| human | Q5 |
| P6178 | Dimensions author ID | 01055745473.64 |
| P496 | ORCID iD | 0000-0002-8414-4647 |
| P166 | award received | Fellow of the Royal Society | Q15631401 |
| P69 | educated at | University of Cambridge | Q35794 |
| P108 | employer | University of Colorado Denver | Q1468161 |
| P734 | family name | Bentley | Q4083870 |
| Bentley | Q4083870 | ||
| Bentley | Q4083870 | ||
| P735 | given name | David | Q18057751 |
| David | Q18057751 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q37620941 | "Cotranscriptionality": the transcription elongation complex as a nexus for nuclear transactions |
| Q35561598 | A 10 residue motif at the C-terminus of the RNA pol II CTD is required for transcription, splicing and 3' end processing. |
| Q59074575 | A block to elongation is largely responsible for decreased transcription of c-myc in differentiated HL60 cells |
| Q38326933 | A protein-binding site in the c-myc promoter functions as a terminator of RNA polymerase II transcription |
| Q34379864 | A ribonucleolytic rat torpedoes RNA polymerase II. |
| Q42178186 | Altered nucleosome occupancy and histone H3K4 methylation in response to 'transcriptional stress'. |
| Q50879143 | Breast Cancer Suppression by Progesterone Receptors Is Mediated by Their Modulation of Estrogen Receptors and RNA Polymerase III. |
| Q24601077 | Capping, splicing, and 3' processing are independently stimulated by RNA polymerase II: different functions for different segments of the CTD |
| Q38822658 | Coordination of RNA Polymerase II Pausing and 3' End Processing Factor Recruitment with Alternative Polyadenylation. |
| Q41920187 | Cotranscriptional recruitment of the mRNA export factor Yra1 by direct interaction with the 3' end processing factor Pcf11. |
| Q35006630 | Coupling mRNA processing with transcription in time and space. |
| Q38815706 | Coupling of RNA Polymerase II Transcription Elongation with Pre-mRNA Splicing |
| Q37103512 | Cyclin-dependent kinase control of the initiation-to-elongation switch of RNA polymerase II |
| Q50335557 | Demethylation of trimethylated histone H3 Lys4 in vivo by JARID1 JmjC proteins. |
| Q41519170 | Distinct modes of transcription read through or terminate at the c-myc attenuator |
| Q38827412 | Effects of Transcription Elongation Rate and Xrn2 Exonuclease Activity on RNA Polymerase II Termination Suggest Widespread Kinetic Competition. |
| Q35697473 | Elevated FMR1 mRNA in premutation carriers is due to increased transcription. |
| Q28267852 | Evolution of immunoglobulin V genes: evidence indicating that recently duplicated human V kappa sequences have diverged by gene conversion |
| Q42574458 | Fast ribozyme cleavage releases transcripts from RNA polymerase II and aborts co-transcriptional pre-mRNA processing. |
| Q44017745 | Functional interaction of yeast pre-mRNA 3' end processing factors with RNA polymerase II. |
| Q42075763 | Gene-specific RNA polymerase II phosphorylation and the CTD code |
| Q41468789 | Human TFIIH Kinase CDK7 Regulates Transcription-Associated Chromatin Modifications |
| Q40127189 | Human antibody genes: V gene variability and CH gene switching strategies. |
| Q36307937 | Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridization. |
| Q24554446 | MCM proteins are associated with RNA polymerase II holoenzyme |
| Q28854607 | Most kappa immunoglobulin mRNA in human lymphocytes is homologous to a small family of germ-line V genes |
| Q47932024 | Optimization of capillary chromatography ion trap-mass spectrometry for identification of gel-separated proteins. |
| Q35170883 | Pre-mRNA splicing is a determinant of histone H3K36 methylation |
| Q34590283 | Pre-mRNA splicing is facilitated by an optimal RNA polymerase II elongation rate. |
| Q50645951 | RNA Pol II Dynamics Modulate Co-transcriptional Chromatin Modification, CTD Phosphorylation, and Transcriptional Direction. |
| Q34590257 | RNA editing and alternative splicing: the importance of co-transcriptional coordination |
| Q40025884 | RNA polymerase II carboxy-terminal domain phosphorylation is required for cotranscriptional pre-mRNA splicing and 3'-end formation |
| Q34009055 | RNA polymerase II pauses and associates with pre-mRNA processing factors at both ends of genes. |
| Q33886335 | Regulation of CDK7 substrate specificity by MAT1 and TFIIH. |
| Q40342109 | Ribozyme cleavage reveals connections between mRNA release from the site of transcription and pre-mRNA processing. |
| Q34419716 | Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factors |
| Q35913831 | Selectable one-step PCR-mediated integration of a degron for rapid depletion of endogenous human proteins |
| Q69824205 | Sequence requirements for premature termination of transcription in the human c-myc gene |
| Q59002438 | Similarity in membrane proteins |
| Q34483551 | Splicing speckles are not reservoirs of RNA polymerase II, but contain an inactive form, phosphorylated on serine2 residues of the C-terminal domain |
| Q39814573 | TFIIH-associated Cdk7 kinase functions in phosphorylation of C-terminal domain Ser7 residues, promoter-proximal pausing, and termination by RNA polymerase II |
| Q28301744 | The C-terminal domain of RNA polymerase II couples mRNA processing to transcription |
| Q39714615 | The C-terminal domain of pol II and a DRB-sensitive kinase are required for 3' processing of U2 snRNA. |
| Q35838270 | The export factor Yra1 modulates mRNA 3' end processing. |
| Q39035516 | The histone-H3K4-specific demethylase KDM5B binds to its substrate and product through distinct PHD fingers |
| Q34511126 | The role of Rat1 in coupling mRNA 3'-end processing to transcription termination: implications for a unified allosteric-torpedo model |
| Q58420465 | The role of gene deletion in the immunoglobulin heavy chain switch |
| Q71823410 | The transcriptional elongation inhibitor 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole inhibits transcription factor IIH-associated protein kinase |
| Q43200546 | The union of transcription and mRNA processing: 20 years of coupling |
| Q87887544 | Transcription elongation rate affects nascent histone pre-mRNA folding and 3' end processing |
| Q34183941 | Transcription elongation: the 'Foggy' is liftingellipsis. |
| Q49101405 | Transcriptional elongation by RNA polymerase II is stimulated by transactivators. |
| Q35495810 | Unrearranged immunoglobulin variable region genes have a functional promoter |
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