scholarly article | Q13442814 |
P50 | author | Guo-Min Li | Q50637024 |
P2093 | author name string | H Watanabe | |
Y Hong | |||
L Gu | |||
S McCulloch | |||
P2860 | cites work | DNA polymerase delta is required for human mismatch repair in vitro | Q24313002 |
hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6 | Q24323176 | ||
Binding of insertion/deletion DNA mismatches by the heterodimer of yeast mismatch repair proteins MSH2 and MSH3. | Q27934985 | ||
Evidence for involvement of yeast proliferating cell nuclear antigen in DNA mismatch repair | Q27938608 | ||
Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis | Q27939891 | ||
D type cyclins associate with multiple protein kinases and the DNA replication and repair factor PCNA | Q28183697 | ||
p21 is a universal inhibitor of cyclin kinases | Q28257305 | ||
Biochemistry and genetics of eukaryotic mismatch repair | Q28282377 | ||
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 | ||
Human strand-specific mismatch repair occurs by a bidirectional mechanism similar to that of the bacterial reaction | Q28610824 | ||
Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
The p21 inhibitor of cyclin-dependent kinases controls DNA replication by interaction with PCNA | Q29615251 | ||
Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines | Q33720790 | ||
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 | ||
Repair tracts in mismatched DNA heteroduplexes | Q35037122 | ||
Cdk-interacting protein 1 directly binds with proliferating cell nuclear antigen and inhibits DNA replication catalyzed by the DNA polymerase delta holoenzyme | Q35739744 | ||
Altering the conserved nucleotide binding motif in the Salmonella typhimurium MutS mismatch repair protein affects both its ATPase and mismatch binding activities | Q35930280 | ||
Nucleotide sequence of the Salmonella typhimurium mutS gene required for mismatch repair: homology of MutS and HexA of Streptococcus pneumoniae | Q36185655 | ||
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 | ||
Molecular matchmakers | Q40885529 | ||
DNA-replication fidelity, mismatch repair and genome instability in cancer cells | Q41016785 | ||
Hypermutability and mismatch repair deficiency in RER+ tumor cells | Q41508298 | ||
MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
Human MutSalpha specifically binds to DNA containing aminofluorene and acetylaminofluorene adducts. | Q53451091 | ||
Isolation and characterization of the Escherichia coli mutL gene product. | Q54734906 | ||
Heteroduplex repair in extracts of human HeLa cells | Q68198738 | ||
Requirement of the yeast MSH3 and MSH6 genes for MSH2-dependent genomic stability | Q71081409 | ||
Inhibition of Nucleotide Excision Repair by the Cyclin-dependent Kinase Inhibitor p21 | Q72036862 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | DNA mismatch repair | Q2984243 |
P304 | page(s) | 1173-1178 | |
P577 | publication date | 1998-03-01 | |
P1433 | published in | Nucleic Acids Research | Q135122 |
P1476 | title | ATP-dependent interaction of human mismatch repair proteins and dual role of PCNA in mismatch repair | |
P478 | volume | 26 |
Q36677284 | A Delicate Balance Between Repair and Replication Factors Regulates Recombination Between Divergent DNA Sequences in Saccharomyces cerevisiae |
Q24298110 | A defined human system that supports bidirectional mismatch-provoked excision |
Q34606404 | A mutation of the yeast gene encoding PCNA destabilizes both microsatellite and minisatellite DNA sequences |
Q36540457 | A personal historical view of DNA mismatch repair with an emphasis on eukaryotic DNA mismatch repair |
Q26769967 | Activation of the DNA Damage Response by RNA Viruses |
Q34614513 | Analysis of conditional mutations in the Saccharomyces cerevisiae MLH1 gene in mismatch repair and in meiotic crossing over. |
Q28383743 | Arsenic Inhibits DNA Mismatch Repair by Promoting EGFR Expression and PCNA Phosphorylation. |
Q36597002 | Beta clamp directs localization of mismatch repair in Bacillus subtilis |
Q58074430 | Bi-directional Processing of DNA Loops by Mismatch Repair-dependent and -independent Pathways in Human Cells |
Q33726437 | Bi-directional routing of DNA mismatch repair protein human exonuclease 1 to replication foci and DNA double strand breaks |
Q38320783 | Biochemical characterization of the interaction between the Saccharomyces cerevisiae MSH2-MSH6 complex and mispaired bases in DNA. |
Q24798955 | Cadmium inhibits mismatch repair by blocking the ATPase activity of the MSH2-MSH6 complex |
Q27934255 | Characterization of nuclease-dependent functions of Exo1p in Saccharomyces cerevisiae |
Q28277364 | Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2 |
Q33559854 | Construction and characterization of mismatch-containing circular DNA molecules competent for assessment of nick-directed human mismatch repair in vitro |
Q40744193 | Contribution of human mlh1 and pms2 ATPase activities to DNA mismatch repair |
Q27640487 | Crystal structure and biochemical analysis of the MutS.ADP.beryllium fluoride complex suggests a conserved mechanism for ATP interactions in mismatch repair |
Q40566115 | DNA damage induces p53-dependent BRCA1 nuclear export |
Q40513970 | DNA methyltransferase Dnmt1 and mismatch repair |
Q28211143 | DNA mismatch repair and mutation avoidance pathways |
Q36453321 | DNA mismatch repair system. Classical and fresh roles |
Q24647002 | DNA mismatch repair: molecular mechanism, cancer, and ageing |
Q34144865 | DNA mismatch repair: the hands of a genome guardian. |
Q35885592 | Deciphering the mismatch recognition cycle in MutS and MSH2-MSH6 using normal-mode analysis |
Q33888905 | Deficiency of a novel mismatch repair activity in a bladder tumor cell line |
Q37491462 | Deoxyribonucleic acid damage induced by doxorubicin in peripheral blood mononuclear cells: possible roles for the stress response and the deoxyribonucleic acid repair process |
Q39111119 | Detection of DNA mismatch repair proteins in fresh human blood lymphocytes--towards a novel method for hereditary non-polyposis colorectal cancer (Lynch syndrome) screening |
Q44761854 | Differential requirement for proliferating cell nuclear antigen in 5' and 3' nick-directed excision in human mismatch repair |
Q24555123 | Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1 |
Q27679146 | Distinct Structural Alterations in Proliferating Cell Nuclear Antigen Block DNA Mismatch Repair |
Q45962906 | DnaN clamp zones provide a platform for spatiotemporal coupling of mismatch detection to DNA replication. |
Q34609730 | EXO1 and MSH6 are high-copy suppressors of conditional mutations in the MSH2 mismatch repair gene of Saccharomyces cerevisiae |
Q37438949 | Epigenetic Enhancement of the Post-replicative DNA Mismatch Repair of Mammalian Genomes by a Hemi-(m)CpG-Np95-Dnmt1 Axis |
Q27939116 | Eukaryotic DNA mismatch repair |
Q77753605 | Eukaryotic mismatch repair: an update |
Q24316068 | Evidence for involvement of HMGB1 protein in human DNA mismatch repair |
Q77495184 | Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer |
Q36623595 | Functional analysis of the mismatch repair system in bladder cancer |
Q24290314 | Functional interaction of proliferating cell nuclear antigen with MSH2-MSH6 and MSH2-MSH3 complexes |
Q34425450 | Functional interactions and signaling properties of mammalian DNA mismatch repair proteins |
Q44068446 | HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions |
Q37022515 | High-fidelity correction of genomic uracil by human mismatch repair activities |
Q34686576 | Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1. |
Q33939108 | Human DNA mismatch repair in vitro operates independently of methylation status at CpG sites |
Q36328799 | Human DNA mismatch repair: coupling of mismatch recognition to strand-specific excision |
Q73794909 | Human DNA repair genes |
Q33343475 | Human MutLalpha: the jack of all trades in MMR is also an endonuclease |
Q24292187 | Human MutY homolog, a DNA glycosylase involved in base excision repair, physically and functionally interacts with mismatch repair proteins human MutS homolog 2/human MutS homolog 6 |
Q24292224 | Human exonuclease I is required for 5' and 3' mismatch repair |
Q33707301 | Human immunodeficiency virus type 1-induced macrophage gene expression includes the p21 gene, a target for viral regulation |
Q33224078 | Human mismatch repair: reconstitution of a nick-directed bidirectional reaction |
Q43002767 | Human mismatch-repair protein MutL homologue 1 (MLH1) interacts with Escherichia coli MutL and MutS in vivo and in vitro: a simple genetic system to assay MLH1 function |
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 |
Q28140727 | Identification of mismatch repair protein complexes in HeLa nuclear extracts and their interaction with heteroduplex DNA |
Q73923892 | Interaction of Escherichia coli MutS and MutL at a DNA mismatch |
Q24553992 | Interaction of mismatch repair protein PMS2 and the p53-related transcription factor p73 in apoptosis response to cisplatin |
Q33933718 | Interactions of Exo1p with components of MutLalpha in Saccharomyces cerevisiae |
Q28209230 | Interactions of the DNA mismatch repair proteins MLH1 and MSH2 with c-MYC and MAX |
Q39675432 | Isolation and characterization of new proliferating cell nuclear antigen (POL30) mutator mutants that are defective in DNA mismatch repair |
Q50287465 | MSH2:MSH3 exchanges ADP for ATP |
Q50287452 | MSH2:MSH6 exchanges ADP for ATP |
Q34614229 | Maternal effect for DNA mismatch repair in the mouse. |
Q28262719 | Mechanisms and functions of DNA mismatch repair |
Q36564560 | Mechanisms in eukaryotic mismatch repair |
Q35910256 | Meiotic recombination intermediates and mismatch repair proteins |
Q33305049 | Mismatch Repair proteins are recruited to replicating DNA through interaction with Proliferating Cell Nuclear Antigen (PCNA) |
Q39656168 | Mismatch recognition-coupled stabilization of Msh2-Msh6 in an ATP-bound state at the initiation of DNA repair |
Q36779731 | Mismatch repair deficiencies transforming stem cells into cancer stem cells and therapeutic implications |
Q38170877 | Mismatch repair deficiency in ovarian cancer -- molecular characteristics and clinical implications |
Q34194518 | Mismatch repair in correction of replication errors and processing of DNA damage |
Q33984294 | Mismatch repair proteins and mitotic genome stability |
Q37483304 | Modulation of mutagenesis in eukaryotes by DNA replication fork dynamics and quality of nucleotide pools |
Q34293069 | Molecular mechanisms of DNA mismatch repair |
Q36057058 | Molecular signaling mechanisms of apoptosis in hereditary non-polyposis colorectal cancer |
Q78681880 | Msh2 deficiency increases the mutation frequency in all parts of the mouse colon |
Q44522189 | Msh2 separation of function mutations confer defects in the initiation steps of mismatch repair |
Q28776215 | Multiple functions of MutS- and MutL-related heterocomplexes |
Q33799870 | MutLalpha and proliferating cell nuclear antigen share binding sites on MutSbeta |
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 |
Q53412320 | Mutator phenotype due to loss of heterozygosity in diploid yeast strains with mutations in MSH2 and MLH1. |
Q35063954 | Mutator phenotypes of yeast strains heterozygous for mutations in the MSH2 gene. |
Q34609246 | Mutual correction of faulty PCNA subunits in temperature-sensitive lethal mus209 mutants of Drosophila melanogaster |
Q52661262 | Mycobacterium tuberculosis class II apurinic/apyrimidinic-endonuclease/3'-5' exonuclease III exhibits DNA regulated modes of interaction with the sliding DNA β-clamp. |
Q24679608 | N-terminus of hMLH1 confers interaction of hMutLalpha and hMutLbeta with hMutSalpha |
Q34097342 | Novel PMS1 alleles preferentially affect the repair of primer strand loops during DNA replication |
Q33643516 | Nuclear reorganization of DNA mismatch repair proteins in response to DNA damage |
Q33961620 | PCNA and Msh2-Msh6 activate an Mlh1-Pms1 endonuclease pathway required for Exo1-independent mismatch repair. |
Q24814841 | PCNA-MutSalpha-mediated binding of MutLalpha to replicative DNA with mismatched bases to induce apoptosis in human cells |
Q28610670 | Partial reconstitution of human DNA mismatch repair in vitro: characterization of the role of human replication protein A |
Q30978715 | Partial reconstitution of human interstrand cross-link repair in vitro: characterization of the roles of RPA and PCNA. |
Q35590357 | Phosphorylation of PCNA by EGFR inhibits mismatch repair and promotes misincorporation during DNA synthesis |
Q92282100 | Phosphorylation of proliferating cell nuclear antigen promotes cancer progression by activating the ATM/Akt/GSK3β/Snail signaling pathway |
Q40309902 | Postreplicative mismatch repair factors are recruited to Epstein-Barr virus replication compartments |
Q28142999 | Proliferating cell nuclear antigen and Msh2p-Msh6p interact to form an active mispair recognition complex |
Q35540109 | Radiation modulates the peptide repertoire, enhances MHC class I expression, and induces successful antitumor immunotherapy |
Q41886077 | Recognition of DNA alterations by the mismatch repair system |
Q42660015 | Replication errors: cha(lle)nging the genome |
Q93063783 | Replication stress triggers microsatellite destabilization and hypermutation leading to clonal expansion in vitro |
Q36687824 | Roles of DNA polymerases in replication, repair, and recombination in eukaryotes. |
Q27932017 | Saccharomyces cerevisiae Msh2p and Msh6p ATPase activities are both required during mismatch repair |
Q39449001 | Saccharomyces cerevisiae pol30 (proliferating cell nuclear antigen) mutations impair replication fidelity and mismatch repair |
Q27938377 | Separation-of-function mutations in Saccharomyces cerevisiae MSH2 that confer mismatch repair defects but do not affect nonhomologous-tail removal during recombination |
Q26999680 | Single-molecule views of MutS on mismatched DNA. |
Q33896699 | Steady-state regulation of the human DNA mismatch repair system. |
Q57784305 | Stochastic Processes and Component Plasticity Governing DNA Mismatch Repair |
Q27933098 | Supercomplex formation between Mlh1-Mlh3 and Sgs1-Top3 heterocomplexes in meiotic yeast cells |
Q38307086 | The DNA strand of chimeric RNA/DNA oligonucleotides can direct gene repair/conversion activity in mammalian and plant cell-free extracts |
Q28551589 | The Eukaryotic Mismatch Recognition Complexes Track with the Replisome during DNA Synthesis |
Q24657814 | The MutSalpha-proliferating cell nuclear antigen interaction in human DNA mismatch repair |
Q36026779 | The N terminus of Saccharomyces cerevisiae Msh6 is an unstructured tether to PCNA |
Q52569390 | The beta sliding clamp binds to multiple sites within MutL and MutS. |
Q44530427 | The coordinated functions of the E. coli MutS and MutL proteins in mismatch repair |
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Q34528290 | The endonuclease domain of MutL interacts with the β sliding clamp |
Q36718848 | The involvement of DNA-damage and -repair defects in neurological dysfunction |
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Q36338245 | Visualization of eukaryotic DNA mismatch repair reveals distinct recognition and repair intermediates. |
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Q52644492 | YB-1 disrupts mismatch repair complex formation, interferes with MutSα recruitment on mismatch and inhibits mismatch repair through interacting with PCNA. |
Q27935389 | exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair |
Q24602221 | hMSH3 and hMSH6 interact with PCNA and colocalize with it to replication foci |
Q24292227 | hMutSalpha forms an ATP-dependent complex with hMutLalpha and hMutLbeta on DNA. |
Q34276816 | hMutSbeta is required for the recognition and uncoupling of psoralen interstrand cross-links in vitro |
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