scholarly article | Q13442814 |
P2093 | author name string | Parker JS | |
Shah R | |||
Zeitlinger J | |||
Grissom SF | |||
Adelman K | |||
Gilchrist DA | |||
Muse GW | |||
Nechaev S | |||
P2860 | cites work | Human transcription elongation factor NELF: identification of novel subunits and reconstitution of the functionally active complex | Q24296462 |
Evidence that negative elongation factor represses transcription elongation through binding to a DRB sensitivity-inducing factor/RNA polymerase II complex and RNA. | Q24537283 | ||
Attenuation of estrogen receptor alpha-mediated transcription through estrogen-stimulated recruitment of a negative elongation factor | Q24562734 | ||
Promoter-associated pausing in promoter architecture and postinitiation transcriptional regulation | Q28138307 | ||
Control of developmental regulators by Polycomb in human embryonic stem cells | Q28235841 | ||
A high-resolution map of active promoters in the human genome | Q29614431 | ||
Genome-wide map of nucleosome acetylation and methylation in yeast | Q29614525 | ||
Elongation by RNA polymerase II: the short and long of it | Q29614529 | ||
The transition from initiation to elongation by RNA polymerase II. | Q33671443 | ||
The RNA polymerase II elongation complex | Q34188475 | ||
Breaking barriers to transcription elongation | Q34561019 | ||
NELF and DSIF cause promoter proximal pausing on the hsp70 promoter in Drosophila | Q35965503 | ||
Transcriptional regulation and the role of diverse coactivators in animal cells | Q36024274 | ||
Transcription Factor and Polymerase Recruitment, Modification, and Movement on dhsp70 In Vivo in the Minutes following Heat Shock | Q36139169 | ||
In vivo transcriptional pausing and cap formation on three Drosophila heat shock genes | Q36499506 | ||
Postinitiation transcriptional control in Drosophila melanogaster | Q36733771 | ||
RNA polymerase II interacts with the promoter region of the noninduced hsp70 gene in Drosophila melanogaster cells | Q36899837 | ||
High-resolution computational models of genome binding events. | Q38310716 | ||
Transcriptional pausing caused by NELF plays a dual role in regulating immediate-early expression of the junB gene | Q38408801 | ||
The ability of positive transcription elongation factor B to transactivate human immunodeficiency virus transcription depends on a functional kinase domain, cyclin T1, and Tat. | Q39580108 | ||
Direct cloning of DNA that interacts in vivo with a specific protein: application to RNA polymerase II and sites of pausing in Drosophila | Q39722928 | ||
Transcriptional regulation of the Ig kappa gene by promoter-proximal pausing of RNA polymerase II. | Q40924990 | ||
Promoter-proximal pausing of RNA polymerase II defines a general rate-limiting step after transcription initiation | Q41365790 | ||
Hold back of RNA polymerase II at the transcription start site mediates down-regulation of c-myc in vivo | Q41535694 | ||
Transcription elongation controls cell fate specification in the Drosophila embryo | Q42846574 | ||
Efficient release from promoter-proximal stall sites requires transcript cleavage factor TFIIS. | Q45209737 | ||
The block to transcriptional elongation within the human c-myc gene is determined in the promoter-proximal region | Q49162171 | ||
The RNA polymerase II molecule at the 5' end of the uninduced hsp70 gene of D. melanogaster is transcriptionally engaged. | Q52459657 | ||
Short transcripts of the ternary complex provide insight into RNA polymerase II elongational pausing. | Q52536804 | ||
Genome-wide analyses of steroid- and radiation-triggered programmed cell death in Drosophila. | Q53658652 | ||
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1507-11 | |
P577 | publication date | 2007-12-01 | |
P1433 | published in | Nature Genetics | Q976454 |
P1476 | title | RNA polymerase is poised for activation across the genome | |
P478 | volume | 39 |
Q33598533 | 14-3-3 mediates histone cross-talk during transcription elongation in Drosophila |
Q33813311 | 4sUDRB-seq: measuring genomewide transcriptional elongation rates and initiation frequencies within cells |
Q92797796 | A 50 year history of technologies that drove discovery in eukaryotic transcription regulation |
Q37014169 | A Two-Way Street: Regulatory Interplay between RNA Polymerase and Nascent RNA Structure |
Q43155322 | A canonical promoter organization of the transcription machinery and its regulators in the Saccharomyces genome |
Q37333813 | A conserved protein motif is required for full modulatory activity of negative elongation factor subunits NELF-A and NELF-B in modifying glucocorticoid receptor-regulated gene induction properties |
Q26823816 | A double take on bivalent promoters |
Q33658615 | A genome-wide gene function prediction resource for Drosophila melanogaster |
Q34109795 | A high-resolution whole-genome map of key chromatin modifications in the adult Drosophila melanogaster |
Q35238267 | A large-scale, in vivo transcription factor screen defines bivalent chromatin as a key property of regulatory factors mediating Drosophila wing development |
Q34881331 | A mathematical model for adaptive prediction of environmental changes by microorganisms. |
Q35315347 | A model for sigma factor competition in bacterial cells |
Q34946814 | A polar barrier to transcription can be circumvented by remodeler-induced nucleosome translocation |
Q43106462 | A role for Chk1 in blocking transcriptional elongation of p21 RNA during the S-phase checkpoint |
Q35342607 | A role for the serine/arginine-rich (SR) protein B52/SRSF6 in cell growth and myc expression in Drosophila |
Q36788279 | A stimulation-dependent alternate core promoter links lymphotoxin α expression with TGF-β1 and fibroblast growth factor-7 signaling in primary human T cells |
Q37218488 | A streamlined method for rapid and sensitive chromatin immunoprecipitation |
Q37475277 | AFF1 is a ubiquitous P-TEFb partner to enable Tat extraction of P-TEFb from 7SK snRNP and formation of SECs for HIV transactivation |
Q33857407 | AFF4, a component of the ELL/P-TEFb elongation complex and a shared subunit of MLL chimeras, can link transcription elongation to leukemia |
Q37606074 | Acetylation of RNA polymerase II regulates growth-factor-induced gene transcription in mammalian cells |
Q27933190 | Activation of a poised RNAPII-dependent promoter requires both SAGA and mediator |
Q35168257 | Activation of inactive hepatocytes through histone acetylation: a mechanism for functional compensation after massive loss of hepatocytes |
Q34357060 | Activation-induced cytidine deaminase targets DNA at sites of RNA polymerase II stalling by interaction with Spt5 |
Q34016223 | Active promoters and insulators are marked by the centrosomal protein 190. |
Q91828810 | Acute NelfA knockdown restricts compensatory gene expression and precipitates ventricular dysfunction during cardiac hypertrophy |
Q35673793 | Aire unleashes stalled RNA polymerase to induce ectopic gene expression in thymic epithelial cells |
Q35225247 | Allele-specific distribution of RNA polymerase II on female X chromosomes |
Q35269902 | Alternative applications for distinct RNA sequencing strategies |
Q47073911 | Antagonistic regulation of PAF1C and p-TEFb is required for oligodendrocyte differentiation. |
Q42426276 | Architecture and RNA binding of the human negative elongation factor. |
Q36978246 | BRD4 coordinates recruitment of pause release factor P-TEFb and the pausing complex NELF/DSIF to regulate transcription elongation of interferon-stimulated genes |
Q35762970 | Bidirectional Transcription Arises from Two Distinct Hubs of Transcription Factor Binding and Active Chromatin |
Q34961966 | Binding of TFIIIC to sine elements controls the relocation of activity-dependent neuronal genes to transcription factories |
Q54729413 | Biochemistry. Nudging through a nucleosome. |
Q37144184 | Biogenesis of mRNPs: integrating different processes in the eukaryotic nucleus |
Q57634686 | Biogenic mechanisms and utilization of small RNAs derived from human protein-coding genes |
Q88609298 | Born to run: control of transcription elongation by RNA polymerase II |
Q37586824 | Brd4 and HEXIM1: multiple roles in P-TEFb regulation and cancer |
Q37453336 | CD69 gene is differentially regulated in T and B cells by evolutionarily conserved promoter-distal elements. |
Q59352420 | CDK9: a signaling hub for transcriptional control |
Q41888533 | CRP-cyclic AMP dependent inhibition of the xylene-responsive σ(54)-promoter Pu in Escherichia coli |
Q37740906 | CYCLINg through transcription: posttranslational modifications of P-TEFb regulate transcription elongation |
Q37036327 | Capturing the dynamic nascent transcriptome during acute cellular responses: The serum response |
Q47108063 | Cdk7 Is Required for Activity-Dependent Neuronal Gene Expression, Long-Lasting Synaptic Plasticity and Long-Term Memory |
Q37207706 | ChIP-Seq of ERalpha and RNA polymerase II defines genes differentially responding to ligands |
Q34342266 | Characteristic bimodal profiles of RNA polymerase II at thousands of active mammalian promoters |
Q37374740 | Chromatin architecture and transcription factor binding regulate expression of erythrocyte membrane protein genes |
Q37395194 | Chromatin poises miRNA- and protein-coding genes for expression |
Q34306290 | Chromatin remodeling in the aging genome of Drosophila |
Q40694812 | Chromatin signature of embryonic pluripotency is established during genome activation |
Q37135175 | Chromatin state marks cell-type- and gender-specific replication of the Drosophila genome |
Q55299954 | Classification of Transcription Boundary-Associated RNAs (TBARs) in Animals and Plants. |
Q36019901 | Co-transcriptional regulation of alternative pre-mRNA splicing |
Q37233367 | Coactivator function defines the active estrogen receptor alpha cistrome |
Q38708191 | Cohesin selectively binds and regulates genes with paused RNA polymerase |
Q35814984 | Compensatory induction of MYC expression by sustained CDK9 inhibition via a BRD4-dependent mechanism |
Q35920526 | Complex effects of flavopiridol on the expression of primary response genes |
Q33797835 | Composite effects of polymorphisms near multiple regulatory elements create a major-effect QTL |
Q35208578 | Construction of mate pair full-length cDNAs libraries and characterization of transcriptional start sites and termination sites |
Q33521283 | Contrasting patterns of transposable element insertions in Drosophila heat-shock promoters |
Q41941777 | Control of Transcriptional Elongation by RNA Polymerase II: A Retrospective |
Q39285490 | Control of inducible gene expression by signal-dependent transcriptional elongation |
Q34038245 | Control of transcriptional elongation |
Q37952115 | Controlling gene expression in response to stress. |
Q37727635 | Core promoter functions in the regulation of gene expression of Drosophila dorsal target genes |
Q33963951 | Corepressor-directed preacetylation of histone H3 in promoter chromatin primes rapid transcriptional switching of cell-type-specific genes in yeast |
Q36019786 | Coupling polymerase pausing and chromatin landscapes for precise regulation of transcription. |
Q37351796 | Curled encodes the Drosophila homolog of the vertebrate circadian deadenylase Nocturnin |
Q38003504 | Cyclin K goes with Cdk12 and Cdk13 |
Q40370696 | Cyclin-dependent kinase 8 module expression profiling reveals requirement of mediator subunits 12 and 13 for transcription of Serpent-dependent innate immunity genes in Drosophila. |
Q37274531 | DNA-binding specificity and in vivo targets of Caenorhabditis elegans nuclear factor I. |
Q53038876 | DSIF and NELF interact with Integrator to specify the correct post-transcriptional fate of snRNA genes. |
Q33708432 | Defining mechanisms that regulate RNA polymerase II transcription in vivo |
Q30491968 | Defining the chromatin signature of inducible genes in T cells |
Q38069828 | Defining the molecular blueprint that drives CD8(+) T cell differentiation in response to infection |
Q36354477 | Defining the status of RNA polymerase at promoters |
Q51776964 | Detecting transcriptionally engaged RNA polymerase in eukaryotic cells with permanganate genomic footprinting. |
Q33815482 | Detection and removal of biases in the analysis of next-generation sequencing reads |
Q90663956 | Determinants of enhancer and promoter activities of regulatory elements |
Q37666209 | Developmental gene regulation in the era of genomics |
Q37669961 | Different modes of enhancer-specific regulation by Runt and Even-skipped during Drosophila segmentation |
Q38751095 | Differential Incorporation of β-actin as A Component of RNA Polymerase II into Regulatory Regions of Stemness/Differentiation Genes in Retinoic Acid-Induced Differentiated Human Embryonic Carcinoma Cells. |
Q34575885 | Differential glucocorticoid receptor-mediated transcription mechanisms |
Q98286423 | Differentiating Drosophila female germ cells initiate Polycomb silencing by regulating PRC2-interacting proteins |
Q35216990 | Differentiation-dependent functional and epigenetic landscapes for cytokine genes in virus-specific CD8+ T cells |
Q21184027 | Discovery of active enhancers through bidirectional expression of short transcripts |
Q26851212 | Disengaging polymerase: terminating RNA polymerase II transcription in budding yeast |
Q34926054 | Distinct mechanisms for induction and tolerance regulate the immediate early genes encoding interleukin 1β and tumor necrosis factor α. |
Q38678210 | Distinct mechanisms of transcriptional pausing orchestrated by GAGA factor and M1BP, a novel transcription factor |
Q35569660 | Drosophila CLOCK target gene characterization: implications for circadian tissue-specific gene expression |
Q41866613 | Drosophila HP1c isoform interacts with the zinc-finger proteins WOC and Relative-of-WOC to regulate gene expression |
Q33375061 | Drosophila Kismet regulates histone H3 lysine 27 methylation and early elongation by RNA polymerase II |
Q35177234 | Drosophila Set1 is the major histone H3 lysine 4 trimethyltransferase with role in transcription. |
Q39310118 | Drosophila dosage compensation involves enhanced Pol II recruitment to male X-linked promoters |
Q28308228 | Drosophila heat shock system as a general model to investigate transcriptional regulation |
Q33702832 | Drosophila melanogaster positive transcriptional elongation factors regulate metabolic and sex-biased expression in adults. |
Q88903638 | Dynamic Change of Transcription Pausing through Modulating NELF Protein Stability Regulates Granulocytic Differentiation |
Q37429059 | Dynamic bookmarking of primary response genes by p300 and RNA polymerase II complexes. |
Q35128809 | Dynamic transcriptional events in embryonic stem cells mediated by the super elongation complex (SEC). |
Q64901530 | Dynamic turnover of paused Pol II complexes at human promoters. |
Q47571126 | Dynamics of RNA Polymerase II Pausing and Bivalent Histone H3 Methylation during Neuronal Differentiation in Brain Development |
Q49844069 | Dynamics of promoter bivalency and RNAP II pausing in mouse stem and differentiated cells |
Q38101203 | Dysregulation of the basal RNA polymerase transcription apparatus in cancer |
Q47380191 | Effects of Arsenic Trioxide on INF-gamma Gene Expression in MRL/lpr Mice and Human Lupus. |
Q37832956 | Elongator: an ancestral complex driving transcription and migration through protein acetylation |
Q49646234 | Emerging themes in neuronal activity-dependent gene expression |
Q37075889 | Enforcing the pause: transcription factor Sp3 limits productive elongation by RNA polymerase II. |
Q34426602 | Enrichment of HP1a on Drosophila chromosome 4 genes creates an alternate chromatin structure critical for regulation in this heterochromatic domain |
Q38886548 | Epigenetic Mechanisms Governing Innate Inflammatory Responses. |
Q37961801 | Epigenetic control of inducible gene expression in the immune system. |
Q38100221 | Epigenetic regulation of pregnane X receptor activity |
Q37875255 | Epigenetic reprogramming during tissue regeneration |
Q33941308 | Epigenomics of T cell activation, differentiation, and memory |
Q33553323 | Erk1/2 activity promotes chromatin features and RNAPII phosphorylation at developmental promoters in mouse ESCs |
Q38338265 | Erythropoiesis is regulated by the transcription elongation factor Foggy/Spt5 through gata1 gene regulation |
Q37615737 | Establishing legitimacy and function in the new transcriptome |
Q57232452 | Eukaryotic core promoters and the functional basis of transcription initiation |
Q34008734 | Evidence that gene activation and silencing during stem cell differentiation requires a transcriptionally paused intermediate state |
Q34790876 | Evolution of insect dorsoventral patterning mechanisms |
Q28818754 | Experimental reconstitution of chronic ER stress in the liver reveals feedback suppression of BiP mRNA expression |
Q42272959 | Extensive cooperation of immune master regulators IRF3 and NFκB in RNA Pol II recruitment and pause release in human innate antiviral transcription |
Q36902919 | Extensive polymerase pausing during Drosophila axis patterning enables high-level and pliable transcription |
Q24310508 | FACT facilitates chromatin transcription by RNA polymerases I and III |
Q39687705 | Factor binding and chromatin modification in the promoter of murine Egr1 gene upon induction |
Q26860339 | From stem cell to red cell: regulation of erythropoiesis at multiple levels by multiple proteins, RNAs, and chromatin modifications |
Q36017203 | Functional Interaction between HEXIM and Hedgehog Signaling during Drosophila Wing Development |
Q24608025 | Functional association of Gdown1 with RNA polymerase II poised on human genes |
Q36794841 | Functional interplay between PPM1G and the transcription elongation machinery |
Q42905470 | Functional relevance of the IRF-1 promoter polymorphism rs2549009 on transcriptional activity in a native genomic environment |
Q35588343 | GAGA factor maintains nucleosome-free regions and has a role in RNA polymerase II recruitment to promoters |
Q37129691 | GAGA factor, a positive regulator of global gene expression, modulates transcriptional pausing and organization of upstream nucleosomes |
Q35485914 | Gene induction and repression during terminal erythropoiesis are mediated by distinct epigenetic changes |
Q42121552 | Gene silencing induced by oxidative DNA base damage: association with local decrease of histone H4 acetylation in the promoter region |
Q35975449 | Gene trapping uncovers sex-specific mechanisms for upstream stimulatory factors 1 and 2 in angiotensinogen expression |
Q37932011 | Gene-specific transcription activation via long-range allosteric shape-shifting |
Q35378348 | Genetic and genomic analyses of RNA polymerase II-pausing factor in regulation of mammalian transcription and cell growth |
Q90482460 | Genome-Wide Maps of Transcription Regulatory Elements and Transcription Enhancers in Development and Disease |
Q92663614 | Genome-wide RNA pol II initiation and pausing in neural progenitors of the rat |
Q90236056 | Genome-wide RNAi screen in Drosophila reveals Enok as a novel trithorax group regulator |
Q36652760 | Genome-wide analysis of KAP1, the 7SK snRNP complex, and RNA polymerase II. |
Q38326754 | Genome-wide analysis of interferon regulatory factor I binding in primary human monocytes |
Q34649901 | Genome-wide control of RNA polymerase II activity by cohesin |
Q47293908 | Genome-wide dose-dependent inhibition of histone deacetylases studies reveal their roles in enhancer remodeling and suppression of oncogenic super-enhancers. |
Q36684862 | Genome-wide localization of exosome components to active promoters and chromatin insulators in Drosophila |
Q40001784 | Genome-wide mapping of allele-specific protein-DNA interactions in human cells. |
Q41349094 | Genome-wide mapping of boundary element-associated factor (BEAF) binding sites in Drosophila melanogaster links BEAF to transcription |
Q28473490 | Genome-wide modeling of transcription preinitiation complex disassembly mechanisms using ChIP-chip data |
Q35969015 | Genome-wide profiling of RNA polymerase transcription at nucleotide resolution in human cells with native elongating transcript sequencing. |
Q37142037 | Genome-wide profiling of salt fractions maps physical properties of chromatin |
Q33954563 | Genomic organization of H2Av containing nucleosomes in Drosophila heterochromatin |
Q36214878 | Global analysis of short RNAs reveals widespread promoter-proximal stalling and arrest of Pol II in Drosophila |
Q36935665 | Global regulation of promoter melting in naive lymphocytes |
Q47146098 | Global unleashing of transcription elongation waves in response to genotoxic stress restricts somatic mutation rate |
Q37157412 | Glucocorticoid receptor represses proinflammatory genes at distinct steps of the transcription cycle |
Q84346986 | Guest Editor's Introduction. Controlling which genes are transcriptionally expressed is key to the generation and maintenance of the repertoire of cell types needed to support the mammalian lifestyle |
Q34637938 | H2A.Z nucleosomes enriched over active genes are homotypic |
Q42355543 | H3K4me3 inversely correlates with DNA methylation at a large class of non-CpG-island-containing start sites |
Q34439368 | H3S28 phosphorylation is a hallmark of the transcriptional response to cellular stress. |
Q28535456 | HEXIM1 induces differentiation of human pluripotent stem cells |
Q37226490 | HEXIM1, a New Player in the p53 Pathway |
Q24294721 | HIF1A employs CDK8-mediator to stimulate RNAPII elongation in response to hypoxia |
Q36535347 | HIV-1 Tat recruits transcription elongation factors dispersed along a flexible AFF4 scaffold |
Q35569664 | Heat shock reduces stalled RNA polymerase II and nucleosome turnover genome-wide |
Q35634495 | High-resolution mapping of open chromatin in the rice genome |
Q38273698 | High-wire act: the poised genome and cellular memory. |
Q34044777 | Histone cross-talk connects protein phosphatase 1α (PP1α) and histone deacetylase (HDAC) pathways to regulate the functional transition of bromodomain-containing 4 (BRD4) for inducible gene expression |
Q24317522 | Histone crosstalk between H3S10ph and H4K16ac generates a histone code that mediates transcription elongation |
Q34496093 | Homozygous mdm2 SNP309 cancer cells with compromised transcriptional elongation at p53 target genes are sensitive to induction of p53-independent cell death |
Q34737713 | Hormone-induced and DNA demethylation-induced relief of a tissue-specific and developmentally regulated block in transcriptional elongation. |
Q37514183 | How eukaryotic genes are transcribed |
Q34310275 | How to stop: the mysterious links among RNA polymerase II occupancy 3' of genes, mRNA 3' processing and termination |
Q35202721 | Human Polymerase-Associated Factor complex (PAFc) connects the Super Elongation Complex (SEC) to RNA polymerase II on chromatin |
Q24310867 | Human mediator subunit MED26 functions as a docking site for transcription elongation factors |
Q33783758 | Human mutations in integrator complex subunits link transcriptome integrity to brain development |
Q33673701 | Human negative elongation factor activates transcription and regulates alternative transcription initiation |
Q33565273 | Identification and characterization of putative methylation targets in the MAOA locus using bioinformatic approaches |
Q24297975 | Identification of HEXIM1 as a positive regulator of p53 |
Q47071011 | Identification of Regions in the Spt5 Subunit of DRB Sensitivity-inducing Factor (DSIF) That Are Involved in Promoter-proximal Pausing |
Q33382118 | Identification of Spt5 target genes in zebrafish development reveals its dual activity in vivo |
Q38810955 | Identification of active miRNA promoters from nuclear run-on RNA sequencing |
Q37416607 | Immediate mediators of the inflammatory response are poised for gene activation through RNA polymerase II stalling. |
Q37737546 | Inducible gene expression: diverse regulatory mechanisms |
Q37181838 | Inhibition of a transcriptional pause by RNA anchoring to RNA polymerase |
Q35036881 | Inhibition of cdk9 during herpes simplex virus 1 infection impedes viral transcription |
Q24611607 | Insights from genomic profiling of transcription factors |
Q37532346 | Integrated transcriptome analysis of mouse spermatogenesis |
Q34938254 | Integrator regulates transcriptional initiation and pause release following activation |
Q27934482 | Interaction of transcriptional regulators with specific nucleosomes across the Saccharomyces genome |
Q42137229 | Interactions between DNA, transcriptional regulator Dreb2a and the Med25 mediator subunit from Arabidopsis thaliana involve conformational changes |
Q33953149 | Interactions between DSIF (DRB sensitivity inducing factor), NELF (negative elongation factor), and the Drosophila RNA polymerase II transcription elongation complex |
Q34536954 | Interferon antagonist NSs of La Crosse virus triggers a DNA damage response-like degradation of transcribing RNA polymerase II. |
Q35125991 | Interferon regulatory factor 1 marks activated genes and can induce target gene expression in systemic lupus erythematosus |
Q34140931 | Interferon γ-inducible protein (IFI) 16 transcriptionally regulates type i interferons and other interferon-stimulated genes and controls the interferon response to both DNA and RNA viruses |
Q37724099 | Interferon-γ resets muscle cell fate by stimulating the sequential recruitment of JARID2 and PRC2 to promoters to repress myogenesis |
Q38024157 | Interplay between chromatin modifications and paused RNA polymerase II in dynamic transition between stalled and activated genes |
Q33659597 | Intrinsic histone-DNA interactions are not the major determinant of nucleosome positions in vivo |
Q33671329 | Intron delays and transcriptional timing during development |
Q37367998 | Isolation and functional analysis of RNA polymerase II elongation complexes. |
Q36467037 | KAP1 Recruitment of the 7SK snRNP Complex to Promoters Enables Transcription Elongation by RNA Polymerase II. |
Q91595828 | Kethoxal-assisted single-stranded DNA sequencing captures global transcription dynamics and enhancer activity in situ |
Q37488718 | Kinetics of promoter Pol II on Hsp70 reveal stable pausing and key insights into its regulation. |
Q24646322 | LARP7 is a stable component of the 7SK snRNP while P-TEFb, HEXIM1 and hnRNP A1 are reversibly associated |
Q34019641 | LARP7 suppresses P-TEFb activity to inhibit breast cancer progression and metastasis |
Q85036285 | Licensed to elongate: a molecular mechanism for MLL-based leukaemogenesis |
Q36098618 | Linking Core Promoter Classes to Circadian Transcription |
Q34934209 | Linking stochastic fluctuations in chromatin structure and gene expression |
Q35897282 | Local chromatin dynamics of transcription factors imply cell-lineage specific functions during cellular differentiation |
Q37356218 | Location, location, (ChIP-)location! Mapping chromatin landscapes one immunoprecipitation at a time |
Q37528860 | Long non-coding RNA identification over mouse brain development by integrative modeling of chromatin and genomic features |
Q33531810 | Lsh mediated RNA polymerase II stalling at HoxC6 and HoxC8 involves DNA methylation |
Q33353263 | MINIYO and transcriptional elongation: lifting the roadblock to differentiation. |
Q37406282 | MYC and transcription elongation. |
Q27309085 | Maintenance of Tissue Pluripotency by Epigenetic Factors Acting at Multiple Levels |
Q42881078 | Maintenance of cell fates through acetylated histone and the histone variant H2A.z in C. elegans |
Q37992785 | Making sense of transcribing chromatin |
Q37331003 | Mapping key features of transcriptional regulatory circuitry in embryonic stem cells. |
Q33826920 | Mechanism and factors that control HIV-1 transcription and latency activation |
Q37211398 | Mechanism of sequence-specific pausing of bacterial RNA polymerase |
Q26830860 | Mechanism of transcription through a nucleosome by RNA polymerase II |
Q40969997 | Mechanisms and Developmental Roles of Promoter-proximal Pausing of RNA Polymerase II. |
Q53606806 | Mechanisms of Evolutionary Innovation Point to Genetic Control Logic as the Key Difference Between Prokaryotes and Eukaryotes. |
Q36293078 | Mechanisms of Groucho-mediated repression revealed by genome-wide analysis of Groucho binding and activity |
Q41769072 | Mechanisms of HIV Transcriptional Regulation and Their Contribution to Latency |
Q36710552 | Mechanisms of backtrack recovery by RNA polymerases I and II. |
Q39206646 | Mediator MED23 regulates basal transcription in vivo via an interaction with P-TEFb |
Q37843610 | Mediator and post-recruitment regulation of RNA polymerase II |
Q47073703 | Mediator subunit 12 coordinates intrinsic and extrinsic control of epithalamic development |
Q38029260 | Menin as a hub controlling mixed lineage leukemia |
Q33679131 | Metal transcription factor-1 regulation via MREs in the transcribed regions of selenoprotein H and other metal-responsive genes |
Q34258857 | Metazoan promoters: emerging characteristics and insights into transcriptional regulation |
Q28084780 | Minireview: nuclear receptor coregulators of the p160 family: insights into inflammation and metabolism |
Q34556377 | Mll3 and Mll4 Facilitate Enhancer RNA Synthesis and Transcription from Promoters Independently of H3K4 Monomethylation |
Q37615912 | Modifications of RNA polymerase II are pivotal in regulating gene expression states |
Q38161393 | Molecular and Epigenetic Mechanisms of MLL in Human Leukemogenesis |
Q42472280 | Molecular maps of the reorganization of genome-nuclear lamina interactions during differentiation |
Q33909578 | Monovalent and unpoised status of most genes in undifferentiated cell-enriched Drosophila testis |
Q100559556 | Motif 1 Binding Protein suppresses wingless to promote eye fate in Drosophila |
Q28475186 | Mouse cofactor of BRCA1 (Cobra1) is required for early embryogenesis. |
Q33576499 | Multifunctional enhancers regulate mouse and human vitamin D receptor gene transcription |
Q37211018 | Multiple P-TEFbs cooperatively regulate the release of promoter-proximally paused RNA polymerase II. |
Q90187891 | NELF Regulates a Promoter-Proximal Step Distinct from RNA Pol II Pause-Release |
Q36710845 | NELF and GAGA factor are linked to promoter-proximal pausing at many genes in Drosophila |
Q28474810 | NELF potentiates gene transcription in the Drosophila embryo |
Q36802956 | NELF-mediated stalling of Pol II can enhance gene expression by blocking promoter-proximal nucleosome assembly |
Q92535255 | Nascent RNA analyses: tracking transcription and its regulation |
Q58713866 | Nascent RNA sequencing analysis provides insights into enhancer-mediated gene regulation |
Q28302903 | Nascent RNA sequencing reveals widespread pausing and divergent initiation at human promoters |
Q35927818 | Native elongating transcript sequencing reveals human transcriptional activity at nucleotide resolution |
Q38629873 | Negative elongation factor accelerates the rate at which heat shock genes are shut off by facilitating dissociation of heat shock factor |
Q33602605 | Negative elongation factor is required for the maintenance of proviral latency but does not induce promoter-proximal pausing of RNA polymerase II on the HIV long terminal repeat |
Q42776375 | Neuronal identity genes regulated by super-enhancers are preferentially down-regulated in the striatum of Huntington's disease mice |
Q34919381 | New insights into the control of HIV-1 transcription: when Tat meets the 7SK snRNP and super elongation complex (SEC). |
Q33565208 | Noncanonical transcript forms in yeast and their regulation during environmental stress |
Q47158530 | Nuclear EGFR and Integrator/Super Elongation Complex concurrently binds to Immediate Early Genes for gene transactivation |
Q34499614 | Nuclear RNA sequencing of the mouse erythroid cell transcriptome |
Q27348460 | Nuclear pore proteins nup153 and megator define transcriptionally active regions in the Drosophila genome |
Q37091501 | Nuclear receptor location analyses in mammalian genomes: from gene regulation to regulatory networks |
Q37326387 | Nucleosome organization in the Drosophila genome. |
Q36883122 | Nucleosome positioning and gene regulation: advances through genomics |
Q39416252 | O-GlcNAcase Is an RNA Polymerase II Elongation Factor Coupled to Pausing Factors SPT5 and TIF1β. |
Q38327596 | Oct-1 cooperates with the TATA binding initiation complex to control rapid transcription of human iNOS. |
Q38028210 | One step back before moving forward: regulation of transcription elongation by arrest and backtracking. |
Q27311517 | P-TEFb, the super elongation complex and mediator regulate a subset of non-paused genes during early Drosophila embryo development |
Q37356131 | P-TEFb- the final frontier |
Q36371761 | PAF1, a Molecular Regulator of Promoter-Proximal Pausing by RNA Polymerase II |
Q92661276 | PARylation During Transcription: Insights into the Fine-Tuning Mechanism and Regulation |
Q38955475 | Pathogenesis of Börjeson-Forssman-Lehmann syndrome: Insights from PHF6 function |
Q39211326 | Pause & go: from the discovery of RNA polymerase pausing to its functional implications. |
Q38364406 | Paused Pol II captures enhancer activity and acts as a potent insulator |
Q37874803 | Paused RNA polymerase II as a developmental checkpoint |
Q36974098 | Pausing for thought: disrupting the early transcription elongation checkpoint leads to developmental defects and tumourigenesis. |
Q34346839 | Pausing of RNA polymerase II disrupts DNA-specified nucleosome organization to enable precise gene regulation |
Q35470656 | Pausing of RNA polymerase II regulates mammalian developmental potential through control of signaling networks. |
Q35950455 | Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression |
Q33348473 | Plant Elongator regulates auxin-related genes during RNA polymerase II transcription elongation |
Q36611111 | Poised RNA polymerase II changes over developmental time and prepares genes for future expression |
Q33522209 | Poised transcription factories prime silent uPA gene prior to activation. |
Q34048002 | Pol II and its associated epigenetic marks are present at Pol III-transcribed noncoding RNA genes. |
Q33631279 | Pol II docking and pausing at growth and stress genes in C. elegans |
Q34494012 | Pol II waiting in the starting gates: Regulating the transition from transcription initiation into productive elongation. |
Q35248792 | Pol III binding in six mammals shows conservation among amino acid isotypes despite divergence among tRNA genes. |
Q34570800 | Polycomb group complexes--many combinations, many functions |
Q34548266 | Polycomb preferentially targets stalled promoters of coding and noncoding transcripts |
Q37875927 | Polycomb proteins in mammalian cell differentiation and plasticity |
Q47556292 | Polymorphism in Tmem132d regulates expression and anxiety-related behavior through binding of RNA polymerase II complex |
Q42609408 | Post-transcription initiation function of the ubiquitous SAGA complex in tissue-specific gene activation |
Q37099958 | Postrecruitment regulation of RNA polymerase II directs rapid signaling responses at the promoters of estrogen target genes |
Q38606913 | Precise maps of RNA polymerase reveal how promoters direct initiation and pausing |
Q42137507 | Predicting promoter activities of primary human DNA sequences |
Q34065439 | Prediction of RNA Polymerase II recruitment, elongation and stalling from histone modification data |
Q36821394 | Premature termination of transcription by RNAP II: the beginning of the end. |
Q41902743 | Prevalence of RNA polymerase stalling at Escherichia coli promoters after open complex formation |
Q36549002 | Probabilistic modelling of chromatin code landscape reveals functional diversity of enhancer-like chromatin states |
Q36676820 | Promoter elements associated with RNA Pol II stalling in the Drosophila embryo |
Q37284766 | Promoter proximal pausing on genes in metazoans |
Q37993419 | Promoter-associated RNAs and promoter-targeted RNAs |
Q33779012 | Promoter-bound p300 complexes facilitate post-mitotic transmission of transcriptional memory |
Q37764482 | Promoter-proximal pausing and its release: molecular mechanisms and physiological functions |
Q92254256 | Promoter-proximal pausing of RNA polymerase II: a nexus of gene regulation |
Q29394946 | Promoter-proximal pausing of RNA polymerase II: emerging roles in metazoans |
Q38435681 | RNA Pol II accumulates at promoters of growth genes during developmental arrest. |
Q37056307 | RNA Polymerase II cluster dynamics predict mRNA output in living cells |
Q37992154 | RNA polymerase II elongation control |
Q36505626 | RNA polymerase II pausing as a context-dependent reader of the genome |
Q35562114 | RNA polymerase II pausing can be retained or acquired during activation of genes involved in the epithelial to mesenchymal transition. |
Q34305741 | RNA polymerase II pausing downstream of core histone genes is different from genes producing polyadenylated transcripts |
Q37618666 | RNA polymerase II pausing during development |
Q41663773 | RNA polymerase II pausing modulates hematopoietic stem cell emergence in zebrafish |
Q36739436 | RNA polymerase II stalling: loading at the start prepares genes for a sprint |
Q34046663 | RNA polymerase II transcription elongation and Pol II CTD Ser2 phosphorylation: A tail of two kinases |
Q34960186 | RNA polymerase II transcription elongation control |
Q27666396 | RNA polymerase and transcription elongation factor Spt4/5 complex structure |
Q93927358 | RNA polymerase caught loitering |
Q33953340 | RNA polymerase complexes cooperate to relieve the nucleosomal barrier and evict histones |
Q34080284 | RNA polymerase mapping during stress responses reveals widespread nonproductive transcription in yeast |
Q38341092 | RNA polymerase trafficking in Bacillus subtilis cells. |
Q37031722 | RNA splicing regulates the temporal order of TNF-induced gene expression |
Q33578947 | RNAi screen in Drosophila larvae identifies histone deacetylase 3 as a positive regulator of the hsp70 heat shock gene expression during heat shock |
Q28576463 | Rapid activity-induced transcription of Arc and other IEGs relies on poised RNA polymerase II |
Q27302880 | Rapid transcriptional pulsing dynamics of high expressing retroviral transgenes in embryonic stem cells |
Q41944247 | Rapid, transcription-independent loss of nucleosomes over a large chromatin domain at Hsp70 loci |
Q38562823 | Ready, pause, go: regulation of RNA polymerase II pausing and release by cellular signaling pathways |
Q33564189 | Real-time observation of the transition from transcription initiation to elongation of the RNA polymerase |
Q29392187 | Regulating RNA polymerase pausing and transcription elongation in embryonic stem cells |
Q35945067 | Regulating the regulators: the pervasive effects of Pol II pausing on stimulus-responsive gene networks |
Q42045280 | Regulation of Hox gene activity by transcriptional elongation in Drosophila |
Q41767088 | Regulation of an inducible promoter by an HP1beta-HP1gamma switch |
Q54188370 | Regulation of chromatin states and gene expression during HSN neuronal maturation is mediated by EOR-1/PLZF, MAU-2/cohesin loader, and SWI/SNF complex. |
Q36735223 | Regulation of the transcriptional activity of poised RNA polymerase II by the elongation factor ELL |
Q24650920 | Regulator trafficking on bacterial transcription units in vivo |
Q21144996 | Regulon-specific control of transcription elongation across the yeast genome |
Q64088219 | Reporter-ChIP-nexus reveals strong contribution of the initiator sequence to RNA polymerase pausing |
Q36042582 | Repression of Hox genes by LMP1 in nasopharyngeal carcinoma and modulation of glycolytic pathway genes by HoxC8. |
Q33501748 | Repression of RNA polymerase II elongation in vivo is critically dependent on the C-terminus of Spt5. |
Q37631411 | Role of noncoding RNAs in the regulation of P-TEFb availability and enzymatic activity |
Q37292763 | S region sequence, RNA polymerase II, and histone modifications create chromatin accessibility during class switch recombination |
Q42552805 | SAGA function in tissue-specific gene expression |
Q35077092 | SUV420H2-mediated H4K20 trimethylation enforces RNA polymerase II promoter-proximal pausing by blocking hMOF-dependent H4K16 acetylation |
Q47876829 | Selective expression of the transcription elongation factor ELL3 in B cells prior to ELL2 drives proliferation and survival |
Q35001684 | Sequential changes at differentiation gene promoters as they become active in a stem cell lineage |
Q35770298 | Ser-634 and Ser-636 of Kaposi's Sarcoma-Associated Herpesvirus RTA are Involved in Transactivation and are Potential Cdk9 Phosphorylation Sites |
Q30491199 | Single molecule transcription elongation |
Q38043827 | Single-molecule studies of RNAPII elongation |
Q36545639 | Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells |
Q90132296 | Spatial organization of RNA polymerase and its relationship with transcription in Escherichia coli |
Q38109752 | Splitting hares and tortoises: a classification of neuronal immediate early gene transcription based on poised RNA polymerase II. |
Q37196147 | Spt6 enhances the elongation rate of RNA polymerase II in vivo |
Q37352913 | Stable pausing by RNA polymerase II provides an opportunity to target and integrate regulatory signals |
Q34799963 | Stably paused genes revealed through inhibition of transcription initiation by the TFIIH inhibitor triptolide |
Q42241186 | Stalled Hox promoters as chromosomal boundaries |
Q80113569 | Stalled polymerases and transcriptional regulation |
Q52859841 | Stochastic resetting in backtrack recovery by RNA polymerases. |
Q36811094 | Stress from Nucleotide Depletion Activates the Transcriptional Regulator HEXIM1 to Suppress Melanoma. |
Q36238292 | Structural analysis of nucleosomal barrier to transcription |
Q40275061 | Super elongation complex promotes early HIV transcription and its function is modulated by P-TEFb |
Q37083712 | TAF4 takes flight |
Q90229016 | TCEA1 regulates the proliferative potential of mouse myeloid cells |
Q24337625 | TIF1gamma controls erythroid cell fate by regulating transcription elongation |
Q34307694 | TRIM28 regulates RNA polymerase II promoter-proximal pausing and pause release |
Q35967446 | Targeting DOT1L and HOX gene expression in MLL-rearranged leukemia and beyond |
Q38297247 | Temporal Dissection of Rate Limiting Transcriptional Events Using Pol II ChIP and RNA Analysis of Adrenergic Stress Gene Activation. |
Q36776327 | The Bin3 RNA methyltransferase targets 7SK RNA to control transcription and translation |
Q36444189 | The Central Region of the Drosophila Co-repressor Groucho as a Regulatory Hub. |
Q36435140 | The DUBm subunit Sgf11 is required for mRNA export and interacts with Cbp80 in Drosophila |
Q24597477 | The Drosophila 7SK snRNP and the essential role of dHEXIM in development |
Q47251709 | The Drosophila CLAMP protein associates with diverse proteins on chromatin |
Q47857382 | The Hox proteins Ubx and AbdA collaborate with the transcription pausing factor M1BP to regulate gene transcription |
Q38140886 | The JAK-STAT pathway in hypertrophic stress signaling and genomic stress response |
Q28068962 | The Many Faces of Elongator in Neurodevelopment and Disease |
Q38043907 | The Mediator complex and transcription elongation |
Q28299679 | The Mediator complex and transcription regulation |
Q26849595 | The Mediator complex: a central integrator of transcription |
Q34313744 | The NSL complex regulates housekeeping genes in Drosophila. |
Q51547007 | The Pisum sativum psp54 gene requires ABI3 and a chromatin remodeller to switch from a poised to a transcriptionally active state. |
Q64054855 | The RNA helicase UPF1 associates with mRNAs co-transcriptionally and is required for the release of mRNAs from gene loci |
Q34303212 | The RNA polymerase II CTD coordinates transcription and RNA processing. |
Q50141694 | The Role of Noncoding RNA Pseudouridylation in Nuclear Gene Expression Events. |
Q27664689 | The Transcription Factor Spn1 Regulates Gene Expression via a Highly Conserved Novel Structural Motif |
Q35910444 | The Transition of Poised RNA Polymerase II to an Actively Elongating State Is a "Complex" Affair |
Q55492193 | The Ubx Polycomb response element bypasses an unpaired Fab-8 insulator via cis transvection in Drosophila. |
Q36959286 | The X-linked intellectual disability protein PHF6 associates with the PAF1 complex and regulates neuronal migration in the mammalian brain. |
Q37200232 | The ZFP-1(AF10)/DOT-1 complex opposes H2B ubiquitination to reduce Pol II transcription |
Q36107018 | The chromatin remodeling and mRNA splicing functions of the Brahma (SWI/SNF) complex are mediated by the SNR1/SNF5 regulatory subunit |
Q37634306 | The complex eukaryotic transcriptome: unexpected pervasive transcription and novel small RNAs |
Q35035409 | The elongin complex antagonizes the chromatin factor Corto for vein versus intervein cell identity in Drosophila wings |
Q89901315 | The embryonic linker histone dBigH1 alters the functional state of active chromatin |
Q39005055 | The emerging picture of CDK9/P-TEFb: more than 20 years of advances since PITALRE. |
Q24336460 | The euchromatic and heterochromatic landscapes are shaped by antagonizing effects of transcription on H2A.Z deposition |
Q33369072 | The genomic distribution and function of histone variant HTZ-1 during C. elegans embryogenesis |
Q36070586 | The histone H3 Lys 27 demethylase JMJD3 regulates gene expression by impacting transcriptional elongation |
Q27930846 | The histone H3K36 demethylase Rph1/KDM4 regulates the expression of the photoreactivation gene PHR1 |
Q28276700 | The human Mediator complex: a versatile, genome-wide regulator of transcription |
Q21136168 | The mechanism of release of P-TEFb and HEXIM1 from the 7SK snRNP by viral and cellular activators includes a conformational change in 7SK |
Q37809563 | The next generation: using new sequencing technologies to analyse gene regulation |
Q50459532 | The origins of developmental gene regulation |
Q36052947 | The pathogenesis of mixed-lineage leukemia |
Q92534361 | The pause-initiation limit restricts transcription activation in human cells |
Q42046257 | The polycomb group mutant esc leads to augmented levels of paused Pol II in the Drosophila embryo |
Q37417300 | The presence of RNA polymerase II, active or stalled, predicts epigenetic fate of promoter CpG islands |
Q37455573 | The structure-function link of compensated chromatin in Drosophila |
Q27692038 | The super elongation complex (SEC) and MLL in development and disease |
Q36210873 | The super elongation complex family of RNA polymerase II elongation factors: gene target specificity and transcriptional output |
Q41680259 | The transcriptional coactivators SAGA, SWI/SNF, and mediator make distinct contributions to activation of glucose-repressed genes |
Q29035794 | The transition from transcriptional initiation to elongation |
Q38837437 | There goes the neighborhood: Assembly of transcriptional complexes during the regulation of metabolism and inflammation by the glucocorticoid receptor. |
Q36520899 | TiF1-gamma plays an essential role in murine hematopoiesis and regulates transcriptional elongation of erythroid genes |
Q36972178 | To grow or not to grow: nutritional control of development during Caenorhabditis elegans L1 arrest |
Q37156727 | Topoisomerases facilitate transcription of long genes linked to autism |
Q26801362 | Transcription Blockage Leads to New Beginnings |
Q42137522 | Transcription control by long non-coding RNAs |
Q37603622 | Transcription dynamics |
Q34499436 | Transcription elongation and tissue-specific somatic CAG instability |
Q37194356 | Transcription elongation control by the 7SK snRNP complex: Releasing the pause. |
Q48731754 | Transcription elongation factors represent in vivo cancer dependencies in glioblastoma |
Q39069527 | Transcription elongation regulator 1 (TCERG1) regulates competent RNA polymerase II-mediated elongation of HIV-1 transcription and facilitates efficient viral replication. |
Q34426416 | Transcription elongation. Heterogeneous tracking of RNA polymerase and its biological implications |
Q36759836 | Transcription factor Sp3 represses expression of p21CIP¹ via inhibition of productive elongation by RNA polymerase II. |
Q26864339 | Transcription goes digital |
Q36804846 | Transcription induces strand-specific mutations at the 5' end of human genes |
Q47653997 | Transcription pausing: biological significance of thermal fluctuations biased by repetitive genomic sequences. |
Q39442921 | Transcription regulation through promoter-proximal pausing of RNA polymerase II. |
Q50301036 | Transcription start site profiling uncovers divergent transcription and enhancer-associated RNAs in Drosophila melanogaster |
Q37626318 | Transcription-generated torsional stress destabilizes nucleosomes. |
Q63433321 | Transcriptional Burst Initiation and Polymerase Pause Release Are Key Control Points of Transcriptional Regulation |
Q36435072 | Transcriptional activation of yeast genes disrupts intragenic nucleosome phasing |
Q37961880 | Transcriptional control of embryonic and induced pluripotent stem cells |
Q37622051 | Transcriptional control of the inflammatory response |
Q34539909 | Transcriptional dynamics elicited by a short pulse of notch activation involves feed-forward regulation by E(spl)/Hes genes |
Q36902905 | Transcriptional elongation checkpoint control in development and disease |
Q36438053 | Transcriptional elongation requires DNA break-induced signalling |
Q36343296 | Transcriptional pausing controls a rapid antiviral innate immune response in Drosophila |
Q47624989 | Transcriptional precision and accuracy in development: from measurements to models and mechanisms |
Q40442784 | Transcriptional regulation by Pol II(G) involving mediator and competitive interactions of Gdown1 and TFIIF with Pol II. |
Q36562036 | Transcriptional regulation patterns revealed by high resolution chromatin immunoprecipitation during cardiac hypertrophy |
Q42428241 | Transcriptional regulation. Meeting on regulatory mechanisms in eukaryotic transcription |
Q28478116 | Transcriptional regulation: effects of promoter proximal pausing on speed, synchrony and reliability |
Q36066304 | Transcriptional repression via antilooping in the Drosophila embryo |
Q35641521 | Translational Initiation at a Non-AUG Start Codon for Human and Mouse Negative Elongation Factor-B |
Q37203938 | Tuning gene expression to changing environments: from rapid responses to evolutionary adaptation |
Q37238973 | Two roles for the Drosophila IKK complex in the activation of Relish and the induction of antimicrobial peptide genes |
Q28587655 | UTX mediates demethylation of H3K27me3 at muscle-specific genes during myogenesis |
Q33945643 | UVB induces a genome-wide acting negative regulatory mechanism that operates at the level of transcription initiation in human cells |
Q36021678 | Unusual combinatorial involvement of poly-A/T tracts in organizing genes and chromatin in Dictyostelium |
Q36456815 | UpSET recruits HDAC complexes and restricts chromatin accessibility and acetylation at promoter regions |
Q33728129 | UpSET-ting the balance: modulating open chromatin features in metazoan genomes |
Q35989796 | Ups and Downs of Poised RNA Polymerase II in B-Cells |
Q36201678 | Using ChIP-chip and ChIP-seq to study the regulation of gene expression: genome-wide localization studies reveal widespread regulation of transcription elongation |
Q36517932 | Using ChIP-chip technology to reveal common principles of transcriptional repression in normal and cancer cells |
Q55097752 | Viral targeting of TFIIB impairs de novo polymerase II recruitment and affects antiviral immunity. |
Q35026881 | Viral-host interactions that control HIV-1 transcriptional elongation |
Q37068274 | Wnt signaling targets ETO coactivation domain of TAF4/TFIID in vivo |
Q92217036 | Writing a wrong: Coupled RNA polymerase II transcription and RNA quality control |
Q39582674 | X chromosome dosage compensation via enhanced transcriptional elongation in Drosophila |
Q28508693 | beta-Catenin primes organizer gene expression by recruiting a histone H3 arginine 8 methyltransferase, Prmt2 |
Q28275988 | c-Myc is a universal amplifier of expressed genes in lymphocytes and embryonic stem cells |
Q24629119 | c-Myc regulates transcriptional pause release |
Q45954525 | dDsk2 regulates H2Bub1 and RNA polymerase II pausing at dHP1c complex target genes. |
Q30980309 | groHMM: a computational tool for identifying unannotated and cell type-specific transcription units from global run-on sequencing data |
Q42177062 | mRNA decapping factors and the exonuclease Xrn2 function in widespread premature termination of RNA polymerase II transcription |
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