review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0027-5107(00)00044-0 |
P698 | PubMed publication ID | 10915869 |
P2093 | author name string | Borts RH | |
Chambers SR | |||
Abdullah MF | |||
P2860 | cites work | Isolation and characterization of Dam+ revertants and suppressor mutations that modify secondary phenotypes of dam-3 strains of Escherichia coli K-12 | Q72141249 |
EXO1 and MSH4 differentially affect crossing-over and segregation | Q73899517 | ||
Marker effects and the nature of the recombination event at the his1 locus of Saccharomyces cerevisiae | Q86644787 | ||
Identification and characterization of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2 | Q24314329 | ||
A pivotal role for the structure of the Holliday junction in DNA branch migration | Q24568301 | ||
Isolation of Deoxyribonucleic Acid Methylase Mutants of Escherichia coli K-12 | Q24596515 | ||
Molecular keys to speciation: DNA polymorphism and the control of genetic exchange in enterobacteria | Q24643432 | ||
Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 | ||
Meiotic chromosomes: it takes two to tango | Q27930023 | ||
The Saccharomyces cerevisiae Msh2 and Msh6 proteins form a complex that specifically binds to duplex oligonucleotides containing mismatched DNA base pairs | Q27930815 | ||
Conserved properties between functionally distinct MutS homologs in yeast | Q27931606 | ||
Saccharomyces cerevisiae MSH2, a mispaired base recognition protein, also recognizes Holliday junctions in DNA. | Q27932061 | ||
DMC1: a meiosis-specific yeast homolog of E. coli recA required for recombination, synaptonemal complex formation, and cell cycle progression | Q27933115 | ||
Heteroduplex DNA correction in Saccharomyces cerevisiae is mismatch specific and requires functional PMS genes | Q27934736 | ||
Viability of Escherichia coli K-12 DNA adenine methylase (dam) mutants requires increased expression of specific genes in the SOS regulon | Q69970405 | ||
Requirement of the yeast MSH3 and MSH6 genes for MSH2-dependent genomic stability | Q71081409 | ||
Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II | Q71835124 | ||
MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair | Q71919357 | ||
'Saccharomyces cerevisiae MSH2/6 complex interacts with Holliday junctions and facilitates their cleavage by phage resolution enzymes | Q27934895 | ||
Binding of insertion/deletion DNA mismatches by the heterodimer of yeast mismatch repair proteins MSH2 and MSH3. | Q27934985 | ||
The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations | Q27935158 | ||
The yeast gene MSH3 defines a new class of eukaryotic MutS homologues. | Q27937756 | ||
Eukaryotic DNA mismatch repair | Q27939116 | ||
Functional specificity of MutL homologs in yeast: evidence for three Mlh1-based heterocomplexes with distinct roles during meiosis in recombination and mismatch correction | Q27939611 | ||
Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis | Q27939891 | ||
Characterization of single-nucleotide polymorphisms in coding regions of human genes | Q28138557 | ||
The repair of double-strand breaks in DNA; a model involving recombination | Q28256950 | ||
The double-strand-break repair model for recombination | Q28267259 | ||
Biochemistry and genetics of eukaryotic mismatch repair | Q28282377 | ||
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
Identification of mismatch repair genes and their role in the development of cancer | Q28288647 | ||
Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer | Q28294774 | ||
Mammalian MutS homologue 5 is required for chromosome pairing in meiosis | Q28295022 | ||
Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
A mechanism for gene conversion in fungi | Q30052741 | ||
The swi4+ gene of Schizosaccharomyces pombe encodes a homologue of mismatch repair enzymes | Q31160628 | ||
The role of mismatch repair in the prevention of base pair mutations in Saccharomyces cerevisiae | Q33592366 | ||
Roles of the DNA mismatch repair and nucleotide excision repair proteins during meiosis | Q33608248 | ||
Sex and the single cell: meiosis in yeast | Q33775500 | ||
Mismatch repair proteins regulate heteroduplex formation during mitotic recombination in yeast | Q33781506 | ||
Specificity of mismatch repair following transformation of Saccharomyces cerevisiae with heteroduplex plasmid DNA. | Q33857769 | ||
The msh2 gene of Schizosaccharomyces pombe is involved in mismatch repair, mating-type switching, and meiotic chromosome organization. | Q33957081 | ||
A general model for genetic recombination | Q34505532 | ||
Mismatch repair proteins MutS and MutL inhibit RecA-catalyzed strand transfer between diverged DNAs | Q35163740 | ||
Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis | Q35190411 | ||
Mismatch-stimulated killing | Q35600080 | ||
Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HexB. | Q36182527 | ||
Inviability of dam recA and dam recB cells of Escherichia coli is correlated with their inability to repair DNA double-strand breaks produced by mismatch repair | Q36283193 | ||
Escherichia coli mutator mutants deficient in methylation-instructed DNA mismatch correction | Q36357026 | ||
Mitotic crossovers between diverged sequences are regulated by mismatch repair proteins in Saccaromyces cerevisiae | Q36557503 | ||
Saccharomyces cerevisiae pms2 mutations are alleles of MLH1, and pms2-2 corresponds to a hereditary nonpolyposis colorectal carcinoma-causing missense mutation | Q36560284 | ||
Exonuclease I of Saccharomyces cerevisiae functions in mitotic recombination in vivo and in vitro | Q36568265 | ||
Functional domains of the Saccharomyces cerevisiae Mlh1p and Pms1p DNA mismatch repair proteins and their relevance to human hereditary nonpolyposis colorectal cancer-associated mutations | Q36570003 | ||
Dual roles for DNA sequence identity and the mismatch repair system in the regulation of mitotic crossing-over in yeast | Q36574453 | ||
Barriers to recombination between closely related bacteria: MutS and RecBCD inhibit recombination between Salmonella typhimurium and Salmonella typhi. | Q36574936 | ||
Dual requirement in yeast DNA mismatch repair for MLH1 and PMS1, two homologs of the bacterial mutL gene | Q36643609 | ||
Timing of molecular events in meiosis in Saccharomyces cerevisiae: stable heteroduplex DNA is formed late in meiotic prophase | Q36659309 | ||
Physical detection of heteroduplexes during meiotic recombination in the yeast Saccharomyces cerevisiae | Q36678511 | ||
Clustering of meiotic double-strand breaks on yeast chromosome III | Q36769301 | ||
Expansions and contractions of the genetic map relative to the physical map of yeast chromosome III. | Q36782718 | ||
Repair of heteroduplex plasmid DNA after transformation into Saccharomyces cerevisiae | Q36897365 | ||
Meiosis: how could it work? | Q37394575 | ||
Requirement for DNA mismatch repair proteins in the transcription-coupled repair of thymine glycols in Saccharomyces cerevisiae | Q38336291 | ||
Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis | Q38344945 | ||
Mismatch repair and the fidelity of genetic recombination | Q38730984 | ||
Mismatch repair in Escherichia coli | Q39480893 | ||
Recombination in the eukaryotic nucleus | Q39560014 | ||
DNA mismatch correction | Q39664959 | ||
The mismatch repair system reduces meiotic homeologous recombination and stimulates recombination-dependent chromosome loss | Q40020196 | ||
Meiotic Gene Conversion: A Signal of the Basic Recombination Event in Yeast | Q40613842 | ||
Aberrant 4:4 Asci, Disparity in the Direction of Conversion, and Frequencies of Conversion in Ascobolus immersus | Q40613844 | ||
Measurements of excision repair tracts formed during meiotic recombination in Saccharomyces cerevisiae | Q40678599 | ||
Polarity of meiotic gene conversion in fungi: contrasting views | Q40733619 | ||
Mismatch recognition in chromosomal interactions and speciation | Q40843091 | ||
The mismatch repair system contributes to meiotic sterility in an interspecific yeast hybrid. | Q41064501 | ||
Measurement of restoration and conversion: its meaning for the mismatch repair hypothesis of conversion | Q41569095 | ||
Origin and mechanisms of non-disjunction in human autosomal trisomies | Q41747895 | ||
A 5'-3' exonuclease from Saccharomyces cerevisiae is required for in vitro recombination between linear DNA molecules with overlapping homology | Q42151362 | ||
MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
Repair of specific base pair mismatches formed during meiotic recombination in the yeast Saccharomyces cerevisiae | Q43182601 | ||
A meiotic gene conversion gradient opposite to the direction of transcription | Q45189857 | ||
Involvement of nucleotide-excision repair in msh2 pms1-independent mismatch repair | Q47979502 | ||
Recombination at work for meiosis | Q48018607 | ||
Mutation of a meiosis-specific MutS homolog decreases crossing over but not mismatch correction | Q48076989 | ||
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 | ||
Crossing over analysis at pachytene in man. | Q50335535 | ||
Dependence on RAD52 and RAD1 for anticancer drug resistance mediated by inactivation of mismatch repair genes. | Q54108643 | ||
Identification of double Holliday junctions as intermediates in meiotic recombination. | Q54599520 | ||
A physical comparison of chromosome III in six strains of Saccharomyces cerevisiae. | Q54643772 | ||
Formation of a single base mismatch impedes spontaneous DNA branch migration. | Q54660357 | ||
Palindromic sequences in heteroduplex DNA inhibit mismatch repair in yeast | Q58998172 | ||
Repair of DNA loops involves DNA-mismatch and nucleotide-excision repair proteins | Q59040284 | ||
Double-strand breaks at an initiation site for meiotic gene conversion | Q59068287 | ||
Gene conversion, recombination nodules, and the initiation of meiotic synapsis | Q69114349 | ||
Effect of base pair mismatches on recombination via the RecBCD pathway | Q69356233 | ||
Meiotic recombination in yeast: alteration by multiple heterozygosities | Q69806097 | ||
Mismatch-specific post-meiotic segregation frequency in yeast suggests a heteroduplex recombination intermediate | Q69893763 | ||
P433 | issue | 1-2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | DNA mismatch repair | Q2984243 |
P304 | page(s) | 129-150 | |
P577 | publication date | 2000-06-01 | |
P1433 | published in | Mutation Research | Q6943732 |
P1476 | title | The many faces of mismatch repair in meiosis | |
P478 | volume | 451 |
Q27931208 | A role for the MutL homologue MLH2 in controlling heteroduplex formation and in regulating between two different crossover pathways in budding yeast. |
Q30884706 | A role for the mismatch repair system during incipient speciation in Saccharomyces. |
Q21092188 | An expanded inventory of conserved meiotic genes provides evidence for sex in Trichomonas vaginalis |
Q35791561 | Analysis of Arabidopsis genome-wide variations before and after meiosis and meiotic recombination by resequencing Landsberg erecta and all four products of a single meiosis |
Q44780934 | Analysis of crossover breakpoints yields new insights into the nature of the gene conversion events associated with large NF1 deletions mediated by nonallelic homologous recombination |
Q35152220 | Biased gene conversion: implications for genome and sex evolution |
Q42614571 | Characterization of components of the mismatch repair machinery in Trypanosoma brucei |
Q34573494 | Cis-effects on meiotic recombination across distinct a1-sh2 intervals in a common Zea genetic background |
Q34569381 | Competing crossover pathways act during meiosis in Saccharomyces cerevisiae |
Q37157456 | Completion of meiosis in male zebrafish (Danio rerio) despite lack of DNA mismatch repair gene mlh1. |
Q34441535 | Crossover formation during rice meiosis relies on interaction of OsMSH4 and OsMSH5. |
Q53044279 | Cryptic sex in Symbiodinium (Alveolata, Dinoflagellata) is supported by an inventory of meiotic genes. |
Q37415040 | Cytological basis of sterility in male and female hybrids between sibling species of grey voles Microtus arvalis and M. levis. |
Q34440683 | Deep genome-wide measurement of meiotic gene conversion using tetrad analysis in Arabidopsis thaliana |
Q35038757 | Effects of trans-acting genetic modifiers on meiotic recombination across the a1-sh2 interval of maize |
Q24530701 | Extreme heterogeneity in the molecular events leading to the establishment of chiasmata during meiosis i in human oocytes |
Q35844854 | Heteroduplex DNA in meiotic recombination in Drosophila mei-9 mutants |
Q38731600 | Homoeologous chromosome pairing across the eukaryote phylogeny |
Q34375685 | Homologous recombination occurs in Entamoeba and is enhanced during growth stress and stage conversion |
Q42030100 | Length and sequence heterozygosity differentially affect HRAS1 minisatellite stability during meiosis in yeast |
Q35684970 | Lessons from the genome sequence of Neurospora crassa: tracing the path from genomic blueprint to multicellular organism |
Q27936830 | MLH1 and MSH2 promote the symmetry of double-strand break repair events at the HIS4 hotspot in Saccharomyces cerevisiae. |
Q34617068 | MLH1 mutations differentially affect meiotic functions in Saccharomyces cerevisiae |
Q30750101 | Meiosis, recombination and chromosomes: a review of gene isolation and fluorescent in situ hybridization data in plants |
Q35905065 | Meiotic Recombination in Neurospora crassa Proceeds by Two Pathways with Extensive Holliday Junction Migration |
Q35844948 | Meiotic recombination in Drosophila Msh6 mutants yields discontinuous gene conversion tracts |
Q35910256 | Meiotic recombination intermediates and mismatch repair proteins |
Q48015429 | Meiotic segregation of a homeologous chromosome pair |
Q42150238 | Minisatellite variants generated in yeast meiosis involve DNA removal during gene conversion |
Q28587810 | Mlh1 Can Function in Antibody Class Switch Recombination Independently of Msh2 |
Q34570971 | MuDR transposase increases the frequency of meiotic crossovers in the vicinity of a Mu insertion in the maize a1 gene |
Q34464620 | Regulation of meiotic recombination and prophase I progression in mammals |
Q37224322 | Reproductive isolation in Saccharomyces |
Q44791057 | Sequence heterology and gene conversion at his-3 of Neurospora crassa |
Q37592729 | Structure of the MutL C-terminal domain: a model of intact MutL and its roles in mismatch repair |
Q34463536 | Systematic mutagenesis of the Saccharomyces cerevisiae MLH1 gene reveals distinct roles for Mlh1p in meiotic crossing over and in vegetative and meiotic mismatch repair |
Q21183986 | The genome and transcriptome of the enteric parasite Entamoeba invadens, a model for encystation |
Q37398314 | The genomic landscape of meiotic crossovers and gene conversions in Arabidopsis thaliana |
Q42828810 | The large loop repair and mismatch repair pathways of Saccharomyces cerevisiae act on distinct substrates during meiosis |
Q35038773 | The meiotic bouquet promotes homolog interactions and restricts ectopic recombination in Schizosaccharomyces pombe |
Q29618523 | The single-end invasion: an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination |
Q33868221 | The surprising negative correlation of gene length and optimal codon use--disentangling translational selection from GC-biased gene conversion in yeast. |
Q60958197 | Where to Cross Over? Defining Crossover Sites in Plants |
Q48139440 | Why are young and old repetitive elements distributed differently in the human genome? |
Q51791906 | miRNA and piRNA localization in the male mammalian meiotic nucleus. |
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