scholarly article | Q13442814 |
P2093 | author name string | M Lieb | |
S Rehmat | |||
P2860 | cites work | Analysis of the Escherichia coli genome: DNA sequence of the region from 84.5 to 86.5 minutes | Q54060980 |
A DNA repair process in Escherichia coli corrects U:G and T:G mismatches to C:G at sites of cytosine methylation. | Q54635965 | ||
Isolation and characterization of the Escherichia coli mutL gene product. | Q54734906 | ||
Mismatch repair and recombination in E. coli. | Q54762491 | ||
Mismatch repair of deaminated 5-methyl-cytosine. | Q54766647 | ||
DNA sequences required to induce localized conversion in Streptococcus pneumoniae transformation | Q58197696 | ||
The vsr gene product of E. coli K-12 is a strand- and sequence-specific DNA mismatch endonuclease | Q59087847 | ||
Mapping missense and nonsense mutation in gene cI of bacteriophage lambda: marker effects | Q67499055 | ||
Location of DNA methylation genes on the Escherichia coli K-12 genetic map | Q69313428 | ||
Conservation of Chi cutting activity in terrestrial and marine enteric bacteria | Q69666883 | ||
Recombination in the lambda repressor gene: evidence that very short patch (VSP) mismatch correction restores a specific sequence | Q70098082 | ||
Specific mismatch correction in bacteriophage lambda crosses by very short patch repair | Q72793019 | ||
Some mismatch repair activities in Escherichia coli | Q24642459 | ||
Repetitive extragenic palindromic sequences: a major component of the bacterial genome | Q28267206 | ||
Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs | Q28287503 | ||
DNA gyrase binds to the family of prokaryotic repetitive extragenic palindromic sequences | Q33676488 | ||
Escherichia coli mutY gene product is required for specific A-G----C.G mismatch correction | Q33680797 | ||
Pedigrees of some mutant strains of Escherichia coli K-12 | Q33851231 | ||
Very short patch mismatch repair in phage lambda: repair sites and length of repair tracts. | Q33952578 | ||
Repair of a mismatch is influenced by the base composition of the surrounding nucleotide sequence | Q33952892 | ||
Spontaneous mutation at a 5-methylcytosine hotspot is prevented by very short patch (VSP) mismatch repair | Q33957852 | ||
Molecular basis of base substitution hotspots in Escherichia coli | Q34183770 | ||
DNA Sequence and Analysis of 136 Kilobases of the Escherichia coli Genome: Organizational Symmetry around the Origin of Replication | Q34306353 | ||
DNA mismatch correction by Very Short Patch repair may have altered the abundance of oligonucleotides in the E. coli genome | Q35066166 | ||
Systematic sequencing of theEscherichia coligenome: analysis of the 0 – 2.4 min region | Q35072782 | ||
Physical mapping of repetitive extragenic palindromic sequences in Escherichia coli and phylogenetic distribution among Escherichia coli strains and other enteric bacteria | Q36114018 | ||
A gene required for very short patch repair in Escherichia coli is adjacent to the DNA cytosine methylase gene | Q36254421 | ||
Bacterial genes mutL, mutS, and dcm participate in repair of mismatches at 5-methylcytosine sites | Q36272166 | ||
Deoxyribonucleic acid-cytosine methylation by host- and plasmid-controlled enzymes | Q36604638 | ||
Over- and under-representation of short oligonucleotides in DNA sequences | Q36835268 | ||
Mechanisms and biological effects of mismatch repair | Q37041860 | ||
Homologous recombination in procaryotes. | Q37054728 | ||
Hyperrecombination at a specific DNA sequence in pneumococcal transformation | Q37563787 | ||
Special sites in generalized recombination | Q39854468 | ||
Statistical evaluation and biological interpretation of non-random abundance in the E. coli K-12 genome of tetra- and pentanucleotide sequences related to VSP DNA mismatch repair | Q40421606 | ||
Characterization of DNA adenine methylation mutants of Escherichia coli K12 | Q41039288 | ||
DNA mismatch-repair in Escherichia coli counteracting the hydrolytic deamination of 5-methyl-cytosine residues | Q41342744 | ||
Heteroduplex DNA formation is associated with replication and recombination in poxvirus-infected cells | Q41833539 | ||
Genetic studies of the lac repressor. III. Additional correlation of mutational sites with specific amino acid residues | Q42028460 | ||
Some features of base pair mismatch and heterology repair in Escherichia coli | Q42083526 | ||
Repair of single base-pair transversion mismatches of Escherichia coli in vitro: correction of certain A/G mismatches is independent of dam methylation and host mutHLS gene functions | Q42960484 | ||
Marker-dependent recombination in T4 bacteriophage. III. Structural prerequisites for marker discrimination | Q42962420 | ||
Genetic requirements for hyper-recombination by very short patch mismatch repair: involvement of Escherichia coli DNA polymerase I. | Q44658321 | ||
Recombinational hotspot activity of chi-like sequences | Q44665383 | ||
Significant dispersed recurrent DNA sequences in the Escherichia coli genome. Several new groups. | Q52400704 | ||
P433 | issue | 3 | |
P304 | page(s) | 660-666 | |
P577 | publication date | 1995-02-01 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Very short patch repair of T:G mismatches in vivo: importance of context and accessory proteins | |
P478 | volume | 177 |
Q35966643 | 5-Methylcytosine is not a mutation hot spot in nondividing Escherichia coli |
Q39741220 | A DNA methyltransferase can protect the genome from postdisturbance attack by a restriction-modification gene complex. |
Q36849562 | Codon bias in Escherichia coli: the influence of codon context on mutation and selection. |
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 |
Q34509028 | DNA Mismatch Repair |
Q39841075 | Depletion of the cellular amounts of the MutS and MutH methyl-directed mismatch repair proteins in stationary-phase Escherichia coli K-12 cells |
Q33555210 | Interaction of MutS and Vsr: some dominant-negative mutS mutations that disable methyladenine-directed mismatch repair are active in very-short-patch repair |
Q33750656 | Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases |
Q35190848 | Mismatch repair protein MutL becomes limiting during stationary-phase mutation |
Q24605441 | Mismatch repair proteins collaborate with methyltransferases in the repair of O(6)-methylguanine |
Q35633546 | Negative regulation of mutS and mutH repair gene expression by the Hfq and RpoS global regulators of Escherichia coli K-12. |
Q34045547 | Neisseria gonorrhoeae FA1090 carries genes encoding two classes of Vsr endonucleases |
Q35609925 | Overexpression of vsr in Escherichia coli is mutagenic |
Q37127818 | Properties of HflX, an enigmatic protein from Escherichia coli. |
Q36294768 | Reconstitution of the very short patch repair pathway from Escherichia coli |
Q34934889 | Repair of deaminated bases in DNA. |
Q39744405 | Repair of hydrolytic DNA deamination damage in thermophilic bacteria: cloning and characterization of a Vsr endonuclease homolog from Bacillus stearothermophilus |
Q34657088 | The Escherichia coli MutL protein stimulates binding of Vsr and MutS to heteroduplex DNA. |
Q33941852 | The structural basis of damaged DNA recognition and endonucleolytic cleavage for very short patch repair endonuclease |
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 |
Q34603730 | Transient and heritable mutators in adaptive evolution in the lab and in nature |
Q37776339 | Wot the ‘L—Does MutL do? |
Search more.