| P2093 | author name string | van der Burg B | |
| | van der Saag PT | |
| | Folkers GE | |
| P2860 | cites work | Identification of a retinoic acid responsive element in the retinoic acid receptor beta gene | Q24300919 |
| | An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita | Q24310501 |
| | Adenovirus E1A functions as a cofactor for retinoic acid receptor beta (RAR beta) through direct interaction with RAR beta | Q24311404 |
| | Interaction of thyroid-hormone receptor with a conserved transcriptional mediator | Q24314697 |
| | Nuclear protein CBP is a coactivator for the transcription factor CREB | Q24319801 |
| | UTF1, a novel transcriptional coactivator expressed in pluripotent embryonic stem cells and extra-embryonic cells | Q24533198 |
| | Retinoid X receptor-COUP-TF interactions modulate retinoic acid signaling | Q24563064 |
| | Sequence and characterization of a coactivator for the steroid hormone receptor superfamily | Q27860465 |
| | A CBP integrator complex mediates transcriptional activation and AP-1 inhibition by nuclear receptors | Q27860552 |
| | Molecular cloning and functional analysis of the adenovirus E1A-associated 300-kD protein (p300) reveals a protein with properties of a transcriptional adaptor | Q28286827 |
| | A novel pathway for vitamin A signaling mediated by RXR heterodimerization with NGFI-B and NURR1 | Q28299331 |
| | A dynamic balance between ARP-1/COUP-TFII, EAR-3/COUP-TFI, and retinoic acid receptor:retinoid X receptor heterodimers regulates Oct-3/4 expression in embryonal carcinoma cells | Q28584892 |
| | Characterization of a negative retinoic acid response element in the murine Oct4 promoter | Q28646103 |
| | The RXR heterodimers and orphan receptors | Q29547867 |
| | The role of general initiation factors in transcription by RNA polymerase II | Q29616442 |
| | Role of CBP/P300 in nuclear receptor signalling | Q29616443 |
| | COUP orphan receptors are negative regulators of retinoic acid response pathways | Q30984728 |
| | Characterization of an autoregulated response element in the mouse retinoic acid receptor type beta gene | Q33691459 |
| | Modulation of retinoic acid sensitivity in lung cancer cells through dynamic balance of orphan receptors nur77 and COUP-TF and their heterodimerization | Q33886347 |
| | The promoter context is a decisive factor in establishing selective responsiveness to nuclear class II receptors | Q33886680 |
| | Teratocarcinomas and mammalian embryogenesis | Q34055108 |
| | Direct recognition of initiator elements by a component of the transcription factor IID complex | Q34323438 |
| | DNA sequence requirements for transcriptional initiator activity in mammalian cells | Q34346613 |
| | Weight matrix descriptions of four eukaryotic RNA polymerase II promoter elements derived from 502 unrelated promoter sequences | Q34538483 |
| | Cooperation between core promoter elements influences transcriptional activity in vivo | Q34555034 |
| | Multiplicity generates diversity in the retinoic acid signalling pathways | Q35236424 |
| | Restriction of interferon gamma responsiveness and basal expression of the myeloid human Fc gamma R1b gene is mediated by a functional PU.1 site and a transcription initiator consensus | Q36363233 |
| | Ligand-dependent occupancy of the retinoic acid receptor beta 2 promoter in vivo | Q36672002 |
| | Chicken ovalbumin upstream promoter transcription factor (COUP-TF) dimers bind to different GGTCA response elements, allowing COUP-TF to repress hormonal induction of the vitamin D3, thyroid hormone, and retinoic acid receptors | Q36701525 |
| | Transcription of the lymphocyte-specific terminal deoxynucleotidyltransferase gene requires a specific core promoter structure | Q37636436 |
| | Core promoter specificities of the Sp1 and VP16 transcriptional activation domains | Q38289947 |
| | The orphan receptor TAK1 acts as a repressor of RAR-, RXR- and T3R-mediated signaling pathways | Q38294384 |
| | Retinoid-dependent in vitro transcription mediated by the RXR/RAR heterodimer | Q38301241 |
| | Molecular mechanisms of COUP-TF-mediated transcriptional repression: evidence for transrepression and active repression | Q38358466 |
| | Evidence for impaired retinoic acid receptor-thyroid hormone receptor AF-2 cofactor activity in human lung cancer | Q40016745 |
| | COUP-TF II homodimers are formed in preference to heterodimers with RXR alpha or TR beta in intact cells | Q40396342 |
| | Common themes in assembly and function of eukaryotic transcription complexes | Q40422045 |
| | A cyclic AMP response element is involved in retinoic acid-dependent RAR beta 2 promoter activation | Q40535955 |
| | Properties of initiator-associated transcription mediated by GAL4-VP16. | Q40656959 |
| | Nonsteroid nuclear receptors: what are genetic studies telling us about their role in real life? | Q40922764 |
| | A role for cofactors in synergistic and cell-specific activation by retinoic acid receptors and retinoid X receptor | Q41253956 |
| | TAFs and TFIIA mediate differential utilization of the tandem Adh promoters | Q41308314 |
| | An initiator element is required for maximal human chorionic somatomammotropin gene promoter and enhancer function | Q41368096 |
| | Retinoic acid receptor and retinoid X receptor expression in retinoic acid—resistant human tumor cell lines | Q41587627 |
| | Cooperativity in transactivation between retinoic acid receptor and TFIID requires an activity analogous to E1A | Q41627610 |
| | Aggregation and cell cycle dependent retinoic acid receptor mRNA expression in P19 embryonal carcinoma cells | Q41642559 |
| | Implication of RARB in epidermoid (Squamous) lung cancer | Q41668039 |
| | Contribution of sequences downstream of the TATA element to a protein-DNA complex containing the TATA-binding protein | Q42065380 |
| | Basal promoter elements as a selective determinant of transcriptional activator function | Q42484764 |
| | CIF, an essential cofactor for TFIID-dependent initiator function | Q42524660 |
| | Differential orientations of the DNA-binding domain and carboxy-terminal dimerization interface regulate binding site selection by nuclear receptor heterodimers. | Q46039694 |
| | Roles of SWI1, SWI2, and SWI3 proteins for transcriptional enhancement by steroid receptors | Q46160477 |
| | Determinants for selective RAR and TR recognition of direct repeat HREs. | Q46177795 |
| | Expression of a retinoic acid response element-hsplacZ transgene defines specific domains of transcriptional activity during mouse embryogenesis | Q46255940 |
| | Cloning and expression during development of three murine members of the COUP family of nuclear orphan receptors | Q48081437 |
| | Transcriptional regulation of retinoic acid receptor β in retinoic acid-sensitive and -resistant P19 embryocarcinoma cells | Q52237758 |
| | TFIID sequence recognition of the initiator and sequences farther downstream in Drosophila class II genes. | Q52541449 |
| | Differential expression of genes encoding α, β and γ retinoic acid receptors and CRABP in the developing limbs of the mouse | Q59062799 |
| P433 | issue | 48 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | tretinoin | Q29417 |
| P304 | page(s) | 32200-32212 | |
| P577 | publication date | 1998-11-01 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Promoter architecture, cofactors, and orphan receptors contribute to cell-specific activation of the retinoic acid receptor beta2 promoter. | |
| P478 | volume | 273 | |