarcinoma cells |
| Q43691949 | Acetylation of steroidogenic factor 1 protein regulates its transcriptional activity and recruits the coactivator GCN5. |
| Q33964757 | Adenovirus E1B 55-kilodalton oncoprotein inhibits p53 acetylation by PCAF. |
| Q24530608 | An RNA polymerase II complex containing all essential initiation factors binds to the activation domain of PAR leucine zipper transcription factor thyroid embryonic factor |
| Q38320487 | AnCF, the CCAAT binding complex of Aspergillus nidulans, is essential for the formation of a DNase I-hypersensitive site in the 5' region of the amdS gene |
| Q77892623 | Analysis of activity and regulation of hGcn5, a human histone acetyltransferase |
| Q24310576 | And-1 is required for the stability of histone acetyltransferase Gcn5 |
| Q22254743 | Androgen receptor interacts with a novel MYST protein, HBO1 |
| Q73445322 | Cell growth inhibition by the Mad/Max complex through recruitment of histone deacetylase activity |
| Q34064159 | Chromatin-remodeling complexes involved in gene activation by the glucocorticoid receptor |
| Q39729515 | Cloning and analysis of a Toxoplasma gondii histone acetyltransferase: a novel chromatin remodelling factor in Apicomplexan parasites |
| Q46623959 | Co-activators and co-repressors in the integration of transcriptional responses |
| Q27932566 | Combinatorial depletion analysis to assemble the network architecture of the SAGA and ADA chromatin remodeling complexes |
| Q35193069 | Critical residues for histone acetylation by Gcn5, functioning in Ada and SAGA complexes, are also required for transcriptional function in vivo |
| Q38331920 | Critical structural elements and multitarget protein interactions of the transcriptional activator AF-1 of hepatocyte nuclear factor 4. |
| Q27619265 | Crystal structure and mechanism of histone acetylation of the yeast GCN5 transcriptional coactivator |
| Q27644364 | Crystal structure of a binary complex between human GCN5 histone acetyltransferase domain and acetyl coenzyme A |
| Q48294220 | Deletion of ADA2 increases antifungal drug susceptibility and virulence in Candida glabrata |
| Q34478777 | Distinct regulatory mechanisms of eukaryotic transcriptional activation by SAGA and TFIID |
| Q34831586 | Distinct roles of the Gcn5 histone acetyltransferase revealed during transient stress-induced reprogramming of the genome |
| Q24319748 | E1A directly binds and regulates the P/CAF acetyltransferase |
| Q90470355 | Epigenetic Regulation of MDR1 and BCRP Transporters by HDAC Inhibition |
| Q41913369 | Essential and redundant functions of histone acetylation revealed by mutation of target lysines and loss of the Gcn5p acetyltransferase |
| Q28140995 | Estrogen receptor interaction with co-activators and co-repressors |
| Q28203389 | Full Activation of Estrogen Receptor α Activation Function-1 Induces Proliferation of Breast Cancer Cells |
| Q58514612 | Gcn5p, a Transcription-related Histone Acetyltransferase, Acetylates Nucleosomes and Folded Nucleosomal Arrays in the Absence of Other Protein Subunits |
| Q33546141 | Genome-wide characterisation of the Gcn5 histone acetyltransferase in budding yeast during stress adaptation reveals evolutionarily conserved and diverged roles |
| Q35192911 | Histone acetyltransferase activity of yeast Gcn5p is required for the activation of target genes in vivo |
| Q33959141 | Histone acetyltransferase complexes can mediate transcriptional activation by the major glucocorticoid receptor activation domain |
| Q35199451 | Histone acetyltransferases regulate HIV-1 enhancer activity in vitro |
| Q35253477 | Histone chaperones, histone acetylation, and the fluidity of the chromogenome |
| Q77109285 | How do histone acetyltransferases select lysine residues in core histones? |
| Q22010568 | Identification of a human histone acetyltransferase related to monocytic leukemia zinc finger protein |
| Q30437262 | Identification of histone H3 lysine 36 acetylation as a highly conserved histone modification |
| Q34338533 | Inhibition of histone deacetylases induces bovine leukemia virus expression in vitro and in vivo |
| Q58692929 | Inhibitor of CBP Histone Acetyltransferase Downregulates p53 Activation and Facilitates Methylation at Lysine 27 on Histone H3 |
| Q38976614 | KATapulting toward Pluripotency and Cancer |
| Q47926688 | Life with nucleosomes: chromatin remodelling in gene regulation |
| Q28593423 | Loss of Gcn5 acetyltransferase activity leads to neural tube closure defects and exencephaly in mouse embryos |
| Q24522706 | Mammalian GCN5 and P/CAF acetyltransferases have homologous amino-terminal domains important for recognition of nucleosomal substrates |
| Q36319684 | Maternal programming of steroid receptor expression and phenotype through DNA methylation in the rat. |
| Q30443104 | Multi-tasking on chromatin with the SAGA coactivator complexes |
| Q34608754 | Mutational analysis of a histone deacetylase in Drosophila melanogaster: missense mutations suppress gene silencing associated with position effect variegation |
| Q35486433 | Myc and SAGA rewire an alternative splicing network during early somatic cell reprogramming |
| 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. |
| Q34452475 | NF-Y is associated with the histone acetyltransferases GCN5 and P/CAF. |
| Q28574433 | Nerve growth factor receptor signaling induces histone acetyltransferase domain-dependent nuclear translocation of p300/CREB-binding protein-associated factor and hGCN5 acetyltransferases |
| Q42071678 | Nucleosome positioning and histone H3 acetylation are independent processes in the Aspergillus nidulans prnD-prnB bidirectional promoter |
| Q36222404 | On the epigenetics of vascular regulation and disease |
| Q43569963 | Paradoxical effects of trichostatin A: inhibition of NF-Y-associated histone acetyltransferase activity, phosphorylation of hGCN5 and downregulation of cyclin A and B1 mRNA. |
| Q27934501 | Plasmodium falciparum histone acetyltransferase, a yeast GCN5 homologue involved in chromatin remodeling |
| Q55920649 | RETRACTED: Nuclear Receptor Function Requires a TFTC-Type Histone Acetyl Transferase Complex |
| Q38177727 | Regulation of ISWI chromatin remodelling activity |
| Q40580833 | Regulation of transforming growth factor-beta and bone morphogenetic protein signalling by transcriptional coactivator GCN5. |
| Q33336341 | Regulators of cellular levels of histone acetylation in Saccharomyces cerevisiae |
| Q24522344 | Repression of GCN5 histone acetyltransferase activity via bromodomain-mediated binding and phosphorylation by the Ku-DNA-dependent protein kinase complex |
| Q36164767 | Role of histone acetylation in the control of gene expression |
| Q39858162 | Screen for DNA-damage-responsive histone modifications identifies H3K9Ac and H3K56Ac in human cells |
| Q27930044 | Sgf29p facilitates the recruitment of TATA box binding protein but does not alter SAGA's global structural integrity in vivo |
| Q30833764 | Site-specific acetylation of ISWI by GCN5. |
| Q27618997 | Solution structure of the catalytic domain of GCN5 histone acetyltransferase bound to coenzyme A |
| Q28742062 | Stemming epigenetics in marine stramenopiles |
| Q34197768 | TFIIB and subunits of the SAGA complex are involved in transcriptional activation of phospholipid biosynthetic genes by the regulatory protein Ino2 in the yeast Saccharomyces cerevisiae |
| 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 |
| Q91529794 | The Fungal Histone Acetyl Transferase Gcn5 Controls Virulence of the Human Pathogen Candida albicans through Multiple Pathways |
| Q33772811 | The Gcn4p activation domain interacts specifically in vitro with RNA polymerase II holoenzyme, TFIID, and the Adap-Gcn5p coactivator complex |
| Q33667278 | The Myc oncoprotein: a critical evaluation of transactivation and target gene regulation |
| Q27935220 | The N-terminus and Tudor domains of Sgf29 are important for its heterochromatin boundary formation function |
| Q28513184 | The PCAF acetylase complex as a potential tumor suppressor |
| Q51492828 | The SAGA complex in the rice pathogen Fusarium fujikuroi: structure and functional characterization. |
| Q42459431 | The SAGA unfolds: convergence of transcription regulators in chromatin-modifying complexes. |
| Q24310327 | The TAF(II)250 subunit of TFIID has histone acetyltransferase activity |
| Q22010950 | The cloning, mapping and expression of a novel gene, BRL, related to the AF10 leukaemia gene |
| Q35666251 | The diverse superfamily of lysine acetyltransferases and their roles in leukemia and other diseases |
| Q24310357 | The double-histone-acetyltransferase complex ATAC is essential for mammalian development |
| 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 |
| Q37405061 | The p38-interacting protein (p38IP) regulates G2/M progression by promoting α-tubulin acetylation via inhibiting ubiquitination-induced degradation of the acetyltransferase GCN5. |
| Q37571931 | The role of the double bromodomain-containing BET genes during mammalian spermatogenesis |
| Q36569298 | Transcription of the HS2 enhancer toward a cis-linked gene is independent of the orientation, position, and distance of the enhancer relative to the gene |
| Q33775085 | Transcriptional regulation of the MDR1 gene by histone acetyltransferase and deacetylase is mediated by NF-Y. |
| Q42490012 | Transforming growth factor-beta and bone morphogenetic proteins: cooperative players in chick and murine programmed retinal cell death |
| Q50924153 | Trichoderma reesei histone acetyltransferase Gcn5 regulates fungal growth, conidiation, and cellulase gene expression. |
| Q39594198 | Trichostatin A up-regulates human papillomavirus type 11 upstream regulatory region-E6 promoter activity in undifferentiated primary human keratinocytes |
| Q92719155 | Two factor authentication: Asf1 mediates crosstalk between H3 K14 and K56 acetylation |
| Q40902813 | c-Myb acetylation at the carboxyl-terminal conserved domain by transcriptional co-activator p300. |
| Q35698749 | dbHiMo: a web-based epigenomics platform for histone-modifying enzymes. |
| Q33738453 | p300 and CBP: partners for life and death |