Transcription reinitiation rate: a special role for the TATA box.
about
Structure and expression of the human p68 RNA helicase gene.Genomic organization, 5'-flanking region and chromosomal localization of the human glutathione transferase A4 geneDifferential transcription of the orphan receptor RORbeta in nuclear extracts derived from Neuro2A and HeLa cellsSingle-RNA counting reveals alternative modes of gene expression in yeastInvestigating transcription reinitiation through in vitro approachesThe unexpected traits associated with core promoter elementsA single-molecule view of transcription reveals convoys of RNA polymerases and multi-scale bursting.Intermediates in formation and activity of the RNA polymerase II preinitiation complex: holoenzyme recruitment and a postrecruitment role for the TATA box and TFIIB.Stepwise bending of DNA by a single TATA-box binding protein.Robust simplifications of multiscale biochemical networksPrecise regulation of gene expression dynamics favors complex promoter architectures.TATA-binding protein mutants that increase transcription from enhancerless and repressed promoters in vivoRoles for non-TATA core promoter sequences in transcription and factor bindingGenetic selection for context-dependent stochastic phenotypes: Sp1 and TATA mutations increase phenotypic noise in HIV-1 gene expression.A downstream element in the human beta-globin promoter: evidence of extended sequence-specific transcription factor IID contactsp300 and estrogen receptor cooperatively activate transcription via differential enhancement of initiation and reinitiation.Multiplex Eukaryotic Transcription (In)activation: Timing, Bursting and Cycling of a Ratchet Clock MechanismIdentification of cis-Regulatory Elements in the dmyc Gene of Drosophila Melanogaster.Linking Core Promoter Classes to Circadian TranscriptionAffinity and competition for TBP are molecular determinants of gene expression noise.Sequence features of yeast and human core promoters that are predictive of maximal promoter activityDNA signals at isoform promotersA global change in RNA polymerase II pausing during the Drosophila midblastula transition.Assembly of the transcription machinery: ordered and stable, random and dynamic, or both?Distinct roles for Ku protein in transcriptional reinitiation and DNA repair.Potential effect on cellular response to cadmium of a single-nucleotide A --> G polymorphism in the promoter of the human gene for metallothionein IIA.DTIE, a novel core promoter element that directs start site selection in TATA-less genes.A genomic model of condition-specific nucleosome behavior explains transcriptional activity in yeast.Multiple rounds of transcription by RNA polymerase II at covalently cross-linked templatesImmediate-early and delayed primary response genes are distinct in function and genomic architecture.Promoter activation via a cyclic AMP response element in vitro.Co-occurrence of transcription and translation gene regulatory features underlies coordinated mRNA and protein synthesis.The transcriptional activator GAL4-VP16 regulates the intra-molecular interactions of the TATA-binding protein.Comparative expression and transcript initiation of three peach dehydrin genes.TATA-flanking sequences influence the rate and stability of TATA-binding protein and TFIIB binding.Disparity between microRNA levels and promoter strength is associated with initiation rate and Pol II pausing.The TATA motif, the CAA motif and the poly(T) transcription termination motif are all important for transcription re-initiation on plant tRNA genesA transcription reinitiation intermediate that is stabilized by activator
P2860
Q24515332-BD0253D5-2C1A-446F-9684-8CDF914497A5Q24531325-E94A6ABB-9EC1-49DD-B5F0-8374343E3A05Q24555410-AD02CEF0-155E-4767-AABD-C9658B24B073Q24619115-7D5BA334-5A63-4531-B851-FE80F616AD0EQ26824513-926302CE-416B-49E1-8073-71DBC0B8AE65Q26862549-EF9C3CCE-3667-4130-A7EC-89C53AEAFDA1Q27334977-1D369B4F-6A68-400C-BA5A-38D38D9468C8Q27940351-25383DBD-86D7-47A9-B8C4-D5CCE35E4827Q30477147-62CBEAA5-6EE0-4F31-87AC-BA62158F2C6BQ33375863-B5C8F45B-6085-48E8-9E53-0EE72E614FF2Q33404059-97C433B1-7173-4721-AF6A-1D4FD230BE62Q33962132-085FE2FA-1A36-4C84-AD57-89373388A925Q33963402-FF18D368-244E-4E72-A408-31E021D7B9F0Q34845153-0529D38A-48AC-4B78-B447-B5251A19F4F7Q35154603-310EB54B-B0C5-4A95-84D5-839DF9763D58Q35189958-7267291A-F961-4A52-9AD6-78DDF1208A6CQ35613455-C58D9DB2-BB7A-4701-A024-0B2FEF3181E0Q35669176-9E5F4278-BBAE-4D23-B22D-BCCA0B8ED9AEQ36098618-267376F1-2405-419E-A9E7-3CC67EFDB816Q36542390-4DD69D52-8CEC-4A60-9142-9EF65A9CF407Q36909766-80DA368A-F036-4CDC-B29B-FF6405958CC0Q37050196-6C6376B9-A9D3-4638-A4C8-D17189208352Q37094528-E7781AFF-3F72-4AA9-A44E-E09C27553278Q37952066-C2E7FD3B-DB9F-472B-A96E-CBD161D9EA79Q38302594-A9B6AC06-E5D5-4B97-8CD9-79EF5B8AFD27Q38310397-F0173053-ADA7-494E-8513-27F0E105B9E2Q38530549-4B95ECE3-5670-40C8-AC57-8CFB3F20DEB3Q39706090-0692F1C1-E247-4951-88E3-03FD53E09206Q39724044-F39E638D-42B8-4F4C-A5BA-968CC2E50FFAQ42040118-8A1F4CC5-9FBA-477D-8D5A-B36DC00C36E5Q42669452-7D0A2CB6-87F7-4BA2-AF4C-FE03A612DFDBQ42869375-093B8E6F-5BAB-43F4-9E62-97F718D72D28Q44061142-3013A057-CB8B-43F2-A650-4C63A9B4489AQ44472633-2D216E28-8AA4-488F-A945-4364CF005BDBQ46145585-64F95AE1-96AF-4760-BF4F-A8A86F49A592Q46833286-4E5C34D0-8FE6-4DAD-92F9-B341DDCA228EQ58065473-F396C508-3A94-4E8B-A287-32680710AB69Q59071495-A2EF132A-74F1-4569-9063-B2249E3EBFDD
P2860
Transcription reinitiation rate: a special role for the TATA box.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Transcription reinitiation rate: a special role for the TATA box.
@en
type
label
Transcription reinitiation rate: a special role for the TATA box.
@en
prefLabel
Transcription reinitiation rate: a special role for the TATA box.
@en
P2860
P356
P1476
Transcription reinitiation rate: a special role for the TATA box.
@en
P2860
P304
P356
10.1128/MCB.17.7.3809
P407
P577
1997-07-01T00:00:00Z