| Q37620941 | "Cotranscriptionality": the transcription elongation complex as a nexus for nuclear transactions |
| Q92532794 | A CRISPR/Cas9 screen identifies the histone demethylase MINA53 as a novel HIV-1 latency-promoting gene (LPG) |
| Q38615900 | A novel SH2 recognition mechanism recruits Spt6 to the doubly phosphorylated RNA polymerase II linker at sites of transcription. |
| Q40191175 | A quantitative and multiplexed approach to uncover the fitness landscape of tumor suppression in vivo |
| Q92133908 | Analog-sensitive cell line identifies cellular substrates of CDK9 |
| Q33734638 | Arabidopsis IWS1 interacts with transcription factor BES1 and is involved in plant steroid hormone brassinosteroid regulated gene expression |
| Q35067664 | Cap-binding protein complex links pre-mRNA capping to transcription elongation and alternative splicing through positive transcription elongation factor b (P-TEFb) |
| Q64884468 | Casein kinase 2 mediated phosphorylation of Spt6 modulates histone dynamics and regulates spurious transcription. |
| Q95297489 | Chemotherapy-induced S100A10 recruits KDM6A to facilitate OCT4-mediated breast cancer stemness |
| Q95355768 | Chromatin Regulation and the Histone Code in HIV Latency |
| Q26999294 | Chromatin and epigenetic regulation of pre-mRNA processing |
| Q35748234 | Chromatin and transcription in yeast |
| Q38286121 | Chromatin modification by the RNA Polymerase II elongation complex |
| Q42059823 | Chromatin reassembly factors are involved in transcriptional interference promoting HIV latency |
| Q36736210 | Clinical and pathologic impact of select chromatin-modulating tumor suppressors in clear cell renal cell carcinoma |
| Q38052877 | Connections between chromatin signatures and splicing |
| Q27937813 | Control of chromatin structure by spt6: different consequences in coding and regulatory regions |
| Q27934029 | Cooperation between the INO80 complex and histone chaperones determines adaptation of stress gene transcription in the yeast Saccharomyces cerevisiae |
| Q38815706 | Coupling of RNA Polymerase II Transcription Elongation with Pre-mRNA Splicing |
| Q27024720 | Coupling pre-mRNA processing to transcription on the RNA factory assembly line |
| Q27667298 | Crystal Structures of the S. cerevisiae Spt6 Core and C-Terminal Tandem SH2 Domain |
| Q33627681 | Crystallization and preliminary crystallographic analysis of eukaryotic transcription and mRNA export factor Iws1 from Encephalitozoon cuniculi |
| Q58748277 | Cycles of gene expression and genome response during mammalian tissue regeneration |
| Q89558876 | DNA mismatch repair in the context of chromatin |
| Q34883246 | Depletion of REF/Aly alters gene expression and reduces RNA polymerase II occupancy |
| Q36406402 | Dynamic changes in histone modifications precede de novo DNA methylation in oocytes. |
| Q38166840 | Dynamic changes of the epigenetic landscape during cellular differentiation. |
| Q37742439 | Epigenetic regulation of development by histone lysine methylation. |
| Q58747998 | Genetic ablation of interacting with Spt6 (Iws1) causes early embryonic lethality |
| Q34310604 | Genetic organization, length conservation, and evolution of RNA polymerase II carboxyl-terminal domain |
| Q57288714 | Genome Instability Is Promoted by the Chromatin-Binding Protein Spn1 in |
| Q35711242 | Genome Scan for Parent-of-Origin QTL Effects on Bovine Growth and Carcass Traits |
| Q24299046 | Genome instability and transcription elongation impairment in human cells depleted of THO/TREX |
| Q34588508 | Genome-wide map of quantified epigenetic changes during in vitro chondrogenic differentiation of primary human mesenchymal stem cells |
| Q37255665 | Genomic disruption of the histone methyltransferase SETD2 in chronic lymphocytic leukaemia. |
| Q96610153 | Genomic profiling in renal cell carcinoma |
| Q38329818 | H3K36 methylation is critical for brassinosteroid-regulated plant growth and development in rice. |
| Q24319622 | HDGF-related protein-2 (HRP-2) acts as an oncogene to promote cell growth in hepatocellular carcinoma |
| Q47781545 | HIV Latency Gets a New Histone Mark. |
| Q35164614 | High nitrogen insensitive 9 (HNI9)-mediated systemic repression of root NO3- uptake is associated with changes in histone methylation |
| Q41500628 | High-throughput assessment of context-dependent effects of chromatin proteins |
| Q35910655 | Histone Chaperones Spt6 and FACT: Similarities and Differences in Modes of Action at Transcribed Genes |
| Q28587253 | Histone H3 lysine 36 methyltransferase Hypb/Setd2 is required for embryonic vascular remodeling |
| Q35238231 | Histone H3 lysine 36 methyltransferase Whsc1 promotes the association of Runx2 and p300 in the activation of bone-related genes |
| Q26865965 | Histone H3 mutations--a special role for H3.3 in tumorigenesis? |
| Q36914566 | Histone H3K36 trimethylation is essential for multiple silencing mechanisms in fission yeast |
| Q24300395 | Histone chaperone Spt6 is required for class switch recombination but not somatic hypermutation |
| Q38343838 | Histone exchange, chromatin structure and the regulation of transcription |
| Q45966440 | Host Methyltransferases and Demethylases: Potential New Epigenetic Targets for HIV Cure Strategies and Beyond. |
| Q41468789 | Human TFIIH Kinase CDK7 Regulates Transcription-Associated Chromatin Modifications |
| Q38715367 | Intragenic DNA methylation prevents spurious transcription initiation |
| Q64054525 | Iws1 and Spt6 Regulate Trimethylation of Histone H3 on Lysine 36 through Akt Signaling and are Essential for Mouse Embryonic Genome Activation |
| Q41147954 | MRG15-mediated tethering of PALB2 to unperturbed chromatin protects active genes from genotoxic stress. |
| Q30794597 | Molecular basis for oncohistone H3 recognition by SETD2 methyltransferase |
| Q27701733 | Multiple cellular proteins interact with LEDGF/p75 through a conserved unstructured consensus motif |
| Q50660807 | Mutations in SETD2 cause a novel overgrowth condition. |
| Q26852971 | New insights into establishment and maintenance of DNA methylation imprints in mammals |
| Q27664927 | Noncanonical Tandem SH2 Enables Interaction of Elongation Factor Spt6 with RNA Polymerase II |
| Q37809760 | Nucleocytoplasmic mRNP export is an integral part of mRNP biogenesis |
| Q41863525 | Nucleosomes are well positioned in exons and carry characteristic histone modifications |
| Q41880113 | Phosphoproteomics screen reveals akt isoform-specific signals linking RNA processing to lung cancer. |
| Q35170883 | Pre-mRNA splicing is a determinant of histone H3K36 methylation |
| Q46110457 | Processing the H3K36me3 signature |
| Q39648288 | Promoter-exon relationship of H3 lysine 9, 27, 36 and 79 methylation on pluripotency-associated genes |
| Q50645951 | RNA Pol II Dynamics Modulate Co-transcriptional Chromatin Modification, CTD Phosphorylation, and Transcriptional Direction. |
| Q37873568 | Recent advances in the regulation of brassinosteroid signaling and biosynthesis pathways |
| Q39634800 | Reciprocal intronic and exonic histone modification regions in humans. |
| Q34258783 | Regulation of the nuclear activities of brassinosteroid signaling |
| Q33883693 | Relationship between gene body DNA methylation and intragenic H3K9me3 and H3K36me3 chromatin marks |
| Q52361188 | Repeat-Specific Functions for the C-Terminal Domain of RNA Polymerase II in Budding Yeast. |
| Q46273301 | Repetitive sequences in malaria parasite proteins. |
| Q51696368 | SETD2 and DNMT3A screen in the Sotos-like syndrome French cohort. |
| Q57472357 | SETD2-dependent H3K36me3 plays a critical role in epigenetic regulation of the HPV31 life cycle |
| Q35188529 | SETD2-dependent histone H3K36 trimethylation is required for homologous recombination repair and genome stability |
| Q28075731 | SETD2: an epigenetic modifier with tumor suppressor functionality |
| Q39118911 | SETting the Stage for Cancer Development: SETD2 and the Consequences of Lost Methylation |
| Q37577424 | SPOP-containing complex regulates SETD2 stability and H3K36me3-coupled alternative splicing. |
| Q99572030 | SPT6-driven error-free DNA repair safeguards genomic stability of glioblastoma cancer stem-like cells |
| Q37158054 | Set2 mediated H3 lysine 36 methylation: regulation of transcription elongation and implications in organismal development |
| Q39225775 | Shaping the cellular landscape with Set2/SETD2 methylation |
| Q35310103 | Solution structure of tandem SH2 domains from Spt6 protein and their binding to the phosphorylated RNA polymerase II C-terminal domain |
| Q30300037 | Spt6 Is Essential for rRNA Synthesis by RNA Polymerase I. |
| Q57491805 | Spt6 Is Required for the Fidelity of Promoter Selection |
| Q96303190 | Spt6 is a maintenance factor for centromeric CENP-A |
| Q38629913 | Spt6 is required for heterochromatic silencing in the fission yeast Schizosaccharomyces pombe. |
| Q37469459 | Spt6 regulates intragenic and antisense transcription, nucleosome positioning, and histone modifications genome-wide in fission yeast |
| Q41975283 | Spt6: two fundamentally distinct functions in the regulation of histone modification |
| Q27665995 | Structure and Biological Importance of the Spn1-Spt6 Interaction, and Its Regulatory Role in Nucleosome Binding |
| Q59070952 | Structure of activated transcription complex Pol II–DSIF–PAF–SPT6 |
| Q60300334 | Structure of transcribing RNA polymerase II-nucleosome complex |
| Q38751593 | Structure/Function Analysis of Recurrent Mutations in SETD2 Protein Reveals a Critical and Conserved Role for a SET Domain Residue in Maintaining Protein Stability and Histone H3 Lys-36 Trimethylation |
| Q64120695 | Supplementing Genistein for Breeder Hens Alters the Fatty Acid Metabolism and Growth Performance of Offsprings by Epigenetic Modification |
| Q39814573 | TFIIH-associated Cdk7 kinase functions in phosphorylation of C-terminal domain Ser7 residues, promoter-proximal pausing, and termination by RNA polymerase II |
| Q36291340 | The Abundant Histone Chaperones Spt6 and FACT Collaborate to Assemble, Inspect, and Maintain Chromatin Structure in Saccharomyces cerevisiae. |
| Q47650921 | The Elongation Factor Spt6 Maintains ESC Pluripotency by Controlling Super-Enhancers and Counteracting Polycomb Proteins. |
| Q46356479 | The Genetic Basis of Hepatosplenic T-cell Lymphoma. |
| Q38043907 | The Mediator complex and transcription elongation |
| Q34303212 | The RNA polymerase II CTD coordinates transcription and RNA processing. |
| 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 |
| Q39156173 | The code and beyond: transcription regulation by the RNA polymerase II carboxy-terminal domain |
| Q91651165 | The elongation factor Elof1 is required for mammalian gastrulation |
| Q47232619 | The elongation factor Spn1 is a multi-functional chromatin binding protein |
| Q52319133 | The essential and multi-functional TFIIH complex. |
| Q36070586 | The histone H3 Lys 27 demethylase JMJD3 regulates gene expression by impacting transcriptional elongation |
| Q24336631 | The histone chaperone Spt6 coordinates histone H3K27 demethylation and myogenesis |
| Q24294424 | The histone chaperone Spt6 is required for activation-induced cytidine deaminase target determination through H3K4me3 regulation |
| Q24339204 | The histone mark H3K36me3 regulates human DNA mismatch repair through its interaction with MutSα |
| Q47370934 | The ribosome assembly gene network is controlled by the feedback regulation of transcription elongation |
| Q27665628 | The structure of an Iws1/Spt6 complex reveals an interaction domain conserved in TFIIS, Elongin A and Med26 |
| Q33677160 | Transcription and chromatin determinants of de novo DNA methylation timing in oocytes |
| Q34539956 | Transcription-coupled changes to chromatin underpin gene silencing by transcriptional interference |
| Q42133855 | Transcriptional elongation and mRNA export are coregulated processes. |
| Q34257867 | Transcriptional provirus silencing as a crosstalk of de novo DNA methylation and epigenomic features at the integration site |
| Q99207801 | Two HIRA-dependent pathways mediate H3.3 de novo deposition and recycling during transcription |
| Q24336514 | UIF, a New mRNA export adaptor that works together with REF/ALY, requires FACT for recruitment to mRNA |
| Q42133715 | Updating the CTD Story: From Tail to Epic. |
| Q37550216 | Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects |
| Q61813696 | loss sensitizes cells to PI3Kβ and AKT inhibition |