| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1996PNAS...93.1292M |
| P356 | DOI | 10.1073/PNAS.93.3.1292 |
| P932 | PMC publication ID | 40073 |
| P698 | PubMed publication ID | 8577757 |
| P5875 | ResearchGate publication ID | 14622298 |
| P2093 | author name string | G N Champe | |
| I Mellon | |||
| P2860 | cites work | RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6. | Q27937381 |
| Mutation of a mutL homolog in hereditary colon cancer | Q28114939 | ||
| ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes | Q28213725 | ||
| The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
| Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer | Q28257360 | ||
| Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template | Q28628394 | ||
| Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene | Q30054509 | ||
| The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA. | Q33640104 | ||
| Mutator phenotypes in human colorectal carcinoma cell lines | Q35568305 | ||
| Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome | Q36658207 | ||
| Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes | Q36728551 | ||
| Repair of DNA heteroduplexes containing small heterologous sequences in Escherichia coli | Q36856385 | ||
| Mechanisms and biological effects of mismatch repair | Q37041860 | ||
| Preferential repair of cyclobutane pyrimidine dimers in the transcribed strand of a gene in yeast chromosomes and plasmids is dependent on transcription | Q37293401 | ||
| Transcription-repair coupling determines the strandedness of ultraviolet mutagenesis in Escherichia coli | Q37306203 | ||
| Escherichia coli mfd mutant deficient in "mutation frequency decline" lacks strand-specific repair: in vitro complementation with purified coupling factor | Q37653163 | ||
| 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 | ||
| Differential repair of UV damage in Saccharomyces cerevisiae | Q40450525 | ||
| Repair and transcription. Collision or collusion? | Q40598246 | ||
| Microsatellite instability: marker of a mutator phenotype in cancer. | Q40630726 | ||
| Mechanisms of transcription-repair coupling and mutation frequency decline | Q40693785 | ||
| Inhibition of transcription and strand-specific DNA repair by alpha-amanitin in Chinese hamster ovary cells | Q41093258 | ||
| Defective mismatch repair in extracts of colorectal and endometrial cancer cell lines exhibiting microsatellite instability | Q41467421 | ||
| Hypermutability and mismatch repair deficiency in RER+ tumor cells | Q41508298 | ||
| Effects of DNA damaging agents on cultured fibroblasts derived from patients with Cockayne syndrome | Q41514231 | ||
| SOS mutator effect in E. coli mutants deficient in mismatch correction | Q41566221 | ||
| Recombinagenic processing of UV-light photoproducts in nonreplicating phage DNA by the Escherichia coli methyl-directed mismatch repair system | Q42031121 | ||
| Transcription preferentially inhibits nucleotide excision repair of the template DNA strand in vitro | Q43762201 | ||
| Mispair specificity of methyl-directed DNA mismatch correction in vitro | Q44909730 | ||
| Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation | Q46049171 | ||
| Induction of the Escherichia coli lactose operon selectively increases repair of its transcribed DNA strand | Q46437555 | ||
| Preferential repair of DNA damage on the transcribed strand of the human metallothionein genes requires RNA polymerase II. | Q46636730 | ||
| Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
| Strand bias in mutation involving 5-methylcytosine deamination in the human hprt gene | Q48087003 | ||
| Site-specific DNA repair at the nucleosome level in a yeast minichromosome. | Q52483708 | ||
| Selective repair of specific chromatin domains in UV-irradiated cells from xeroderma pigmentosum complementation group C. | Q54324697 | ||
| 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 | ||
| Strand-selective repair of DNA damage in the yeast GAL7 gene requires RNA polymerase II | Q67926162 | ||
| UvrABC incision of N-methylmitomycin A-DNA monoadducts and cross-links | Q69555135 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Escherichia coli | Q25419 |
| DNA mismatch repair | Q2984243 | ||
| P304 | page(s) | 1292-1297 | |
| P577 | publication date | 1996-02-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide-excision repair of the lactose operon in Escherichia coli | |
| P478 | volume | 93 |
| Q39033344 | A Magic Spot in Genome Maintenance |
| Q35626161 | Characterization of Lactococcus lactis UV-sensitive mutants obtained by ISS1 transposition |
| Q24532391 | Cockayne syndrome: defective repair of transcription? |
| Q34244233 | Controlling the efficiency of excision repair |
| Q34509028 | DNA Mismatch Repair |
| Q41441658 | DNA excision repair pathways |
| Q33772428 | DNA mismatch repair catalyzed by extracts of mitotic, postmitotic, and senescent Drosophila tissues and involvement of mei-9 gene function for full activity |
| Q34568596 | DNA mismatch repair defects: role in colorectal carcinogenesis |
| Q53391114 | DNA mismatch repair enzyme hMSH2 in malignant melanoma: increased immunoreactivity as compared to acquired melanocytic nevi and strong mRNA expression in melanoma cell lines. |
| Q92267314 | DNA mismatch repair is required for the host innate response and controls cellular fate after influenza virus infection |
| Q54120570 | DNA repair in Mycobacterium tuberculosis. What have we learnt from the genome sequence? |
| Q46002898 | DNA replication and postreplication mismatch repair in cell-free extracts from cultured human neuroblastoma and fibroblast cells. |
| Q74623145 | Decreased cisplatin damage-dependent DNA synthesis in cellular extracts of mismatch repair deficient cells |
| Q33868100 | Defective nucleotide excision repair in xpc mutant mice and its association with cancer predisposition |
| Q62594873 | Determinants of Base-Pair Substitution Patterns Revealed by Whole-Genome Sequencing of DNA Mismatch Repair Defective |
| Q28586687 | Different mismatch repair deficiencies all have the same effects on somatic hypermutation: intact primary mechanism accompanied by secondary modifications |
| Q33601079 | Effect of DNA lesions on transcription elongation |
| Q47724007 | Effects of nonbulky DNA base damages on Escherichia coli RNA polymerase-mediated elongation and promoter clearance |
| Q32108861 | Evidence for a physical interaction between the Escherichia coli methyl-directed mismatch repair proteins MutL and UvrD. |
| Q28238561 | Evolution of mutation rates in bacteria |
| Q35351447 | Folate depletion impairs DNA excision repair in the colon of the rat. |
| Q36565069 | Functional nucleotide excision repair is required for the preferential removal of N-ethylpurines from the transcribed strand of the dihydrofolate reductase gene of Chinese hamster ovary cells |
| Q33943516 | Genomic heterogeneity of nucleotide excision repair |
| Q58874713 | Genotoxic Effect and Carcinogenic Potential of a Mixture of As and Cd in Zebrafish at Permissible Maximum Contamination Levels for Drinking Water |
| Q39682097 | Global genome removal of thymine glycol in Escherichia coli requires endonuclease III but the persistence of processed repair intermediates rather than thymine glycol correlates with cellular sensitivity to high doses of hydrogen peroxide |
| Q37522716 | Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adduct |
| Q58074493 | Human MutSα Specifically Binds to DNA Containing Aminofluorene and Acetylaminofluorene Adducts |
| Q38363713 | Human cells bearing homozygous mutations in the DNA mismatch repair genes hMLH1 or hMSH2 are fully proficient in transcription-coupled nucleotide excision repair |
| Q37606952 | Identification of genes involved in low aminoglycoside-induced SOS response in Vibrio cholerae: a role for transcription stalling and Mfd helicase |
| Q54064735 | Immunohistochemical analysis of DNA 'mismatch-repair' enzyme human Mut-S-Homologon-2 in ovarian carcinomas. |
| Q42488176 | Immunohistochemical analysis of DNA mismatch repair enzyme hMSH-2 in normal human skin and basal cell carcinomas |
| Q36235057 | In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair |
| Q33732387 | Induction of the SOS response increases the efficiency of global nucleotide excision repair of cyclobutane pyrimidine dimers, but not 6-4 photoproducts, in UV-irradiated Escherichia coli. |
| Q60680560 | Intracistronic transcription termination in polysialyltransferase gene (siaD ) affects phase variation in Neisseria meningitidis |
| Q36615131 | Involvement of mismatch repair in transcription-coupled nucleotide excision repair |
| Q39384000 | Mechanistic insights into transcription coupled DNA repair |
| Q35943160 | Mfd is required for rapid recovery of transcription following UV-induced DNA damage but not oxidative DNA damage in Escherichia coli |
| Q47684794 | Mfd translocase is necessary and sufficient for transcription-coupled repair in Escherichia coli |
| Q44280420 | Mice defective in the mismatch repair gene Msh2 show increased predisposition to UVB radiation-induced skin cancer |
| Q35063842 | Microsatellite instability in Drosophila spellchecker1 (MutS homolog) mutants |
| Q34194518 | Mismatch repair in correction of replication errors and processing of DNA damage |
| Q33967893 | Mismatch repair mutants in yeast are not defective in transcription-coupled DNA repair of UV-induced DNA damage. |
| Q33960642 | Mismatch repair processing of carcinogen-DNA adducts triggers apoptosis |
| Q35190848 | Mismatch repair protein MutL becomes limiting during stationary-phase mutation |
| Q33984294 | Mismatch repair proteins and mitotic genome stability |
| Q73093625 | Mismatch repair provokes chromosome aberrations in hamster cells treated with methylating agents or 6-thioguanine, but not with ethylating agents |
| Q38301649 | Mouse mismatch repair gene Msh2 is not essential for transcription-coupled repair of UV-induced cyclobutane pyrimidine dimers |
| Q40744422 | Multiple mutations are common at mouse Aprt in genotoxin-exposed mismatch repair deficient cells |
| Q28303186 | MutS homologs in mammalian cells |
| Q54598216 | Mutation frequency decline in Escherichia coli. I. Effects of defects in mismatch repair. |
| Q54598212 | Mutation frequency decline in Escherichia coli. II. Kinetics support the involvement of transcription-coupled excision repair. |
| Q28235642 | Mutations predisposing to hereditary nonpolyposis colorectal cancer |
| Q36733353 | Physical interaction between components of DNA mismatch repair and nucleotide excision repair |
| Q34675663 | Preferential repair of oxidized base damage in the transcribed genes of mammalian cells |
| Q37127818 | Properties of HflX, an enigmatic protein from Escherichia coli. |
| Q36339832 | Rate and molecular spectrum of spontaneous mutations in the bacterium Escherichia coli as determined by whole-genome sequencing. |
| Q36565271 | Recognition and repair of compound DNA lesions (base damage and mismatch) by human mismatch repair and excision repair systems |
| Q57752804 | Regulation of UvrD Helicase Activity by MutL |
| Q35132508 | Regulation of nucleotide excision repair in bacteria and mammalian cells. |
| Q42660015 | Replication errors: cha(lle)nging the genome |
| Q38336291 | Requirement for DNA mismatch repair proteins in the transcription-coupled repair of thymine glycols in Saccharomyces cerevisiae |
| Q46663864 | Resistance of Deinococcus radiodurans to mutagenesis is facilitated by pentose phosphate pathway in the mutS1 mutant background |
| Q26999076 | Rethinking transcription coupled DNA repair |
| Q43915766 | SN2 DNA-alkylating agent-induced phosphorylation of p53 and activation of p21 gene expression |
| Q40124687 | Single-molecule FRET TACKLE reveals highly dynamic mismatched DNA-MutS complexes |
| Q38324036 | Specific binding of human MSH2.MSH6 mismatch-repair protein heterodimers to DNA incorporating thymine- or uracil-containing UV light photoproducts opposite mismatched bases. |
| Q36961669 | Stationary phase mutagenesis in B. subtilis: a paradigm to study genetic diversity programs in cells under stress |
| Q27635053 | Structure and function of the N-terminal 40 kDa fragment of human PMS2: a monomeric GHL ATPase |
| Q43755592 | The SOS-dependent upregulation of uvrD is not required for efficient nucleotide excision repair of ultraviolet light induced DNA photoproducts in Escherichia coli |
| Q46129337 | The microsatellites of Escherichia coli: rapidly evolving repetitive DNAs in a non-pathogenic prokaryote |
| Q40605233 | The nucleotide excision repair system of Borrelia burgdorferi is the sole pathway involved in repair of DNA damage by UV light |
| Q36642237 | The role of the human DNA mismatch repair gene hMSH2 in DNA repair, cell cycle control and apoptosis: implications for pathogenesis, progression and therapy of cancer |
| Q34640431 | Transcription and DNA damage: a link to a kink |
| Q36962799 | Transcription coupled nucleotide excision repair in Escherichia coli can be affected by changing the arginine at position 529 of the beta subunit of RNA polymerase. |
| Q35614147 | Transcription of the mutL repair, miaA tRNA modification, hfq pleiotropic regulator, and hflA region protease genes of Escherichia coli K-12 from clustered Esigma32-specific promoters during heat shock |
| Q34088373 | Transcription-coupled nucleotide excision repair of a gene transcribed by bacteriophage T7 RNA polymerase in Escherichia coli |
| Q33594900 | Transcription-coupled repair of DNA damage: unanticipated players, unexpected complexities |
| Q35132516 | Transcription-coupled repair of oxidative DNA damage in human cells: mechanisms and consequences |
| Q35132666 | Transcription-coupled repair: a multifunctional signaling pathway |
| Q38934194 | Transcription-coupled repair: an update |
| Q64388371 | Transcriptional effects on double-strand break-induced gene conversion tracts |
| Q44633186 | Transcriptional mutagenesis induced by uracil and 8-oxoguanine in Escherichia coli. |
| Q27617873 | Transformation of MutL by ATP binding and hydrolysis: a switch in DNA mismatch repair |
| Q34603730 | Transient and heritable mutators in adaptive evolution in the lab and in nature |
| Q44267645 | Ultraviolet-sensitive syndrome cells are defective in transcription-coupled repair of cyclobutane pyrimidine dimers |
| Q41749824 | Understanding bias in DNA repair. |
| Q35120155 | Who's on first in the cellular response to DNA damage? |
| Q64389529 | Why Is DNA Double Stranded? The Discovery of DNA Excision Repair Mechanisms |
| Q37776339 | Wot the ‘L—Does MutL do? |
| Q33963455 | p53-mediated DNA repair responses to UV radiation: studies of mouse cells lacking p53, p21, and/or gadd45 genes |
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