scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1019075047 |
P356 | DOI | 10.1038/365274A0 |
P3181 | OpenCitations bibliographic resource ID | 1294547 |
P698 | PubMed publication ID | 8371783 |
P2093 | author name string | Strand M | |
Petes TD | |||
Liskay RM | |||
Prolla TA | |||
P2860 | cites work | Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis | Q22122362 |
Eukaryotic DNA polymerase amino acid sequence required for 3'----5' exonuclease activity | Q27931124 | ||
A positive selection for mutants lacking orotidine-5'-phosphate decarboxylase activity in yeast: 5-fluoro-orotic acid resistance | Q28131606 | ||
Pathway correcting DNA replication errors in Saccharomyces cerevisiae | Q28263175 | ||
The distribution of the numbers of mutants in bacterial populations | Q29620123 | ||
Microsatellite instability in cancer of the proximal colon | Q29620692 | ||
Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday | Q34229913 | ||
Triplet repeat mutations in human disease | Q36129554 | ||
Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HexB. | Q36182527 | ||
A novel repeated element with Z-DNA-forming potential is widely found in evolutionarily diverse eukaryotic genomes | Q36317993 | ||
Repair of DNA heteroduplexes containing small heterologous sequences in Escherichia coli | Q36856385 | ||
Genetic Mapping of Ty Elements in Saccharomyces cerevisiae | Q36941423 | ||
High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12. | Q40388905 | ||
Instability of simple sequence DNA in Saccharomyces cerevisiae | Q40655124 | ||
Clues to the pathogenesis of familial colorectal cancer | Q42622043 | ||
Unequal crossover and the evolution of multigene families | Q69047999 | ||
P2507 | corrigendum / erratum | Erratum: Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair | Q59041973 |
P433 | issue | 6443 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | DNA mismatch repair | Q2984243 |
P304 | page(s) | 274-6 | |
P577 | publication date | 1993-09-16 | |
P1433 | published in | Nature | Q180445 |
P1476 | title | Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair | |
P478 | volume | 365 |
Q40443279 | (CA/GT)(n) microsatellites affect homologous recombination during yeast meiosis |
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Q54567733 | A direct role for DNA polymerase III in adaptive reversion of a frameshift mutation in Escherichia coli. |
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Q36756806 | A genome-wide view of the spectrum of spontaneous mutations in yeast. |
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Q34096157 | Microsatellite mutations in the germline: implications for evolutionary inference |
Q39559220 | Microsatellites and the genetics of highly selfing populations in the freshwater snail Bulinus truncatus |
Q26771472 | Microsatellites in Pursuit of Microbial Genome Evolution |
Q34057384 | Microsatellites: consensus and controversy |
Q28262642 | Microsatellites: simple sequences with complex evolution |
Q43864989 | Milestones of Lynch syndrome: 1895-2015. |
Q24545497 | Mini- and microsatellites |
Q58883739 | Minireview |
Q36623156 | Minisatellite instability is found in colorectal tumours with mismatch repair deficiency |
Q41347026 | Mismatch Repair Deficiency in Phenotypically Normal Human Cells |
Q57956407 | Mismatch repair and cancer |
Q33756019 | Mismatch repair and immunoglobulin gene hypermutation: did we learn something? |
Q36540568 | Mismatch repair defects and Lynch syndrome: The role of the basic scientist in the battle against cancer |
Q28507129 | Mismatch repair deficiency interferes with the accumulation of mutations in chronically stimulated B cells and not with the hypermutation process |
Q31081839 | Mismatch repair genes identified using genetic screens in Blm-deficient embryonic stem cells |
Q33750656 | Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases |
Q33970449 | Mismatch repair in Schizosaccharomyces pombe requires the mutL homologous gene pms1: molecular cloning and functional analysis. |
Q33967893 | Mismatch repair mutants in yeast are not defective in transcription-coupled DNA repair of UV-induced DNA damage. |
Q33984294 | Mismatch repair proteins and mitotic genome stability |
Q39723543 | Mismatched nucleotides may facilitate expansion of trinucleotide repeats in genetic diseases |
Q36557503 | Mitotic crossovers between diverged sequences are regulated by mismatch repair proteins in Saccaromyces cerevisiae |
Q50975967 | Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice. |
Q37281033 | Molecular Markers for Biomass Traits: Association, Interaction and Genetic Divergence in Silkworm Bombyx mori |
Q38618241 | Molecular Population Genetics of the Northern Elephant Seal Mirounga angustirostris |
Q40939438 | Molecular alterations in head and neck squamous cell carcinoma |
Q41626535 | Molecular aspects of neuro-oncology |
Q36600301 | Molecular characterization of phosphorylcholine expression on the lipooligosaccharide of Histophilus somni |
Q33670210 | Molecular diagnostics of cancer predisposition: hereditary non-polyposis colorectal carcinoma and mismatch repair defects |
Q36478733 | Molecular fingerprinting methods for the discrimination between C. albicans and C. dubliniensis |
Q56990379 | Molecular identification of mycorrhizal fungi by direct amplification of microsatellite regions |
Q35763450 | Molecular tumor clocks and dynamic phenotype |
Q30980447 | Molecular typing of Salmonella enterica serovar typhi isolates from various countries in Asia by a multiplex PCR assay on variable-number tandem repeats |
Q43087650 | Morphology of sporadic colorectal cancer with DNA replication errors |
Q26774627 | Mouse models for the discovery of colorectal cancer driver genes |
Q37420112 | Multilocus short sequence repeat sequencing approach for differentiating among Mycobacterium avium subsp. paratuberculosis strains |
Q27012760 | Multiple cellular mechanisms prevent chromosomal rearrangements involving repetitive DNA |
Q40345428 | Multiple forms of genetic instability within a 2-Mb chromosomal segment of 3q26.3-q27 are associated with development of esophageal adenocarcinoma |
Q40707366 | Multiple pathways leading to genomic instability and tumorigenesis |
Q24548535 | Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae |
Q28303186 | MutS homologs in mammalian cells |
Q28138127 | Mutability of microsatellites developed for the ant Camponotus consobrinus |
Q45976982 | Mutagenesis of yeast MW104-1B strain has identified the uncharacterized PMS6 DNA mismatch repair gene locus and additional alleles of existing PMS1, PMS2 and MSH2 genes |
Q33758490 | Mutants with temperature-sensitive defects in the Escherichia coli mismatch repair system: sensitivity to mispairs generated in vivo |
Q34643894 | Mutation accumulation in populations of varying size: the distribution of mutational effects for fitness correlates in Caenorhabditis elegans |
Q34569677 | Mutation and evolution of microsatellite loci in Neurospora |
Q47676846 | Mutation frequency analysis of mononucleotide and dinucleotide repeats after oxidative stress |
Q48084125 | Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer |
Q24318892 | Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair |
Q39542902 | Mutational analyses of dinucleotide and tetranucleotide microsatellites in Escherichia coli: influence of sequence on expansion mutagenesis |
Q37655530 | Mutational dynamics of microsatellites |
Q39408460 | Mutational mechanisms, phylogeny, and evolution of a repetitive region within a clock gene of Drosophila melanogaster |
Q52720227 | Mutational signatures of DNA mismatch repair deficiency in C. elegans and human cancers. |
Q33842093 | Mutations in the MSH3 gene preferentially lead to deletions within tracts of simple repetitive DNA in Saccharomyces cerevisiae |
Q36573422 | Mutations in yeast proliferating cell nuclear antigen define distinct sites for interaction with DNA polymerase delta and DNA polymerase epsilon |
Q24320018 | Mutations of mitotic checkpoint genes in human cancers |
Q24318484 | Mutations of two PMS homologues in hereditary nonpolyposis colon cancer |
Q28235642 | Mutations predisposing to hereditary nonpolyposis colorectal cancer |
Q35568305 | Mutator phenotypes in human colorectal carcinoma cell lines |
Q34055320 | Mutator suppression and escape from replication error-induced extinction in yeast |
Q46057951 | Mutators in Escherichia coli |
Q41671780 | Natural mismatch repair mutations mediate phenotypic diversity and drug resistance in Cryptococcus deuterogattii |
Q44605177 | Nick-dependent and -independent processing of large DNA loops in human cells |
Q36287766 | Ninety-six haploid yeast strains with individual disruptions of open reading frames between YOR097C and YOR192C, constructed for the Saccharomyces genome deletion project, have an additional mutation in the mismatch repair gene MSH3 |
Q40490322 | No association of CpG island methylator phenotype and colorectal cancer survival: population-based study. |
Q43728888 | Non-truncating hMLH1 variants identified in Slovenian gastric cancer patients are not associated with Lynch Syndrome: a functional analysis report |
Q33572538 | Normally lethal amino acid substitutions suppress an ultramutator DNA Polymerase δ variant |
Q57617226 | North Eurasian origin of the myotonic dystrophy mutation |
Q40744789 | Occurrence and consequences of coding sequence insertions and deletions in Mammalian genomes |
Q33966750 | Opposing roles of the holliday junction processing systems of Escherichia coli in recombination-dependent adaptive mutation |
Q36563938 | Orientation dependence of trinucleotide CAG repeat instability in Saccharomyces cerevisiae |
Q44158339 | Origin and instability of GAA repeats: insights from Alu elements |
Q34975960 | Pathogenesis and clinical management of hereditary non-polyposis colorectal cancer |
Q78732134 | Pathogenesis of colorectal cancer |
Q35983656 | Pathophysiological dynamics of human ovarian surface epithelial cells in epithelial ovarian carcinogenesis |
Q38289363 | Pausing of DNA synthesis in vitro at specific loci in CTG and CGG triplet repeats from human hereditary disease genes. |
Q36594447 | Phylogenetic assessment of length variation at a microsatellite locus |
Q34984592 | Plastid genome sequence of a wild woody oil species, Prinsepia utilis, provides insights into evolutionary and mutational patterns of Rosaceae chloroplast genomes |
Q40821912 | Polar alteration of short tandem repeats (STRs) in mammalian cells |
Q28299236 | Polymerase delta variants in RER colorectal tumours |
Q34818604 | Polymorphisms in DNA repair genes, recreational physical activity and breast cancer risk |
Q37876895 | Polypurine.polypyrimidine sequences in complete bacterial genomes: preference for polypurines in protein-coding regions |
Q47408874 | Possible ancient origin of heterochromatic JNK sequences in chromosomes 2R of Secale vavilovii Grossh |
Q58194052 | Postzygotic instability of the myotonic dystrophy p[AGC]n repeat supported by larger expansions in muscle and reduced amplifications in sperm |
Q35020831 | Predicting human minisatellite polymorphism |
Q43694707 | Prediction of the immunogenic potential of frameshift-mutated antigens in microsatellite instable cancer |
Q62977764 | Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry |
Q28597264 | Prevalence and Dynamics of Ribosomal DNA Micro-heterogeneity Are Linked to Population History in Two Contrasting Yeast Species |
Q77206910 | Probing immunoglobulin gene hypermutation with microsatellites suggests a nonreplicative short patch DNA synthesis process |
Q28241736 | Promoter methylation status of hMLH1, hMSH2, and MGMT genes in colorectal cancer associated with adenoma-carcinoma sequence |
Q41982548 | Proofreading and secondary structure processing determine the orientation dependence of CAG x CTG trinucleotide repeat instability in Escherichia coli |
Q34589559 | Recognition of DNA insertion/deletion mismatches by an activity in Saccharomyces cerevisiae |
Q28254808 | Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1 |
Q50492858 | Reduction of stability of arabidopsis genomic and transgenic DNA-repeat sequences (microsatellites) by inactivation of AtMSH2 mismatch-repair function. |
Q35062359 | Relative rates of insertion and deletion mutations in a microsatellite sequence in cultured cells |
Q33865368 | Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae |
Q36368731 | Repeat or not repeat?--Statistical validation of tandem repeat prediction in genomic sequences |
Q42660015 | Replication errors: cha(lle)nging the genome |
Q36555338 | Replication slippage between distant short repeats in Saccharomyces cerevisiae depends on the direction of replication and the RAD50 and RAD52 genes. |
Q34612512 | Requirement for Msh6, but not for Swi4 (Msh3), in Msh2-dependent repair of base-base mismatches and mononucleotide loops in Schizosaccharomyces pombe |
Q27939891 | Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis |
Q27930027 | Requirement of mismatch repair genes MSH2 and MSH3 in the RAD1-RAD10 pathway of mitotic recombination in Saccharomyces cerevisiae. |
Q24610838 | Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications |
Q24338799 | Ribonucleotides misincorporated into DNA act as strand-discrimination signals in eukaryotic mismatch repair |
Q34626118 | Role of proofreading and mismatch repair in maintaining the stability of nucleotide repeats in DNA. |
Q42965264 | Role of reciprocal exchange, one-ended invasion crossover and single-strand annealing on inverted and direct repeat recombination in yeast: different requirements for the RAD1, RAD10, and RAD52 genes |
Q45150040 | Role of tumor suppressor genes in the development of adult T cell leukemia/lymphoma (ATLL). |
Q41099585 | Saccharomyces cerevisiae DNA repair processes: an update |
Q28242820 | Sensitivity to phosphonoacetic acid: a new phenotype to probe DNA polymerase delta in Saccharomyces cerevisiae. |
Q27938377 | Separation-of-function mutations in Saccharomyces cerevisiae MSH2 that confer mismatch repair defects but do not affect nonhomologous-tail removal during recombination |
Q39716960 | Sequence analysis and characterization of stutter products at the tetranucleotide repeat locus vWA. |
Q28650519 | Sequence differences at orthologous microsatellites inflate estimates of human-chimpanzee differentiation |
Q48959890 | Sequence simplicity and evolution of the 3' untranslated region of the histone H1o gene |
Q24548611 | Short-sequence DNA repeats in prokaryotic genomes |
Q37419898 | Significance of amplified fragment length polymorphism in identification and epidemiological examination of Candida species colonization in children undergoing allogeneic stem cell transplantation |
Q72372652 | Simple repeat DNA is not replicated simply |
Q40959218 | Simple repetitive sequences in the genome: structure and functional significance |
Q37634942 | Simple sequence repeat polymorphisms (SSRPs) for evaluation of molecular diversity and germplasm classification of minor crops. |
Q24792439 | Simple sequence repeats and compositional bias in the bipartite Ralstonia solanacearum GMI1000 genome |
Q40412255 | Simple sequence repeats in Escherichia coli: abundance, distribution, composition, and polymorphism |
Q24561717 | Simple tandem DNA repeats and human genetic disease |
Q30725562 | Single cell analysis of CAG repeat in brains of dentatorubral-pallidoluysian atrophy (DRPLA). |
Q35611290 | Single-stranded DNA-binding protein enhances the stability of CTG triplet repeats in Escherichia coli |
Q33935026 | Size comparisons among integral membrane transport protein homologues in bacteria, Archaea, and Eucarya |
Q59070212 | Slippery DNA and diseases |
Q72048107 | Slippery DNA runs on and on and on… |
Q42496337 | Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm. |
Q24652779 | Somatic hypermutation introduces insertions and deletions into immunoglobulin V genes |
Q71937479 | Somatic mutations in VNTR-locus D1S7 in human colorectal carcinomas are associated with microsatellite instability |
Q40733625 | Some features of base pair mismatch repair and its role in the formation of genetic recombinants. |
Q35610606 | Spontaneous and induced mutations in a single open reading frame alter both virulence and avirulence in Xanthomonas campestris pv. vesicatoria avrBs2. |
Q40021880 | Stability of a CTG/CAG trinucleotide repeat in yeast is dependent on its orientation in the genome |
Q72161217 | Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice |
Q33964874 | Stability of tandem repeats in the Drosophila melanogaster Hsr-omega nuclear RNA. |
Q33958980 | Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism |
Q42967686 | Stabilization of microsatellite sequences by variant repeats in the yeast Saccharomyces cerevisiae |
Q33338279 | Stabilization of the genome of the mismatch repair deficient Mycobacterium tuberculosis by context-dependent codon choice |
Q74463085 | Stabilization of the intermediate in frameshift mutation |
Q28507252 | Stepwise deletions of polyA sequences in mismatch repair-deficient colorectal cancers |
Q73176036 | Strand asymmetry of +1 frameshift mutagenesis at a homopolymeric run by DNA polymerase III holoenzyme of Escherichia coli |
Q35132473 | Streisinger revisited: DNA synthesis errors mediated by substrate misalignments |
Q73247971 | Strong association between microsatellites and an HLA-B, DR haplotype (B18-DR3): implication for microsatellite evolution |
Q71144093 | TTA.TAA triplet repeats in plasmids form a non-H bonded structure |
Q28600879 | Tandem amino acid repeats in the green anole (Anolis carolinensis) and other squamates may have a role in increasing genetic variability |
Q35080842 | Tandem repeat modification during double-strand break repair induced by an engineered TAL effector nuclease in zebrafish genome |
Q34299527 | Tandem-repeat patterns and mutation rates in microsatellites of the nematode model organism Pristionchus pacificus |
Q40631911 | Telomeric repeat sequences |
Q28289880 | The 2013 Thomas Hunt Morgan Medal: Thomas Douglas Petes |
Q46237519 | The 9-bp deletion in region V of mitochondrial DNA: evidence of mutation recurrence |
Q42291850 | The Devil is in the details for DNA mismatch repair |
Q40958116 | The SKM-1 leukemic cell line established from a patient with progression to myelomonocytic leukemia in myelodysplastic syndrome (MDS)-contribution to better understanding of MDS. |
Q27930815 | The Saccharomyces cerevisiae Msh2 and Msh6 proteins form a complex that specifically binds to duplex oligonucleotides containing mismatched DNA base pairs |
Q55193718 | The annotation of repetitive elements in the genome of channel catfish (Ictalurus punctatus). |
Q40606207 | The clinical and genetic manifestations of hereditary nonpolyposis colorectal carcinoma |
Q89700458 | The competing mini-dumbbell mechanism: new insights into CCTG repeat expansion |
Q35020600 | The complex mutation pattern of a microsatellite |
Q34609052 | The consequences of growth of a mutator strain of Escherichia coli as measured by loss of function among multiple gene targets and loss of fitness |
Q34263814 | The contribution of endogenous sources of DNA damage to the multiple mutations in cancer |
Q48068829 | The contribution of slippage-like processes to genome evolution |
Q32122960 | The distribution and frequency of microsatellite loci in Drosophila melanogaster |
Q38246275 | The dual nature of mismatch repair as antimutator and mutator: for better or for worse |
Q34607157 | The effect of DNA replication mutations on CAG tract stability in yeast. |
Q59090793 | The evolutionary dynamics of repetitive DNA in eukaryotes |
Q73200819 | The genetics of colorectal cancer |
Q40849233 | The genetics of inherited colon cancer |
Q34223787 | The genomic diversity and phylogenetic relationship in the family iridoviridae |
Q24814928 | The immunogenicity of colorectal cancers with high-degree microsatellite instability |
Q35064113 | The in vitro fidelity of yeast DNA polymerase δ and polymerase ε holoenzymes during dinucleotide microsatellite DNA synthesis |
Q79198468 | The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours |
Q42694402 | The insertion of palindromic repeats in the evolution of proteins. |
Q31833517 | The instability within: problems in current analyses of microsatellite instability |
Q34533276 | The mechanism of mismatch repair and the functional analysis of mismatch repair defects in Lynch syndrome |
Q44166483 | The microsatellites and minisatellites in the genome of Fenneropenaeus chinensis |
Q46129337 | The microsatellites of Escherichia coli: rapidly evolving repetitive DNAs in a non-pathogenic prokaryote |
Q33957081 | The msh2 gene of Schizosaccharomyces pombe is involved in mismatch repair, mating-type switching, and meiotic chromosome organization. |
Q33199915 | The origin of malaria: mixed messages from genetic diversity |
Q24681035 | The origins and early evolution of DNA mismatch repair genes--multiple horizontal gene transfers and co-evolution |
Q34551905 | The oxidized deoxynucleoside triphosphate pool is a significant contributor to genetic instability in mismatch repair-deficient cells |
Q34660994 | The paradoxical population genetics of Plasmodium falciparum |
Q41736108 | The pattern of sensitivity of yeast dna2 mutants to DNA damaging agents suggests a role in DSB and postreplication repair pathways |
Q35199876 | The preference for GT-rich DNA by the yeast Rad51 protein defines a set of universal pairing sequences |
Q33968093 | The prevention of repeat-associated deletions in Saccharomyces cerevisiae by mismatch repair depends on size and origin of deletions. |
Q36571784 | The rate and spectrum of microsatellite mutation in Caenorhabditis elegans and Daphnia pulex |
Q80381157 | The relative significance of mechanisms of antigenic variation in African trypanosomes |
Q35589077 | The rise and fall of genomic methylation in cancer. |
Q33811934 | The role of DNA mismatch repair in cisplatin mutagenicity |
Q41193565 | The role of DNA repair in the prevention of cancer |
Q36282861 | The role of SOS and flap processing in microsatellite instability in Escherichia coli. |
Q41347770 | The role of constrained self-organization in genome structural evolution |
Q34614165 | The roles of Klenow processing and flap processing activities of DNA polymerase I in chromosome instability in Escherichia coli K12 strains |
Q71806485 | The stabilization of repetitive tracts of DNA by variant repeats requires a functional DNA mismatch repair system |
Q80998259 | Toward a unified theory for repeat expansions |
Q35753529 | Tracing cell fates in human colorectal tumors from somatic microsatellite mutations: evidence of adenomas with stem cell architecture |
Q39026764 | Traditional Approaches to Molecular Genetic Analysis |
Q27617873 | Transformation of MutL by ATP binding and hydrolysis: a switch in DNA mismatch repair |
Q80101353 | Treatment of Hereditary Colorectal Cancer Syndromes |
Q72345831 | Triad-DNA: a model for trinucleotide repeats |
Q41527084 | Trinucleotide Repeat Instability: Genetic Features and Molecular Mechanisms |
Q40959214 | Trinucleotide repeat expansion and human disease |
Q35550042 | Trinucleotide repeat instability: a hairpin curve at the crossroads of replication, recombination, and repair |
Q73839003 | Trinucleotide repeats affect DNA replication in vivo |
Q33836548 | Trinucleotide repeats and other microsatellites in yeasts |
Q42683838 | Trinucleotide repeats in yeast |
Q24614511 | Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancer |
Q39847637 | Two distinct models account for short and long deletions within sequence repeats in Escherichia coli |
Q38940317 | Understanding how mismatch repair proteins participate in the repair/anti-recombination decision |
Q48540221 | Updated summary of genome editing technology in human cultured cells linked to human genetics studies |
Q36246500 | Use of microsatellite instability and immunohistochemistry testing for the identification of individuals at risk for Lynch syndrome |
Q38324281 | Using tumour phylogenetics to identify the roots of metastasis in humans. |
Q44499081 | Utility of microsatellite markers and amplified fragment length polymorphism in the study of potentially ochratoxigenic black aspergilli |
Q35608492 | VNTRDB: a bacterial variable number tandem repeat locus database |
Q33854065 | Variation in efficiency of DNA mismatch repair at different sites in the yeast genome |
Q34420775 | What controls the length of noncoding DNA? |
Q33877330 | Whole-Genome Sequence and Variant Analysis of W303, a Widely-Used Strain of Saccharomyces cerevisiae |
Q24621750 | Yeast as a model organism |
Q48066231 | Yeast genes and human disease |
Q24630038 | Yeast: an experimental organism for 21st Century biology |
Q35788174 | hMLH1 promoter hypermethylation in microsatellite instability-positive endometrial carcinoma. Cause or consequence? |
Q59041973 | Erratum: Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair | main subject | P921 |
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