| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1999PNAS...96.2964F |
| P356 | DOI | 10.1073/PNAS.96.6.2964 |
| P932 | PMC publication ID | 15878 |
| P698 | PubMed publication ID | 10077620 |
| P5875 | ResearchGate publication ID | 13212580 |
| P2093 | author name string | W Engels | |
| C Flores | |||
| P2860 | cites work | DNA sequencing with chain-terminating inhibitors | Q22066207 |
| Mutations of two PMS homologues in hereditary nonpolyposis colon cancer | Q24318484 | ||
| Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis | Q38344945 | ||
| Low mutation rates of microsatellite loci in Drosophila melanogaster | Q38559869 | ||
| X-ray-induced mutations affecting the level of the enzyme alcohol dehydrogenase in Drosophila melanogaster: Frequency and genetic analysis of null-enzyme mutants | Q39705758 | ||
| The mismatch repair system reduces meiotic homeologous recombination and stimulates recombination-dependent chromosome loss | Q40020196 | ||
| Microsatellite instability in yeast: dependence on repeat unit size and DNA mismatch repair genes | Q40022200 | ||
| High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12. | Q40388905 | ||
| High mutation rate of a long microsatellite allele in Drosophila melanogaster provides evidence for allele-specific mutation rates | Q40838369 | ||
| DNA mismatch binding defects, DNA damage tolerance, and mutator phenotypes in human colorectal carcinoma cell lines | Q41338982 | ||
| The molecular analysis of the el-noc complex of Drosophila melanogaster | Q42117676 | ||
| Clues to the pathogenesis of familial colorectal cancer | Q42622043 | ||
| Mutation of a meiosis-specific MutS homolog decreases crossing over but not mismatch correction | Q48076989 | ||
| The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants | Q50192890 | ||
| Targeted gene replacement in Drosophila via P element-induced gap repair. | Q52444406 | ||
| Molecular analysis of the Adh region of the genome of Drosophila melanogaster. | Q52457568 | ||
| N-(2-chloroethyl)-N'-cyclohexyl-N-nitrosourea sensitivity in mismatch repair-defective human cells. | Q54150269 | ||
| Differential involvement of the human mismatch repair proteins, hMLH1 and hMSH2, in transcription-coupled repair | Q56765940 | ||
| Differential effects of the mismatch repair genes MSH2 and MSH3 on homeologous recombination in Saccharomyces cerevisiae | Q57451646 | ||
| Repair of DNA loops involves DNA-mismatch and nucleotide-excision repair proteins | Q59040284 | ||
| Chromosomal instability, reproductive cell death and apoptosis induced by O6-methylguanine in Mex-, Mex+ and methylation-tolerant mismatch repair compromised cells: facts and models | Q74063639 | ||
| Role of MutS ATPase activity in MutS,L-dependent block of in vitro strand transfer | Q77172147 | ||
| A comprehensive set of sequence analysis programs for the VAX | Q26778432 | ||
| Requirement of mismatch repair genes MSH2 and MSH3 in the RAD1-RAD10 pathway of mitotic recombination in Saccharomyces cerevisiae. | Q27930027 | ||
| Interaction between mismatch repair and genetic recombination in Saccharomyces cerevisiae | Q27930781 | ||
| The Saccharomyces cerevisiae Msh2 and Msh6 proteins form a complex that specifically binds to duplex oligonucleotides containing mismatched DNA base pairs | Q27930815 | ||
| Role of Saccharomyces cerevisiae Msh2 and Msh3 repair proteins in double-strand break-induced recombination | Q27931976 | ||
| Saccharomyces cerevisiae MSH2, a mispaired base recognition protein, also recognizes Holliday junctions in DNA. | Q27932061 | ||
| Characterization of insertion mutations in the Saccharomyces cerevisiae MSH1 and MSH2 genes: evidence for separate mitochondrial and nuclear functions | Q27932283 | ||
| 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 | ||
| Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
| Induction of microsatellite instability by oxidative DNA damage | Q28285253 | ||
| Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer | Q28294774 | ||
| Mouse models for hereditary nonpolyposis colorectal cancer | Q28585761 | ||
| hMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA | Q28610839 | ||
| Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
| Genetic Transformation of Drosophila with Transposable Element Vectors | Q29618208 | ||
| Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair | Q29618879 | ||
| The distribution and frequency of microsatellite loci in Drosophila melanogaster | Q32122960 | ||
| 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 | ||
| DNA mismatch repair catalyzed by extracts of mitotic, postmitotic, and senescent Drosophila tissues and involvement of mei-9 gene function for full activity | Q33772428 | ||
| Hyper-recombining recipient strains in bacterial conjugation | Q33951934 | ||
| A stable genomic source of P element transposase in Drosophila melanogaster. | Q33953857 | ||
| Isolation and characterization of X-linked mutants of Drosophila melanogaster which are sensitive to mutagens | Q33991662 | ||
| The genetics of a small autosomal region of Drosophila melanogaster containing the structural gene for alcohol dehydrogenase. II. Lethal mutations in the region | Q33993339 | ||
| FlyBase: the Drosophila database | Q34586086 | ||
| Mismatch repair proteins MutS and MutL inhibit RecA-catalyzed strand transfer between diverged DNAs | Q35163740 | ||
| Tissues of MSH2-deficient mice demonstrate hypermutability on exposure to a DNA methylating agent. | Q35795316 | ||
| Rapid kinetics of mismatch repair of heteroduplex DNA that is formed during recombination in yeast | Q36240053 | ||
| Mouse embryonic stem cells carrying one or two defective Msh2 alleles respond abnormally to oxidative stress inflicted by low-level radiation | Q36325598 | ||
| Mitotic crossovers between diverged sequences are regulated by mismatch repair proteins in Saccaromyces cerevisiae | Q36557503 | ||
| Physical interaction between components of DNA mismatch repair and nucleotide excision repair | Q36733353 | ||
| P-element-induced interallelic gene conversion of insertions and deletions in Drosophila melanogaster | Q36825877 | ||
| Requirement for DNA mismatch repair proteins in the transcription-coupled repair of thymine glycols in Saccharomyces cerevisiae | Q38336291 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | microsatellite | Q265193 |
| Drosophila | Q312154 | ||
| Spellchecker1 Dmel_CG4215 | Q29814740 | ||
| P304 | page(s) | 2964-2969 | |
| P577 | publication date | 1999-03-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Microsatellite instability in Drosophila spellchecker1 (MutS homolog) mutants | |
| P478 | volume | 96 |
| Q42673462 | A UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase is essential for viability in Drosophila melanogaster |
| Q34012568 | Caenorhabditis elegans DNA mismatch repair gene msh-2 is required for microsatellite stability and maintenance of genome integrity |
| Q33202907 | Characterization of a UDP-N-acetyl-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase with an unusual lectin domain from the platyhelminth parasite Echinococcus granulosus |
| Q90557319 | Compound Dynamics and Combinatorial Patterns of Amino Acid Repeats Encode a System of Evolutionary and Developmental Markers |
| Q26864268 | Control of mucin-type O-glycosylation: a classification of the polypeptide GalNAc-transferase gene family |
| Q39116605 | DNA Repair in Drosophila: Mutagens, Models, and Missing Genes |
| Q28211143 | DNA mismatch repair and mutation avoidance pathways |
| Q30887437 | DNA repair in Drosophila: insights from the Drosophila genome sequence. |
| Q39922450 | Drosophila bloom helicase maintains genome integrity by inhibiting recombination between divergent DNA sequences. |
| Q38755812 | Functional and physical interaction between the mismatch repair and FA-BRCA pathways |
| Q31046911 | Functional conservation of subfamilies of putative UDP-N-acetylgalactosamine:polypeptide N-acetylgalactosaminyltransferases in Drosophila, Caenorhabditis elegans, and mammals. One subfamily composed of l(2)35Aa is essential in Drosophila |
| Q43869182 | Germ cells microsatellite instability. The effect of different mutagens in a mismatch repair mutant of Drosophila (spel1). |
| Q52551102 | Germline mutations at microsatellite loci in homozygous and heterozygous mutants for mismatch repair and PCNA genes in Drosophila. |
| Q24535964 | MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens |
| Q35844948 | Meiotic recombination in Drosophila Msh6 mutants yields discontinuous gene conversion tracts |
| Q34160987 | Microsatellites: genomic distribution, putative functions and mutational mechanisms: a review |
| Q47070082 | Mismatch repair-driven mutational bias in D. melanogaster |
| Q28469182 | Multiple-pathway analysis of double-strand break repair mutations in Drosophila |
| Q34643894 | Mutation accumulation in populations of varying size: the distribution of mutational effects for fitness correlates in Caenorhabditis elegans |
| Q30497522 | Pickpocket is a DEG/ENaC protein required for mechanical nociception in Drosophila larvae. |
| Q52704657 | Rescue of Drosophila Melanogaster l(2)35Aa lethality is only mediated by polypeptide GalNAc-transferase pgant35A, but not by the evolutionary conserved human ortholog GalNAc-transferase-T11. |
| Q52548942 | Spontaneous and bleomycin-induced genomic alterations in the progeny of Drosophila treated males depends on the Msh2 status. DNA fingerprinting analysis. |
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