| Q24519069 | A 57-nucleotide upstream early polyadenylation element in human papillomavirus type 16 interacts with hFip1, CstF-64, hnRNP C1/C2, and polypyrimidine tract binding protein |
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| Q30308297 | A potential role for mini-chromosome maintenance (MCM) proteins in initiation at the dihydrofolate reductase replication origin |
| Q34594614 | A unified model of transcription elongation: what have we learned from single-molecule experiments? |
| Q26864222 | Alternative cleavage and polyadenylation: the long and short of it |
| Q33832891 | Alternative polyadenylation of mRNA precursors. |
| Q34283461 | An RNA polymerase pause site is associated with the immunoglobulin mus poly(A) site |
| Q33612479 | An exonic splicing silencer in the testes-specific DNA ligase III beta exon |
| Q41922554 | Comparative investigation of the genomic regions involved in antigenic variation of the TprK antigen among treponemal species, subspecies, and strains |
| Q33680184 | Complex exon-intron marking by histone modifications is not determined solely by nucleosome distribution |
| Q51890620 | Conditional knockdown of target gene expression by tetracycline regulated transcription of double strand RNA. |
| Q39630267 | Construction, modification and evaluation of apolipoprotein A-I promoter-driven shRNA expression vectors against hTERT |
| Q38822658 | Coordination of RNA Polymerase II Pausing and 3' End Processing Factor Recruitment with Alternative Polyadenylation. |
| Q39756702 | Cotranscriptional processing of Drosophila histone mRNAs. |
| Q34759787 | Downstream elements of mammalian pre-mRNA polyadenylation signals: primary, secondary and higher-order structures. |
| Q33827197 | Downstream sequence elements with different affinities for the hnRNP H/H' protein influence the processing efficiency of mammalian polyadenylation signals |
| Q39175067 | Epigenomic and RNA structural correlates of polyadenylation |
| Q34650438 | Functional coupling of RNAP II transcription to spliceosome assembly |
| Q46616243 | Functional coupling of cleavage and polyadenylation with transcription of mRNA. |
| Q41911100 | Functional coupling of last-intron splicing and 3'-end processing to transcription in vitro: the poly(A) signal couples to splicing before committing to cleavage |
| Q41847081 | G-quadruplexes: the beginning and end of UTRs |
| Q35965403 | Generation of Ski-knockdown mice by expressing a long double-strand RNA from an RNA polymerase II promoter. |
| Q34310275 | How to stop: the mysterious links among RNA polymerase II occupancy 3' of genes, mRNA 3' processing and termination |
| Q39940501 | In Vivo Evidence that Defects in the Transcriptional Elongation Factors RPB2, TFIIS, and SPT5 Enhance Upstream Poly(A) Site Utilization |
| Q34353647 | In vitro activity of the baculovirus late expression factor LEF-5 |
| Q37272736 | Independent and high-level dual-gene expression in adult stem-progenitor cells from a single lentiviral vector |
| Q27933119 | Independent functions of yeast Pcf11p in pre-mRNA 3' end processing and in transcription termination |
| Q40819762 | Independent repression of a GC-rich housekeeping gene by Sp1 and MAZ involves the same cis-elements |
| Q24657651 | Interaction between a poly(A)-specific ribonuclease and the 5' cap influences mRNA deadenylation rates in vitro |
| Q39864208 | Local character of readthrough activation in adenovirus type 5 early region 1 transcription control |
| Q40559049 | MAZ elements alter transcription elongation and silencing of the fibroblast growth factor receptor 2 exon IIIb |
| Q39528777 | Mechanism of poly(A) signal transduction to RNA polymerase II in vitro |
| Q40819110 | Messenger RNAs that are not synthesized by RNA polymerase II can be 3' end cleaved and polyadenylated |
| Q24536127 | Mice lacking ghrelin receptors resist the development of diet-induced obesity |
| Q33871092 | Molecular mechanisms of eukaryotic pre-mRNA 3' end processing regulation |
| Q26851218 | Mutual relationships between transcription and pre-mRNA processing in the synthesis of mRNA |
| Q35748217 | Novel transcript truncating function of Rap1p revealed by synthetic codon-optimized Ty1 retrotransposon |
| Q40607399 | Orientation-dependent gene expression with Epstein-Barr virus-derived vectors |
| Q35893857 | PAF Complex Plays Novel Subunit-Specific Roles in Alternative Cleavage and Polyadenylation |
| Q24548945 | Pause sites promote transcriptional termination of mammalian RNA polymerase II |
| Q37645638 | Physical and functional association of RNA polymerase II and the proteasome |
| Q28592770 | Quantitative proteomic identification of MAZ as a transcriptional regulator of muscle-specific genes in skeletal and cardiac myocytes |
| Q34401522 | RNA G-Quadruplexes in the model plant species Arabidopsis thaliana: prevalence and possible functional roles |
| Q37996957 | RNA biology in a test tube--an overview of in vitro systems/assays |
| Q40222409 | RNA polymerase II C-terminal domain mediates regulation of alternative splicing by SRp20. |
| Q28221126 | RNA polymerase II conducts a symphony of pre-mRNA processing activities |
| Q34009055 | RNA polymerase II pauses and associates with pre-mRNA processing factors at both ends of genes. |
| Q34305741 | RNA polymerase II pausing downstream of core histone genes is different from genes producing polyadenylated transcripts |
| Q80176355 | Regulation of T cell receptor-alpha gene recombination by transcription |
| Q40056936 | Regulatory mechanisms for 3'-end alternative splicing and polyadenylation of the Glial Fibrillary Acidic Protein, GFAP, transcript |
| Q41665782 | Sequence-resolved detection of pausing by single RNA polymerase molecules. |
| Q35671541 | Signals for pre-mRNA cleavage and polyadenylation |
| Q30491199 | Single molecule transcription elongation |
| Q37137880 | Single-molecule studies of RNA polymerase: motoring along |
| Q37835470 | Single-molecule studies of RNA polymerase: one singular sensation, every little step it takes |
| Q38043827 | Single-molecule studies of RNAPII elongation |
| Q36990770 | Species-specific factors mediate extensive heterogeneity of mRNA 3' ends in yeasts |
| Q30436775 | Specific signals at the 3' end of the DHFR gene define one boundary of the downstream origin of replication |
| Q45084538 | Spurious polyadenylation of Norovirus Narita 104 capsid protein mRNA in transgenic plants. |
| Q42104053 | Strong polyadenylation and weak pausing combine to cause efficient termination of transcription in the human Ggamma-globin gene. |
| Q36406071 | Subcellular RNA profiling links splicing and nuclear DICER1 to alternative cleavage and polyadenylation. |
| Q24670418 | Systematic variation in mRNA 3'-processing signals during mouse spermatogenesis |
| Q74353662 | The cleavage/polyadenylation activity triggered by a U-rich motif sequence is differently required depending on the poly(A) site location at either the first or last 3'-terminal exon of the 2'-5' oligo(A) synthetase gene |
| Q24671920 | The multifunctional protein p54nrb/PSF recruits the exonuclease XRN2 to facilitate pre-mRNA 3' processing and transcription termination |
| Q46370210 | The poly(A) signal, without the assistance of any downstream element, directs RNA polymerase II to pause in vivo and then to release stochastically from the template |
| Q34511126 | The role of Rat1 in coupling mRNA 3'-end processing to transcription termination: implications for a unified allosteric-torpedo model |
| Q29541446 | Transcription termination by nuclear RNA polymerases |
| Q33302220 | Transcriptional regulation of human eosinophil RNases by an evolutionary- conserved sequence motif in primate genome |
| Q38310504 | Transcriptional termination and coupled polyadenylation in vitro |
| Q37251886 | Transcriptional termination enhances protein expression in human cells |
| Q40190265 | Two G-rich regulatory elements located adjacent to and 440 nucleotides downstream of the core poly(A) site of the intronless melanocortin receptor 1 gene are critical for efficient 3' end processing |
| Q35171631 | Unraveling the mechanistic features of RNA polymerase II termination by the 5'-3' exoribonuclease Rat1 |
| Q34252430 | Vezf1 protein binding sites genome-wide are associated with pausing of elongating RNA polymerase II. |