| scholarly article | Q13442814 |
| P356 | DOI | 10.1074/JBC.M002989200 |
| P698 | PubMed publication ID | 10896937 |
| P50 | author | Naoko Tanese | Q56015691 |
| P2093 | author name string | Furukawa T | |
| Tanese N | |||
| P2860 | cites work | Novel cofactors and TFIIA mediate functional core promoter selectivity by the human TAFII150-containing TFIID complex | Q22003968 |
| Human transcription factor hTAF(II)150 (CIF150) is involved in transcriptional regulation of cell cycle progression | Q22010401 | ||
| Cloning and expression of human TAFII250: a TBP-associated factor implicated in cell-cycle regulation | Q24308057 | ||
| Human TAF(II)135 potentiates transcriptional activation by the AF-2s of the retinoic acid, vitamin D3, and thyroid hormone receptors in mammalian cells | Q24311726 | ||
| Histone-like TAFs within the PCAF histone acetylase complex | Q24317520 | ||
| Function of TAF(II)-containing complex without TBP in transcription by RNA polymerase II | Q24320008 | ||
| Specific interactions and potential functions of human TAFII100 | Q24322534 | ||
| Distinct subdomains of human TAFII130 are required for interactions with glutamine-rich transcriptional activators | Q24522713 | ||
| DNA binding site selection by RNA polymerase II TAFs: a TAF(II)250-TAF(II)150 complex recognizes the initiator | Q24534381 | ||
| 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 | Q24554357 | ||
| The human CCG1 gene, essential for progression of the G1 phase, encodes a 210-kilodalton nuclear DNA-binding protein | Q24601947 | ||
| Molecular cloning and analysis of two subunits of the human TFIID complex: hTAFII130 and hTAFII100 | Q24682969 | ||
| Solution structure of a TBP-TAF(II)230 complex: protein mimicry of the minor groove surface of the TATA box unwound by TBP | Q27765345 | ||
| The histone H3-like TAF is broadly required for transcription in yeast | Q27930236 | ||
| A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation | Q27936635 | ||
| 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 | ||
| Functional domains and upstream activation properties of cloned human TATA binding protein | Q28116604 | ||
| Dissecting the regulatory circuitry of a eukaryotic genome | Q28131632 | ||
| Transcription factor IIA derepresses TATA-binding protein (TBP)-associated factor inhibition of TBP-DNA binding | Q28272088 | ||
| The TAFs in the HAT | Q28277194 | ||
| The general transcription factors of RNA polymerase II | Q28298663 | ||
| Regulation of gene expression by TBP-associated proteins | Q28679170 | ||
| The role of general initiation factors in transcription by RNA polymerase II | Q29616442 | ||
| Biochemistry and structural biology of transcription factor IID (TFIID) | Q29620209 | ||
| Mechanism of transcriptional activation by Sp1: evidence for coactivators | Q29620214 | ||
| Transcription activation by the adenovirus E1a protein | Q29620538 | ||
| Product review. New mammalian expression vectors | Q29620743 | ||
| Different functional domains of TAFII250 modulate expression of distinct subsets of mammalian genes | Q30846886 | ||
| Simian virus 40 large T antigen stabilizes the TATA-binding protein-TFIIA complex on the TATA element | Q33774811 | ||
| TBP-associated factors (TAFIIs): multiple, selective transcriptional mediators in common complexes | Q33832058 | ||
| Purification and analysis of RNA polymerase II transcription factors by using wheat germ agglutinin affinity chromatography | Q33842710 | ||
| Human TAFII 105 is a cell type-specific TFIID subunit related to hTAFII130. | Q34401793 | ||
| 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 | ||
| TAFII250-dependent transcription of cyclin A is directed by ATF activator proteins | Q35193620 | ||
| The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAFII60 of Drosophila | Q35196382 | ||
| Considerations of transcriptional control mechanisms: do TFIID-core promoter complexes recapitulate nucleosome-like functions? | Q36035094 | ||
| The Drosophila 110-kDa transcription factor TFIID subunit directly interacts with the N-terminal region of the 230-kDa subunit | Q36382074 | ||
| Mechanisms for flexibility in DNA sequence recognition and VP16-induced complex formation by the Oct-1 POU domain | Q36550439 | ||
| Drosophila TFIIA-L is processed into two subunits that are associated with the TBP/TAF complex | Q36754140 | ||
| TAFII mutations disrupt Dorsal activation in the Drosophila embryo | Q36792176 | ||
| Use of a hybrid vaccinia virus-T7 RNA polymerase system for expression of target genes | Q36843702 | ||
| Factors involved in specific transcription by mammalian RNA polymerase II: purification, genetic specificity, and TATA box-promoter interactions of TFIID. | Q36846156 | ||
| Broad, but not universal, transcriptional requirement for yTAFII17, a histone H3-like TAFII present in TFIID and SAGA. | Q38330677 | ||
| 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 | ||
| TAF-like function of SV40 large T antigen | Q41196723 | ||
| Mechanisms of transcriptional activation: differences and similarities between yeast, Drosophila, and man. | Q41441677 | ||
| Molecular cloning of Drosophila TFIID subunits | Q41488440 | ||
| Coactivators for a proline-rich activator purified from the multisubunit human TFIID complex | Q42468497 | ||
| Assembly of recombinant TFIID reveals differential coactivator requirements for distinct transcriptional activators | Q42491732 | ||
| Drosophila TFIIA directs cooperative DNA binding with TBP and mediates transcriptional activation | Q42492930 | ||
| The p250 subunit of native TATA box-binding factor TFIID is the cell-cycle regulatory protein CCG1. | Q42510472 | ||
| TBP-associated factors are not generally required for transcriptional activation in yeast | Q42522148 | ||
| CIF, an essential cofactor for TFIID-dependent initiator function | Q42524660 | ||
| Largest subunit of Drosophila transcription factor IID directs assembly of a complex containing TBP and a coactivator. | Q44826917 | ||
| Transcription activation in cells lacking TAFIIS. | Q48060189 | ||
| Monoclonal antibodies directed against the amino-terminal domain of human TBP cross-react with TBP from other species. | Q52552566 | ||
| GAL4 derivatives function alone and synergistically with mammalian activators in vitro | Q58422721 | ||
| Topology and reorganization of a human TFIID–promoter complex | Q60083846 | ||
| A small-scale procedure for preparation of nuclear extracts that support efficient transcription and pre-mRNA splicing | Q67970168 | ||
| Yeast TAF(II)90 is required for cell-cycle progression through G2/M but not for general transcription activation | Q71574610 | ||
| TFIIA regulates TBP and TFIID dimers | Q73075615 | ||
| Global transcription regulators of eukaryotes | Q74670392 | ||
| TATA box mimicry by TFIID: autoinhibition of pol II transcription | Q77313418 | ||
| 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 | ||
| The role of TAFs in RNA polymerase II transcription | Q77654626 | ||
| P433 | issue | 38 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 29847-29856 | |
| P577 | publication date | 2000-09-01 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Assembly of partial TFIID complexes in mammalian cells reveals distinct activities associated with individual TATA box-binding protein-associated factors | |
| P478 | volume | 275 |
| Q33850179 | Complete genome sequence of the shrimp white spot bacilliform virus |
| Q27644713 | Conserved region I of human coactivator TAF4 binds to a short hydrophobic motif present in transcriptional regulators |
| Q39645792 | Distinct requirements for C.elegans TAF(II)s in early embryonic transcription |
| Q38716923 | Egr-1 and RNA POL II facilitate glioma cell GDNF transcription induced by histone hyperacetylation in promoter II. |
| Q77665569 | Enhanced apoptosis of B and T lymphocytes in TAFII105 dominant-negative transgenic mice is linked to nuclear factor-kappa B |
| Q27937030 | Fluorescence-based analyses of the effects of full-length recombinant TAF130p on the interaction of TATA box-binding protein with TATA box DNA. |
| Q33558899 | Human Taf(II)130 is a coactivator for NFATp |
| Q44562084 | Identification of a novel TATA element-binding protein binding region at the N terminus of the Saccharomyces cerevisiae TAF1 protein |
| Q47878452 | Identification of heteromolecular binding sites in transcription factors Sp1 and TAF4 using high-resolution nuclear magnetic resonance spectroscopy. |
| Q24534176 | Isoform-specific interaction of HP1 with human TAFII130. |
| Q27930749 | Protein-protein interaction map for yeast TFIID. |
| Q38363849 | Sp1 is a key regulator of the PDGF beta-receptor transcription |
| Q35033681 | TAF4 nucleates a core subcomplex of TFIID and mediates activated transcription from a TATA-less promoter |
| Q37083712 | TAF4 takes flight |
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