scholarly article | Q13442814 |
P356 | DOI | 10.1128/MCB.17.5.2859 |
P8608 | Fatcat ID | release_zstbkykglrc73hzpxttgrwh2xy |
P932 | PMC publication ID | 232138 |
P698 | PubMed publication ID | 9111358 |
P5875 | ResearchGate publication ID | 14107518 |
P50 | author | Dmitry A. Gordenin | Q55130852 |
Michael A Resnick | Q62124589 | ||
P2093 | author name string | H T Tran | |
J D Keen | |||
M Kricker | |||
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Frameshift mutagenesis by eucaryotic DNA polymerases in vitro | Q69620654 | ||
Spectrum of spontaneous frameshift mutations. Sequences of bacteriophage T4 rII gene frameshifts | Q69729456 | ||
Exonucleolytic proofreading during replication of repetitive DNA | Q70862403 | ||
Molecular analysis of mutations in mutator colorectal carcinoma cell lines | Q70972736 | ||
Requirement of the yeast MSH3 and MSH6 genes for MSH2-dependent genomic stability | Q71081409 | ||
Microsatellite instability and mismatch repair defects in cancer | Q71133326 | ||
The 3'-->5' exonucleases of both DNA polymerases delta and epsilon participate in correcting errors of DNA replication in Saccharomyces cerevisiae | Q72240900 | ||
Lessons from hereditary colorectal cancer | Q28131788 | ||
Pathway correcting DNA replication errors in Saccharomyces cerevisiae | Q28263175 | ||
Increased mutation rate at the hprt locus accompanies microsatellite instability in colon cancer | Q28305622 | ||
Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair | Q29618879 | ||
Adaptive mutation sequences reproduced by mismatch repair deficiency | Q33640315 | ||
Mutations in the MSH3 gene preferentially lead to deletions within tracts of simple repetitive DNA in Saccharomyces cerevisiae | Q33842093 | ||
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Spontaneous mutation in the Escherichia coli lacI gene | Q33958486 | ||
The prevention of repeat-associated deletions in Saccharomyces cerevisiae by mismatch repair depends on size and origin of deletions. | Q33968093 | ||
Selection of lys2 Mutants of the Yeast SACCHAROMYCES CEREVISIAE by the Utilization of alpha-AMINOADIPATE. | Q34002073 | ||
Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday | Q34229913 | ||
Z-DNA-forming sequences are spontaneous deletion hot spots | Q34307496 | ||
Differential expression of RNA transcripts encoding unique carboxy-terminal sequences of human parathyroid hormone-related peptide | Q34307994 | ||
Spectra of spontaneous mutations in Escherichia coli strains defective in mismatch correction: the nature of in vivo DNA replication errors. | Q34343418 | ||
Temperature-sensitive mutations in the yeast DNA polymerase I gene | Q34618611 | ||
Mutator phenotypes in human colorectal carcinoma cell lines | Q35568305 | ||
Error-prone replication of repeated DNA sequences by T7 DNA polymerase in the absence of its processivity subunit | Q35598571 | ||
An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair. | Q36412005 | ||
Replication slippage between distant short repeats in Saccharomyces cerevisiae depends on the direction of replication and the RAD50 and RAD52 genes. | Q36555338 | ||
Altered replication and inverted repeats induce mismatch repair-independent recombination between highly diverged DNAs in yeast. | Q36565513 | ||
Frameshift intermediates in homopolymer runs are removed efficiently by yeast mismatch repair proteins | Q36568343 | ||
Dual requirement in yeast DNA mismatch repair for MLH1 and PMS1, two homologs of the bacterial mutL gene | Q36643609 | ||
APC mutations in colorectal tumors with mismatch repair deficiency | Q37383704 | ||
Parathyroid hormone-related protein: biochemistry and molecular biology | Q37436735 | ||
Mutator phenotype may be required for multistage carcinogenesis | Q37732904 | ||
Differences in the spectrum of spontaneous mutations in the hprt gene between tumor cells of the microsatellite mutator phenotype | Q38358374 | ||
Depletion of the cellular amounts of the MutS and MutH methyl-directed mismatch repair proteins in stationary-phase Escherichia coli K-12 cells | Q39841075 | ||
DNA polymerases required for repair of UV-induced damage in Saccharomyces cerevisiae | Q40016053 | ||
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 | ||
Microsatellite instability in inherited and sporadic neoplasms | Q40493550 | ||
DNA polymerase II, the epsilon polymerase of Saccharomyces cerevisiae | Q40777457 | ||
Diverse hypermutability of multiple expressed sequence motifs present in a cancer with microsatellite instability. | Q41206728 | ||
Cell-specific and regulator-induced promoter usage and messenger ribonucleic acid splicing for parathyroid hormone-related protein | Q41211109 | ||
Demonstration That Mutation of the Type II Transforming Growth Factor β Receptor Inactivates Its Tumor Suppressor Activity in Replication Error-positive Colon Carcinoma Cells | Q41294837 | ||
DNA mismatch binding defects, DNA damage tolerance, and mutator phenotypes in human colorectal carcinoma cell lines | Q41338982 | ||
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Mechanisms of spontaneous and induced frameshift mutation in bacteriophage T4. | Q41879395 | ||
3'-->5' exonucleases of DNA polymerases epsilon and delta correct base analog induced DNA replication errors on opposite DNA strands in Saccharomyces cerevisiae | Q42117167 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | DNA mismatch repair | Q2984243 |
P304 | page(s) | 2859-2865 | |
P577 | publication date | 1997-05-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | Hypermutability of homonucleotide runs in mismatch repair and DNA polymerase proofreading yeast mutants | |
P478 | volume | 17 |
Q58696745 | A Case Study of Genomic Instability in an Industrial Strain of |
Q64070379 | A Compendium of Mutational Signatures of Environmental Agents |
Q35729697 | A Genetic Incompatibility Accelerates Adaptation in Yeast |
Q63965569 | A Novel, Drug Resistance-Independent, Fluorescence-Based Approach To Measure Mutation Rates in Microbial Pathogens |
Q36756806 | A genome-wide view of the spectrum of spontaneous mutations in yeast. |
Q42266867 | A molecular characterization of spontaneous frameshift mutagenesis within the trpA gene of Escherichia coli. |
Q36724317 | A mutation in the putative MLH3 endonuclease domain confers a defect in both mismatch repair and meiosis in Saccharomyces cerevisiae |
Q58695959 | A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and proficient tumours |
Q33958881 | A novel role in DNA metabolism for the binding of Fen1/Rad27 to PCNA and implications for genetic risk. |
Q28534685 | A reversible histone H3 acetylation cooperates with mismatch repair and replicative polymerases in maintaining genome stability |
Q48188761 | Abundance, distribution, and mutation rates of homopolymeric nucleotide runs in the genome of Caenorhabditis elegans |
Q35038676 | Accumulation of recessive lethal mutations in Saccharomyces cerevisiae mlh1 mismatch repair mutants is not associated with gross chromosomal rearrangements |
Q73793665 | Analysis of microsatellites in 13 hemiascomycetous yeast species: mechanisms involved in genome dynamics |
Q50332644 | Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system. |
Q33384119 | Anc1, a protein associated with multiple transcription complexes, is involved in postreplication repair pathway in S. cerevisiae. |
Q44939272 | Arabidopsis thaliana AtPOLK encodes a DinB-like DNA polymerase that extends mispaired primer termini and is highly expressed in a variety of tissues |
Q40597558 | Assembly of a phased diploid Candida albicans genome facilitates allele-specific measurements and provides a simple model for repeat and indel structure |
Q34285681 | Avoidance of long mononucleotide repeats in codon pair usage |
Q34443496 | Base composition of mononucleotide runs affects DNA polymerase slippage and removal of frameshift intermediates by mismatch repair in Saccharomyces cerevisiae |
Q38320783 | Biochemical characterization of the interaction between the Saccharomyces cerevisiae MSH2-MSH6 complex and mispaired bases in DNA. |
Q33828325 | Break-induced replication is highly inaccurate |
Q37142738 | Cadmium is a mutagen that acts by inhibiting mismatch repair. |
Q34194253 | Carcinogenesis in the GI tract: from morphology to genetics and back again |
Q37237633 | Cdc28/Cdk1 positively and negatively affects genome stability in S. cerevisiae. |
Q34606398 | Characterization of the repeat-tract instability and mutator phenotypes conferred by a Tn3 insertion in RFC1, the large subunit of the yeast clamp loader |
Q46691965 | Checkpoint-dependent activation of mutagenic repair in Saccharomyces cerevisiae pol3-01 mutants |
Q35865056 | Chimeric Saccharomyces cerevisiae Msh6 protein with an Msh3 mispair-binding domain combines properties of both proteins. |
Q38297805 | Chromosome targeting at short polypurine sites by cationic triplex-forming oligonucleotides. |
Q34612185 | Cis-elements governing trinucleotide repeat instability in Saccharomyces cerevisiae. |
Q27936220 | Cmr1/WDR76 defines a nuclear genotoxic stress body linking genome integrity and protein quality control |
Q28474763 | Cohesin Is limiting for the suppression of DNA damage-induced recombination between homologous chromosomes |
Q24650948 | Comparative genomics and molecular dynamics of DNA repeats in eukaryotes |
Q40806587 | Concerted action of the MutLβ heterodimer and Mer3 helicase regulates the global extent of meiotic gene conversion. |
Q64387724 | Cooperation between non-essential DNA polymerases contributes to genome stability in Saccharomyces cerevisiae |
Q41216018 | DNA mutation motifs in the genes associated with inherited diseases. |
Q73357737 | DNA polymerase III proofreading mutants enhance the expansion and deletion of triplet repeat sequences in Escherichia coli |
Q41670559 | DNA polymerase epsilon catalytic domains are dispensable for DNA replication, DNA repair, and cell viability |
Q36457026 | DNA polymerase kappa produces interrupted mutations and displays polar pausing within mononucleotide microsatellite sequences |
Q89983002 | DNA polymerase δ proofreads errors made by DNA polymerase ε |
Q33754229 | DNA polymerases as potential therapeutic targets for cancers deficient in the DNA mismatch repair proteins MSH2 or MLH1 |
Q28295863 | DNA replication fidelity and cancer |
Q33537493 | DNA secondary structure: a common and causative factor for expansion in human disease |
Q25255444 | DNA sequences shaped by selection for stability |
Q34196484 | Detection of heterozygous mutations in the genome of mismatch repair defective diploid yeast using a Bayesian approach |
Q35562130 | Differences in genome-wide repeat sequence instability conferred by proofreading and mismatch repair defects |
Q27934236 | Discrete in vivo roles for the MutL homologs Mlh2p and Mlh3p in the removal of frameshift intermediates in budding yeast |
Q36371989 | Distinct DNA-binding surfaces in the ATPase and linker domains of MutLγ determine its substrate specificities and exert separable functions in meiotic recombination and mismatch repair |
Q40895728 | Distinct regulation of Mlh1p heterodimers in meiosis and mitosis in Saccharomyces cerevisiae. |
Q28277921 | Division of labor at the eukaryotic replication fork |
Q92203157 | Effective mismatch repair depends on timely control of PCNA retention on DNA by the Elg1 complex |
Q90480019 | Effects of OsMSH6 Mutations on Microsatellite Stability and Homeologous Recombination in Rice |
Q36764079 | Endonuclease activities of MutLα and its homologs in DNA mismatch repair |
Q43104148 | Escherichia coli DNA polymerase IV contributes to spontaneous mutagenesis at coding sequences but not microsatellite alleles |
Q33711830 | Eukaryotic Mismatch Repair in Relation to DNA Replication |
Q37420612 | Every microsatellite is different: Intrinsic DNA features dictate mutagenesis of common microsatellites present in the human genome |
Q24796773 | Evidence for interplay among yeast replicative DNA polymerases alpha, delta and epsilon from studies of exonuclease and polymerase active site mutations |
Q36115776 | Evidence that the DNA mismatch repair system removes 1-nucleotide Okazaki fragment flaps |
Q51326292 | Evolution of simple sequence repeat-mediated phase variation in bacterial genomes. |
Q52681774 | Explosive mutation accumulation triggered by heterozygous human Pol ε proofreading-deficiency is driven by suppression of mismatch repair. |
Q34701239 | Extensive microsatellite variation in rice induced by introgression from wild rice (Zizania latifolia Griseb.). |
Q42644527 | Fidelity of replication of repetitive DNA in mutS and repair proficient Escherichia coli |
Q54979482 | Flap endonuclease overexpression drives genome instability and DNA damage hypersensitivity in a PCNA-dependent manner. |
Q36568343 | Frameshift intermediates in homopolymer runs are removed efficiently by yeast mismatch repair proteins |
Q33951115 | Frameshift mutagenesis and microsatellite instability induced by human alkyladenine DNA glycosylase. |
Q35748265 | Frameshift mutagenesis: the roles of primer-template misalignment and the nonhomologous end-joining pathway in Saccharomyces cerevisiae. |
Q33791245 | Frameshift mutation, microsatellites and mismatch repair |
Q49911660 | Functional Analysis of Cancer-Associated DNA Polymerase ε Variants in Saccharomyces cerevisiae |
Q34693488 | Functional analysis of human MutSalpha and MutSbeta complexes in yeast |
Q33739955 | Functional analysis of human mismatch repair gene mutations identifies weak alleles and polymorphisms capable of polygenic interactions |
Q34376982 | Functional analysis of iceA1, a CATG-recognizing restriction endonuclease gene in Helicobacter pylori |
Q34497819 | Functional heterologous protein expression by genetically engineered probiotic yeast Saccharomyces boulardii |
Q24290314 | Functional interaction of proliferating cell nuclear antigen with MSH2-MSH6 and MSH2-MSH3 complexes |
Q27659620 | Functional residues on the surface of the N-terminal domain of yeast Pms1 |
Q56749499 | GINS is a DNA polymerase epsilon accessory factor during chromosomal DNA replication in budding yeast |
Q34750817 | Generation of a strong mutator phenotype in yeast by imbalanced base excision repair |
Q35834445 | Genetic Interactions Implicating Postreplicative Repair in Okazaki Fragment Processing |
Q27932384 | Genetic analysis of mlh3 mutations reveals interactions between crossover promoting factors during meiosis in baker's yeast |
Q34606865 | Genetic factors affecting the impact of DNA polymerase delta proofreading activity on mutation avoidance in yeast. |
Q37271649 | Genome-wide In Silico Analysis, Characterization and Identification of Microsatellites in Spodoptera littoralis Multiple nucleopolyhedrovirus (SpliMNPV). |
Q34618433 | Genomic Instability Induced by Mutations in Saccharomyces cerevisiae POL1 |
Q52589171 | Genomic Instability Promoted by Overexpression of Mismatch Repair Factors in Yeast: A Model for Understanding Cancer Progression. |
Q38273272 | Genomic and global approaches to unravelling how hypermutable sequences influence bacterial pathogenesis. |
Q34187406 | Genomic mutation rates: what high-throughput methods can tell us |
Q52551102 | Germline mutations at microsatellite loci in homozygous and heterozygous mutants for mismatch repair and PCNA genes in Drosophila. |
Q24792585 | Homopolymer tract length dependent enrichments in functional regions of 27 eukaryotes and their novel dependence on the organism DNA (G+C)% composition |
Q40153707 | How a Genetically Stable Extremophile Evolves: Modes of Genome Diversification in the Archaeon Sulfolobus acidocaldarius |
Q34603856 | Hypermutability in carcinogenesis |
Q28215990 | Identification of MARCKS, FLJ11383 and TAF1B as putative novel target genes in colorectal carcinomas with microsatellite instability |
Q27934694 | Identification of RTG2 as a modifier gene for CTG*CAG repeat instability in Saccharomyces cerevisiae |
Q34700410 | Ig gene hypermutation: a mechanism is due. |
Q40988373 | In situ detection of frameshift mutations in mouse cells |
Q39572388 | In vitro expansion of mammalian telomere repeats by DNA polymerase alpha-primase |
Q36177419 | In-silico prediction and deep-DNA sequencing validation indicate phase variation in 115 Neisseria meningitidis genes. |
Q33967139 | Inactivation of DNA mismatch repair by increased expression of yeast MLH1. |
Q57802932 | Incompatibilities in Mismatch Repair Genes Contribute to a Wide Range of Mutation Rates in Human Isolates of Baker's Yeast |
Q33345237 | Incompatibilities involving yeast mismatch repair genes: a role for genetic modifiers and implications for disease penetrance and variation in genomic mutation rates |
Q28285253 | Induction of microsatellite instability by oxidative DNA damage |
Q35728727 | Inefficient proofreading and biased error rates during inaccurate DNA synthesis by a mutant derivative of Saccharomyces cerevisiae DNA polymerase delta. |
Q33719300 | Interaction of proliferating cell nuclear antigen with PMS2 is required for MutLα activation and function in mismatch repair. |
Q90429771 | Intrinsically disordered regions regulate both catalytic and non-catalytic activities of the MutLα mismatch repair complex |
Q60301717 | Involvement of C-terminal truncation mutation of kinesin-5 in resistance to kinesin-5 inhibitor |
Q47135454 | Involvement of DNA mismatch repair in the maintenance of heterochromatic DNA stability in Saccharomyces cerevisiae. |
Q50487055 | Involvement of the Arabidopsis thaliana AtPMS1 gene in somatic repeat instability. |
Q34012877 | Isolation and characterization of point mutations in mismatch repair genes that destabilize microsatellites in yeast |
Q35100950 | Isolation and characterization of polymorphic microsatellites in the genome of yak (Bos grunniens). |
Q43077169 | Large-scale expansions of Friedreich's ataxia GAA repeats in yeast |
Q36132253 | Lesion-Induced Mutation in the Hyperthermophilic Archaeon Sulfolobus acidocaldarius and Its Avoidance by the Y-Family DNA Polymerase Dbh. |
Q34617068 | MLH1 mutations differentially affect meiotic functions in Saccharomyces cerevisiae |
Q28544021 | MMS exposure promotes increased MtDNA mutagenesis in the presence of replication-defective disease-associated DNA polymerase γ variants |
Q27320576 | Mathematical and live meningococcal models for simple sequence repeat dynamics - coherent predictions and observations |
Q36319705 | Mechanisms of glycosylase induced genomic instability |
Q33970339 | Microsatellite Instability in Yeast: Dependence on the Length of the Microsatellite |
Q40022200 | Microsatellite instability in yeast: dependence on repeat unit size and DNA mismatch repair genes |
Q28262642 | Microsatellites: simple sequences with complex evolution |
Q48244295 | Mismatch Repair Incompatibilities in Diverse Yeast Populations |
Q36540568 | Mismatch repair defects and Lynch syndrome: The role of the basic scientist in the battle against cancer |
Q33984294 | Mismatch repair proteins and mitotic genome stability |
Q27937434 | Mismatch repair-independent increase in spontaneous mutagenesis in yeast lacking non-essential subunits of DNA polymerase ε. |
Q47313905 | Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies |
Q28305501 | Mlh1-Mlh3, a meiotic crossover and DNA mismatch repair factor, is a Msh2-Msh3-stimulated endonuclease |
Q36128650 | Mutation hot spots in yeast caused by long-range clustering of homopolymeric sequences |
Q34573244 | Mutation rates, spectra and hotspots in mismatch repair-deficient Caenorhabditis elegans |
Q37128670 | Mutation rates, spectra, and genome-wide distribution of spontaneous mutations in mismatch repair deficient yeast |
Q39542902 | Mutational analyses of dinucleotide and tetranucleotide microsatellites in Escherichia coli: influence of sequence on expansion mutagenesis |
Q28395673 | Mutational landscape of yeast mutator strains |
Q33786781 | Mutational spectrum analysis of RNase H(35) deficient Saccharomyces cerevisiae using fluorescence-based directed termination PCR. |
Q39646894 | Mutations in polI but not mutSLH destabilize Haemophilus influenzae tetranucleotide repeats |
Q53412320 | Mutator phenotype due to loss of heterozygosity in diploid yeast strains with mutations in MSH2 and MLH1. |
Q33957827 | Mutator phenotypes conferred by MLH1 overexpression and by heterozygosity for mlh1 mutations. |
Q34919969 | Mutator phenotypes due to DNA replication infidelity. |
Q35063954 | Mutator phenotypes of yeast strains heterozygous for mutations in the MSH2 gene. |
Q41671780 | Natural mismatch repair mutations mediate phenotypic diversity and drug resistance in Cryptococcus deuterogattii |
Q34480201 | Negative epistasis between natural variants of the Saccharomyces cerevisiae MLH1 and PMS1 genes results in a defect in mismatch repair |
Q36540667 | Non-canonical actions of mismatch repair |
Q34097342 | Novel PMS1 alleles preferentially affect the repair of primer strand loops during DNA replication |
Q57009219 | Nucleosomes around a mismatched base pair are excluded via an Msh2-dependent reaction with the aid of SNF2 family ATPase Smarcad1 |
Q33816436 | Numerous length polymorphisms at short tandem repeats in human cytomegalovirus. |
Q35613347 | POS5 gene of Saccharomyces cerevisiae encodes a mitochondrial NADH kinase required for stability of mitochondrial DNA. |
Q41859611 | Phase variable genes of Campylobacter jejuni exhibit high mutation rates and specific mutational patterns but mutability is not the major determinant of population structure during host colonization |
Q41855884 | PolyA deletions in hereditary nonpolyposis colorectal cancer: mutations before a gatekeeper |
Q77206910 | Probing immunoglobulin gene hypermutation with microsatellites suggests a nonreplicative short patch DNA synthesis process |
Q41982548 | Proofreading and secondary structure processing determine the orientation dependence of CAG x CTG trinucleotide repeat instability in Escherichia coli |
Q53062576 | Proper functioning of the GINS complex is important for the fidelity of DNA replication in yeast. |
Q64388364 | R-loop formation by dCas9 is mutagenic in Saccharomyces cerevisiae |
Q33340572 | Rapid accumulation of mutations during seed-to-seed propagation of mismatch-repair-defective Arabidopsis |
Q50492858 | Reduction of stability of arabidopsis genomic and transgenic DNA-repeat sequences (microsatellites) by inactivation of AtMSH2 mismatch-repair function. |
Q33865368 | Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae |
Q26825747 | Replicative DNA polymerase mutations in cancer |
Q28258327 | Replicative DNA polymerase δ but not ε proofreads errors in Cis and in Trans |
Q35084896 | Role of endogenous retroviruses in autoimmune diseases |
Q33792439 | Role of the dinB gene product in spontaneous mutation in Escherichia coli with an impaired replicative polymerase |
Q46554910 | Saccharomyces cerevisiae DNA polymerase delta: high fidelity for base substitutions but lower fidelity for single- and multi-base deletions. |
Q35653058 | Saccharomyces cerevisiae MSH2-MSH3 and MSH2-MSH6 complexes display distinct requirements for DNA binding domain I in mismatch recognition |
Q36549257 | Saccharomyces cerevisiae MutLalpha is a mismatch repair endonuclease |
Q39449001 | Saccharomyces cerevisiae pol30 (proliferating cell nuclear antigen) mutations impair replication fidelity and mismatch repair |
Q34610604 | Sequence composition and context effects on the generation and repair of frameshift intermediates in mononucleotide runs in Saccharomyces cerevisiae. |
Q42676800 | Simple sequence repeats in the Helicobacter pylori genome |
Q24652779 | Somatic hypermutation introduces insertions and deletions into immunoglobulin V genes |
Q35728306 | Specialized mismatch repair function of Glu339 in the Phe-X-Glu motif of yeast Msh6 |
Q34604252 | Spectra of spontaneous frameshift mutations at the hisD3052 allele of Salmonella typhimurium in four DNA repair backgrounds |
Q34613326 | Spontaneous frameshift mutations in Saccharomyces cerevisiae: accumulation during DNA replication and removal by proofreading and mismatch repair activities. |
Q33338279 | Stabilization of the genome of the mismatch repair deficient Mycobacterium tuberculosis by context-dependent codon choice |
Q28507252 | Stepwise deletions of polyA sequences in mismatch repair-deficient colorectal cancers |
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Q33957467 | The 3'-->5' exonucleases of DNA polymerases delta and epsilon and the 5'-->3' exonuclease Exo1 have major roles in postreplication mutation avoidance in Saccharomyces cerevisiae |
Q53049781 | The Arabidopsis DNA mismatch repair gene PMS1 restricts somatic recombination between homeologous sequences. |
Q34433261 | The C-terminus of Dpb2 is required for interaction with Pol2 and for cell viability |
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Q33254833 | The DNA polymerase activity of Pol epsilon holoenzyme is required for rapid and efficient chromosomal DNA replication in Xenopus egg extracts |
Q43189001 | The G67E mutation in hMLH1 is associated with an unusual presentation of Lynch syndrome |
Q51312086 | The Major Replicative Histone Chaperone CAF-1 Suppresses the Activity of the DNA Mismatch Repair System in the Cytotoxic Response to a DNA-methylating Agent. |
Q36026779 | The N terminus of Saccharomyces cerevisiae Msh6 is an unstructured tether to PCNA |
Q34265917 | The adaptive imbalance in base excision-repair enzymes generates microsatellite instability in chronic inflammation. |
Q33691482 | The baker's yeast diploid genome is remarkably stable in vegetative growth and meiosis |
Q34607157 | The effect of DNA replication mutations on CAG tract stability in yeast. |
Q90084152 | The fitness cost of mismatch repair mutators in Saccharomyces cerevisiae: partitioning the mutational load |
Q35064113 | The in vitro fidelity of yeast DNA polymerase δ and polymerase ε holoenzymes during dinucleotide microsatellite DNA synthesis |
Q27934540 | The in vivo characterization of translesion synthesis across UV-induced lesions in Saccharomyces cerevisiae: insights into Pol zeta- and Pol eta-dependent frameshift mutagenesis |
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Q27932484 | The multiple biological roles of the 3'-->5' exonuclease of Saccharomyces cerevisiae DNA polymerase delta require switching between the polymerase and exonuclease domains |
Q36571784 | The rate and spectrum of microsatellite mutation in Caenorhabditis elegans and Daphnia pulex |
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Q36162012 | The unstructured linker arms of Mlh1-Pms1 are important for interactions with DNA during mismatch repair |
Q42575223 | Topical reversion at the HIS1 locus of Saccharomyces cerevisiae. A tale of three mutants. |
Q93216537 | Transcription-coupled repair and mismatch repair contribute towards preserving genome integrity at mononucleotide repeat tracts |
Q27938847 | Transcriptional networks in S. cerevisiae linked to an accumulation of base excision repair intermediates. |
Q38940317 | Understanding how mismatch repair proteins participate in the repair/anti-recombination decision |
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Q27933894 | YNK1, the yeast homolog of human metastasis suppressor NM23, is required for repair of UV radiation- and etoposide-induced DNA damage |
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Q49043239 | Yeast mutator phenotype enforced by Arabidopsis PMS1 expression |
Q27935389 | exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair |
Q42352313 | mlh3 mutations in baker's yeast alter meiotic recombination outcomes by increasing noncrossover events genome-wide. |
Q28478414 | p53 transactivation and the impact of mutations, cofactors and small molecules using a simplified yeast-based screening system |
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