| scholarly article | Q13442814 |
| P2093 | author name string | K Struhl | |
| L A Stargell | |||
| R T Ranallo | |||
| P2860 | cites work | Interaction with RAP74 subunit of TFIIF is required for transcriptional activation by serum response factor | Q24313335 |
| Histone-like TAFs within the PCAF histone acetylase complex | Q24317520 | ||
| Cloning and expression of Drosophila TAFII60 and human TAFII70 reveal conserved interactions with other subunits of TFIID | Q24322651 | ||
| Molecular cloning of the small (gamma) subunit of human TFIIA reveals functions critical for activated transcription | Q24336744 | ||
| Binding of basal transcription factor TFIIH to the acidic activation domains of VP16 and p53 | Q24609153 | ||
| RNA polymerase II transcription initiation: a structural view | Q24614755 | ||
| Crystal structure of a TFIIB-TBP-TATA-element ternary complex | Q27729899 | ||
| Co-crystal structure of TBP recognizing the minor groove of a TATA element | Q27732068 | ||
| Crystal structure of a yeast TFIIA/TBP/DNA complex | Q27732643 | ||
| The histone H3-like TAF is broadly required for transcription in yeast | Q27930236 | ||
| A multiprotein mediator of transcriptional activation and its interaction with the C-terminal repeat domain of RNA polymerase II. | Q27930548 | ||
| Reduced binding of TFIID to transcriptionally compromised mutants of VP16. | Q54251780 | ||
| Binding of general transcription factor TFIIB to an acidic activating region | Q59058683 | ||
| Stimulation of RNA polymerase II transcription initiation by recruitment of TBP in vivo | Q59065052 | ||
| Direct and selective binding of an acidic transcriptional activation domain to the TATA-box factor TFIID | Q59070657 | ||
| Connecting a promoter-bound protein to TBP bypasses the need for a transcriptional activation domain | Q60078040 | ||
| Crystal structure of the yeast TFIIA/TBP/DNA complex | Q71075240 | ||
| Yeast TAF(II)90 is required for cell-cycle progression through G2/M but not for general transcription activation | Q71574610 | ||
| Conserved and nonconserved functions of the yeast and human TATA-binding proteins | Q72718769 | ||
| Histone-like TAFs are essential for transcription in vivo | Q77652527 | ||
| A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation | Q27936635 | ||
| Synthesis of large rRNAs by RNA polymerase II in mutants of Saccharomyces cerevisiae defective in RNA polymerase I | Q27936714 | ||
| Yeast TAF(II)145 functions as a core promoter selectivity factor, not a general coactivator | Q27937694 | ||
| Yeast TAF(II)145 required for transcription of G1/S cyclin genes and regulated by the cellular growth state | Q27938810 | ||
| The TBP-TFIIA Interaction in the Response to Acidic Activators in Vivo | Q27939451 | ||
| Dissecting the regulatory circuitry of a eukaryotic genome | Q28131632 | ||
| The TAFs in the HAT | Q28277194 | ||
| Transcriptional activation by recruitment | Q29615048 | ||
| TAFs mediate transcriptional activation and promoter selectivity | Q29616441 | ||
| Biochemistry and structural biology of transcription factor IID (TFIID) | Q29620209 | ||
| An RNA polymerase II holoenzyme responsive to activators | Q29620210 | ||
| Molecular cloning and functional analysis of Drosophila TAF110 reveal properties expected of coactivators | Q29620376 | ||
| Core promoter-specific function of a mutant transcription factor TFIID defective in TATA-box binding | Q33729443 | ||
| The Gcn4p activation domain interacts specifically in vitro with RNA polymerase II holoenzyme, TFIID, and the Adap-Gcn5p coactivator complex | Q33772811 | ||
| A wide variety of DNA sequences can functionally replace a yeast TATA element for transcriptional activation | Q33919654 | ||
| The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAFII60 of Drosophila | Q35196382 | ||
| Synergistic and promoter-selective activation of transcription by recruitment of transcription factors TFIID and TFIIB. | Q36300660 | ||
| Recruiting TATA-binding protein to a promoter: transcriptional activation without an upstream activator | Q36555479 | ||
| A new class of activation-defective TATA-binding protein mutants: evidence for two steps of transcriptional activation in vivo | Q36561614 | ||
| Regional codon randomization: defining a TATA-binding protein surface required for RNA polymerase III transcription | Q36752945 | ||
| Yeast homologues of higher eukaryotic TFIID subunits | Q37047781 | ||
| Absolute mRNA levels and transcriptional initiation rates in Saccharomyces cerevisiae | Q37580107 | ||
| Holo-TFIID supports transcriptional stimulation by diverse activators and from a TATA-less promoter | Q38325574 | ||
| Broad, but not universal, transcriptional requirement for yTAFII17, a histone H3-like TAFII present in TFIID and SAGA. | Q38330677 | ||
| Functional differences between yeast and human TFIID are localized to the highly conserved region | Q38335602 | ||
| Structure-function analysis of TAF130: identification and characterization of a high-affinity TATA-binding protein interaction domain in the N terminus of yeast TAF(II)130 | Q40022288 | ||
| The ts13 mutation in the TAF(II)250 subunit (CCG1) of TFIID directly affects transcription of D-type cyclin genes in cells arrested in G1 at the nonpermissive temperature | Q40022378 | ||
| Chromatin structure and RNA polymerase II connection: implications for transcription | Q40948234 | ||
| Binding of TAFs to core elements directs promoter selectivity by RNA polymerase II | Q41333550 | ||
| Promoter-selective transcriptional defect in cell cycle mutant ts13 rescued by hTAFII250. | Q41487995 | ||
| TAFII-independent activation mediated by human TBP in the presence of the positive cofactor PC4 | Q42459088 | ||
| TFIID can be rate limiting in vivo for TATA-containing, but not TATA-lacking, RNA polymerase II promoters | Q42468186 | ||
| Activation domains of stably bound GAL4 derivatives alleviate repression of promoters by nucleosomes | Q42475419 | ||
| Assembly of recombinant TFIID reveals differential coactivator requirements for distinct transcriptional activators | Q42491732 | ||
| Increased recruitment of TATA-binding protein to the promoter by transcriptional activation domains in vivo | Q42492288 | ||
| Drosophila TAFII40 interacts with both a VP16 activation domain and the basal transcription factor TFIIB. | Q42502083 | ||
| TBP-associated factors are not generally required for transcriptional activation in yeast | Q42522148 | ||
| TAF(II)s mediate activation of transcription in the Drosophila embryo | Q42528499 | ||
| Transcription activation via enhanced preinitiation complex assembly in a human cell-free system lacking TAFIIs | Q47858026 | ||
| Activator-mediated recruitment of the RNA polymerase II machinery is the predominant mechanism for transcriptional activation in yeast | Q47858045 | ||
| Transcription activation in cells lacking TAFIIS. | Q48060189 | ||
| Yeast TAFIIS in a multisubunit complex required for activated transcription. | Q52541518 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 3951-3957 | |
| P577 | publication date | 1999-06-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | A TATA-binding protein mutant defective for TFIID complex formation in vivo | |
| P478 | volume | 19 |
| Q40736935 | Autonomous function of the amino-terminal inhibitory domain of TAF1 in transcriptional regulation |
| Q30700508 | Evidence that TAF-TATA box-binding protein interactions are required for activated transcription in mammalian cells |
| Q34609942 | Functional interaction of CCR4-NOT proteins with TATAA-binding protein (TBP) and its associated factors in yeast. |
| Q27938987 | Impaired core promoter recognition caused by novel yeast TAF145 mutations can be restored by creating a canonical TATA element within the promoter region of the TUB2 gene |
| Q27940055 | Molecular and genetic characterization of a Taf1p domain essential for yeast TFIID assembly. |
| Q34011585 | Region of yeast TAF 130 required for TFIID to associate with promoters |
| Q30587319 | TAFs revisited: more data reveal new twists and confirm old ideas |
| Q33967253 | TFIIA interacts with TFIID via association with TATA-binding protein and TAF40 |
| Q34286148 | The Ccr4-not complex and yTAF1 (yTaf(II)130p/yTaf(II)145p) show physical and functional interactions |
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