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RNA polymerase stalling at developmental control genes in the Drosophila melanogaster embryoPreparing the first responders: building the inflammatory transcriptome from the ground upPromoter-proximal pausing of RNA polymerase II: emerging roles in metazoansHistone gene replacement reveals a post-transcriptional role for H3K36 in maintaining metazoan transcriptome fidelity.ORIO (Online Resource for Integrative Omics): a web-based platform for rapid integration of next generation sequencing data.Probing TBP interactions in transcription initiation and reinitiation with RNA aptamers that act in distinct modes.Moonshine illuminates a developmental role for regulated transcription elongationDrosophila Paf1 modulates chromatin structure at actively transcribed genes.Pol II waiting in the starting gates: Regulating the transition from transcription initiation into productive elongation.Mll3 and Mll4 Facilitate Enhancer RNA Synthesis and Transcription from Promoters Independently of H3K4 Monomethylation.Bacteriophage T4 MotA and AsiA proteins suffice to direct Escherichia coli RNA polymerase to initiate transcription at T4 middle promotersPausing of RNA polymerase II regulates mammalian developmental potential through control of signaling networks.Bidirectional Transcription Arises from Two Distinct Hubs of Transcription Factor Binding and Active ChromatinCoupling polymerase pausing and chromatin landscapes for precise regulation of transcription.Global analysis of short RNAs reveals widespread promoter-proximal stalling and arrest of Pol II in DrosophilaDefining the status of RNA polymerase at promoters.Promoter-proximal Pol II: when stalling speeds things up.Spt6 enhances the elongation rate of RNA polymerase II in vivoStable pausing by RNA polymerase II provides an opportunity to target and integrate regulatory signalsImmediate mediators of the inflammatory response are poised for gene activation through RNA polymerase II stalling.Acetylation of RNA polymerase II regulates growth-factor-induced gene transcription in mammalian cells.The Importance of Controlling Transcription Elongation at Coding and Noncoding RNA Loci.Enhanced chromatin accessibility of the dosage compensated Drosophila male X-chromosome requires the CLAMP zinc finger protein.The kinetics of pre-mRNA splicing in the Drosophila genome and the influence of gene architecture.Intragenic Enhancers Attenuate Host Gene Expression.Taking MLL through the MudPIT: identification of novel complexes that bring together MLL-fusion proteins and transcription elongation factors.RNA polymerase II stalling mediates cytokine gene expression.Characterization of the interactions between the bacteriophage T4 AsiA protein and RNA polymerase.Non-coding RNA: More uses for genomic junkNegative elongation factor is essential for endometrial functionThe interaction between the AsiA protein of bacteriophage T4 and the sigma70 subunit of Escherichia coli RNA polymeraseConserved regions 4.1 and 4.2 of sigma(70) constitute the recognition sites for the anti-sigma factor AsiA, and AsiA is a dimer free in solutionHow does Pol II overcome the nucleosome barrier?Interaction of T4 AsiA with its target sites in the RNA polymerase sigma70 subunit leads to distinct and opposite effects on transcriptionEmerging Roles of Non-Coding RNA TranscriptionNF-Y controls fidelity of transcription initiation at gene promoters through maintenance of the nucleosome-depleted regionPromoter-proximal pausing of RNA polymerase II: a nexus of gene regulation
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hulumtuese
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Karen Adelman
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Karen Adelman
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Karen Adelman
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Karen Adelman
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Karen Adelman
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Karen Adelman
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Karen Adelman
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Karen Adelman
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Karen Adelman
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Karen Adelman
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Karen Adelman
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Karen Adelman
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Karen Adelman
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