| P2093 | author name string | Peter Karran | |
| | Shinya Oda | |
| | Katsuhiko Yanaga | |
| | Katsutoshi Kobayashi | |
| P2860 | cites work | A defined human system that supports bidirectional mismatch-provoked excision | Q24298110 |
| | Mechanism of 5'-directed excision in human mismatch repair | Q24300483 |
| | 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 |
| | Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability | Q24319995 |
| | UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells | Q24605185 |
| | Two modes of microsatellite instability in human cancer: differential connection of defective DNA mismatch repair to dinucleotide repeat instability. | Q24804629 |
| | hMSH2-hMSH6 forms a hydrolysis-independent sliding clamp on mismatched DNA | Q28138775 |
| | A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy | Q28142117 |
| | 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 |
| | Transcription-coupled repair deficiency and mutations in human mismatch repair genes | Q28276963 |
| | Sequential assembly of the nucleotide excision repair factors in vivo | Q28610121 |
| | Nucleotide-promoted release of hMutSalpha from heteroduplex DNA is consistent with an ATP-dependent translocation mechanism | Q28610864 |
| | Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 |
| | Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines | Q29620526 |
| | Microsatellite instability in cancer of the proximal colon | Q29620692 |
| | Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene | Q30054509 |
| | Molecular mechanism of nucleotide excision repair. | Q30669716 |
| | The instability within: problems in current analyses of microsatellite instability | Q31833517 |
| | UV light-induced degradation of RNA polymerase II is dependent on the Cockayne's syndrome A and B proteins but not p53 or MLH1. | Q31970093 |
| | Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide-excision repair of the lactose operon in Escherichia coli | Q33555494 |
| | Nucleotide excision repair: from E. coli to man. | Q33601014 |
| | Effect of DNA lesions on transcription elongation | Q33601079 |
| | The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA. | Q33640104 |
| | Mutated gene-specific phenotypes of dinucleotide repeat instability in human colorectal carcinoma cell lines deficient in DNA mismatch repair | Q33861772 |
| | Mismatch repair defects in cancer | Q33885063 |
| | Mismatch repair mutants in yeast are not defective in transcription-coupled DNA repair of UV-induced DNA damage. | Q33967893 |
| | Defective Repair Replication of DNA in Xeroderma Pigmentosum | Q34054000 |
| | Molecular mechanisms of DNA mismatch repair | Q34293069 |
| | Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells | Q34348395 |
| | Mechanisms of transcription-coupled DNA repair | Q34514438 |
| | Nucleotide excision repair and its interplay with transcription | Q35576450 |
| | Functional characterization of global genomic DNA repair and its implications for cancer. | Q35596006 |
| | Mismatch repair and DNA damage signalling | Q35848516 |
| | The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA | Q35907237 |
| | Nucleotide sequence context effect of a cyclobutane pyrimidine dimer upon RNA polymerase II transcription | Q36029964 |
| | Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers. | Q36213486 |
| | An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair. | Q36412005 |
| | Lack of gene- and strand-specific DNA repair in RNA polymerase III-transcribed human tRNA genes | Q36564736 |
| | Recognition and repair of compound DNA lesions (base damage and mismatch) by human mismatch repair and excision repair systems | Q36565271 |
| | Base pair conformation-dependent excision of benzo[a]pyrene diol epoxide-guanine adducts by human nucleotide excision repair enzymes | Q36573952 |
| | Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes | Q36728551 |
| | Physical interaction between components of DNA mismatch repair and nucleotide excision repair | Q36733353 |
| | Precise assessment of microsatellite instability using high resolution fluorescent microsatellite analysis | Q36876038 |
| | Nucleotide excision repair in Escherichia coli | Q37056044 |
| | Ubiquitination of RNA polymerase II large subunit signaled by phosphorylation of carboxyl-terminal domain | Q37195554 |
| | Distribution of methyl and ethyl adducts following alkylation with monofunctional alkylating agents | Q37939678 |
| | Mammalian O6-alkylguanine-DNA alkyltransferase: regulation and importance in response to alkylating carcinogenic and therapeutic agents | Q37952773 |
| | Molecular genetics of eukaryotic DNA excision repair | Q38028472 |
| | Mouse mismatch repair gene Msh2 is not essential for transcription-coupled repair of UV-induced cyclobutane pyrimidine dimers | Q38301649 |
| | Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage | Q38320078 |
| | XPC lymphoblastoid cells defective in the hMutSalpha DNA mismatch repair complex exhibit normal sensitivity to UVC radiation and normal transcription-coupled excision repair of DNA cyclobutane pyrimidine dimers | Q38341371 |
| | Model for XPC-independent transcription-coupled repair of pyrimidine dimers in humans | Q38347606 |
| | Human cells bearing homozygous mutations in the DNA mismatch repair genes hMLH1 or hMSH2 are fully proficient in transcription-coupled nucleotide excision repair | Q38363713 |
| | Differential repair of UV damage in Saccharomyces cerevisiae | Q40450525 |
| | Repair and transcription. Collision or collusion? | Q40598246 |
| | Transcription-coupled repair removes both cyclobutane pyrimidine dimers and 6-4 photoproducts with equal efficiency and in a sequential way from transcribed DNA in xeroderma pigmentosum group C fibroblasts | Q40805549 |
| | The p53-regulated cyclin-dependent kinase inhibitor, p21 (cip1, waf1, sdi1), is not required for global genomic and transcription-coupled nucleotide excision repair of UV-induced DNA photoproducts | Q40809068 |
| | Nucleotide excision repair. II: From yeast to mammals | Q40828389 |
| | Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review | Q40901949 |
| | Ultraviolet radiation-induced ubiquitination and proteasomal degradation of the large subunit of RNA polymerase II. Implications for transcription-coupled DNA repair | Q41056225 |
| | Mismatch repair defects and O6-methylguanine-DNA methyltransferase expression in acquired resistance to methylating agents in human cells | Q41082110 |
| | Nucleotide excision repair in mammalian cells | Q41593250 |
| | Strand-specific mismatch repair in mammalian cells | Q41602506 |
| | Recombinagenic processing of UV-light photoproducts in nonreplicating phage DNA by the Escherichia coli methyl-directed mismatch repair system | Q42031121 |
| | Replication errors: cha(lle)nging the genome | Q42660015 |
| | Mechanisms of tolerance to DNA damaging therapeutic drugs | Q43829355 |
| | Transcription-dependent and independent DNA excision repair pathways in human cells | Q44670059 |
| | Blockage of RNA polymerase II at a cyclobutane pyrimidine dimer and 6-4 photoproduct | Q44974909 |
| | Induction of the Escherichia coli lactose operon selectively increases repair of its transcribed DNA strand | Q46437555 |
| | Lack of transcription-coupled repair in mammalian ribosomal RNA genes | Q46561611 |
| | Detection of an involvement of the human mismatch repair genes hMLH1 and hMSH2 in nucleotide excision repair is dependent on UVC fluence to cells | Q47406954 |
| | Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 |
| | Features of microsatellite instability in colorectal cancer: comparison between colon and rectum. | Q53396073 |
| | 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 |
| | Processing of O6-methylguanine by mismatch correction in human cell extracts | Q71824297 |
| | Genetic instability in intestinal metaplasia is a frequent event leading to well-differentiated early adenocarcinoma of the stomach | Q73898283 |
| | Inhibition of RNA polymerase II as a trigger for the p53 response | Q78171317 |
| P433 | issue | 3 | |
| P921 | main subject | DNA mismatch repair | Q2984243 |
| P304 | page(s) | 103-115 | |
| P577 | publication date | 2005-09-01 | |
| P1433 | published in | Human Cell | Q26853933 |
| P1476 | title | Involvement of mismatch repair in transcription-coupled nucleotide excision repair | |
| P478 | volume | 18 | |