| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | Jiricny J | |
| 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 | ||
| The evolutionarily conserved zinc finger motif in the largest subunit of human replication protein A is required for DNA replication and mismatch repair but not for nucleotide excision repair | Q24321288 | ||
| Purified human MSH2 protein binds to DNA containing mismatched nucleotides | Q24321644 | ||
| hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6 | Q24323176 | ||
| Mismatch repair deficiency associated with overexpression of the MSH3 gene | Q24681589 | ||
| The structure of guanosine-thymidine mismatches in B-DNA at 2.5-A resolution | Q27728623 | ||
| Genetic and biochemical analysis of Msh2p-Msh6p: role of ATP hydrolysis and Msh2p-Msh6p subunit interactions in mismatch base pair recognition. | Q27932001 | ||
| Enhancement of MSH2-MSH3-mediated mismatch recognition by the yeast MLH1-PMS1 complex | Q27932428 | ||
| Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis | Q27939891 | ||
| Mutation of a mutL homolog in hereditary colon cancer | Q28114939 | ||
| 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 | Q28251975 | ||
| 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 | ||
| Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs | Q28287503 | ||
| 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 | ||
| MutS homologs in mammalian cells | Q28303186 | ||
| 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 | ||
| Isolation of MutSbeta from human cells and comparison of the mismatch repair specificities of MutSbeta and MutSalpha | Q28610863 | ||
| Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
| Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
| An atypical topoisomerase II from Archaea with implications for meiotic recombination | Q29618230 | ||
| Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair | Q29618879 | ||
| Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines | Q29620526 | ||
| Genetic analysis of yeast RPA1 reveals its multiple functions in DNA metabolism | Q32068528 | ||
| 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 | ||
| A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches | Q33676586 | ||
| Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines | Q33720790 | ||
| Mutations in the MSH3 gene preferentially lead to deletions within tracts of simple repetitive DNA in Saccharomyces cerevisiae | Q33842093 | ||
| Mismatch repair involving localized DNA synthesis in extracts of Xenopus eggs | Q33861434 | ||
| MutS mediates heteroduplex loop formation by a translocation mechanism | Q33887145 | ||
| DNA ligase I is recruited to sites of DNA replication by an interaction with proliferating cell nuclear antigen: identification of a common targeting mechanism for the assembly of replication factories | Q33889077 | ||
| Meiotic gene conversion mutants in Saccharomyces cerevisiae. I. Isolation and characterization of pms1-1 and pms1-2. | Q33951095 | ||
| Isolation and characterization of two Saccharomyces cerevisiae genes encoding homologs of the bacterial HexA and MutS mismatch repair proteins | Q33960283 | ||
| Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs | Q34554581 | ||
| Adaptive mutation: has the unicorn landed? | Q34603905 | ||
| The Escherichia coli MutL protein stimulates binding of Vsr and MutS to heteroduplex DNA. | Q34657088 | ||
| DNA mismatch correction in a defined system | Q34674714 | ||
| Altering the conserved nucleotide binding motif in the Salmonella typhimurium MutS mismatch repair protein affects both its ATPase and mismatch binding activities | Q35930280 | ||
| Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HexB. | Q36182527 | ||
| Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers. | Q36213486 | ||
| Heteroduplex DNA mismatch repair system of Streptococcus pneumoniae: cloning and expression of the hexA gene | Q36305416 | ||
| Misalignment-mediated DNA synthesis errors | Q36613826 | ||
| Repair of DNA heteroduplexes containing small heterologous sequences in Escherichia coli | Q36856385 | ||
| Mechanisms and biological effects of mismatch repair | Q37041860 | ||
| Mismatch repair in Xenopus egg extracts: DNA strand breaks act as signals rather than excision points. | Q37328984 | ||
| One role for DNA methylation in vertebrate cells is strand discrimination in mismatch repair | Q37553690 | ||
| Loss of expression of the human MSH3 gene in hematological malignancies | Q38291729 | ||
| The Saccharomyces cerevisiae Msh2 protein specifically binds to duplex oligonucleotides containing mismatched DNA base pairs and insertions | Q38299752 | ||
| The purification of a human mismatch-binding protein and identification of its associated ATPase and helicase activities | Q38324324 | ||
| 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 | ||
| Mismatch-containing oligonucleotide duplexes bound by the E. coli mutS-encoded protein | Q38346658 | ||
| Appropriate Partners Make Good Matches | Q40440563 | ||
| Editing DNA replication and recombination by mismatch repair: from bacterial genetics to mechanisms of predisposition to cancer in humans | Q40522942 | ||
| Increased rate of base substitution in a hamster mutator strain obtained during serial selection for gene amplification | Q40647834 | ||
| Microsatellite instability, mismatch repair deficiency, and genetic defects in human cancer cell lines. | Q40962229 | ||
| Conditional mutator phenotypes in hMSH2-deficient tumor cell lines | Q41091724 | ||
| DNA repair and colorectal cancer | Q41264767 | ||
| The Croonian Lecture, 1996: endogenous damage to DNA. | Q41266659 | ||
| Mismatch repair and cancer | Q41284260 | ||
| Strand-specific mismatch repair in mammalian cells | Q41602506 | ||
| The role of DNA mismatch repair in drug resistance. | Q41727728 | ||
| MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
| Mispair specificity of methyl-directed DNA mismatch correction in vitro | Q44909730 | ||
| Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations. | Q48075586 | ||
| Kinetic analysis of nucleotide incorporation and misincorporation by Klenow fragment of Escherichia coli DNA polymerase I. | Q52356212 | ||
| Different base/base mispairs are corrected with different efficiencies and specificities in monkey kidney cells. | Q52868583 | ||
| Selection for beta 2-microglobulin mutation in mismatch repair-defective colorectal carcinomas. | Q54057043 | ||
| Photocross-linking of the NH2-terminal region of Taq MutS protein to the major groove of a heteroduplex DNA. | Q54558924 | ||
| Gap formation is associated with methyl-directed mismatch correction under conditions of restricted DNA synthesis. | Q54735505 | ||
| Mismatch repair and cancer | Q57956407 | ||
| Slippery DNA and diseases | Q59070212 | ||
| Initiation of methyl-directed mismatch repair | Q64389906 | ||
| DNA replication fidelity | Q68047290 | ||
| Heteroduplex repair in extracts of human HeLa cells | Q68198738 | ||
| A specific mismatch repair event protects mammalian cells from loss of 5-methylcytosine | Q70191133 | ||
| P433 | issue | 22 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 6427-6436 | |
| P577 | publication date | 1998-11-01 | |
| P1433 | published in | The EMBO Journal | Q1278554 |
| P1476 | title | Replication errors: cha(lle)nging the genome | |
| P478 | volume | 17 |
| Q28359649 | Affinity of mismatch-binding protein MutS for heteroduplexes containing different mismatches |
| Q39744515 | Amplification of repeat-containing transcribed sequences (ARTS): a transcriptome fingerprinting strategy to detect functionally relevant microsatellite mutations in cancer |
| Q33247666 | Analysis of the excision step in human DNA mismatch repair |
| Q73581932 | Assembly and molecular activities of the MutS tetramer |
| Q39656345 | Asymmetric ATP binding and hydrolysis activity of the Thermus aquaticus MutS dimer is key to modulation of its interactions with mismatched DNA. |
| Q38295596 | Asymmetric recognition of DNA local distortion. Structure-based functional studies of eukaryotic Msh2-Msh6. |
| Q28300063 | Bcl-2 expression suppresses mismatch repair activity through inhibition of E2F transcriptional activity |
| Q35880032 | Biochemical analysis of the human mismatch repair proteins hMutSα MSH2(G674A)-MSH6 and MSH2-MSH6(T1219D) |
| Q22009979 | Characterization of MAD2B and other mitotic spindle checkpoint genes |
| Q40912570 | Characterization of the MEN1 gene product, menin, by site-specific polyclonal antibodies |
| Q34099201 | Clinical and molecular analysis of hereditary non-polyposis colorectal cancer in Chinese colorectal cancer patients |
| Q27629464 | Composite active site of an ABC ATPase: MutS uses ATP to verify mismatch recognition and authorize DNA repair |
| Q40744193 | Contribution of human mlh1 and pms2 ATPase activities to DNA mismatch repair |
| Q34612530 | Control of GT repeat stability in Schizosaccharomyces pombe by mismatch repair factors |
| Q36538311 | DNA damage and repair in epithelium after allogeneic hematopoietic stem cell transplantation |
| Q40513970 | DNA methyltransferase Dnmt1 and mismatch repair |
| Q64387816 | DNA template requirements for human mismatch repair in vitro |
| Q26996542 | DNA triplet repeat expansion and mismatch repair |
| Q43621496 | Different effects of methotrexate on DNA mismatch repair proficient and deficient cells |
| Q44353892 | Differential and simultaneous adenosine di- and triphosphate binding by MutS. |
| Q43675423 | Distinct MutS DNA-binding modes that are differentially modulated by ATP binding and hydrolysis |
| Q57272811 | Dual recognition–incision enzymes might be involved in mismatch repair and meiosis |
| Q53357842 | Effect of Helicobacter pylori infection on the expression of DNA mismatch repair protein. |
| Q50111958 | Effect of chromosome location on bacterial mutation rates |
| Q27939116 | Eukaryotic DNA mismatch repair |
| Q77753605 | Eukaryotic mismatch repair: an update |
| Q24316068 | Evidence for involvement of HMGB1 protein in human DNA mismatch repair |
| Q58698592 | Evidence of response to pembrolizumab in a patient with Lynch syndrome-related metastatic colon cancer |
| Q40978666 | Expression of methylation-modulated tumor-related genes in endoscopically resected early esophageal squamous neoplasia |
| Q35559704 | Folate deficiency, mismatch repair-dependent apoptosis, and human disease |
| Q34425450 | Functional interactions and signaling properties of mammalian DNA mismatch repair proteins |
| Q33959675 | Genetics of hereditary colon cancer - a basis for prevention? |
| Q28131737 | Genome maintenance mechanisms for preventing cancer |
| Q24291378 | HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes |
| Q37411879 | Helicobacter pylori infection and expression of DNA mismatch repair proteins |
| Q33939108 | Human DNA mismatch repair in vitro operates independently of methylation status at CpG sites |
| Q33770256 | Hypermutation in bacteria and other cellular systems |
| Q40762811 | Identification and functional characterization of the promoter region of the human MSH6 gene |
| Q37370959 | Identification of factors influencing strand bias in oligonucleotide-mediated recombination in Escherichia coli |
| 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 |
| Q58048567 | Impact of DNA physical properties on local sequence bias of human mutation |
| Q40746606 | Implication of protein kinase C in the regulation of DNA mismatch repair protein expression and function |
| Q34667117 | In memoriam Bernard Strehler--genomic instability in ageing: a persistent challenge |
| Q28209230 | Interactions of the DNA mismatch repair proteins MLH1 and MSH2 with c-MYC and MAX |
| Q36018122 | Involvement of mismatch repair in the reciprocal control of motility and adherence of uropathogenic Escherichia coli |
| Q36615131 | Involvement of mismatch repair in transcription-coupled nucleotide excision repair |
| Q37438613 | Life without dUTPase |
| Q40020098 | Low-dose metronomic cyclophosphamide treatment mediates ischemia-dependent K-ras mutation in colorectal carcinoma xenografts |
| Q22009114 | MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1 |
| Q38312705 | Measuring motion on DNA by the type I restriction endonuclease EcoR124I using triplex displacement |
| Q42044589 | Mechanisms of dinucleotide repeat instability in Escherichia coli |
| Q73311211 | Mediating mismatch repair |
| Q57742296 | Microsatellite instability |
| Q50335571 | Mismatch recognition and DNA-dependent stimulation of the ATPase activity of hMutSalpha is abolished by a single mutation in the hMSH6 subunit |
| Q39656168 | Mismatch recognition-coupled stabilization of Msh2-Msh6 in an ATP-bound state at the initiation of DNA repair |
| Q39731406 | Mismatch repair activity in mammalian mitochondria |
| Q33756019 | Mismatch repair and immunoglobulin gene hypermutation: did we learn something? |
| Q33885063 | Mismatch repair defects in cancer |
| Q36779731 | Mismatch repair deficiencies transforming stem cells into cancer stem cells and therapeutic implications |
| Q35057393 | Mismatch repair protein expression in colorectal cancer |
| Q33984294 | Mismatch repair proteins and mitotic genome stability |
| Q33947315 | Mitotic recombination in yeast: elements controlling its incidence |
| Q28214396 | Mouse models for human DNA mismatch-repair gene defects |
| Q37253966 | Multiple populations of artemisinin-resistant Plasmodium falciparum in Cambodia |
| Q38292725 | MutS recognition: multiple mismatches and sequence context effects |
| Q34123282 | Mutations within the hMLH1 and hPMS2 subunits of the human MutLalpha mismatch repair factor affect its ATPase activity, but not its ability to interact with hMutSalpha |
| Q24679608 | N-terminus of hMLH1 confers interaction of hMutLalpha and hMutLbeta with hMutSalpha |
| Q35009957 | Non-Hodgkin lymphoma risk and variants in genes controlling lymphocyte development |
| Q53924883 | Overproduction and analysis of eukaryotic multiprotein complexes in Escherichia coli using a dual-vector strategy. |
| Q28610670 | Partial reconstitution of human DNA mismatch repair in vitro: characterization of the role of human replication protein A |
| Q27690911 | Postreplicative mismatch repair |
| Q24805338 | Recognition and binding of mismatch repair proteins at an oncogenic hot spot |
| Q39582800 | Replication-associated mutational asymmetry in the human genome |
| Q34612512 | Requirement for Msh6, but not for Swi4 (Msh3), in Msh2-dependent repair of base-base mismatches and mononucleotide loops in Schizosaccharomyces pombe |
| Q33786744 | Requirement for Phe36 for DNA binding and mismatch repair by Escherichia coli MutS protein |
| Q34194512 | Role of MED1 (MBD4) Gene in DNA repair and human cancer |
| Q46657284 | S-phase checkpoint controls mitosis via an APC-independent Cdc20p function |
| Q35586971 | Soil microbiome responses to the short-term effects of Amazonian deforestation. |
| Q40412801 | Somatic hypermutation and mismatch repair in non-B cells |
| Q33770250 | Somatic hypermutation of immunoglobulin and non-immunoglobulin genes |
| Q34603312 | Somatic mutations at the trinucleotide repeats of androgen receptor gene in male hepatocellular carcinoma |
| Q24793345 | Some Provocative Thoughts on Damage and Repair of DNA. |
| Q34175345 | Spontaneous DNA damage, genome instability, and cancer--when DNA replication escapes control. |
| Q33700987 | Structural maintenance of chromosomes (SMC) proteins: conserved molecular properties for multiple biological functions |
| Q28143945 | Structure and function of mismatch repair proteins |
| Q34048739 | Suppression of genome instability by redundant S-phase checkpoint pathways in Saccharomyces cerevisiae |
| Q46200700 | Suppression of spontaneous chromosomal rearrangements by S phase checkpoint functions in Saccharomyces cerevisiae |
| Q36406986 | The RAD5-dependent postreplication repair pathway is important to suppress gross chromosomal rearrangements |
| Q34608831 | The Saccharomyces cerevisiae DNA recombination and repair functions of the RAD52 epistasis group inhibit Ty1 transposition |
| Q52569390 | The beta sliding clamp binds to multiple sites within MutL and MutS. |
| Q39572450 | The roles of mutS, sbcCD and recA in the propagation of TGG repeats in Escherichia coli |
| Q28145111 | The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites |
| Q44337576 | Transcription-associated mutational asymmetry in mammalian evolution |
| Q33184847 | Transient mismatch repair gene transfection for functional analysis of genetic hMLH1 and hMSH2 variants |
| Q64388803 | [DNA-dependent protein kinase (DNA-PK), a key enzyme in the re-ligation of double-stranded DNA breaks] |
| Q39936198 | hMSH2 expression is driven by AP1-dependent regulation through phorbol-ester exposure |
| Q24299514 | hMutS alpha is protected from ubiquitin-proteasome-dependent degradation by atypical protein kinase C zeta phosphorylation |
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