| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | David L Bentley | Q55137036 |
| P2860 | cites work | A slow RNA polymerase II affects alternative splicing in vivo | Q40627617 |
| P433 | issue | 3 | |
| P304 | page(s) | 251-256 | |
| P577 | publication date | 2005-06-01 | |
| P1433 | published in | Current Opinion in Cell Biology | Q13505682 |
| P1476 | title | Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factors | |
| P478 | volume | 17 |
| Q38290847 | 'Mediator-ing' messenger RNA processing. |
| Q37448767 | 3'-End processing of histone pre-mRNAs in Drosophila: U7 snRNP is associated with FLASH and polyadenylation factors |
| Q33813311 | 4sUDRB-seq: measuring genomewide transcriptional elongation rates and initiation frequencies within cells |
| Q35641869 | A Function for the hnRNP A1/A2 Proteins in Transcription Elongation |
| Q35022331 | A KH-domain RNA-binding protein interacts with FIERY2/CTD phosphatase-like 1 and splicing factors and is important for pre-mRNA splicing in Arabidopsis |
| Q27934649 | A Requirement for the Saccharomyces cerevisiae Paf1 complex in snoRNA 3' end formation |
| Q36424546 | A cis element between the TATA Box and the transcription start site of the major immediate-early promoter of human cytomegalovirus determines efficiency of viral replication |
| Q44863809 | A contemporary, laboratory-intensive course on messenger RNA transcription and processing |
| Q41656652 | A core complex of CPSF73, CPSF100, and Symplekin may form two different cleavage factors for processing of poly(A) and histone mRNAs |
| Q35688363 | A genome-wide analysis indicates that yeast pre-mRNA splicing is predominantly posttranscriptional |
| Q34367969 | A model in vitro system for co-transcriptional splicing |
| Q35220948 | A novel CDX2 isoform regulates alternative splicing |
| Q42736746 | A novel assay identifies transcript elongation roles for the Nup84 complex and RNA processing factors. |
| Q81741002 | A splicing regulator promotes transcriptional elongation |
| Q38787111 | A splicing-dependent transcriptional checkpoint associated with prespliceosome formation. |
| Q33419826 | Activation of host translational control pathways by a viral developmental switch |
| Q36164324 | Aging and Loss of Circulating 17β-Estradiol Alters the Alternative Splicing of ERβ in the Female Rat Brain |
| Q36579430 | Alteration of cyclin D1 transcript elongation by a mutated transcription factor up-regulates the oncogenic D1b splice isoform in cancer |
| Q36141431 | Alternative Splicing of Toll-Like Receptor 9 Transcript in Teleost Fish Grouper Is Regulated by NF-κB Signaling via Phosphorylation of the C-Terminal Domain of the RPB1 Subunit of RNA Polymerase II |
| Q36418590 | Alternative polyadenylation: new insights from global analyses |
| Q33981279 | An interaction between KSHV ORF57 and UIF provides mRNA-adaptor redundancy in herpesvirus intronless mRNA export. |
| Q37652978 | An unexpected ending: noncanonical 3' end processing mechanisms. |
| Q39864591 | Analysis of RNA processing reactions using cell free systems: 3' end cleavage of pre-mRNA substrates in vitro. |
| Q37033318 | Analysis of influenza B Virus NS1 protein trafficking reveals a novel interaction with nuclear speckle domains |
| Q89250483 | Analysis of specific RNA in cultured cells through quantitative integration of q-PCR and N-SIM single cell FISH images: Application to hormonal stimulation of StAR transcription |
| Q21263194 | Arabidopsis mRNA polyadenylation machinery: comprehensive analysis of protein-protein interactions and gene expression profiling |
| Q39867690 | Assembly and mobility of exon-exon junction complexes in living cells |
| Q37355954 | Assembly of an export-competent mRNP is needed for efficient release of the 3'-end processing complex after polyadenylation |
| Q36796433 | Back to the origin: reconsidering replication, transcription, epigenetics, and cell cycle control |
| Q37144184 | Biogenesis of mRNPs: integrating different processes in the eukaryotic nucleus |
| Q37360004 | Bipartite functions of the CREB co-activators selectively direct alternative splicing or transcriptional activation |
| Q24303611 | CDK12 is a transcription elongation-associated CTD kinase, the metazoan ortholog of yeast Ctk1 |
| Q35834049 | CPSF30 at the Interface of Alternative Polyadenylation and Cellular Signaling in Plants |
| Q37348799 | Cdk7 mediates RPB1-driven mRNA synthesis in Toxoplasma gondii |
| Q40116941 | Cell-type-specific expression of the human CD68 gene is associated with changes in Pol II phosphorylation and short-range intrachromosomal gene looping |
| Q24296280 | Characterization of hMTr1, a human Cap1 2'-O-ribose methyltransferase |
| Q37955649 | Chlamydomonas reinhardtii as a viable platform for the production of recombinant proteins: current status and perspectives |
| Q46675833 | Close coupling between transcription and exit of mRNP from the cell nucleus |
| Q42182644 | Co-transcriptional degradation of aberrant pre-mRNA by Xrn2. |
| Q37021156 | Combinatorial incorporation of enhancer-blocking components of the chicken beta-globin 5'HS4 and human T-cell receptor alpha/delta BEAD-1 insulators in self-inactivating retroviral vectors reduces their genotoxic potential |
| Q41870191 | Competition within Introns: Splicing Wins over Polyadenylation via a General Mechanism |
| Q34706714 | Complex and dynamic landscape of RNA polyadenylation revealed by PAS-Seq |
| Q41936701 | Concurrent splicing and transcription are not sufficient to enhance splicing efficiency |
| Q33708655 | Connections between alternative transcription and alternative splicing in mammals |
| Q39544049 | Consensus PP1 binding motifs regulate transcriptional corepression and alternative RNA splicing activities of the steroid receptor coregulators, p54nrb and PSF. |
| Q46908229 | Control and regulation of gene expression: quantitative analysis of the expression of phosphoglycerate kinase in bloodstream form Trypanosoma brucei |
| Q21144446 | Control of pre-mRNA splicing by the general splicing factors PUF60 and U2AF(65) |
| Q27664278 | Cooperative interaction of transcription termination factors with the RNA polymerase II C-terminal domain |
| Q37346740 | Core structure of the yeast spt4-spt5 complex: a conserved module for regulation of transcription elongation |
| Q80143464 | Cotranscriptional coupling of splicing factor recruitment and precursor messenger RNA splicing in mammalian cells |
| Q41920187 | Cotranscriptional recruitment of the mRNA export factor Yra1 by direct interaction with the 3' end processing factor Pcf11. |
| Q79327019 | Cotranscriptional splicing regulation: it's not just about speed |
| Q34592670 | Coupling mRNA synthesis and decay |
| Q39850003 | DNA damage regulates alternative splicing through inhibition of RNA polymerase II elongation. |
| Q35227085 | DNA-Encoded Chromatin Structural Intron Boundary Signals Identify Conserved Genes with Common Function. |
| Q35754282 | Decapping of long noncoding RNAs regulates inducible genes. |
| Q34883246 | Depletion of REF/Aly alters gene expression and reduces RNA polymerase II occupancy |
| Q39998735 | Depolarization-mediated regulation of alternative splicing |
| Q27933085 | Direct interactions between the Paf1 complex and a cleavage and polyadenylation factor are revealed by dissociation of Paf1 from RNA polymerase II. |
| Q39997363 | Distinct requirement of RNA polymerase II CTD phosphorylations in budding and fission yeast |
| Q33568513 | Drosophila melanogaster retrotransposon and inverted repeat-derived endogenous siRNAs are differentially processed in distinct cellular locations. |
| Q35221556 | EMB-4: a predicted ATPase that facilitates lin-12 activity in Caenorhabditis elegans |
| Q24632981 | Editor meets silencer: crosstalk between RNA editing and RNA interference |
| Q36130861 | Effects of ADARs on small RNA processing pathways in C. elegans |
| Q35910114 | Emerging Views on the CTD Code |
| Q39774238 | Enhanced mRNA cap methylation increases cyclin D1 expression and promotes cell transformation |
| Q35791571 | Estimation of alternative splicing variability in human populations |
| Q36052366 | Evidence that the localization of the elongation factor Spt16 across transcribed genes is dependent upon histone H3 integrity in Saccharomyces cerevisiae |
| Q33791162 | Evolution at protein ends: major contribution of alternative transcription initiation and termination to the transcriptome and proteome diversity in mammals |
| Q38148162 | Ewing sarcoma protein: a key player in human cancer |
| Q52699670 | Exclusion of mRNPs and ribosomal particles from a thin zone beneath the nuclear envelope revealed upon inhibition of transport. |
| Q36850001 | Expression of protein-coding genes embedded in ribosomal DNA. |
| Q35739332 | FUS/TLS contributes to replication-dependent histone gene expression by interaction with U7 snRNPs and histone-specific transcription factors |
| Q42574458 | Fast ribozyme cleavage releases transcripts from RNA polymerase II and aborts co-transcriptional pre-mRNA processing. |
| Q34777700 | Finishing touches: post-translational modification of protein factors involved in mammalian pre-mRNA 3' end formation |
| Q28751417 | Formation of the 3' end of histone mRNA: getting closer to the end |
| Q41882250 | From structure to systems: high-resolution, quantitative genetic analysis of RNA polymerase II. |
| Q34650438 | Functional coupling of RNAP II transcription to spliceosome assembly |
| 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 |
| Q37147522 | Functional integration of transcriptional and RNA processing machineries |
| Q41837167 | Functional interaction of the Ess1 prolyl isomerase with components of the RNA polymerase II initiation and termination machineries |
| Q34471112 | Gene-specific requirement for P-TEFb activity and RNA polymerase II phosphorylation within the p53 transcriptional program |
| Q26863342 | Gene-specific requirement of RNA polymerase II CTD phosphorylation |
| Q42272826 | Genetic interaction analysis of point mutations enables interrogation of gene function at a residue-level resolution: exploring the applications of high-resolution genetic interaction mapping of point mutations |
| Q52597287 | Genetics of personalized medicine: cancer and rare diseases. |
| Q24299046 | Genome instability and transcription elongation impairment in human cells depleted of THO/TREX |
| Q33406244 | Genome-wide analysis of factors affecting transcription elongation and DNA repair: a new role for PAF and Ccr4-not in transcription-coupled repair. |
| Q29616717 | Genome-wide analysis of mammalian promoter architecture and evolution |
| Q53135142 | Genome-wide control of polyadenylation site choice by CPSF30 in Arabidopsis. |
| Q34605595 | Global impact of RNA polymerase II elongation inhibition on alternative splicing regulation |
| Q54214251 | HIV latency reversing agents act through Tat post translational modifications. |
| Q38088112 | How cells get the message: dynamic assembly and function of mRNA-protein complexes |
| Q58611909 | Human RNA cap1 methyltransferase CMTr1 cooperates with RNA helicase DHX15 to modify RNAs with highly structured 5' termini |
| Q37186872 | Human cap methyltransferase (RNMT) N-terminal non-catalytic domain mediates recruitment to transcription initiation sites |
| Q24338302 | Human mRNA export machinery recruited to the 5' end of mRNA |
| Q34545620 | ICP27 interacts with the C-terminal domain of RNA polymerase II and facilitates its recruitment to herpes simplex virus 1 transcription sites, where it undergoes proteasomal degradation during infection |
| Q39600021 | Identification of Tat-SF1 cellular targets by exon array analysis reveals dual roles in transcription and splicing |
| Q40851164 | In vitro systems for coupling RNAP II transcription to splicing and polyadenylation |
| Q33252529 | In vivo commitment to yeast cotranscriptional splicing is sensitive to transcription elongation mutants |
| Q37088096 | In vivo dynamics of RNA polymerase II transcription. |
| Q45417487 | Influenza virus inhibits RNA polymerase II elongation |
| Q38355923 | Innate immune restriction and antagonism of viral RNA lacking 2׳-O methylation |
| Q50495729 | Integrating haplotypes and single genetic variability effects of the Pax7 gene on growth traits in two cattle breeds. |
| Q37962775 | Integrating transcription kinetics with alternative polyadenylation and cell cycle control. |
| Q27320819 | Integration of the unfolded protein and oxidative stress responses through SKN-1/Nrf |
| Q35641224 | Interaction of yeast RNA-binding proteins Nrd1 and Nab3 with RNA polymerase II terminator elements |
| Q37101927 | Intragenic epigenetic changes modulate NCAM alternative splicing in neuronal differentiation |
| Q36732545 | Intronic sequence elements impede exon ligation and trigger a discard pathway that yields functional telomerase RNA in fission yeast |
| Q46664772 | Involvement of Pta1, Pcf11 and a KlCYC1 AU-rich element in alternative RNA 3'-end processing selection in yeast |
| Q37367998 | Isolation and functional analysis of RNA polymerase II elongation complexes. |
| Q54588177 | Keeping mRNPs in check during assembly and nuclear export. |
| Q48769916 | Localized co-transcriptional recruitment of the multifunctional RNA-binding protein CELF1 by lampbrush chromosome transcription units |
| Q27333569 | Loss of PTB or negative regulation of Notch mRNA reveals distinct zones of Notch and actin protein accumulation in Drosophila embryo |
| Q35914094 | MYBS: a comprehensive web server for mining transcription factor binding sites in yeast |
| Q50327954 | MYC Mediates mRNA Cap Methylation of Canonical Wnt/β-Catenin Signaling Transcripts By Recruiting CDK7 and RNA Methyltransferase |
| Q37388994 | Meayamycin inhibits pre-messenger RNA splicing and exhibits picomolar activity against multidrug-resistant cells |
| Q35179872 | Mechanism of alternative splicing and its regulation |
| Q36578696 | Mechanism of transcriptional activation by the Myc oncoproteins |
| Q37386626 | Mechanotransduction at a distance: mechanically coupling the extracellular matrix with the nucleus |
| Q42418612 | Molecular architecture of the human pre-mRNA 3' processing complex |
| Q35078202 | Molecular crowding inhibits U-insertion/deletion RNA editing in vitro: consequences for the in vivo reaction |
| Q26783595 | Multiple Export Mechanisms for mRNAs |
| Q34407825 | Myc Regulation of mRNA Cap Methylation |
| Q42789906 | Myc up-regulates formation of the mRNA methyl cap. |
| Q37132771 | Neuronal cell depolarization induces intragenic chromatin modifications affecting NCAM alternative splicing. |
| Q37058515 | Non-coding RNAs regulating the transcriptional machinery |
| Q33840158 | Notch and delta mRNAs in early-stage and mid-stage drosophila embryos exhibit complementary patterns of protein-producing potentials |
| Q30944989 | Notch mRNA expression in Drosophila embryos is negatively regulated at the level of mRNA 3' processing |
| Q24293319 | Novel domains in the hnRNP G/RBMX protein with distinct roles in RNA binding and targeting nascent transcripts |
| Q34499614 | Nuclear RNA sequencing of the mouse erythroid cell transcriptome |
| Q34497927 | Nuclear activity of sperm cells during Hyacinthus orientalis L. in vitro pollen tube growth |
| Q28081155 | Nuclear export of messenger RNA |
| Q37651988 | Nuclear networking fashions pre-messenger RNA and primary microRNA transcripts for function |
| Q27932591 | Nuclear transport factor directs localization of protein synthesis during mitosis |
| Q37809760 | Nucleocytoplasmic mRNP export is an integral part of mRNP biogenesis |
| Q33611294 | Nucleophosmin is selectively deposited on mRNA during polyadenylation |
| Q44504209 | Nucleosome distribution near the 3' ends of genes in the human genome |
| Q46849980 | Nucleosome positioning as a determinant of exon recognition |
| Q26741360 | P-TEFb goes viral |
| Q38896947 | P-TEFb goes viral. |
| Q33565484 | PRDM Proteins: Molecular Mechanisms in Signal Transduction and Transcriptional Regulation |
| Q27313223 | Perturbation of chromatin structure globally affects localization and recruitment of splicing factors |
| Q36909302 | Phylogenetic analysis of mRNA polyadenylation sites reveals a role of transposable elements in evolution of the 3'-end of genes |
| Q42566449 | Pin1 regulates parathyroid hormone mRNA stability |
| Q42144123 | Playing inside the genes: Intragenic histone acetylation after membrane depolarization of neural cells opens a path for alternative splicing regulation |
| Q35613366 | Pol I transcription and pre-rRNA processing are coordinated in a transcription-dependent manner in mammalian cells |
| Q37693565 | Pre-mRNA 3'-end processing complex assembly and function |
| Q37868141 | Pre-mRNA splicing: where and when in the nucleus |
| Q33529075 | Processivity and coupling in messenger RNA transcription |
| Q47714630 | Proteome analysis of protein partners to nucleosomes containing canonical H2A or the variant histones H2A.Z or H2A.X. |
| Q37194592 | Quality control of mRNP in the nucleus |
| Q38679087 | Quick or quality? How mRNA escapes nuclear quality control during stress |
| Q24297879 | RAM/Fam103a1 is required for mRNA cap methylation |
| Q41940904 | RNA Polymerase II Elongation at the Crossroads of Transcription and Alternative Splicing |
| Q47856872 | RNA decay systems enhance reciprocal switching of sense and antisense transcripts in response to glucose starvation. |
| Q37806517 | RNA folding in living cells |
| Q27000261 | RNA helicases in splicing |
| Q40222409 | RNA polymerase II C-terminal domain mediates regulation of alternative splicing by SRp20. |
| Q34498143 | RNA polymerase II CTD phosphopeptides compete with RNA for the interaction with Pcf11. |
| Q37992154 | RNA polymerase II elongation control |
| Q35048913 | RNA polymerase II kinetics in polo polyadenylation signal selection. |
| Q36588947 | RNA polymerase II mutations conferring defects in poly(A) site cleavage and termination in Saccharomyces cerevisiae |
| 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 |
| Q26866134 | RNA-binding proteins and gene regulation in myogenesis |
| Q33758327 | RNA-dependent chromatin association of transcription elongation factors and Pol II CTD kinases. |
| Q37439783 | Rates of in situ transcription and splicing in large human genes |
| Q33713852 | Rational design of antisense oligomers to induce dystrophin exon skipping. |
| Q42911900 | Recruitment of P-TEFb (Cdk9-Pch1) to chromatin by the cap-methyl transferase Pcm1 in fission yeast |
| Q24310689 | Recruitment of the complete hTREX complex is required for Kaposi's sarcoma-associated herpesvirus intronless mRNA nuclear export and virus replication |
| Q36670724 | Reducing the genotoxic potential of retroviral vectors |
| Q36915028 | Reflections on the history of pre-mRNA processing and highlights of current knowledge: a unified picture |
| Q27930283 | Regulation of NAB2 mRNA 3'-end formation requires the core exosome and the Trf4p component of the TRAMP complex |
| Q24644921 | Regulation of mRNA cap methylation |
| Q36873605 | Regulation of primary response genes in B cells |
| Q39262923 | Ribavirin-induced intracellular GTP depletion activates transcription elongation in coagulation factor VII gene expression. |
| Q24631714 | Role of RNA structure in regulating pre-mRNA splicing |
| Q43042769 | Role of poly (A) tail as an identity element for mRNA nuclear export |
| Q38757480 | Roles of Sumoylation in mRNA Processing and Metabolism |
| Q27929974 | Rtf1 is a multifunctional component of the Paf1 complex that regulates gene expression by directing cotranscriptional histone modification |
| Q39791099 | S-adenosyl homocysteine hydrolase is required for Myc-induced mRNA cap methylation, protein synthesis, and cell proliferation. |
| Q24299993 | SON controls cell-cycle progression by coordinated regulation of RNA splicing |
| Q28512917 | SR proteins collaborate with 7SK and promoter-associated nascent RNA to release paused polymerase |
| Q24654094 | SR proteins in vertical integration of gene expression from transcription to RNA processing to translation |
| Q24641891 | Sam68 regulates translation of target mRNAs in male germ cells, necessary for mouse spermatogenesis |
| Q39963552 | Self-splicing of a group I intron reveals partitioning of native and misfolded RNA populations in yeast |
| Q30642490 | Senataxin suppresses the antiviral transcriptional response and controls viral biogenesis |
| Q37008367 | Silencing and transcriptional properties of the imprinted Airn ncRNA are independent of the endogenous promoter |
| Q47270300 | Size matters in RNA export |
| Q27025648 | Small-molecule inhibitors of the Myc oncoprotein |
| Q30493098 | Son is essential for nuclear speckle organization and cell cycle progression |
| Q35672134 | Son maintains accurate splicing for a subset of human pre-mRNAs |
| Q34321074 | Sounds of silence: synonymous nucleotides as a key to biological regulation and complexity |
| Q42262226 | Specific regulation of mRNA cap methylation by the c-Myc and E2F1 transcription factors |
| Q24670536 | Specific trans-acting proteins interact with auxiliary RNA polyadenylation elements in the COX-2 3'-UTR |
| Q33648862 | Splicing factor Spf30 assists exosome-mediated gene silencing in fission yeast |
| Q34864584 | Splicing factors facilitate RNAi-directed silencing in fission yeast |
| Q34353625 | Splicing of a critical exon of human Survival Motor Neuron is regulated by a unique silencer element located in the last intron |
| Q39751851 | Splicing- and cleavage-independent requirement of RNA polymerase II CTD for mRNA release from the transcription site |
| Q36119251 | Splicing-independent recruitment of spliceosomal small nuclear RNPs to nascent RNA polymerase II transcripts |
| Q91753027 | Spt5 modulates cotranscriptional spliceosome assembly in Saccharomyces cerevisiae |
| Q28469151 | Stability of mRNA/DNA and DNA/DNA duplexes affects mRNA transcription |
| Q50607100 | Strategies to facilitate transgene expression in Chlamydomonas reinhardtii. |
| Q27649099 | Structure of the Yeast SR Protein Npl3 and Interaction with mRNA 3′-End Processing Signals |
| Q24321455 | Systematic analysis of the protein interaction network for the human transcription machinery reveals the identity of the 7SK capping enzyme |
| Q36875501 | Systems perspectives on mRNA processing |
| Q40511151 | Systems-level analyses identify extensive coupling among gene expression machines |
| Q33922921 | T-loop phosphorylated Cdk9 localizes to nuclear speckle domains which may serve as sites of active P-TEFb function and exchange between the Brd4 and 7SK/HEXIM1 regulatory complexes. |
| Q39814573 | TFIIH-associated Cdk7 kinase functions in phosphorylation of C-terminal domain Ser7 residues, promoter-proximal pausing, and termination by RNA polymerase II |
| Q35924992 | TLS/FUS (translocated in liposarcoma/fused in sarcoma) regulates target gene transcription via single-stranded DNA response elements |
| Q28266047 | TOR signaling and rapamycin influence longevity by regulating SKN-1/Nrf and DAF-16/FoxO |
| Q36845667 | Targeting of AID-mediated sequence diversification by cis-acting determinants |
| Q41973410 | Targeting tat inhibitors in the assembly of human immunodeficiency virus type 1 transcription complexes |
| Q55092205 | Targeting the Polyadenylation Signal of Pre-mRNA: A New Gene Silencing Approach for Facioscapulohumeral Dystrophy. |
| Q44824953 | The Arabidopsis ortholog of the 77 kDa subunit of the cleavage stimulatory factor (AtCstF-77) involved in mRNA polyadenylation is an RNA-binding protein |
| Q37147259 | The CTD role in cotranscriptional RNA processing and surveillance |
| Q37136812 | The Carboxyl-terminal Domain of RNA Polymerase II Is Not Sufficient to Enhance the Efficiency of Pre-mRNA Capping or Splicing in the Context of a Different Polymerase |
| Q36444189 | The Central Region of the Drosophila Co-repressor Groucho as a Regulatory Hub. |
| Q24316355 | The Iws1:Spt6:CTD complex controls cotranscriptional mRNA biosynthesis and HYPB/Setd2-mediated histone H3K36 methylation |
| Q28567657 | The Myc transactivation domain promotes global phosphorylation of the RNA polymerase II carboxy-terminal domain independently of direct DNA binding |
| Q82264705 | The Sm proteins regulate germ cell specification during early C. elegans embryogenesis |
| Q24293507 | The Spt6 SH2 domain binds Ser2-P RNAPII to direct Iws1-dependent mRNA splicing and export |
| Q36898954 | The T body, a new cytoplasmic RNA granule in Saccharomyces cerevisiae |
| Q33999337 | The TET family of proteins: functions and roles in disease |
| Q34400749 | The TFIIB Tip Domain Couples Transcription Initiation to Events Involved in RNA Processing |
| Q28082339 | The end of the message: multiple protein-RNA interactions define the mRNA polyadenylation site |
| Q30663144 | The essential N terminus of the Pta1 scaffold protein is required for snoRNA transcription termination and Ssu72 function but is dispensable for pre-mRNA 3'-end processing. |
| Q37477468 | The fate of the messenger is pre-determined: a new model for regulation of gene expression |
| Q34064696 | The fission yeast RNA binding protein Mmi1 regulates meiotic genes by controlling intron specific splicing and polyadenylation coupled RNA turnover |
| Q38172436 | The functional consequences of intron retention: alternative splicing coupled to NMD as a regulator of gene expression |
| Q21090175 | The in vivo kinetics of RNA polymerase II elongation during co-transcriptional splicing |
| Q39434281 | The interplay between transcription and mRNA degradation in Saccharomyces cerevisiae |
| Q30494350 | The life of an mRNA in space and time |
| Q37419011 | The long journey of actin and actin-associated proteins from genes to polysomes |
| Q27933267 | The multifunctional Ccr4-Not complex directly promotes transcription elongation |
| Q35074663 | The nucleosome regulates the usage of polyadenylation sites in the human genome |
| Q33826903 | The polyadenylation code: a unified model for the regulation of mRNA alternative polyadenylation |
| Q26750643 | The reciprocal regulation between splicing and 3'-end processing |
| Q48635561 | The recruitment of the U5 snRNP to nascent transcripts requires internal loop 1 of U5 snRNA. |
| Q37821623 | The regulation of parathyroid hormone secretion and synthesis |
| Q28535873 | The role of Ctk1 kinase in termination of small non-coding RNAs |
| Q34066845 | The role of SON in splicing, development, and disease |
| Q27937384 | The role of the putative 3' end processing endonuclease Ysh1p in mRNA and snoRNA synthesis |
| Q24604774 | The roles of PARP1 in gene control and cell differentiation |
| Q36952048 | The splicing factor SC35 has an active role in transcriptional elongation |
| Q35826689 | The spt5 C-terminal region recruits yeast 3' RNA cleavage factor I. |
| Q37649097 | The transcription-splicing protein NonO/p54nrb and three NonO-interacting proteins bind to distal enhancer region and augment rhodopsin expression |
| Q33700143 | The transcriptional transactivator Tat selectively regulates viral splicing. |
| Q34468889 | Theory on the coupled stochastic dynamics of transcription and splice-site recognition |
| Q35319555 | To be or not to be: the regulation of mRNA fate as a survival strategy during mammalian hibernation |
| Q34150385 | To polyadenylate or to deadenylate: that is the question |
| Q42772904 | Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain |
| Q39414832 | Transcription and splicing: when the twain meet |
| Q38381579 | Transcription by the multifunctional RNA polymerase I in Trypanosoma brucei functions independently of RPB7. |
| Q35879126 | Transcription reactivation steps stimulated by oocyte maturation in C. elegans |
| Q37242438 | Transcription-independent functions of MYC: regulation of translation and DNA replication |
| Q35917031 | Transcriptional co-activator protein p100 interacts with snRNP proteins and facilitates the assembly of the spliceosome |
| Q42133855 | Transcriptional elongation and mRNA export are coregulated processes. |
| Q42418720 | Transcripts synthesized by RNA polymerase III can be polyadenylated in an AAUAAA-dependent manner |
| Q35171449 | U2 snRNP is required for expression of the 3' end of genes |
| Q37273040 | UBE2I (UBC9), a SUMO-conjugating enzyme, localizes to nuclear speckles and stimulates transcription in mouse oocytes |
| Q35133832 | Ubiquitin-associated domain of Mex67 synchronizes recruitment of the mRNA export machinery with transcription |
| Q33283913 | Unfolding the mystery of alternative splicing through a unique method of in vivo selection |
| Q27931365 | Unphosphorylated SR-like protein Npl3 stimulates RNA polymerase II elongation |
| Q36714930 | What happens at or after transcription: Insights into circRNA biogenesis and function |
| Q84532003 | When chromatin meets splicing |
| Q27932390 | Yeast arginine methyltransferase Hmt1p regulates transcription elongation and termination by methylating Npl3p |
| Q24318720 | ZIP: a novel transcription repressor, represses EGFR oncogene and suppresses breast carcinogenesis |
| Q80763950 | [Chromatin and transcription regulation] |
| Q57479681 | mRNA cap regulation in mammalian cell function and fate |
| Q37907202 | mRNA export and cancer |
| Q37163404 | mRNA journey to the cytoplasm: attire required |
| Q42127838 | mRNA nuclear export and human disease |
| Q38128469 | mRNA quality control pathways in Saccharomyces cerevisiae |
| Q33531744 | mRNA secondary structures fold sequentially but exchange rapidly in vivo |
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