| P50 | author | Jean-Marc Egly | Q3167372 |
| | Jean-Philippe Lainé | Q125241387 |
| P2860 | cites work | XAB2, a novel tetratricopeptide repeat protein involved in transcription-coupled DNA repair and transcription | Q24290089 |
| | Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome | Q24292732 |
| | The ubiquitin ligase activity in the DDB2 and CSA complexes is differentially regulated by the COP9 signalosome in response to DNA damage | Q24301297 |
| | Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair | Q24312736 |
| | Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II | Q24314310 |
| | Cockayne syndrome group B protein enhances elongation by RNA polymerase II | Q24317053 |
| | Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein | Q24317182 |
| | Cisplatin- and UV-damaged DNA lure the basal transcription factor TFIID/TBP. | Q38339920 |
| | ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor. | Q39455992 |
| | Saccharomyces cerevisiae mms19 mutants are deficient in transcription-coupled and global nucleotide excision repair. | Q39721487 |
| | Dual requirement for the yeast MMS19 gene in DNA repair and RNA polymerase II transcription | Q40020418 |
| | DNA structural elements required for ERCC1-XPF endonuclease activity. | Q41045887 |
| | Excision-repair patch lengths are similar for transcription-coupled repair and global genome repair in UV-irradiated human cells | Q41068797 |
| | Inhibition of transcription and strand-specific DNA repair by alpha-amanitin in Chinese hamster ovary cells | Q41093258 |
| | Effects of DNA damaging agents on cultured fibroblasts derived from patients with Cockayne syndrome | Q41514231 |
| | Fate of RNA polymerase II stalled at a cisplatin lesion | Q44691519 |
| | Transcription elongation by RNA polymerase II: mechanism of SII activation. | Q48375819 |
| | DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall. | Q54455838 |
| | Molecular mechanism of transcription-repair coupling. | Q54659174 |
| | Purification and interaction properties of the human RNA polymerase B(II) general transcription factor BTF2 | Q68041082 |
| | Blockage of RNA polymerase as a possible trigger for u.v. light-induced apoptosis | Q71408610 |
| | U.v.-induced nuclear accumulation of p53 is evoked through DNA damage of actively transcribed genes independent of the cell cycle | Q72185052 |
| | The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH | Q24336968 |
| | Nucleotide excision repair of DNA with recombinant human proteins: definition of the minimal set of factors, active forms of TFIIH, and modulation by CAK | Q24609992 |
| | Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes | Q24644162 |
| | The comings and goings of nucleotide excision repair factors on damaged DNA | Q24672395 |
| | Genome maintenance mechanisms for preventing cancer | Q28131737 |
| | ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes | Q28213725 |
| | RNA polymerase II elongation complexes containing the Cockayne syndrome group B protein interact with a molecular complex containing the transcription factor IIH components xeroderma pigmentosum B and p62 | Q28285490 |
| | A multistep damage recognition mechanism for global genomic nucleotide excision repair | Q28359842 |
| | Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition | Q28585729 |
| | CSB is a component of RNA pol I transcription | Q28610049 |
| | DNA-binding polarity of human replication protein A positions nucleases in nucleotide excision repair | Q28628567 |
| | Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene | Q30054509 |
| | Double-check probing of DNA bending and unwinding by XPA-RPA: an architectural function in DNA repair | Q30684974 |
| | Molecular anatomy of the human excision nuclease assembled at sites of DNA damage | Q31097811 |
| | Order of assembly of human DNA repair excision nuclease | Q31326797 |
| | Ordered conformational changes in damaged DNA induced by nucleotide excision repair factors | Q33198588 |
| | DNA damage stabilizes interaction of CSB with the transcription elongation machinery | Q33204356 |
| | Requirement for yeast RAD26, a homolog of the human CSB gene, in elongation by RNA polymerase II | Q33551567 |
| | The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex | Q33887586 |
| | Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH. | Q33890541 |
| | Transcriptional activators stimulate DNA repair. | Q34167329 |
| | Cockayne syndrome: Review of 140 cases | Q34232807 |
| | Yeast RAD26, a homolog of the human CSB gene, functions independently of nucleotide excision repair and base excision repair in promoting transcription through damaged bases | Q34280857 |
| | Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells | Q34348395 |
| | Rescue of arrested RNA polymerase II complexes | Q35036829 |
| | The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA | Q35907237 |
| | Reduced RNA polymerase II transcription in intact and permeabilized Cockayne syndrome group B cells | Q36128504 |
| | Role of high mobility group (HMG) chromatin proteins in DNA repair. | Q36139621 |
| | The XPA protein is a zinc metalloprotein with an ability to recognize various kinds of DNA damage | Q36676627 |
| | Mammalian DNA nucleotide excision repair reconstituted with purified protein components. | Q36697936 |
| | Nucleotide excision repair DNA synthesis by DNA polymerase epsilon in the presence of PCNA, RFC, and RPA. | Q36699598 |
| | Preferential repair of cyclobutane pyrimidine dimers in the transcribed strand of a gene in yeast chromosomes and plasmids is dependent on transcription | Q37293401 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 387-397 | |
| P577 | publication date | 2006-01-12 | |
| P1433 | published in | The EMBO Journal | Q1278554 |
| P1476 | title | Initiation of DNA repair mediated by a stalled RNA polymerase IIO. | |
| P478 | volume | 25 | |