| Q35000751 | A TBP-containing multiprotein complex (TIF-IB) mediates transcription specificity of murine RNA polymerase I |
| Q61796943 | A cell cycle-coordinated Polymerase II transcription compartment encompasses gene expression before global genome activation |
| Q42657392 | A cell-specific factor represses stimulation of transcription in vitro by transcriptional enhancer factor 1. |
| Q34875163 | A dual role for SAGA-associated factor 29 (SGF29) in ER stress survival by coordination of both histone H3 acetylation and histone H3 lysine-4 trimethylation |
| Q42136897 | A dual role of linker histone H1.4 Lys 34 acetylation in transcriptional activation |
| Q48185247 | A far upstream estrogen response element of the ovalbumin gene contains several half-palindromic 5'-TGACC-3' motifs acting synergistically |
| Q57970989 | A fraction of the transcription factor TAF15 participates in interactions with a subset of the spliceosomal U1 snRNP complex |
| Q31100751 | A new class of transcription initiation factors, intermediate between TATA box-binding proteins (TBPs) and TBP-like factors (TLFs), is present in the marine unicellular organism, the dinoflagellate Crypthecodinium cohnii |
| Q24682174 | A novel human Ada2 homologue functions with Gcn5 or Brg1 to coactivate transcription |
| Q48733526 | A unified nomenclature for TATA box binding protein (TBP)-associated factors (TAFs) involved in RNA polymerase II transcription |
| Q28507988 | ATAC and Mediator coactivators form a stable complex and regulate a set of non-coding RNA genes |
| Q28115512 | An hGCN5/TRRAP histone acetyltransferase complex co-activates BRCA1 transactivation function through histone modification |
| Q28512845 | Analysis of TATA-binding protein 2 (TBP2) and TBP expression suggests different roles for the two proteins in regulation of gene expression during oogenesis and early mouse development |
| Q45373088 | Architecture of TAF11/TAF13/TBP complex suggests novel regulation properties of general transcription factor TFIID. |
| Q28238481 | Assignment of the human TAFII30 gene (TAF2H) to human chromosome band 11p15.3 using somatic cell hybrids |
| Q24338317 | Ataxin-7 is a subunit of GCN5 histone acetyltransferase-containing complexes |
| Q28235480 | Both normal and polyglutamine- expanded ataxin-7 are components of TFTC-type GCN5 histone acetyltransferase- containing complexes |
| Q24544742 | CCAAT binding NF-Y-TBP interactions: NF-YB and NF-YC require short domains adjacent to their histone fold motifs for association with TBP basic residues |
| Q63406920 | Chaperonin CCT checkpoint function in basal transcription factor TFIID assembly |
| Q41368117 | Characterization of a HeLa cell factor which negatively regulates transcriptional activation in vitro by transcriptional enhancer factor-1 (TEF-1). |
| Q48338620 | Characterization of the L1NH repeat family of Novikoff hepatoma |
| Q38166157 | Chromatin and DNA sequences in defining promoters for transcription initiation. |
| Q39680679 | Chromatin interaction of TATA-binding protein is dynamically regulated in human cells |
| Q42502032 | Chromatin is permissive to TATA-binding protein (TBP)-mediated transcription initiation |
| Q24315758 | Cloning and characterization of hTAFII18, hTAFII20 and hTAFII28: three subunits of the human transcription factor TFIID |
| Q64114392 | Co-translational assembly of mammalian nuclear multisubunit complexes |
| Q41040060 | Coactivators and general transcription factors have two distinct dynamic populations dependent on transcription |
| Q34242723 | Collisions between replication and transcription complexes cause common fragile site instability at the longest human genes |
| Q35023042 | Cytoplasmic TAF2-TAF8-TAF10 complex provides evidence for nuclear holo-TFIID assembly from preformed submodules. |
| Q57971039 | Detection of an EcoRI restriction fragment length polymorphism in the gene encoding the human TBP associated factor II 30 (TAF(II)30) |
| Q40404523 | Different TBP-associated factors are required for mediating the stimulation of transcription in vitro by the acidic transactivator GAL-VP16 and the two nonacidic activation functions of the estrogen receptor. |
| Q45295367 | Differential distribution of the normal and mutated forms of huntingtin in the human brain |
| Q36908396 | Distinct GCN5/PCAF-containing complexes function as co-activators and are involved in transcription factor and global histone acetylation. |
| Q24562199 | Distinct domains of hTAFII100 are required for functional interaction with transcription factor TFIIF beta (RAP30) and incorporation into the TFIID complex |
| Q27936344 | Distinct mutations in yeast TAF(II)25 differentially affect the composition of TFIID and SAGA complexes as well as global gene expression patterns. |
| Q45895879 | Distribution of p53 binding protein 1 (53BP1) and phosphorylated H2A.X during mouse preimplantation development in the absence of DNA damage |
| Q28594607 | Dominant and redundant functions of TFIID involved in the regulation of hepatic genes |
| Q24522406 | EWS, but not EWS-FLI-1, is associated with both TFIID and RNA polymerase II: interactions between two members of the TET family, EWS and hTAFII68, and subunits of TFIID and RNA polymerase II complexes. |
| Q57971062 | Estrogen receptor binds to the salmon GnRH gene in a region with long palindromic sequences |
| Q40816896 | Expression of active hormone and DNA-binding domains of the chicken progesterone receptor in E. coli. |
| Q41097922 | Formation of an active tissue-specific chromatin domain initiated by epigenetic marking at the embryonic stem cell stage. |
| Q24320008 | Function of TAF(II)-containing complex without TBP in transcription by RNA polymerase II |
| Q64071997 | Functional interplay between TFIIH and KAT2A regulates higher-order chromatin structure and class II gene expression |
| Q33392490 | GPAT: retrieval of genomic annotation from large genomic position datasets. |
| Q33493740 | Gcn5 and SAGA regulate shelterin protein turnover and telomere maintenance. |
| Q34119741 | Genes of the ecdysone biosynthesis pathway are regulated by the dATAC histone acetyltransferase complex in Drosophila |
| Q57292666 | Global role for coactivator complexes in RNA polymerase II transcription |
| Q28507540 | Glucagon regulates gluconeogenesis through KAT2B- and WDR5-mediated epigenetic effects |
| Q25256616 | Glutamine-expanded ataxin-7 alters TFTC/STAGA recruitment and chromatin structure leading to photoreceptor dysfunction. |
| Q34393141 | H3K9 and H3K14 acetylation co-occur at many gene regulatory elements, while H3K14ac marks a subset of inactive inducible promoters in mouse embryonic stem cells |
| Q28589235 | Heterochromatin formation in the mouse embryo requires critical residues of the histone variant H3.3 |
| Q38229848 | Histone H2B ubiquitination: signaling not scrapping. |
| Q112718707 | Histone H2Bub1 deubiquitylation is essential for mouse development, but does not regulate global RNA polymerase II transcription |
| Q36483487 | Histone H3 tails containing dimethylated lysine and adjacent phosphorylated serine modifications adopt a specific conformation during mitosis and meiosis |
| Q39458102 | Histone folds mediate selective heterodimerization of yeast TAF(II)25 with TFIID components yTAF(II)47 and yTAF(II)65 and with SAGA component ySPT7. |
| Q52323784 | Homozygous TAF8 mutation in a patient with intellectual disability results in undetectable TAF8 protein, but preserved RNA Polymerase II transcription. |
| Q34310275 | How to stop: the mysterious links among RNA polymerase II occupancy 3' of genes, mRNA 3' processing and termination |
| Q24321811 | Human TAFII30 is present in a distinct TFIID complex and is required for transcriptional activation by the estrogen receptor |
| Q37188855 | Human U1 snRNA forms a new chromatin-associated snRNP with TAF15 |
| Q22010008 | Identification of TATA-binding protein-free TAFII-containing complex subunits suggests a role in nucleosome acetylation and signal transduction |
| Q33279534 | Identification of a small TAF complex and its role in the assembly of TAF-containing complexes |
| Q34093393 | Identification of hTAF(II)80 delta links apoptotic signaling pathways to transcription factor TFIID function |
| Q50026152 | Imaging of native transcription factors and histone phosphorylation at high resolution in live cells. |
| Q42772100 | In vivo evidence that TATA-binding protein/SL1 colocalizes with UBF and RNA polymerase I when rRNA synthesis is either active or inactive |
| Q30803435 | Interpreting and visualizing ChIP-seq data with the seqMINER software |
| Q47971112 | Intronic enhancers control expression of zebrafish sonic hedgehog in floor plate and notochord. |
| Q50327263 | KAT2-mediated PLK4 acetylation contributes to genomic stability by preserving centrosome number |
| Q125341597 | KAT2-mediated acetylation switches the mode of PALB2 chromatin association to safeguard genome integrity |
| Q37393746 | KAT2A/KAT2B-targeted acetylome reveals a role for PLK4 acetylation in preventing centrosome amplification |
| Q47692115 | Keys to open chromatin for transcription activation: FACT and Asf1. |
| Q24616312 | Lessons from genome-wide studies: an integrated definition of the coactivator function of histone acetyl transferases |
| Q28294388 | Localization of the gene (TAF2D) encoding the 100-kDa subunit (hTAFII100) of the human TFIID complex to chromosome 10 band q24-q25.2 |
| Q24534373 | Mammalian TAF(II)30 is required for cell cycle progression and specific cellular differentiation programmes |
| Q34089518 | Mapping histone fold TAFs within yeast TFIID. |
| Q37260390 | Mapping key functional sites within yeast TFIID |
| Q35996339 | Mechanisms of antihormone action |
| Q33764210 | Mof-associated complexes have overlapping and unique roles in regulating pluripotency in embryonic stem cells and during differentiation. |
| Q57971028 | NF-Y Recruitment of TFIID, Multiple Interactions with Histone Fold TAFIIs |
| Q36774924 | New problems in RNA polymerase II transcription initiation: matching the diversity of core promoters with a variety of promoter recognition factors. |
| Q28211665 | Novel subunits of the TATA binding protein free TAFII-containing transcription complex identified by matrix-assisted laser desorption/ionization-time of flight mass spectrometry following one-dimensional gel electrophoresis |
| Q34193915 | Occupancy of the Drosophila hsp70 promoter by a subset of basal transcription factors diminishes upon transcriptional activation. |
| Q28271113 | Organization and chromosomal localization of the gene (TAF2H) encoding the human TBP-associated factor II 30 (TAFII30) |
| Q24313443 | PRMT1 mediated methylation of TAF15 is required for its positive gene regulatory function |
| Q41269608 | Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias |
| Q35372325 | Protein kinase A-mediated serine 35 phosphorylation dissociates histone H1.4 from mitotic chromosome |
| Q55920649 | RETRACTED: Nuclear Receptor Function Requires a TFTC-Type Histone Acetyl Transferase Complex |
| Q57971036 | Regulation of Gene Expression by Multiple Forms of TFIID and Other Novel TAFII-Containing Complexes |
| Q57971019 | Rôle d’une désorganisation de la chromatine dans la neurodégénérescence due à une expansion de polyglutamine dans l’ataxine-7 |
| Q57970969 | SAGA Is a General Cofactor for RNA Polymerase II Transcription |
| Q47790116 | SAGA Is a General Cofactor for RNA Polymerase II Transcription. |
| Q36011032 | SAGA unveiled. |
| Q40409585 | Sequence-specific transactivators counteract topoisomerase II-mediated inhibition of in vitro transcription by RNA polymerases I and II. |
| Q47721313 | Sharing the SAGA. |
| Q41995608 | Subunits of ADA-two-A-containing (ATAC) or Spt-Ada-Gcn5-acetyltrasferase (SAGA) Coactivator Complexes Enhance the Acetyltransferase Activity of GCN5. |
| Q35019731 | TAF10 (TAF(II)30) is necessary for TFIID stability and early embryogenesis in mice. |
| Q35626108 | TAF10 Interacts with the GATA1 Transcription Factor and Controls Mouse Erythropoiesis. |
| Q52043541 | TAF10 is required for the establishment of skin barrier function in foetal, but not in adult mouse epidermis. |
| Q39249159 | TAF15 is important for cellular proliferation and regulates the expression of a subset of cell cycle genes through miRNAs |
| Q39720855 | TAF4b and Jun/activating protein-1 collaborate to regulate the expression of integrin alpha6 and cancer cell migration properties |
| Q33526062 | TAF6delta orchestrates an apoptotic transcriptome profile and interacts functionally with p53. |
| Q24299340 | TAF7 (TAFII55) plays a role in the transcription activation by c-Jun |
| Q112747738 | TAF8 regions important for TFIID lobe B assembly or for TAF2 interactions are required for embryonic stem cell survival |
| Q21262979 | TATA binding protein associated factor 3 (TAF3) interacts with p53 and inhibits its function |
| Q39970043 | TATA box-binding protein-associated factor 12 is important for RAS-induced transformation properties of colorectal cancer cells. |
| Q44055102 | TATA-binding protein-free TAF-containing complex (TFTC) and p300 are both required for efficient transcriptional activation |
| Q43543191 | TBP is not universally required for zygotic RNA polymerase II transcription in zebrafish |
| Q24595327 | TBP-associated factors interact with DNA and govern species specificity of RNA polymerase I transcription |
| Q47069152 | TBP-like factor is required for embryonic RNA polymerase II transcription in C. elegans |
| Q36642182 | TBP/TFIID-dependent activation of MyoD target genes in skeletal muscle cells |
| Q33516977 | TBP2 is a general transcription factor specialized for female germ cells. |
| Q37362829 | TBP2 is essential for germ cell development by regulating transcription and chromatin condensation in the oocyte. |
| Q47073694 | TBP2, a vertebrate-specific member of the TBP family, is required in embryonic development of zebrafish. |
| Q27681162 | TFIID TAF6-TAF9 Complex Formation Involves the HEAT Repeat-containing C-terminal Domain of TAF6 and Is Modulated by TAF5 Protein |
| Q53793587 | Targeting the replisome with transduced monoclonal antibodies triggers lethal DNA replication stress in cancer cells. |
| Q24323898 | The ATAC acetyl transferase complex controls mitotic progression by targeting non-histone substrates. |
| Q36465817 | The Drosophila NURF remodelling and the ATAC histone acetylase complexes functionally interact and are required for global chromosome organization |
| Q28142781 | The N-terminal domain of human TAFII68 displays transactivation and oncogenic properties |
| Q43762001 | The N-terminal region of the chicken progesterone receptor specifies target gene activation |
| Q57971012 | The Proteasome Restricts Permissive Transcription at Tissue-Specific Gene Loci in Embryonic Stem Cells |
| Q34235677 | The SAGA coactivator complex acts on the whole transcribed genome and is required for RNA polymerase II transcription. |
| Q47820612 | The TAF10-containing TFIID and SAGA transcriptional complexes are dispensable for early somitogenesis in the mouse embryo. |
| Q54691046 | The TATA box regulates TATA-binding protein (TBP) dynamics in vivo. |
| Q33724309 | The TBP-like factor: an alternative transcription factor in metazoa? |
| Q24291405 | The TFIID components human TAF(II)140 and Drosophila BIP2 (TAF(II)155) are novel metazoan homologues of yeast TAF(II)47 containing a histone fold and a PHD finger |
| Q41611761 | The architecture of human general transcription factor TFIID core complex |
| Q37110561 | The human SPT20-containing SAGA complex plays a direct role in the regulation of endoplasmic reticulum stress-induced genes. |
| Q34339638 | The human TREX-2 complex is stably associated with the nuclear pore basket. |
| Q40416675 | The major histocompatibility complex (MHC) Ea promoter: sequences and factors at the initiation site. |
| Q43236176 | The metazoan ATAC and SAGA coactivator HAT complexes regulate different sets of inducible target genes |
| Q34107355 | The multicoloured world of promoter recognition complexes. |
| Q28274200 | The putative cofactor TIF1alpha is a protein kinase that is hyperphosphorylated upon interaction with liganded nuclear receptors |
| Q36242528 | The role of enhancers as centres for general transcription factor recruitment. |
| Q42871341 | The spectacular landscape of chromatin and ncRNAs under the Tico sunlight |
| Q24338865 | The structural plasticity of SCA7 domains defines their differential nucleosome-binding properties |
| Q39524270 | Three-dimensional structures of the TAFII-containing complexes TFIID and TFTC. |
| Q42114225 | Tip60 complex binds to active Pol II promoters and a subset of enhancers and co-regulates the c-Myc network in mouse embryonic stem cells |
| Q57029673 | Transcript Buffering: A Balancing Act between mRNA Synthesis and mRNA Degradation |
| Q57970965 | Transcription and mRNA export machineries SAGA and TREX-2 maintain monoubiquitinated H2B balance required for DNA repair |
| Q28249862 | Transcription factor TFIID recruits factor CPSF for formation of 3' end of mRNA |
| Q47790162 | Transcription of Nearly All Yeast RNA Polymerase II-Transcribed Genes Is Dependent on Transcription Factor TFIID. |
| Q38095707 | Transcription-replication encounters, consequences and genomic instability |
| Q36566966 | Transcriptional alterations and chromatin remodeling in polyglutamine diseases. |
| Q24556548 | Two distinct estrogen-regulated promoters generate transcripts encoding the two functionally different human progesterone receptor forms A and B |
| Q35131757 | Two isoforms of Drosophila TRF2 are involved in embryonic development, premeiotic chromatin condensation, and proper differentiation of germ cells of both sexes. |
| Q33962278 | Two novel Drosophila TAF(II)s have homology with human TAF(II)30 and are differentially regulated during development |
| Q24550893 | UV-damaged DNA-binding protein in the TFTC complex links DNA damage recognition to nucleosome acetylation |
| Q33945643 | UVB induces a genome-wide acting negative regulatory mechanism that operates at the level of transcription initiation in human cells |
| Q63972398 | Uniform Widespread Nuclear Phosphorylation of Histone H2AX Is an Indicator of Lethal DNA Replication Stress |
| Q36555582 | Widely spaced, directly repeated PuGGTCA elements act as promiscuous enhancers for different classes of nuclear receptors. |
| Q42653067 | YEATS2 links histone acetylation to tumorigenesis of non-small cell lung cancer. |
| Q46728959 | Zinc-finger UBPs: regulators of deubiquitylation |
| Q51989076 | [Suppression of non-specific transcription by the proteasome in embryonic stem cells]. |
| Q27346614 | dTAF10- and dTAF10b-Containing Complexes Are Required for Ecdysone-Driven Larval-Pupal Morphogenesis in Drosophila melanogaster |
| Q33777909 | seqMINER: an integrated ChIP-seq data interpretation platform |