scholarly article | Q13442814 |
retracted paper | Q45182324 |
P356 | DOI | 10.1016/S0921-8777(98)00007-X |
P698 | PubMed publication ID | 9637246 |
P2093 | author name string | S A Leadon | |
A V Avrutskaya | |||
P2860 | cites work | Characterization of insertion mutations in the Saccharomyces cerevisiae MSH1 and MSH2 genes: evidence for separate mitochondrial and nuclear functions | Q27932283 |
The yeast gene MSH3 defines a new class of eukaryotic MutS homologues. | Q27937756 | ||
Evidence for involvement of yeast proliferating cell nuclear antigen in DNA mismatch repair | Q27938608 | ||
Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis | Q27939891 | ||
Mutation of a mutL homolog in hereditary colon cancer | Q28114939 | ||
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 | ||
Transcription-coupled repair deficiency and mutations in human mismatch repair genes | Q28276963 | ||
Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G | Q28302894 | ||
Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene | Q30054509 | ||
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 | ||
Differential repair of DNA damage in specific nucleotide sequences in monkey cells | Q35057451 | ||
Purification of PCNA as a nucleotide excision repair protein | Q35069851 | ||
Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HexB. | Q36182527 | ||
Recognition and repair of compound DNA lesions (base damage and mismatch) by human mismatch repair and excision repair systems | Q36565271 | ||
Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome | Q36658207 | ||
Preferential repair of cyclobutane pyrimidine dimers in the transcribed strand of a gene in yeast chromosomes and plasmids is dependent on transcription | Q37293401 | ||
Gene- and strand-specific repair in vitro: partial purification of a transcription-repair coupling factor | Q37595520 | ||
Double mutants of Saccharomyces cerevisiae with alterations in global genome and transcription-coupled repair | Q38362404 | ||
Transcription-coupled repair and human disease | Q40556402 | ||
Relationships between DNA repair and transcription | Q41114776 | ||
A hPMS2 mutant cell line is defective in strand-specific mismatch repair | Q41313494 | ||
MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
Clues to the pathogenesis of familial colorectal cancer | Q42622043 | ||
Retraction: A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function | Q43057671 | ||
Monoclonal antibody to DNA containing thymine glycol | Q46344136 | ||
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
The yeast RAD2, but not RAD1, gene is involved in the transcription-coupled repair of thymine glycols. | Q52507121 | ||
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 | ||
Structure and function of transcription-repair coupling factor. II. Catalytic properties. | Q54615766 | ||
Molecular mechanism of transcription-repair coupling. | Q54659174 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Saccharomyces cerevisiae | Q719725 |
DNA mismatch repair | Q2984243 | ||
P1104 | number of pages | 11 | |
P304 | page(s) | 177-187 | |
P577 | publication date | 1998-03-01 | |
P1433 | published in | Mutation Research | Q6943732 |
P1476 | title | Requirement for DNA mismatch repair proteins in the transcription-coupled repair of thymine glycols in Saccharomyces cerevisiae | |
P478 | volume | 407 |
Q73893732 | Arabidopsis MutS homologs-AtMSH2, AtMSH3, AtMSH6, and a novel AtMSH7-form three distinct protein heterodimers with different specificities for mismatched DNA |
Q35136087 | BRCA1 gene in breast cancer |
Q34090778 | DNA mismatch repair and genetic instability |
Q35202227 | DNA mismatch repair proteins: potential guardians against genomic instability and tumorigenesis induced by ultraviolet photoproducts |
Q28509765 | Different effects of CSA and CSB deficiency on sensitivity to oxidative DNA damage |
Q77753605 | Eukaryotic mismatch repair: an update |
Q33943516 | Genomic heterogeneity of nucleotide excision repair |
Q38363713 | Human cells bearing homozygous mutations in the DNA mismatch repair genes hMLH1 or hMSH2 are fully proficient in transcription-coupled nucleotide excision repair |
Q24301013 | Identification and characterization of BCL-3-binding protein: implications for transcription and DNA repair or recombination |
Q33967139 | Inactivation of DNA mismatch repair by increased expression of yeast MLH1. |
Q33953558 | Initiation of base excision repair: glycosylase mechanisms and structures |
Q33847720 | Mammalian DNA mismatch repair |
Q44328503 | Mammalian DNA mismatch repair protects cells from UVB-induced DNA damage by facilitating apoptosis and p53 activation |
Q40851055 | Measurement of oxidative DNA damage and repair in specific DNA sequences |
Q35063842 | Microsatellite instability in Drosophila spellchecker1 (MutS homolog) mutants |
Q35848516 | Mismatch repair and DNA damage signalling |
Q34194518 | Mismatch repair in correction of replication errors and processing of DNA damage |
Q33984294 | Mismatch repair proteins and mitotic genome stability |
Q30669716 | Molecular mechanism of nucleotide excision repair. |
Q38301649 | Mouse mismatch repair gene Msh2 is not essential for transcription-coupled repair of UV-induced cyclobutane pyrimidine dimers |
Q37091419 | New applications of the Comet assay: Comet-FISH and transcription-coupled DNA repair |
Q38057404 | Oxidative stress and the DNA mismatch repair pathway |
Q36733353 | Physical interaction between components of DNA mismatch repair and nucleotide excision repair |
Q40785979 | Reduction of spontaneous mutagenesis in mismatch repair-deficient and proficient cells by dietary antioxidants |
Q73132227 | Repair of oxidative DNA damage in vitro: a tool for screening antioxidative compounds |
Q42660015 | Replication errors: cha(lle)nging the genome |
Q73051217 | Retraction |
Q39674772 | Strand bias in targeted gene repair is influenced by transcriptional activity |
Q33984289 | The many faces of mismatch repair in meiosis |
Q33592366 | The role of mismatch repair in the prevention of base pair mutations in Saccharomyces cerevisiae |
Q33594900 | Transcription-coupled repair of DNA damage: unanticipated players, unexpected complexities |
Q35132666 | Transcription-coupled repair: a multifunctional signaling pathway |
Q64388371 | Transcriptional effects on double-strand break-induced gene conversion tracts |
Q78198352 | Transgenic expression of human MGMT blocks the hypersensitivity of PMS2-deficient mice to low dose MNU thymic lymphomagenesis |
Q44267645 | Ultraviolet-sensitive syndrome cells are defective in transcription-coupled repair of cyclobutane pyrimidine dimers |
Q74624259 | [Hereditary nonpolyposis colorectal carcinoma (HNPCC). Current review of etiology, clinical aspects, diagnosis and therapy] |
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