| scholarly article | Q13442814 |
| P2093 | author name string | Shisheng Li | |
| Michael J Smerdon | |||
| P2860 | cites work | Trichothiodystrophy, a transcription syndrome | Q24291198 |
| Six human RNA polymerase subunits functionally substitute for their yeast counterparts | Q24310655 | ||
| Analysis of the interaction of the novel RNA polymerase II (pol II) subunit hsRPB4 with its partner hsRPB7 and with pol II. | Q24321388 | ||
| Structural basis of transcription: RNA polymerase II at 2.8 angstrom resolution | Q27631276 | ||
| Structural basis of transcription: an RNA polymerase II elongation complex at 3.3 A resolution | Q27631280 | ||
| RAD25 is a DNA helicase required for DNA repair and RNA polymerase II transcription | Q27930190 | ||
| Transcription elongation through DNA arrest sites. A multistep process involving both RNA polymerase II subunit RPB9 and TFIIS. | Q27930400 | ||
| The yeast TFB1 and SSL1 genes, which encode subunits of transcription factor IIH, are required for nucleotide excision repair and RNA polymerase II transcription | Q27934367 | ||
| Molecular cloning and characterization of Saccharomyces cerevisiae RAD28, the yeast homolog of the human Cockayne syndrome A (CSA) gene | Q27936483 | ||
| RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6. | Q27937381 | ||
| Deletion of the RNA polymerase subunit RPB4 acts as a global, not stress-specific, shut-off switch for RNA polymerase II transcription at high temperatures | Q27939981 | ||
| The Rpb9 subunit of RNA polymerase II binds transcription factor TFIIE and interferes with the SAGA and elongator histone acetyltransferases | Q27940159 | ||
| A positive selection for mutants lacking orotidine-5'-phosphate decarboxylase activity in yeast: 5-fluoro-orotic acid resistance | Q28131606 | ||
| Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template | Q28628394 | ||
| The sequence, and its evolutionary implications, of a Thermococcus celer protein associated with transcription | Q28775998 | ||
| Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene | Q30054509 | ||
| Yeast chromatin structure and regulation of GAL gene expression | Q31441059 | ||
| Fractions to functions: RNA polymerase II thirty years later | Q33671449 | ||
| Structure of wild-type yeast RNA polymerase II and location of Rpb4 and Rpb7. | Q33888711 | ||
| Architecture of RNA polymerase II and implications for the transcription mechanism | Q33899775 | ||
| Deletion of the CSB homolog, RAD26, yields Spt(-) strains with proficient transcription-coupled repair | Q33940642 | ||
| E. coli Transcription repair coupling factor (Mfd protein) rescues arrested complexes by promoting forward translocation | Q34135671 | ||
| Controlling the efficiency of excision repair | Q34244233 | ||
| Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells | Q34348395 | ||
| Mechanisms of transcription-coupled DNA repair | Q34514438 | ||
| Multisubunit RNA polymerases | Q34525904 | ||
| The RNA polymerase II machinery: structure illuminates function | Q34574312 | ||
| Transitions in the coupling of transcription and nucleotide excision repair within RNA polymerase II-transcribed genes of Saccharomyces cerevisiae | Q36300531 | ||
| RNA polymerase II subunit RPB4 is essential for high- and low-temperature yeast cell growth | Q36769195 | ||
| Sequence-specific and domain-specific DNA repair in xeroderma pigmentosum and Cockayne syndrome cells | Q36875627 | ||
| The RAD7 and RAD16 genes, which are essential for pyrimidine dimer removal from the silent mating type loci, are also required for repair of the nontranscribed strand of an active gene in Saccharomyces cerevisiae | Q38304692 | ||
| DNA repair rates mapped along the human PGK1 gene at nucleotide resolution | Q38310213 | ||
| Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repair | Q38313225 | ||
| Double mutants of Saccharomyces cerevisiae with alterations in global genome and transcription-coupled repair | Q38362404 | ||
| Excision repair at the level of the nucleotide in the upstream control region, the coding sequence and in the region where transcription terminates of the Saccharomyces cerevisiae MFA2 gene and the role of RAD26. | Q39542527 | ||
| A portion of RNA polymerase II molecules has a component essential for stress responses and stress survival | Q40656654 | ||
| The transcription-repair coupling factor CSA is required for efficient repair only during the elongation stages of RNA polymerase II transcription | Q41020602 | ||
| Two-dimensional and epitaxial crystallization of a mutant form of yeast RNA polymerase II. | Q43842832 | ||
| Different forms of TFIIH for transcription and DNA repair: holo-TFIIH and a nucleotide excision repairosome | Q46391372 | ||
| Induction of the Escherichia coli lactose operon selectively increases repair of its transcribed DNA strand | Q46437555 | ||
| Yeast RNA polymerase II subunit RPB9 is essential for growth at temperature extremes. | Q48206014 | ||
| Site-specific DNA repair at the nucleosome level in a yeast minichromosome. | Q52483708 | ||
| RNA polymerase II subunit Rpb9 regulates transcription elongation in vivo. | Q52540398 | ||
| Nucleotide level detection of cyclobutane pyrimidine dimers using oligonucleotides and magnetic beads to facilitate labelling of DNA fragments incised at the dimers and chemical sequencing reference ladders. | Q53452426 | ||
| Modulation of DNA damage and DNA repair in chromatin. | Q53937922 | ||
| Two conformations of RNA polymerase II revealed by electron crystallography. | Q53963713 | ||
| Molecular mechanism of transcription-repair coupling. | Q54659174 | ||
| Transcription factor b (TFIIH) is required during nucleotide-excision repair in yeast | Q58318854 | ||
| DNA repair gene RAD3 of S. cerevisiae is essential for transcription by RNA polymerase II | Q59097138 | ||
| The Saccharomyces cerevisiae DNA repair gene RAD25 is required for transcription by RNA polymerase II | Q72102254 | ||
| RNA polymerase II subunit RPB9 is required for accurate start site selection | Q72613078 | ||
| Low- and high-resolution mapping of DNA damage at specific sites | Q73044796 | ||
| Transcription elongation factor S-II is not required for transcription-coupled repair in yeast | Q73337593 | ||
| The initiation of DNA base excision repair of dipyrimidine photoproducts | Q77949977 | ||
| P4510 | describes a project that uses | ImageQuant | Q112270642 |
| P433 | issue | 21 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Saccharomyces cerevisiae | Q719725 |
| P304 | page(s) | 5921-5929 | |
| P577 | publication date | 2002-11-01 | |
| P1433 | published in | The EMBO Journal | Q1278554 |
| P1476 | title | Rpb4 and Rpb9 mediate subpathways of transcription-coupled DNA repair in Saccharomyces cerevisiae | |
| P478 | volume | 21 |
| Q28543050 | A genetic assay for transcription errors reveals multilayer control of RNA polymerase II fidelity |
| Q27931906 | A new connection of mRNP biogenesis and export with transcription-coupled repair |
| Q35563943 | A role for SUMO in nucleotide excision repair |
| Q42876928 | A role for checkpoint kinase-dependent Rad26 phosphorylation in transcription-coupled DNA repair in Saccharomyces cerevisiae. |
| Q36740171 | A single amino acid change in histone H4 enhances UV survival and DNA repair in yeast |
| Q37830691 | Archaeal RNA polymerase and transcription regulation. |
| Q34570125 | Ccr4-not complex mRNA deadenylase activity contributes to DNA damage responses in Saccharomyces cerevisiae |
| Q27936277 | Cleavage factor I links transcription termination to DNA damage response and genome integrity maintenance in Saccharomyces cerevisiae |
| Q33905274 | Cockayne syndrome group B cellular and biochemical functions |
| Q24817079 | Crystal structure and RNA binding of the Rpb4/Rpb7 subunits of human RNA polymerase II |
| Q73346957 | Current Awareness on Yeast |
| Q28709604 | DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae |
| Q50994474 | Def1 and Dst1 play distinct roles in repair of AP lesions in highly transcribed genomic regions |
| Q34293940 | Dissecting transcription-coupled and global genomic repair in the chromatin of yeast GAL1-10 genes |
| Q27934457 | Diverse roles of RNA polymerase II-associated factor 1 complex in different subpathways of nucleotide excision repair |
| Q40695120 | Domainal organization of the lower eukaryotic homologs of the yeast RNA polymerase II core subunit Rpb7 reflects functional conservation |
| Q27938606 | Evidence that the histone methyltransferase Dot1 mediates global genomic repair by methylating histone H3 on lysine 79. |
| Q27930103 | Evidence that the transcription elongation function of Rpb9 is involved in transcription-coupled DNA repair in Saccharomyces cerevisiae |
| Q38994555 | Facilitators and Repressors of Transcription-coupled DNA Repair in Saccharomyces cerevisiae |
| Q36579359 | Five repair pathways in one context: chromatin modification during DNA repair |
| Q39012214 | From Mfd to TRCF and Back Again-A Perspective on Bacterial Transcription-coupled Nucleotide Excision Repair |
| Q91828974 | Functional interplay between Mediator and RNA polymerase II in Rad2/XPG loading to the chromatin |
| Q33406244 | Genome-wide analysis of factors affecting transcription elongation and DNA repair: a new role for PAF and Ccr4-not in transcription-coupled repair. |
| Q47982607 | Genome-wide maps of alkylation damage, repair, and mutagenesis in yeast reveal mechanisms of mutational heterogeneity. |
| Q34655042 | Genomic location of the human RNA polymerase II general machinery: evidence for a role of TFIIF and Rpb7 at both early and late stages of transcription |
| Q37128155 | Histone H3 Lys79 methylation is required for efficient nucleotide excision repair in a silenced locus of Saccharomyces cerevisiae |
| Q92203088 | Histone H4 H75E mutation attenuates global genomic and Rad26-independent transcription-coupled nucleotide excision repair |
| Q42844928 | Homologous recombination is involved in transcription-coupled repair of UV damage in Saccharomyces cerevisiae |
| Q33791149 | Insights into how Spt5 functions in transcription elongation and repressing transcription coupled DNA repair |
| Q37592638 | Members of the SAGA and Mediator complexes are partners of the transcription elongation factor TFIIS. |
| Q27939686 | Modulation of Rad26- and Rpb9-mediated DNA repair by different promoter elements. |
| Q36107008 | Mutations at the Subunit Interface of Yeast Proliferating Cell Nuclear Antigen Reveal a Versatile Regulatory Domain |
| Q38056492 | Nucleotide excision repair in cellular chromatin: studies with yeast from nucleotide to gene to genome |
| Q51276964 | RNA Polymerase-I-Dependent Transcription-coupled Nucleotide Excision Repair of UV-Induced DNA Lesions at Transcription Termination Sites, in Saccharomyces cerevisiae |
| Q98237728 | RNA polymerase II subunit D is essential for zebrafish development |
| Q31132336 | Rad26, the transcription-coupled repair factor in yeast, is required for removal of stalled RNA polymerase-II following UV irradiation |
| Q33719420 | Rad26p, a transcription-coupled repair factor, is recruited to the site of DNA lesion in an elongating RNA polymerase II-dependent manner in vivo |
| Q27932672 | Rad4-Rad23 interaction with SWI/SNF links ATP-dependent chromatin remodeling with nucleotide excision repair |
| Q90110326 | Regulation of the RNAPII Pool Is Integral to the DNA Damage Response |
| Q27930029 | Requirement of ELC1 for RNA polymerase II polyubiquitylation and degradation in response to DNA damage in Saccharomyces cerevisiae |
| Q25256763 | Roles for Gcn5p and Ada2p in transcription and nucleotide excision repair at the Saccharomyces cerevisiae MET16 gene |
| Q37156247 | Rpb1 sumoylation in response to UV radiation or transcriptional impairment in yeast |
| Q38037139 | Rpb4 and Rpb7: multifunctional subunits of RNA polymerase II. |
| Q49222219 | Rpb9-deficient cells are defective in DNA damage response and require histone H3 acetylation for survival. |
| Q27932885 | Rtr1 is the Saccharomyces cerevisiae homolog of a novel family of RNA polymerase II-binding proteins. |
| Q34268990 | Running with RNA polymerase: eukaryotic transcript elongation |
| Q39939479 | Schizosaccharomyces pombe Ddb1 recruits substrate-specific adaptor proteins through a novel protein motif, the DDB-box |
| Q27932689 | Sen1, the yeast homolog of human senataxin, plays a more direct role than Rad26 in transcription coupled DNA repair |
| Q88181627 | Single-nucleotide resolution dynamic repair maps of UV damage in Saccharomyces cerevisiae genome |
| Q36174139 | Tfb5 is partially dispensable for Rad26 mediated transcription coupled nucleotide excision repair in yeast. |
| Q27930568 | The C-terminal repeat domain of Spt5 plays an important role in suppression of Rad26-independent transcription coupled repair |
| Q52560605 | The Cellular Response to Transcription-Blocking DNA Damage. |
| Q27935757 | The Rad4 homologue YDR314C is essential for strand-specific repair of RNA polymerase I-transcribed rDNA in Saccharomyces cerevisiae |
| Q34580247 | The Rpb4/7 module of RNA polymerase II is required for carbon catabolite repressor protein 4-negative on TATA (Ccr4-not) complex to promote elongation |
| Q46659790 | The dissociable RPB4 subunit of RNA Pol II has vital functions in Drosophila |
| Q36643870 | The mechanism of nucleotide excision repair-mediated UV-induced mutagenesis in nonproliferating cells |
| Q37398643 | The molecular basis of chromatin dynamics during nucleotide excision repair |
| Q36173014 | The roles of Rad16 and Rad26 in repairing repressed and actively transcribed genes in yeast |
| Q26801362 | Transcription Blockage Leads to New Beginnings |
| Q34579775 | Transcription bypass of DNA lesions enhances cell survival but attenuates transcription coupled DNA repair |
| Q38934194 | Transcription-coupled repair: an update |
| Q35948156 | Yeast Rpb9 plays an important role in ubiquitylation and degradation of Rpb1 in response to UV-induced DNA damage |
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