scholarly article | Q13442814 |
review article | Q7318358 |
P356 | DOI | 10.1016/S0921-8777(98)00056-1 |
P698 | PubMed publication ID | 9875287 |
P2093 | author name string | J Jiricny | |
P2860 | cites work | DNA polymerase delta is required for human mismatch repair in vitro | Q24313002 |
Identification and characterization of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2 | Q24314329 | ||
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer | Q24318484 | ||
Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair | Q24318892 | ||
hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6 | Q24323176 | ||
Mismatch repair deficiency associated with overexpression of the MSH3 gene | Q24681589 | ||
Genetic and biochemical analysis of Msh2p-Msh6p: role of ATP hydrolysis and Msh2p-Msh6p subunit interactions in mismatch base pair recognition. | Q27932001 | ||
Saccharomyces cerevisiae Msh2p and Msh6p ATPase activities are both required during mismatch repair | Q27932017 | ||
Saccharomyces cerevisiae MSH2, a mispaired base recognition protein, also recognizes Holliday junctions in DNA. | Q27932061 | ||
Heteroduplex DNA correction in Saccharomyces cerevisiae is mismatch specific and requires functional PMS genes | Q27934736 | ||
'Saccharomyces cerevisiae MSH2/6 complex interacts with Holliday junctions and facilitates their cleavage by phage resolution enzymes | Q27934895 | ||
Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis | Q27939891 | ||
Binding of mismatched microsatellite DNA sequences by the human MSH2 protein | Q28241673 | ||
The amino-terminal domain of heat shock protein 90 (hsp90) that binds geldanamycin is an ATP/ADP switch domain that regulates hsp90 conformation | Q28248831 | ||
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 | ||
The human mismatch recognition complex hMSH2-hMSH6 functions as a novel molecular switch | Q28258968 | ||
Genetic mapping of a locus predisposing to human colorectal cancer | Q28268634 | ||
Mismatch repair: mechanisms and relationship to cancer susceptibility | Q28271480 | ||
Transcription-coupled repair deficiency and mutations in human mismatch repair genes | Q28276963 | ||
Biochemistry and genetics of eukaryotic mismatch repair | Q28282377 | ||
Identification of mismatch repair genes and their role in the development of cancer | Q28288647 | ||
Isolation of an hMSH2-p160 Heterodimer That Restores DNA Mismatch Repair to Tumor Cells | Q28292781 | ||
GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells | Q28292790 | ||
Mutations of GTBP in genetically unstable cells | Q28292802 | ||
Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair | Q28508905 | ||
Mutation in the mismatch repair gene Msh6 causes cancer susceptibility | Q28592583 | ||
hMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA | Q28610839 | ||
DHFR/MSH3 amplification in methotrexate-resistant cells alters the hMutSalpha/hMutSbeta ratio and reduces the efficiency of base-base mismatch repair | Q28610848 | ||
ATP-dependent interaction of human mismatch repair proteins and dual role of PCNA in mismatch repair | Q28610858 | ||
Gap formation is associated with methyl-directed mismatch correction under conditions of restricted DNA synthesis. | Q54735505 | ||
Alterations in DNA Methylation: A Fundamental Aspect of Neoplasia | Q56418625 | ||
Mismatch correction at O 6 -methylguanine residues in E. coli DNA | Q59049241 | ||
Slippery DNA and diseases | Q59070212 | ||
Mismatch-specific post-meiotic segregation frequency in yeast suggests a heteroduplex recombination intermediate | Q69893763 | ||
Different base/base mismatches are corrected with different efficiencies by the methyl-directed DNA mismatch-repair system of E. coli | Q70387562 | ||
Molecular analysis of mutations in mutator colorectal carcinoma cell lines | Q70972736 | ||
The mismatch-repair protein hMSH2 binds selectively to DNA adducts of the anticancer drug cisplatin | Q71533749 | ||
MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair | Q71919357 | ||
DNA mismatch binding and incision at modified guanine bases by extracts of mammalian cells: implications for tolerance to DNA methylation damage | Q72371545 | ||
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 | ||
Isolation of MutSbeta from human cells and comparison of the mismatch repair specificities of MutSbeta and MutSalpha | Q28610863 | ||
Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
Evidence for a physical interaction between the Escherichia coli methyl-directed mismatch repair proteins MutL and UvrD. | Q32108861 | ||
A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches | Q33676586 | ||
A naturally occurring hPMS2 mutation can confer a dominant negative mutator phenotype | Q33772742 | ||
Specificity of mismatch repair following transformation of Saccharomyces cerevisiae with heteroduplex plasmid DNA. | Q33857769 | ||
MutS mediates heteroduplex loop formation by a translocation mechanism | Q33887145 | ||
Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs | Q34554581 | ||
Requirement for d(GATC) sequences in Escherichia coli mutHLS mismatch correction | Q34603979 | ||
Selective recognition of a cisplatin-DNA adduct by human mismatch repair proteins. | Q34625095 | ||
Differential human nucleotide excision repair of paired and mispaired cisplatin-DNA adducts | Q34625375 | ||
DNA mismatch correction in a defined system | Q34674714 | ||
Mismatch repair proteins MutS and MutL inhibit RecA-catalyzed strand transfer between diverged DNAs | Q35163740 | ||
Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers. | Q36213486 | ||
Mitotic crossovers between diverged sequences are regulated by mismatch repair proteins in Saccaromyces cerevisiae | Q36557503 | ||
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 | ||
Mechanisms and biological effects of mismatch repair | Q37041860 | ||
Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adduct | Q37522716 | ||
One role for DNA methylation in vertebrate cells is strand discrimination in mismatch repair | Q37553690 | ||
The Saccharomyces cerevisiae Msh2 protein specifically binds to duplex oligonucleotides containing mismatched DNA base pairs and insertions | Q38299752 | ||
Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage | Q38320078 | ||
Requirement for DNA mismatch repair proteins in the transcription-coupled repair of thymine glycols in Saccharomyces cerevisiae | Q38336291 | ||
hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSalpha | Q38336441 | ||
Mismatch-, MutS-, MutL-, and helicase II-dependent unwinding from the single-strand break of an incised heteroduplex | Q38337751 | ||
MutS and MutL activate DNA helicase II in a mismatch-dependent manner | Q38337755 | ||
Increased somatic recombination in methylation tolerant human cells with defective DNA mismatch repair | Q38338039 | ||
The great GATC: DNA methylation in E. coli | Q38670595 | ||
Mismatch repair, genetic stability, and cancer | Q40556409 | ||
DNA damage tolerance, mismatch repair and genome instability | Q40582064 | ||
Cisplatin and adriamycin resistance are associated with MutLalpha and mismatch repair deficiency in an ovarian tumor cell line | Q41174585 | ||
Drug-related killings: a case of mistaken identity | Q41239275 | ||
Hypermutability and mismatch repair deficiency in RER+ tumor cells | Q41508298 | ||
Strand-specific mismatch repair in mammalian cells | Q41602506 | ||
MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
Replication errors: cha(lle)nging the genome | Q42660015 | ||
Involvement of the mismatch repair system in temozolomide-induced apoptosis | Q47752780 | ||
Frameshift mismatch recognition by the human MutS alpha complex | Q47791002 | ||
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 | ||
Different base/base mispairs are corrected with different efficiencies and specificities in monkey kidney cells. | Q52868583 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | DNA mismatch repair | Q2984243 |
P304 | page(s) | 107-121 | |
P577 | publication date | 1998-12-01 | |
P1433 | published in | Mutation Research | Q6943732 |
P1476 | title | Eukaryotic mismatch repair: an update | |
P478 | volume | 409 |
Q34047820 | A coordinated interplay: proteins with multiple functions in DNA replication, DNA repair, cell cycle/checkpoint control, and transcription |
Q77758189 | A polymorphism in the hMSH2 gene (gIVS12-6T>C) associated with non-Hodgkin lymphomas |
Q28359649 | Affinity of mismatch-binding protein MutS for heteroduplexes containing different mismatches |
Q58074430 | Bi-directional Processing of DNA Loops by Mismatch Repair-dependent and -independent Pathways in Human Cells |
Q28275089 | Cancer genes and the pathways they control |
Q35895420 | Carcinogen-specific induction of genetic instability. |
Q34194253 | Carcinogenesis in the GI tract: from morphology to genetics and back again |
Q27934255 | Characterization of nuclease-dependent functions of Exo1p in Saccharomyces cerevisiae |
Q36997235 | Chlamydomonas reinhardtii: a convenient model system for the study of DNA repair in photoautotrophic eukaryotes |
Q40700534 | Combined effects of adenovirus-mediated wild-type p53 transduction, temozolomide and poly (ADP-ribose) polymerase inhibitor in mismatch repair deficient and non-proliferating tumor cells. |
Q27934370 | Components of a Fanconi-like pathway control Pso2-independent DNA interstrand crosslink repair in yeast |
Q27629464 | Composite active site of an ABC ATPase: MutS uses ATP to verify mismatch recognition and authorize DNA repair |
Q27652436 | Crystal Structure of MutS2 Endonuclease Domain and the Mechanism of Homologous Recombination Suppression |
Q27627633 | Crystal structures of mismatch repair protein MutS and its complex with a substrate DNA |
Q53906544 | Cytotoxic and clastogenic effects of a DNA minor groove binding methyl sulfonate ester in mismatch repair deficient leukemic cells. |
Q42280794 | DNA interstrand cross-link repair in the Saccharomyces cerevisiae cell cycle: overlapping roles for PSO2 (SNM1) with MutS factors and EXO1 during S phase |
Q34144865 | DNA mismatch repair: the hands of a genome guardian. |
Q64387816 | DNA template requirements for human mismatch repair in vitro |
Q33888905 | Deficiency of a novel mismatch repair activity in a bladder tumor cell line |
Q24337694 | Differential specificities and simultaneous occupancy of human MutSalpha nucleotide binding sites |
Q24555123 | Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1 |
Q26822552 | Electrochemistry of nonconjugated proteins and glycoproteins. Toward sensors for biomedicine and glycomics |
Q28592033 | Elevated mutant frequencies and increased C : G-->T : A transitions in Mlh1-/- versus Pms2-/- murine small intestinal epithelial cells |
Q27929951 | Functional studies on the candidate ATPase domains of Saccharomyces cerevisiae MutLalpha. |
Q35026407 | Gene silencing in phenomena related to DNA repair |
Q26810051 | Genetic and epigenetic interactions in allopolyploid plants |
Q33943516 | Genomic heterogeneity of nucleotide excision repair |
Q24291378 | HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes |
Q24292224 | Human exonuclease I is required for 5' and 3' mismatch repair |
Q43514135 | Human mismatch repair and G*T mismatch binding by hMutSalpha in vitro is inhibited by adriamycin, actinomycin D, and nogalamycin |
Q33224078 | Human mismatch repair: reconstitution of a nick-directed bidirectional reaction |
Q22254324 | Identification of factors interacting with hMSH2 in the fetal liver utilizing the yeast two-hybrid system. In vivo interaction through the C-terminal domains of hEXO1 and hMSH2 and comparative expression analysis |
Q39093868 | Initiation of strand incision at G:T and O(6)-methylguanine:T base mismatches in DNA by human cell extracts |
Q73923892 | Interaction of Escherichia coli MutS and MutL at a DNA mismatch |
Q33933718 | Interactions of Exo1p with components of MutLalpha in Saccharomyces cerevisiae |
Q50487055 | Involvement of the Arabidopsis thaliana AtPMS1 gene in somatic repeat instability. |
Q24300483 | Mechanism of 5'-directed excision in human mismatch repair |
Q33885063 | Mismatch repair defects in cancer |
Q40711388 | Mismatch repair deficiency in hematological malignancies with microsatellite instability |
Q34293069 | Molecular mechanisms of DNA mismatch repair |
Q78239852 | MutS recognition of exocyclic DNA adducts that are endogenous products of lipid oxidation |
Q28202414 | Mutation processes at the protein level: is Lamarck back? |
Q34097342 | Novel PMS1 alleles preferentially affect the repair of primer strand loops during DNA replication |
Q42942768 | Nuclease activity of the MutS homologue MutS2 from Thermus thermophilus is confined to the Smr domain |
Q28307657 | Oligo/polynucleotide-based gene modification: strategies and therapeutic potential |
Q43722359 | Poly (ADP-ribose) polymerase inhibitor increases apoptosis and reduces necrosis induced by a DNA minor groove binding methyl sulfonate ester |
Q28256131 | Prokaryotic DNA mismatch repair |
Q31390340 | Role of DNA repair in carcinogen-induced ras mutation |
Q24793345 | Some Provocative Thoughts on Damage and Repair of DNA. |
Q28143945 | Structure and function of mismatch repair proteins |
Q42413459 | The 1999 Reginald Thomson Lecture. Custom-built mice: unique discovery tools in biomedical research. |
Q39456907 | The Immune Biology of Microsatellite-Unstable Cancer |
Q31833517 | The instability within: problems in current analyses of microsatellite instability |
Q24596494 | The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2 |
Q24291370 | The interaction of DNA mismatch repair proteins with human exonuclease I |
Q28512554 | The mammalian mismatch repair protein MSH2 is required for correct MRE11 and RAD51 relocalization and for efficient cell cycle arrest induced by ionizing radiation in G2 phase |
Q30043983 | The role of DNA mismatch repair in generating genetic diversity and drug resistance in malaria parasites |
Q35880273 | The role of OsMSH4 in male and female gamete development in rice meiosis |
Q35559695 | Two common forms of the human MLH1 gene may be associated with functional differences |
Q30465158 | Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency |
Q52956515 | Why do mammalian mitochondria possess a mismatch repair activity? |
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