Published in Proc Natl Acad Sci U S A on February 06, 1996
p53-mediated DNA repair responses to UV radiation: studies of mouse cells lacking p53, p21, and/or gadd45 genes. Mol Cell Biol (2000) 6.23
Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adduct. Proc Natl Acad Sci U S A (1996) 2.57
Rate and molecular spectrum of spontaneous mutations in the bacterium Escherichia coli as determined by whole-genome sequencing. Proc Natl Acad Sci U S A (2012) 2.47
In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair. Proc Natl Acad Sci U S A (2001) 2.18
Mismatch repair protein MutL becomes limiting during stationary-phase mutation. Genes Dev (1997) 2.03
Recognition and repair of compound DNA lesions (base damage and mismatch) by human mismatch repair and excision repair systems. Mol Cell Biol (1997) 1.79
Evidence for a physical interaction between the Escherichia coli methyl-directed mismatch repair proteins MutL and UvrD. EMBO J (1998) 1.66
Replication errors: cha(lle)nging the genome. EMBO J (1998) 1.62
Characterization of Lactococcus lactis UV-sensitive mutants obtained by ISS1 transposition. J Bacteriol (1997) 1.61
Transient and heritable mutators in adaptive evolution in the lab and in nature. Genetics (1998) 1.43
Cockayne syndrome: defective repair of transcription? EMBO J (1997) 1.40
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. J Bacteriol (1996) 1.39
Structure and function of the N-terminal 40 kDa fragment of human PMS2: a monomeric GHL ATPase. EMBO J (2001) 1.35
Different mismatch repair deficiencies all have the same effects on somatic hypermutation: intact primary mechanism accompanied by secondary modifications. J Exp Med (1999) 1.28
Physical interaction between components of DNA mismatch repair and nucleotide excision repair. Proc Natl Acad Sci U S A (1998) 1.24
Preferential repair of oxidized base damage in the transcribed genes of mammalian cells. J Biol Chem (2010) 1.22
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. J Bacteriol (1998) 1.21
Mismatch repair processing of carcinogen-DNA adducts triggers apoptosis. Mol Cell Biol (1999) 1.12
Single-molecule FRET TACKLE reveals highly dynamic mismatched DNA-MutS complexes. Biochemistry (2010) 1.04
Folate depletion impairs DNA excision repair in the colon of the rat. Gut (1998) 1.02
Microsatellite instability in Drosophila spellchecker1 (MutS homolog) mutants. Proc Natl Acad Sci U S A (1999) 0.98
Transcription-coupled repair of DNA damage: unanticipated players, unexpected complexities. Am J Hum Genet (1999) 0.95
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. J Mol Histol (2006) 0.91
Mfd is required for rapid recovery of transcription following UV-induced DNA damage but not oxidative DNA damage in Escherichia coli. J Bacteriol (2012) 0.90
Transcription and DNA damage: a link to a kink. Environ Health Perspect (1997) 0.86
Rethinking transcription coupled DNA repair. Curr Opin Microbiol (2015) 0.86
Properties of HflX, an enigmatic protein from Escherichia coli. J Bacteriol (2009) 0.85
Mismatch repair mutants in yeast are not defective in transcription-coupled DNA repair of UV-induced DNA damage. Genetics (1996) 0.84
The nucleotide excision repair system of Borrelia burgdorferi is the sole pathway involved in repair of DNA damage by UV light. J Bacteriol (2013) 0.84
DNA mismatch repair catalyzed by extracts of mitotic, postmitotic, and senescent Drosophila tissues and involvement of mei-9 gene function for full activity. Mol Cell Biol (1998) 0.82
Identification of genes involved in low aminoglycoside-induced SOS response in Vibrio cholerae: a role for transcription stalling and Mfd helicase. Nucleic Acids Res (2013) 0.81
Transcription-coupled repair: an update. Arch Toxicol (2016) 0.81
Transcription-coupled nucleotide excision repair of a gene transcribed by bacteriophage T7 RNA polymerase in Escherichia coli. DNA Repair (Amst) (2010) 0.80
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. DNA Repair (Amst) (2007) 0.80
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. Mol Cell Biol (1997) 0.80
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. Nucleic Acids Res (2002) 0.79
DNA Mismatch Repair. Ecosal Plus (2012) 0.77
A Magic Spot in Genome Maintenance. Trends Genet (2016) 0.77
Resistance of Deinococcus radiodurans to mutagenesis is facilitated by pentose phosphate pathway in the mutS1 mutant background. Curr Microbiol (2008) 0.75
Understanding bias in DNA repair. Proc Natl Acad Sci U S A (2017) 0.75
Mechanistic insights into transcription coupled DNA repair. DNA Repair (Amst) (2017) 0.75
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell (1993) 13.54
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell (1993) 9.93
Molecular mechanism of transcription-repair coupling. Science (1993) 9.55
Mutation of a mutL homolog in hereditary colon cancer. Science (1994) 9.04
Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene. Cell (1987) 8.23
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature (1994) 8.04
Mechanisms and biological effects of mismatch repair. Annu Rev Genet (1991) 7.86
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. Cell (1985) 7.62
Hypermutability and mismatch repair deficiency in RER+ tumor cells. Cell (1993) 6.61
Induction of the Escherichia coli lactose operon selectively increases repair of its transcribed DNA strand. Nature (1989) 5.07
ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes. Cell (1992) 4.80
Mispair specificity of methyl-directed DNA mismatch correction in vitro. J Biol Chem (1988) 4.20
The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA. Proc Natl Acad Sci U S A (1990) 4.04
Repair of DNA heteroduplexes containing small heterologous sequences in Escherichia coli. Proc Natl Acad Sci U S A (1992) 3.21
Mutator phenotypes in human colorectal carcinoma cell lines. Proc Natl Acad Sci U S A (1994) 3.10
Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template. Proc Natl Acad Sci U S A (1994) 3.02
Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation. Nat Genet (1994) 2.95
Microsatellite instability: marker of a mutator phenotype in cancer. Cancer Res (1994) 2.89
Defective mismatch repair in extracts of colorectal and endometrial cancer cell lines exhibiting microsatellite instability. J Biol Chem (1994) 2.82
Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes. Mol Cell Biol (1991) 2.53
Site-specific DNA repair at the nucleosome level in a yeast minichromosome. Cell (1990) 2.47
RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6. EMBO J (1994) 2.46
Preferential repair of cyclobutane pyrimidine dimers in the transcribed strand of a gene in yeast chromosomes and plasmids is dependent on transcription. Proc Natl Acad Sci U S A (1992) 2.41
Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome. Proc Natl Acad Sci U S A (1993) 2.38
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. Mol Cell Biol (1994) 2.26
Escherichia coli mfd mutant deficient in "mutation frequency decline" lacks strand-specific repair: in vitro complementation with purified coupling factor. Proc Natl Acad Sci U S A (1991) 2.12
Transcription preferentially inhibits nucleotide excision repair of the template DNA strand in vitro. J Biol Chem (1990) 1.94
Strand-selective repair of DNA damage in the yeast GAL7 gene requires RNA polymerase II. J Biol Chem (1992) 1.94
Mechanisms of transcription-repair coupling and mutation frequency decline. Microbiol Rev (1994) 1.68
Differential repair of UV damage in Saccharomyces cerevisiae. Nucleic Acids Res (1989) 1.67
Preferential repair of DNA damage on the transcribed strand of the human metallothionein genes requires RNA polymerase II. Mutat Res (1991) 1.58
Repair and transcription. Collision or collusion? Curr Biol (1994) 1.50
Inhibition of transcription and strand-specific DNA repair by alpha-amanitin in Chinese hamster ovary cells. Mutat Res (1992) 1.42
Transcription-repair coupling determines the strandedness of ultraviolet mutagenesis in Escherichia coli. Proc Natl Acad Sci U S A (1992) 1.31
Selective repair of specific chromatin domains in UV-irradiated cells from xeroderma pigmentosum complementation group C. Mutat Res (1990) 1.26
SOS mutator effect in E. coli mutants deficient in mismatch correction. EMBO J (1984) 1.25
Recombinagenic processing of UV-light photoproducts in nonreplicating phage DNA by the Escherichia coli methyl-directed mismatch repair system. Genetics (1991) 1.25
Effects of DNA damaging agents on cultured fibroblasts derived from patients with Cockayne syndrome. Mutat Res (1979) 1.15
Strand bias in mutation involving 5-methylcytosine deamination in the human hprt gene. Mutat Res (1994) 1.09
UvrABC incision of N-methylmitomycin A-DNA monoadducts and cross-links. J Biol Chem (1989) 0.97