scholarly article | Q13442814 |
P2093 | author name string | G Feng | |
M E Winkler | |||
H C Tsui | |||
P2860 | cites work | Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis | Q22122362 |
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer | Q24318484 | ||
Biochemical characterization of gapB-encoded erythrose 4-phosphate dehydrogenase of Escherichia coli K-12 and its possible role in pyridoxal 5'-phosphate biosynthesis | Q24673234 | ||
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 | ||
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 | ||
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
Mismatch repair: mechanisms and relationship to cancer susceptibility | Q28271480 | ||
Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs | Q28287503 | ||
The physical map of the whole E. coli chromosome: application of a new strategy for rapid analysis and sorting of a large genomic library | Q29618185 | ||
Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair | Q29618879 | ||
The extreme mutator effect of Escherichia coli mutD5 results from saturation of mismatch repair by excessive DNA replication errors | Q33586319 | ||
Adaptive mutation sequences reproduced by mismatch repair deficiency | Q33640315 | ||
Homeologous recombination and mismatch repair during transformation in Streptococcus pneumoniae: saturation of the Hex mismatch repair system | Q33883002 | ||
Adaptive reversion of a frameshift mutation in Escherichia coli | Q33958142 | ||
Isolation and characterization of two Saccharomyces cerevisiae genes encoding homologs of the bacterial HexA and MutS mismatch repair proteins | Q33960283 | ||
Proofreading-defective DNA polymerase II increases adaptive mutation in Escherichia coli. | Q34019746 | ||
Adaptive reversion of an episomal frameshift mutation in Escherichia coli requires conjugal functions but not actual conjugation | Q34229499 | ||
Adaptive mutation in Escherichia coli: a role for conjugation. | Q34308488 | ||
DNA mismatch correction in a defined system | Q34674714 | ||
Nonconserved segment of the MutL protein from Escherichia coli K-12 and Salmonella typhimurium | Q35069420 | ||
Mismatch repair proteins MutS and MutL inhibit RecA-catalyzed strand transfer between diverged DNAs | Q35163740 | ||
Kinetic limitation and cellular amount of pyridoxine (pyridoxamine) 5'-phosphate oxidase of Escherichia coli K-12. | Q35579386 | ||
Alignment of Escherichia coli K12 DNA sequences to a genomic restriction map. | Q35827342 | ||
Altering the conserved nucleotide binding motif in the Salmonella typhimurium MutS mismatch repair protein affects both its ATPase and mismatch binding activities | Q35930280 | ||
Inactivation of mismatch repair overcomes the barrier to transduction between Salmonella typhimurium and Salmonella typhi | Q36105804 | ||
Saturation of mismatch repair in the mutD5 mutator strain of Escherichia coli | Q36180968 | ||
Dual requirement in yeast DNA mismatch repair for MLH1 and PMS1, two homologs of the bacterial mutL gene | Q36643609 | ||
Single-step purifications of His6-MutH, His6-MutL and His6-MutS repair proteins of escherichia coli K-12. | Q36812322 | ||
Repair of DNA heteroduplexes containing small heterologous sequences in Escherichia coli | Q36856385 | ||
Mechanisms and biological effects of mismatch repair | Q37041860 | ||
Methyl-directed mismatch repair is bidirectional | Q38318556 | ||
Mismatch-containing oligonucleotide duplexes bound by the E. coli mutS-encoded protein | Q38346658 | ||
Very short patch repair of T:G mismatches in vivo: importance of context and accessory proteins | Q39835453 | ||
Redundant transfer of F' plasmids occurs between Escherichia coli cells during nonlethal selections | Q39835578 | ||
Analysis of cell size and DNA content in exponentially growing and stationary-phase batch cultures of Escherichia coli | Q39839306 | ||
Quantitation of Dam methyltransferase in Escherichia coli | Q39936541 | ||
The Escherichia coli fdv gene probably encodes mutS and is located at minute 58.8 adjacent to the hyc-hyp gene cluster | Q39958045 | ||
Mismatch repair, genetic stability and tumour avoidance | Q40522939 | ||
Editing DNA replication and recombination by mismatch repair: from bacterial genetics to mechanisms of predisposition to cancer in humans | Q40522942 | ||
Mismatch repair, genetic stability, and cancer | Q40556409 | ||
Nucleotide sequence of the Escherichia coli mutH gene | Q40566134 | ||
Molecular matchmakers | Q40885529 | ||
Mechanisms of directed mutation | Q41110210 | ||
DNA mismatch-repair in Escherichia coli counteracting the hydrolytic deamination of 5-methyl-cytosine residues | Q41342744 | ||
Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs | Q41572901 | ||
The mutL repair gene of Escherichia coli K-12 forms a superoperon with a gene encoding a new cell-wall amidase | Q42673927 | ||
Transcriptional patterns of the mutL-miaA superoperon of Escherichia coli K-12 suggest a model for posttranscriptional regulation | Q42684164 | ||
Control of large chromosomal duplications in Escherichia coli by the mismatch repair system | Q42962535 | ||
Structure of recombinants from conjugational crosses between Escherichia coli donor and mismatch-repair deficient Salmonella typhimurium recipients | Q42964416 | ||
Mispair specificity of methyl-directed DNA mismatch correction in vitro | Q44909730 | ||
Multicopy single-stranded DNA of Escherichia coli enhances mutation and recombination frequencies by titrating MutS protein | Q50140322 | ||
Interspecies gene exchange in bacteria: the role of SOS and mismatch repair systems in evolution of species. | Q50144938 | ||
The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants | Q50192890 | ||
Isolation and characterization of the Escherichia coli mutH gene product. | Q54397103 | ||
Evidence that F plasmid transfer replication underlies apparent adaptive mutation. | Q54613748 | ||
Adaptive mutation by deletions in small mononucleotide repeats. | Q54630365 | ||
Base selection, proofreading, and mismatch repair during DNA replication in Escherichia coli. | Q54648245 | ||
Mechanism for induction of adaptive mutations in Escherichia coli. | Q54715058 | ||
Isolation and characterization of the Escherichia coli mutL gene product. | Q54734906 | ||
A unicorn in the garden | Q59085860 | ||
Initiation of methyl-directed mismatch repair | Q64389906 | ||
Multicopy single-stranded DNAs with mismatched base pairs are mutagenic in Escherichia coli | Q72618648 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | DNA mismatch repair | Q2984243 |
Escherichia coli K-12 | Q21399437 | ||
P304 | page(s) | 2388-2396 | |
P577 | publication date | 1996-04-01 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Depletion of the cellular amounts of the MutS and MutH methyl-directed mismatch repair proteins in stationary-phase Escherichia coli K-12 cells | |
P478 | volume | 178 |
Q35966643 | 5-Methylcytosine is not a mutation hot spot in nondividing Escherichia coli |
Q54567733 | A direct role for DNA polymerase III in adaptive reversion of a frameshift mutation in Escherichia coli. |
Q42968100 | A genetic strategy to demonstrate the occurrence of spontaneous mutations in nondividing cells within colonies of Escherichia coli |
Q34088211 | Adaptive mutation in Escherichia coli |
Q34603905 | Adaptive mutation: has the unicorn landed? |
Q24623723 | Adaptive mutation: implications for evolution |
Q35629407 | An editing-defective aminoacyl-tRNA synthetase is mutagenic in aging bacteria via the SOS response |
Q42557075 | Antagonism of ultraviolet-light mutagenesis by the methyl-directed mismatch-repair system of Escherichia coli |
Q47652171 | Antibiotic resistance mutations induced in growing cells of Bacillus-related thermophiles. |
Q33545737 | Are adaptive mutations due to a decline in mismatch repair? The evidence is lacking |
Q73581932 | Assembly and molecular activities of the MutS tetramer |
Q38254948 | Atomic force microscopy captures MutS tetramers initiating DNA mismatch repair. |
Q36296925 | Atomic force microscopy captures the initiation of methyl-directed DNA mismatch repair |
Q36913761 | Bacterial physiology, regulation and mutational adaptation in a chemostat environment |
Q24548990 | Barriers to genetic exchange between bacterial species: Streptococcus pneumoniae transformation |
Q39847729 | Carbon starvation of Salmonella typhimurium does not cause a general increase of mutation rates |
Q51324871 | Cascading MutS and MutL sliding clamps control DNA diffusion to activate mismatch repair. |
Q36905565 | Causes and consequences of DNA repair activity modulation during stationary phase in Escherichia coli |
Q40257785 | Changes in Gene Transcription Induced by Hydrogen Peroxide Treatment of Verotoxin-Producing Escherichia coli O157:H7 and Non-O157 Serotypes on Romaine Lettuce |
Q34617418 | Conjugational Hyperrecombination Achieved by Derepressing the LexA Regulon, Altering the Properties of RecA Protein and Inactivating Mismatch Repair in Escherichia coli K-12 |
Q34133630 | Cooperation and competition in mismatch repair: very short-patch repair and methyl-directed mismatch repair in Escherichia coli |
Q26825267 | Culture history and population heterogeneity as determinants of bacterial adaptation: the adaptomics of a single environmental transition |
Q53054701 | DNA Methylation. |
Q34509028 | DNA Mismatch Repair |
Q33772428 | DNA mismatch repair catalyzed by extracts of mitotic, postmitotic, and senescent Drosophila tissues and involvement of mei-9 gene function for full activity |
Q36328709 | DNA mismatch repair-induced double-strand breaks |
Q46002898 | DNA replication and postreplication mismatch repair in cell-free extracts from cultured human neuroblastoma and fibroblast cells. |
Q37210972 | Dual daughter strand incision is processive and increases the efficiency of DNA mismatch repair |
Q41915989 | Elevated mutation frequency in surviving populations of carbon-starved rpoS-deficient Pseudomonas putida is caused by reduced expression of superoxide dismutase and catalase |
Q38321350 | Enzymatic repair of 5-formyluracil. II. Mismatch formation between 5-formyluracil and guanine during dna replication and its recognition by two proteins involved in base excision repair (AlkA) and mismatch repair (MutS). |
Q35582961 | Error-Prone DNA Polymerases: When Making a Mistake is the Only Way to Get Ahead |
Q39753960 | Error-prone polymerase, DNA polymerase IV, is responsible for transient hypermutation during adaptive mutation in Escherichia coli. |
Q34091159 | Escherichia coli DNA glycosylase Mug: a growth-regulated enzyme required for mutation avoidance in stationary-phase cells |
Q27644397 | Escherichia coli MutS tetramerization domain structure reveals that stable dimers but not tetramers are essential for DNA mismatch repair in vivo |
Q33791245 | Frameshift mutation, microsatellites and mismatch repair |
Q43208620 | Functional analyses of Escherichia coli MutS-beta clamp interaction in vitro and in vivo |
Q34643555 | General stress response regulator RpoS in adaptive mutation and amplification in Escherichia coli |
Q41620371 | Genetic variability and adaptation to stress. |
Q58571303 | Heterogeneity in efflux pump expression predisposes antibiotic-resistant cells to mutation |
Q55258904 | Heterogeneity of spontaneous DNA replication errors in single isogenic Escherichia coli cells. |
Q47104096 | Hfq links translation repression to stress-induced mutagenesis in E. coli |
Q24672935 | High fidelity of RecA-catalyzed recombination: a watchdog of genetic diversity |
Q43002767 | Human mismatch-repair protein MutL homologue 1 (MLH1) interacts with Escherichia coli MutL and MutS in vivo and in vitro: a simple genetic system to assay MLH1 function |
Q36568353 | Hypermutability of homonucleotide runs in mismatch repair and DNA polymerase proofreading yeast mutants. |
Q33770256 | Hypermutation in bacteria and other cellular systems |
Q37191467 | Influences of capsule on cell shape and chain formation of wild-type and pcsB mutants of serotype 2 Streptococcus pneumoniae. |
Q35547555 | Intact mutS in laboratory-derived and clinical glycopeptide-intermediate Staphylococcus aureus strains |
Q33543179 | Interplay between pleiotropy and secondary selection determines rise and fall of mutators in stress response |
Q34697729 | Involvement of Y-family DNA polymerases in mutagenesis caused by oxidized nucleotides in Escherichia coli |
Q40763644 | Involvement of error-prone DNA polymerase IV in stationary-phase mutagenesis in Pseudomonas putida |
Q37363643 | Irreversibility of cellular aging and neoplastic transformation: a clonal analysis |
Q33692291 | Mechanisms of mutation in nondividing cells. Insights from the study of adaptive mutation in Escherichia coli |
Q33847662 | Mechanisms of stationary phase mutation: a decade of adaptive mutation |
Q28270244 | Mechanisms of, and barriers to, horizontal gene transfer between bacteria |
Q50097388 | Method for Detecting and Studying Genome-Wide Mutations in Single Living Cells in Real Time |
Q35190848 | Mismatch repair protein MutL becomes limiting during stationary-phase mutation |
Q48248666 | Molecular analysis of mutS expression and mutation in natural isolates of pathogenic Escherichia coli |
Q24643432 | Molecular keys to speciation: DNA polymorphism and the control of genetic exchange in enterobacteria |
Q91404367 | MutL sliding clamps coordinate exonuclease-independent Escherichia coli mismatch repair |
Q37642675 | MutL: conducting the cell's response to mismatched and misaligned DNA. |
Q50989071 | MutS stimulates the endonuclease activity of MutL in an ATP-hydrolysis-dependent manner. |
Q35869358 | Mutation as a stress response and the regulation of evolvability |
Q41703503 | Mutation for survival |
Q39145276 | Mutation rate plasticity in rifampicin resistance depends on Escherichia coli cell-cell interactions. |
Q47722399 | Natural transformation and phase variation modulation in Neisseria meningitidis |
Q35633546 | Negative regulation of mutS and mutH repair gene expression by the Hfq and RpoS global regulators of Escherichia coli K-12. |
Q34531199 | Nucleoid-associated proteins affect mutation dynamics in E. coli in a growth phase-specific manner |
Q37261476 | Photoaffinity isolation and identification of proteins in cancer cell extracts that bind to platinum-modified DNA. |
Q42574539 | Physical and functional interactions between Escherichia coli MutL and the Vsr repair endonuclease |
Q37716243 | Rate and effects of spontaneous mutations that affect fitness in mutator Escherichia coli |
Q36339832 | Rate and molecular spectrum of spontaneous mutations in the bacterium Escherichia coli as determined by whole-genome sequencing. |
Q39587858 | Reduction of GC --> TA transversion mutation by overexpression of MutS in Escherichia coli K-12. |
Q34425903 | Regulation of substrate recognition by the MiaA tRNA prenyltransferase modification enzyme of Escherichia coli K-12. |
Q34077198 | Stability of EcoRI restriction-modification enzymes in vivo differentiates the EcoRI restriction-modification system from other postsegregational cell killing systems. |
Q35544150 | Stationary phase mutagenesis: mechanisms that accelerate adaptation of microbial populations under environmental stress |
Q57784305 | Stochastic Processes and Component Plasticity Governing DNA Mismatch Repair |
Q42160273 | Stoichiometry of MutS and MutL at unrepaired mismatches in vivo suggests a mechanism of repair |
Q35986593 | Stress responses and genetic variation in bacteria. |
Q40459862 | Stress-Induced Mutagenesis. |
Q36961683 | Stress-induced mutagenesis in bacteria. |
Q57742436 | The LipB protein is a negative regulator of dam gene expression in Escherichia coli |
Q34048440 | The MutS C terminus is essential for mismatch repair activity in vivo |
Q44530427 | The coordinated functions of the E. coli MutS and MutL proteins in mismatch repair |
Q24547729 | The effect of mismatch repair and heteroduplex formation on sexual isolation in Bacillus |
Q39502867 | The miaA mutator phenotype of Escherichia coli K-12 requires recombination functions |
Q34348467 | The msDNAs of bacteria |
Q35177659 | The role of mutators in the emergence of antibiotic-resistant bacteria |
Q36384221 | The role of transient hypermutators in adaptive mutation in Escherichia coli |
Q36491712 | Too many mutants with multiple mutations |
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 |
Q41445233 | Transcriptional de-repression and Mfd are mutagenic in stressed Bacillus subtilis cells |
Q34603730 | Transient and heritable mutators in adaptive evolution in the lab and in nature |
Q27678892 | Using stable MutS dimers and tetramers to quantitatively analyze DNA mismatch recognition and sliding clamp formation |
Q37776339 | Wot the ‘L—Does MutL do? |
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