| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Petra Schwertman | Q55149621 |
| Jurgen A Marteijn | Q55149624 | ||
| P2093 | author name string | Wim Vermeulen | |
| P2860 | cites work | Blockage of RNA polymerase as a possible trigger for u.v. light-induced apoptosis | Q71408610 |
| Clinical characteristics of three patients with UVs syndrome, a photosensitive disorder with defective DNA repair | Q71415736 | ||
| Cockayne syndrome without typical clinical manifestations including neurologic abnormalities | Q77429600 | ||
| Transcription - guarding the genome by sensing DNA damage | Q80518102 | ||
| Repair of 8-oxoguanine in DNA is deficient in Cockayne syndrome group B cells | Q22001461 | ||
| Deubiquitination of p53 by HAUSP is an important pathway for p53 stabilization | Q24292930 | ||
| The role of CSA in the response to oxidative DNA damage in human cells | Q24297071 | ||
| Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo | Q24300037 | ||
| Damage-induced ubiquitylation of human RNA polymerase II by the ubiquitin ligase Nedd4, but not Cockayne syndrome proteins or BRCA1 | Q24300146 | ||
| The ubiquitin ligase activity in the DDB2 and CSA complexes is differentially regulated by the COP9 signalosome in response to DNA damage | Q24301297 | ||
| Loss of HAUSP-mediated deubiquitination contributes to DNA damage-induced destabilization of Hdmx and Hdm2 | Q24303581 | ||
| Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair | Q24310583 | ||
| UV-sensitive syndrome protein UVSSA recruits USP7 to regulate transcription-coupled repair | Q24310704 | ||
| Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair | Q24310767 | ||
| 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 | ||
| CSA-dependent degradation of CSB by the ubiquitin-proteasome pathway establishes a link between complementation factors of the Cockayne syndrome | Q24338620 | ||
| Molecular cloning of the human DNA excision repair gene ERCC-6 | Q24596936 | ||
| UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells | Q24605185 | ||
| Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes | Q24644162 | ||
| Early steps in the DNA base excision/single-strand interruption repair pathway in mammalian cells | Q24650179 | ||
| USP7 counteracts SCFbetaTrCP- but not APCCdh1-mediated proteolysis of Claspin | Q24652867 | ||
| STAM proteins bind ubiquitinated proteins on the early endosome via the VHS domain and ubiquitin-interacting motif | Q24669647 | ||
| Structural basis for acidic-cluster-dileucine sorting-signal recognition by VHS domains | Q27638015 | ||
| CPD damage recognition by transcribing RNA polymerase II | Q27643778 | ||
| Molecular Basis of Transcriptional Mutagenesis at 8-Oxoguanine | Q27657438 | ||
| Cockayne syndrome group B protein (CSB) plays a general role in chromatin maintenance and remodeling | Q28245824 | ||
| Effect of thymine glycol on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II | Q28360336 | ||
| Different effects of CSA and CSB deficiency on sensitivity to oxidative DNA damage | Q28509765 | ||
| Retinal degeneration and ionizing radiation hypersensitivity in a mouse model for Cockayne syndrome | Q28587576 | ||
| Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template | Q28628394 | ||
| A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage | Q29541053 | ||
| Accumulation of mitochondrial DNA damage and bioenergetic dysfunction in CSB defective cells. | Q46039182 | ||
| Host cell reactivation of plasmids containing oxidative DNA lesions is defective in Cockayne syndrome but normal in UV-sensitive syndrome fibroblasts | Q46675864 | ||
| Photosensitivity syndrome brings to light a new transcription-coupled DNA repair cofactor | Q46841191 | ||
| Cockayne syndrome B protein (CSB): linking p53, HIF-1 and p300 to robustness, lifespan, cancer and cell fate decisions. | Q51817829 | ||
| Reinvestigation of the classification of five cell strains of xeroderma pigmentosum group E with reclassification of three of them. | Q53438317 | ||
| Assignment of 2 patients with xeroderma pigmentosum to complementation group E | Q55898414 | ||
| A New Human Photosensitive Subject with a Defect in the Recovery of DNA Synthesis after Ultraviolet-light Irradiation | Q59242136 | ||
| Xeroderma pigmentosum complementation group E: a case report | Q69649198 | ||
| Clinical syndromes associated with DNA repair deficiency and enhanced sun sensitivity | Q70596036 | ||
| Transcription-coupled DNA repair: two decades of progress and surprises | Q29614662 | ||
| DNA damage stabilizes interaction of CSB with the transcription elongation machinery | Q33204356 | ||
| Impaired genome maintenance suppresses the growth hormone--insulin-like growth factor 1 axis in mice with Cockayne syndrome | Q33275830 | ||
| Proteins of nucleotide and base excision repair pathways interact in mitochondria to protect from loss of subcutaneous fat, a hallmark of aging | Q33656093 | ||
| The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex | Q33887586 | ||
| Cockayne syndrome: Review of 140 cases | Q34232807 | ||
| Recognition of RNA polymerase II carboxy-terminal domain by 3'-RNA-processing factors | Q34331986 | ||
| Reduced RNA polymerase II transcription in extracts of cockayne syndrome and xeroderma pigmentosum/Cockayne syndrome cells | Q34636040 | ||
| Translesion synthesis by RNA polymerases: occurrence and biological implications for transcriptional mutagenesis | Q35013058 | ||
| RNA polymerase II bypass of oxidative DNA damage is regulated by transcription elongation factors | Q35191105 | ||
| Cockayne syndrome group B protein prevents the accumulation of damaged mitochondria by promoting mitochondrial autophagy. | Q35894155 | ||
| The conserved Cockayne syndrome B-piggyBac fusion protein (CSB-PGBD3) affects DNA repair and induces both interferon-like and innate antiviral responses in CSB-null cells. | Q35923273 | ||
| Transcription regulation and human diseases. | Q35981295 | ||
| Reduced RNA polymerase II transcription in intact and permeabilized Cockayne syndrome group B cells | Q36128504 | ||
| UV-sensitive syndrome | Q36139544 | ||
| Nucleotide excision repair-initiating proteins bind to oxidative DNA lesions in vivo | Q36486570 | ||
| Genome maintenance mechanisms are critical for preventing cancer as well as other aging-associated diseases | Q36858337 | ||
| The role of Cockayne Syndrome group B (CSB) protein in base excision repair and aging. | Q36882150 | ||
| Transcription-coupled nucleotide excision repair in mammalian cells: molecular mechanisms and biological effects | Q37048164 | ||
| New applications of the Comet assay: Comet-FISH and transcription-coupled DNA repair | Q37091419 | ||
| UV-induced inhibition of transcription involves repression of transcription initiation and phosphorylation of RNA polymerase II. | Q37249463 | ||
| Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome | Q37593459 | ||
| The multifaceted roles of USP7: new therapeutic opportunities | Q37862125 | ||
| Ubiquitylation and degradation of elongating RNA polymerase II: the last resort | Q38041910 | ||
| ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor. | Q39455992 | ||
| BRCA1 contributes to transcription-coupled repair of DNA damage through polyubiquitination and degradation of Cockayne syndrome B protein | Q39506911 | ||
| Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome. | Q39931897 | ||
| Primary fibroblasts of Cockayne syndrome patients are defective in cellular repair of 8-hydroxyguanine and 8-hydroxyadenine resulting from oxidative stress | Q40660412 | ||
| Mitochondrial repair of 8-oxoguanine is deficient in Cockayne syndrome group B. | Q40683322 | ||
| UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I. | Q41342786 | ||
| A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations | Q41472419 | ||
| Deletion of 5' sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome | Q41939477 | ||
| UVSSA and USP7: new players regulating transcription-coupled nucleotide excision repair in human cells | Q42107148 | ||
| KIAA1530 protein is recruited by Cockayne syndrome complementation group protein A (CSA) to participate in transcription-coupled repair (TCR). | Q42121575 | ||
| ATM-dependent downregulation of USP7/HAUSP by PPM1G activates p53 response to DNA damage | Q42243995 | ||
| An altered redox balance mediates the hypersensitivity of Cockayne syndrome primary fibroblasts to oxidative stress. | Q42503209 | ||
| Elongating RNA polymerase II is disassembled through specific degradation of its largest but not other subunits in response to DNA damage in vivo | Q42642375 | ||
| USP7/HAUSP stimulates repair of oxidative DNA lesions | Q42714232 | ||
| P275 | copyright license | Creative Commons Attribution-NonCommercial 2.0 Generic | Q44128984 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | transcription | Q177900 |
| DNA repair | Q210538 | ||
| Cockayne syndrome | Q914389 | ||
| transport protein | Q2111029 | ||
| photosensitivity | Q2944236 | ||
| ubiquitin C-terminal hydrolase L1 | Q7876540 | ||
| P304 | page(s) | 275-284 | |
| P577 | publication date | 2013-06-13 | |
| 2013-08-01 | |||
| P1433 | published in | Chromosoma | Q15765851 |
| P1476 | title | UVSSA and USP7, a new couple in transcription-coupled DNA repair | |
| P478 | volume | 122 |
| Q92072668 | A Bioinformatics Approach to Explore MicroRNAs as Tools to Bridge Pathways Between Plants and Animals. Is DNA Damage Response (DDR) a Potential Target Process? |
| Q38721258 | Amplification of unscheduled DNA synthesis signal enables fluorescence-based single cell quantification of transcription-coupled nucleotide excision repair. |
| Q64236078 | FACT subunit Spt16 controls UVSSA recruitment to lesion-stalled RNA Pol II and stimulates TC-NER |
| Q35729124 | Imprinting genes associated with endometriosis |
| Q38240374 | Insight in the multilevel regulation of NER. |
| Q38970691 | Nucleotide Excision Repair: Finely Tuned Molecular Orchestra of Early Pre-incision Events |
| Q50428930 | Nucleotide Excision Repair: From Neurodegeneration to Cancer. |
| Q28084088 | Nucleotide excision repair in humans |
| Q26773800 | Role of Deubiquitinating Enzymes in DNA Repair |
| Q38989377 | Targeting Deubiquitinating Enzymes in Glioblastoma Multiforme: Expectations and Challenges. |
| Q39032808 | Timing of DNA lesion recognition: Ubiquitin signaling in the NER pathway |
| Q34579775 | Transcription bypass of DNA lesions enhances cell survival but attenuates transcription coupled DNA repair |
| Q38934194 | Transcription-coupled repair: an update |
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