| Q94204092 | 3' end formation and regulation of eukaryotic mRNAs |
| Q41983938 | 3' end formation of pre-mRNA and phosphorylation of Ser2 on the RNA polymerase II CTD are reciprocally coupled in human cells |
| Q37448767 | 3'-End processing of histone pre-mRNAs in Drosophila: U7 snRNP is associated with FLASH and polyadenylation factors |
| Q34485087 | A Subset of Drosophila Integrator Proteins Is Essential for Efficient U7 snRNA and Spliceosomal snRNA 3′-End Formation |
| Q36506583 | A complex containing the CPSF73 endonuclease and other polyadenylation factors associates with U7 snRNP and is recruited to histone pre-mRNA for 3'-end processing |
| Q50982781 | A distal auxiliary element facilitates cleavage and polyadenylation of Dux4 mRNA in the pathogenic haplotype of FSHD. |
| Q39722557 | A functional human Poly(A) site requires only a potent DSE and an A-rich upstream sequence. |
| Q54561571 | A novel plant in vitro assay system for pre-mRNA cleavage during 3'-end formation. |
| Q36021683 | A quantitative atlas of polyadenylation in five mammals |
| Q39142495 | A short conserved motif in ALYREF directs cap- and EJC-dependent assembly of export complexes on spliced mRNAs |
| Q41626584 | A snoRNA modulates mRNA 3' end processing and regulates the expression of a subset of mRNAs |
| Q34810369 | A systems genetic analysis of alcohol drinking by mice, rats and men: influence of brain GABAergic transmission |
| Q91725525 | A unified allosteric/torpedo mechanism for transcriptional termination on human protein-coding genes |
| Q37308761 | A viral genome landscape of RNA polyadenylation from KSHV latent to lytic infection |
| Q64066717 | Activation of the Endonuclease that Defines mRNA 3' Ends Requires Incorporation into an 8-Subunit Core Cleavage and Polyadenylation Factor Complex |
| Q46559090 | Activity-Dependent Regulation of Alternative Cleavage and Polyadenylation During Hippocampal Long-Term Potentiation. |
| Q93253561 | Aire-dependent genes undergo Clp1-mediated 3'UTR shortening associated with higher transcript stability in the thymus |
| Q36824347 | Alterations in polyadenylation and its implications for endocrine disease |
| Q47126679 | Alternative Polyadenylation in Human Diseases. |
| Q89051609 | Alternative Polyadenylation of Mammalian Transcripts Is Generally Deleterious, Not Adaptive |
| Q91565524 | Alternative cleavage and polyadenylation in health and disease |
| Q35902018 | Alternative cleavage and polyadenylation in spermatogenesis connects chromatin regulation with post-transcriptional control |
| Q34037217 | Alternative cleavage and polyadenylation: extent, regulation and function |
| Q26864222 | Alternative cleavage and polyadenylation: the long and short of it |
| Q34530421 | Alternative mRNA polyadenylation in eukaryotes: an effective regulator of gene expression |
| Q58556962 | Alternative polyadenylation factors link cell cycle to migration |
| Q37775673 | Alternative polyadenylation of antisense RNAs and flowering time control. |
| Q33832891 | Alternative polyadenylation of mRNA precursors. |
| Q36418590 | Alternative polyadenylation: new insights from global analyses |
| Q46587967 | An Mtr4/ZFC3H1 complex facilitates turnover of unstable nuclear RNAs to prevent their cytoplasmic transport and global translational repression. |
| Q37940429 | An active role for splicing in 3'-end formation |
| Q35740539 | An essential role for Clp1 in assembly of polyadenylation complex CF IA and Pol II transcription termination |
| Q37652978 | An unexpected ending: noncanonical 3' end processing mechanisms. |
| Q36106993 | Analysis of C. elegans intestinal gene expression and polyadenylation by fluorescence-activated nuclei sorting and 3'-end-seq |
| Q39864591 | Analysis of RNA processing reactions using cell free systems: 3' end cleavage of pre-mRNA substrates in vitro. |
| Q36575994 | Analysis of alternative cleavage and polyadenylation by 3' region extraction and deep sequencing. |
| Q34107359 | Analysis of spliceosomal proteins in Trypanosomatids reveals novel functions in mRNA processing |
| Q33665562 | Antisense-mediated FLC transcriptional repression requires the P-TEFb transcription elongation factor |
| Q90681248 | Arabidopsis CRL4 Complexes: Surveying Chromatin States and Gene Expression |
| Q36559217 | Archaeal β-CASP ribonucleases of the aCPSF1 family are orthologs of the eukaryal CPSF-73 factor |
| Q34002244 | Arginine methylation in subunits of mammalian pre-mRNA cleavage factor I. |
| Q50335775 | CBC-ARS2 stimulates 3'-end maturation of multiple RNA families and favors cap-proximal processing |
| Q33778704 | CPF-associated phosphatase activity opposes condensin-mediated chromosome condensation |
| Q34430715 | CPSF30 and Wdr33 directly bind to AAUAAA in mammalian mRNA 3' processing |
| Q35834049 | CPSF30 at the Interface of Alternative Polyadenylation and Cellular Signaling in Plants |
| Q36531711 | Case study on the evolution of hetero-oligomer interfaces based on the differences in paralogous proteins |
| Q91651291 | Characterization and Functional Analysis of Polyadenylation Sites in Fast and Slow Muscles |
| Q34648489 | Characterization of the distal polyadenylation site of the ß-adducin (Add2) pre-mRNA. |
| Q90226583 | Chromosomal Density of Cancer Up-Regulated Genes, Aberrant Enhancer Activity and Cancer Fitness Genes Are Associated with Transcriptional Cis-Effects of Broad Copy Number Gains in Colorectal Cancer |
| Q39269835 | Cleavage and polyadenylation: Ending the message expands gene regulation |
| Q50320383 | Cleavage factor Im is a key regulator of 3' UTR length |
| Q57810978 | Common mechanism of transcription termination at coding and noncoding RNA genes in fission yeast |
| Q46306192 | Comparative analysis of alternative polyadenylation in S. cerevisiae and S. pombe |
| Q31109375 | Complex Selection on Human Polyadenylation Signals Revealed by Polymorphism and Divergence Data |
| Q50140656 | Comprehensive Characterization of Alternative Polyadenylation in Human Cancer |
| Q91807464 | Comprehensive in vivo identification of the c-Myc mRNA protein interactome using HyPR-MS |
| Q35588235 | Connections between 3'-end processing and DNA damage response |
| Q34193290 | Construction of a full transcription map of human papillomavirus type 18 during productive viral infection |
| Q36406376 | Context-dependent modulation of Pol II CTD phosphatase SSUP-72 regulates alternative polyadenylation in neuronal development |
| Q26866106 | Control of poly(A) tail length |
| Q37130394 | Coupling between alternative polyadenylation and alternative splicing is limited to terminal introns |
| Q27646447 | Crystal Structure of the HEAT Domain from the Pre-mRNA Processing Factor Symplekin |
| Q24338977 | Crystal structure of a human cleavage factor CFI(m)25/CFI(m)68/RNA complex provides an insight into poly(A) site recognition and RNA looping |
| Q24337433 | Crystal structure of human poly(A) polymerase gamma reveals a conserved catalytic core for canonical poly(A) polymerases |
| Q24300716 | Crystal structure of the human symplekin-Ssu72-CTD phosphopeptide complex |
| Q38825492 | CstF-64 and 3'-UTR cis-element determine Star-PAP specificity for target mRNA selection by excluding PAPα. |
| Q53228284 | Cytoplasmic parafibromin/hCdc73 targets and destabilizes p53 mRNA to control p53-mediated apoptosis. |
| Q36817549 | Definition of RNA polymerase II CoTC terminator elements in the human genome. |
| Q33602636 | Delineating the structural blueprint of the pre-mRNA 3'-end processing machinery |
| Q39312680 | Developmental transitions in Arabidopsis are regulated by antisense RNAs resulting from bidirectionally transcribed genes |
| Q55279990 | Differential 3' Processing of Specific Transcripts Expands Regulatory and Protein Diversity Across Neuronal Cell Types. |
| Q26851212 | Disengaging polymerase: terminating RNA polymerase II transcription in budding yeast |
| Q34985077 | Distinct polyadenylation landscapes of diverse human tissues revealed by a modified PA-seq strategy |
| Q33628402 | Drosophila translational elongation factor-1gamma is modified in response to DOA kinase activity and is essential for cellular viability. |
| Q41845276 | Dual roles for PARP1 during heat shock: transcriptional activator and posttranscriptional inhibitor of gene expression |
| Q42128098 | Dynamic analyses of alternative polyadenylation from RNA-seq reveal a 3'-UTR landscape across seven tumour types. |
| Q39090047 | Dynamic landscape of alternative polyadenylation during retinal development |
| Q36378005 | E2F mediates enhanced alternative polyadenylation in proliferation |
| Q27935349 | Efficient mRNA polyadenylation requires a ubiquitin-like domain, a zinc knuckle, and a RING finger domain, all contained in the Mpe1 protein |
| Q38748176 | Evidence that a threshold of serine/arginine-rich (SR) proteins recruits CFIm to promote rous sarcoma virus mRNA 3' end formation |
| Q28507441 | Feedback regulation of transcriptional termination by the mammalian circadian clock PERIOD complex |
| Q34324573 | Fip1 regulates mRNA alternative polyadenylation to promote stem cell self-renewal |
| Q39913133 | Fluorescent protein tagging confirms the presence of ribosomal proteins at Drosophila polytene chromosomes. |
| Q34997983 | Fox-1 family of RNA-binding proteins |
| Q36791576 | From polyadenylation to splicing: Dual role for mRNA 3' end formation factors |
| Q52337741 | Full-length mRNA sequencing uncovers a widespread coupling between transcription initiation and mRNA processing. |
| Q34109773 | Fungal virulence and development is regulated by alternative pre-mRNA 3'end processing in Magnaporthe oryzae |
| Q40207521 | Genome-Wide Polyadenylation Maps Reveal Dynamic mRNA 3'-End Formation in the Failing Human Heart |
| Q37461596 | Genome-wide dynamics of alternative polyadenylation in rice. |
| Q34787276 | Genome-wide identification and predictive modeling of tissue-specific alternative polyadenylation |
| Q40922556 | Genome-wide promoter binding profiling of protein phosphatase-1 and its major nuclear targeting subunits. |
| Q42073319 | HIV-1 mRNA 3' end processing is distinctively regulated by eIF3f, CDK11, and splice factor 9G8. |
| Q92668748 | Herpes simplex virus blocks host transcription termination via the bimodal activities of ICP27 |
| Q33838515 | Heterogeneity in mammalian RNA 3' end formation |
| Q37333940 | Host shutoff is a conserved phenotype of gammaherpesvirus infection and is orchestrated exclusively from the cytoplasm |
| Q85641371 | How bidirectional becomes unidirectional |
| Q42152221 | Identification of 3' gene ends using transcriptional and genomic conservation across vertebrates |
| Q36189648 | Implications of polyadenylation in health and disease |
| Q90019860 | Importance of amino acids Leu135 and Tyr236 for the interaction between EhCFIm25 and RNA: a molecular dynamics simulation study |
| Q52808328 | In cell mutational interference mapping experiment (in cell MIME) identifies the 5' polyadenylation signal as a dual regulator of HIV-1 genomic RNA production and packaging. |
| Q24608252 | Inhibition of polyadenylation reduces inflammatory gene induction |
| Q99614240 | Integrator Recruits Protein Phosphatase 2A to Prevent Pause Release and Facilitate Transcription Termination |
| Q34471019 | Interactions of CstF-64, CstF-77, and symplekin: implications on localisation and function. |
| Q37001441 | Intronic cleavage and polyadenylation regulates gene expression during DNA damage response through U1 snRNA |
| Q38791134 | Isolation of the protein and RNA content of active sites of transcription from mammalian cells |
| Q35363252 | Juxtaposition of two distant, serine-arginine-rich protein-binding elements is required for optimal polyadenylation in Rous sarcoma virus |
| Q35169858 | Long conserved fragments upstream of Mammalian polyadenylation sites. |
| Q37748073 | Long noncoding RNAs: implications for antigen receptor diversification |
| Q47753117 | Major splice variants and multiple polyadenylation site utilization in mRNAs encoding human translation initiation factors eIF4E1 and eIF4E3 regulate the translational regulators? |
| Q38085601 | Making ends meet: coordination between RNA 3'-end processing and transcription initiation. |
| Q26852725 | Means to an end: mechanisms of alternative polyadenylation of messenger RNA precursors |
| Q26852702 | Mechanisms and consequences of alternative polyadenylation |
| Q93199445 | Mechanistic insights into mRNA 3'-end processing |
| Q42427869 | Merging molecular electron microscopy and mass spectrometry by carbon film-assisted endoproteinase digestion |
| Q45761998 | Message ends: RNA 3' processing and flowering time control |
| Q47256963 | Molecular Mechanisms for CFIm-Mediated Regulation of mRNA Alternative Polyadenylation |
| Q42632922 | Molecular Regulation of Alternative Polyadenylation (APA) within the Drosophila Nervous System |
| Q46335657 | Molecular basis for the recognition of the human AAUAAA polyadenylation signal. |
| Q33871092 | Molecular mechanisms of eukaryotic pre-mRNA 3' end processing regulation |
| Q49965976 | Mtr4/ZFC3H1 protects polysomes through nuclear RNA surveillance |
| Q34883412 | Multilayer regulatory mechanisms control cleavage factor I proteins in filamentous fungi. |
| Q37723733 | Mutually Exclusive CBC-Containing Complexes Contribute to RNA Fate |
| Q88742264 | NUDT21 negatively regulates PSMB2 and CXXC5 by alternative polyadenylation and contributes to hepatocellular carcinoma suppression |
| Q34042969 | New facets in the regulation of gene expression by ADP-ribosylation and poly(ADP-ribose) polymerases |
| Q38235716 | New links between mRNA polyadenylation and diverse nuclear pathways |
| Q93200397 | Non-translational Connections of eEF1B in the Cytoplasm and Nucleus of Cancer Cells |
| Q42681796 | Noncanonical translation initiation of the Arabidopsis flowering time and alternative polyadenylation regulator FCA. |
| Q91764661 | Novel insights into PARPs in gene expression: regulation of RNA metabolism |
| Q34190177 | Nuclear import of cytoplasmic poly(A) binding protein restricts gene expression via hyperadenylation and nuclear retention of mRNA. |
| Q38301627 | Nuclear matrix protein Matrin3 regulates alternative splicing and forms overlapping regulatory networks with PTB. |
| Q38084750 | Nuclear organization of RNA polymerase II transcription. |
| Q33899506 | Nuclear pre-mRNA 3'-end processing regulates synapse and axon development in C. elegans |
| Q24319827 | Nucleophosmin deposition during mRNA 3' end processing influences poly(A) tail length |
| Q38434984 | Optimizing In Vitro Pre-mRNA 3' Cleavage Efficiency: Reconstitution from Anion-Exchange Separated HeLa Cleavage Factors and from Adherent HeLa Cell Nuclear Extract |
| Q47107706 | Overexpressed HSF1 cancer signature genes cluster in human chromosome 8q. |
| Q37448736 | Overlapping and distinct functions of CstF64 and CstF64τ in mammalian mRNA 3' processing |
| Q37649496 | Oxidative stress controls the choice of alternative last exons via a Brahma-BRCA1-CstF pathway |
| Q36010483 | PABPN1-Dependent mRNA Processing Induces Muscle Wasting. |
| Q36800743 | PAPERCLIP Identifies MicroRNA Targets and a Role of CstF64/64tau in Promoting Non-canonical poly(A) Site Usage. |
| Q39231132 | PARP1 represses PAP and inhibits polyadenylation during heat shock |
| Q89581152 | PARPs and ADP-ribosylation in RNA biology: from RNA expression and processing to protein translation and proteostasis |
| Q35772782 | PSF: nuclear busy-body or nuclear facilitator? |
| Q92080506 | Pan-tissue analysis of allelic alternative polyadenylation suggests widespread functional regulation |
| Q34483300 | Plant polyadenylation factors: conservation and variety in the polyadenylation complex in plants. |
| Q36305636 | Poly(A) binding protein nuclear 1 levels affect alternative polyadenylation |
| Q36931456 | Poly(A) code analyses reveal key determinants for tissue-specific mRNA alternative polyadenylation |
| Q26991894 | Poly(A) polymerase (PAP) diversity in gene expression--star-PAP vs canonical PAP |
| Q24650853 | Poly(A) signal-dependent degradation of unprocessed nascent transcripts accompanies poly(A) signal-dependent transcriptional pausing in vitro |
| Q24633294 | Poly(A) signals located near the 5' end of genes are silenced by a general mechanism that prevents premature 3'-end processing |
| Q41806905 | Poly(A) tail length is controlled by the nuclear poly(A)-binding protein regulating the interaction between poly(A) polymerase and the cleavage and polyadenylation specificity factor |
| Q42872039 | Poly(A) tail-mediated gene regulation by opposing roles of Nab2 and Pab2 nuclear poly(A)-binding proteins in pre-mRNA decay |
| Q28568965 | Polyadenylation site-specific differences in the activity of the neuronal βCstF-64 protein in PC-12 cells |
| Q28485193 | Polyadenylation-dependent control of long noncoding RNA expression by the poly(A)-binding protein nuclear 1 |
| Q38940602 | Polymorphisms in Non-coding RNA Genes and Their Targets Sites as Risk Factors of Sporadic Colorectal Cancer |
| Q37139138 | Post-transcriptional regulation by poly(ADP-ribosyl)ation of the RNA-binding proteins |
| Q37693565 | Pre-mRNA 3'-end processing complex assembly and function |
| Q45983188 | Precursor microRNA-122 inhibits synthesis of Insig1 isoform mRNA by modulating polyadenylation site usage. |
| Q38513793 | Principles of miRNA-mRNA interactions: beyond sequence complementarity |
| Q26746120 | Processing and transcriptome expansion at the mRNA 3' end in health and disease: finding the right end |
| Q37160188 | Progressive lengthening of 3' untranslated regions of mRNAs by alternative polyadenylation during mouse embryonic development. |
| Q37418456 | Protein kinase Darkener of apricot and its substrate EF1γ regulate organelle transport along microtubules. |
| Q34426176 | Protein kinase WNK3 regulates the neuronal splicing factor Fox-1 |
| Q46331666 | Purification of mRNA Processing Complexes Using an RNA Affinity Approach |
| Q38170575 | Putting an 'End' to HIV mRNAs: capping and polyadenylation as potential therapeutic targets |
| Q36002383 | RAX2: a genome-wide detection method of condition-associated transcription variation. |
| Q34360775 | RBBP6 isoforms regulate the human polyadenylation machinery and modulate expression of mRNAs with AU-rich 3' UTRs |
| Q36871074 | RBFOX1 and RBFOX2 are dispensable in iPSCs and iPSC-derived neurons and do not contribute to neural-specific paternal UBE3A silencing. |
| Q64114377 | RNA Biology Provides New Therapeutic Targets for Human Disease |
| Q38852154 | RNA Dynamics in the Control of Circadian Rhythm |
| Q38741213 | RNA Processing and Genome Stability: Cause and Consequence |
| Q100750569 | RNA in cancer |
| Q35048913 | RNA polymerase II kinetics in polo polyadenylation signal selection. |
| Q34960186 | RNA polymerase II transcription elongation control |
| Q34085158 | RNA sequencing: from tag-based profiling to resolving complete transcript structure |
| Q52599402 | RNA surveillance by the nuclear RNA exosome: mechanisms and significance. |
| Q97546454 | RNA-binding proteins in tumor progression |
| Q33833844 | Ratio-based analysis of differential mRNA processing and expression of a polyadenylation factor mutant pcfs4 using arabidopsis tiling microarray. |
| Q34430722 | Reconstitution of CPSF active in polyadenylation: recognition of the polyadenylation signal by WDR33. |
| Q47351875 | Reconstitution of the CstF complex unveils a regulatory role for CstF-50 in recognition of 3'-end processing signals |
| Q36915028 | Reflections on the history of pre-mRNA processing and highlights of current knowledge: a unified picture |
| Q64061683 | Regulation of Intronic Polyadenylation by PCF11 Impacts mRNA Expression of Long Genes |
| Q33520920 | Reprogramming of 3' untranslated regions of mRNAs by alternative polyadenylation in generation of pluripotent stem cells from different cell types |
| Q33365612 | Role of cleavage and polyadenylation specificity factor 100: anchoring poly(A) sites and modulating transcription termination. |
| Q26777328 | Roles for SUMO in pre-mRNA processing |
| Q38757480 | Roles of Sumoylation in mRNA Processing and Metabolism |
| Q38788828 | SR proteins are NXF1 adaptors that link alternative RNA processing to mRNA export. |
| Q64077206 | Selective Roles of Vertebrate PCF11 in Premature and Full-Length Transcript Termination |
| Q35671541 | Signals for pre-mRNA cleavage and polyadenylation |
| Q47734878 | Small Nuclear Ribonucleoprotein Polypeptide A-Mediated Alternative Polyadenylation of STAT5B during Th1 Cell Differentiation |
| Q27675892 | Solution Structure of RING Finger-like Domain of Retinoblastoma-binding Protein-6 (RBBP6) Suggests It Functions as a U-box |
| Q34351577 | Specificity factors in cytoplasmic polyadenylation |
| Q41824813 | Splicing-coupled 3' end formation requires a terminal splice acceptor site, but not intron excision |
| Q55339687 | Structural basis for MTR4-ZCCHC8 interactions that stimulate the MTR4 helicase in the nuclear exosome-targeting complex. |
| Q48190052 | Structural basis of AAUAAA polyadenylation signal recognition by the human CPSF complex. |
| Q24313447 | Structural basis of UGUA recognition by the Nudix protein CFI(m)25 and implications for a regulatory role in mRNA 3' processing |
| Q28245082 | Structural biology of poly(A) site definition |
| Q43518701 | Structural biology: Spliceosome subunit revealed |
| Q47258918 | Structural insights into the assembly and polyA signal recognition mechanism of the human CPSF complex |
| Q38195095 | Structure and function of pre-mRNA 5'-end capping quality control and 3'-end processing |
| Q53386945 | Survey of rice proteins interacting with OsFCA and OsFY proteins which are homologous to the Arabidopsis flowering time proteins, FCA and FY. |
| Q35532398 | Systematic profiling of poly(A)+ transcripts modulated by core 3' end processing and splicing factors reveals regulatory rules of alternative cleavage and polyadenylation |
| Q41826039 | TDP-43 regulates β-adducin (Add2) transcript stability. |
| Q38440904 | TNIP2 is a Hub Protein in the NF-κB Network with Both Protein and RNA Mediated Interactions. |
| Q99720182 | TREND-DB-a transcriptome-wide atlas of the dynamic landscape of alternative polyadenylation |
| Q47776194 | Targeting a Single Alternative Polyadenylation Site Coordinately Blocks Expression of Androgen Receptor mRNA Splice Variants in Prostate Cancer |
| Q55092205 | Targeting the Polyadenylation Signal of Pre-mRNA: A New Gene Silencing Approach for Facioscapulohumeral Dystrophy. |
| Q52597741 | Targeting the polyadenylation factor EhCFIm25 with RNA aptamers controls survival in Entamoeba histolytica. |
| Q46024315 | The Arabidopsis CPSF30-L gene plays an essential role in nitrate signaling and regulates the nitrate transceptor gene NRT1.1. |
| Q36182348 | The Cstf2t Polyadenylation Gene Plays a Sex-Specific Role in Learning Behaviors in Mice |
| Q42705246 | The N-terminal domains of FLASH and Lsm11 form a 2:1 heterotrimer for histone pre-mRNA 3'-end processing |
| Q37671309 | The Paf1 complex: platform or player in RNA polymerase II transcription? |
| Q24294529 | The RBBP6/ZBTB38/MCM10 axis regulates DNA replication and common fragile site stability |
| Q34303212 | The RNA polymerase II CTD coordinates transcription and RNA processing. |
| Q52335114 | The TORC1-Regulated CPA Complex Rewires an RNA Processing Network to Drive Autophagy and Metabolic Reprogramming. |
| Q42150115 | The Y3** ncRNA promotes the 3' end processing of histone mRNAs |
| Q34845721 | The conserved intronic cleavage and polyadenylation site of CstF-77 gene imparts control of 3' end processing activity through feedback autoregulation and by U1 snRNP |
| Q47715179 | The contribution of alternative polyadenylation to the cancer phenotype |
| Q33789087 | The eEF1γ subunit contacts RNA polymerase II and binds vimentin promoter region |
| Q28082339 | The end of the message: multiple protein-RNA interactions define the mRNA polyadenylation site |
| Q33581465 | The hinge domain of the cleavage stimulation factor protein CstF-64 is essential for CstF-77 interaction, nuclear localization, and polyadenylation |
| Q37581812 | The human cap-binding complex is functionally connected to the nuclear RNA exosome |
| Q92020674 | The mRNA Export Receptor NXF1 Coordinates Transcriptional Dynamics, Alternative Polyadenylation, and mRNA Export |
| Q36765062 | The novel poly(A) polymerase Star-PAP is a signal-regulated switch at the 3'-end of mRNAs |
| Q91790975 | The oncogenic potential of small nuclear ribonucleoprotein polypeptide G: a comprehensive and perspective view |
| Q64069116 | The p53 mRNA: an integral part of the cellular stress response |
| Q33826903 | The polyadenylation code: a unified model for the regulation of mRNA alternative polyadenylation |
| Q40090853 | The polyadenylation complex of Trypanosoma brucei: Characterization of the functional poly(A) polymerase |
| Q64082993 | The polyadenylation inhibitor cordycepin reduces pain, inflammation and joint pathology in rodent models of osteoarthritis |
| Q34219352 | The proteomes of transcription factories containing RNA polymerases I, II or III. |
| Q28078160 | The role of TREX in gene expression and disease |
| Q37676346 | The role of alternative polyadenylation in the antiviral innate immune response |
| Q38012032 | The role of the 3' untranslated region in post-transcriptional regulation of protein expression in mammalian cells |
| Q53348104 | The spen family protein FPA controls alternative cleavage and polyadenylation of RNA. |
| Q41896597 | The stem-loop luciferase assay for polyadenylation (SLAP) method for determining CstF-64-dependent polyadenylation activity |
| Q37924519 | The structure of human cleavage factor I(m) hints at functions beyond UGUA-specific RNA binding: a role in alternative polyadenylation and a potential link to 5' capping and splicing |
| Q34461180 | The τCstF-64 polyadenylation protein controls genome expression in testis |
| Q33637722 | Tissue-specific mechanisms of alternative polyadenylation: testis, brain, and beyond. |
| Q39021067 | Tissue-specific regulation of alternative polyadenylation represses expression of a neuronal ankyrin isoform in C. elegans epidermal development |
| Q34150385 | To polyadenylate or to deadenylate: that is the question |
| Q35092483 | Toward a systematic understanding of mRNA 3' untranslated regions. |
| Q37408113 | Transcription elongation factor ELL2 directs immunoglobulin secretion in plasma cells by stimulating altered RNA processing. |
| Q29541446 | Transcription termination by nuclear RNA polymerases |
| Q40339336 | Transcriptional activators enhance polyadenylation of mRNA precursors. |
| Q35458713 | Transcriptional activity regulates alternative cleavage and polyadenylation |
| Q26862917 | Transcriptional stalling in B-lymphocytes: a mechanism for antibody diversification and maintenance of genomic integrity |
| Q59884668 | Transcriptome 3'end organization by PCF11 links alternative polyadenylation to formation and neuronal differentiation of neuroblastoma |
| Q35195969 | Transcriptome dynamics through alternative polyadenylation in developmental and environmental responses in plants revealed by deep sequencing. |
| Q36414738 | Transcriptome-wide analyses of CstF64-RNA interactions in global regulation of mRNA alternative polyadenylation |
| Q36510112 | Triplex DNA-binding proteins are associated with clinical outcomes revealed by proteomic measurements in patients with colorectal cancer |
| Q36684834 | UV damage regulates alternative polyadenylation of the RPB2 gene in yeast. |
| Q42633493 | Unique features of plant cleavage and polyadenylation specificity factor revealed by proteomic studies |
| Q37864536 | Unravelling the means to an end: RNA polymerase II transcription termination. |
| Q92217036 | Writing a wrong: Coupled RNA polymerase II transcription and RNA quality control |
| Q50064038 | Xrn2 accelerates termination by RNA polymerase II, which is underpinned by CPSF73 activity |
| Q27933667 | Yeast transcription termination factor Rtt103 functions in DNA damage response |
| Q37263272 | eEF1Bγ binds the Che-1 and TP53 gene promoters and their transcripts. |
| Q41569819 | mRNA 3' end processing factors: a phylogenetic comparison |
| Q24601240 | mRNA 3'end processing: A tale of the tail reaches the clinic |
| Q39579705 | p53 inhibits mRNA 3' processing through its interaction with the CstF/BARD1 complex |
| Q36419865 | period-1 encodes an ATP-dependent RNA helicase that influences nutritional compensation of the Neurospora circadian clock |
| Q47214605 | snoRNAs associate with mRNA 3' processing complex: New wine in old bottles. |
| Q36978280 | αCP Poly(C) binding proteins act as global regulators of alternative polyadenylation |