Pages that link to "Q28610839"
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The following pages link to hMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA (Q28610839):
Displaying 50 items.
- Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer (Q22003969) (← links)
- MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1 (Q22009114) (← links)
- Multiple mutations and frameshifts are the hallmark of defective hPMS2 in pZ189-transfected human tumor cells (Q22254326) (← links)
- 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 (Q24292187) (← links)
- Human exonuclease I is required for 5' and 3' mismatch repair (Q24292224) (← links)
- DNA polymerase delta is required for human mismatch repair in vitro (Q24313002) (← links)
- Evidence for involvement of HMGB1 protein in human DNA mismatch repair (Q24316068) (← links)
- Differential specificities and simultaneous occupancy of human MutSalpha nucleotide binding sites (Q24337694) (← links)
- Physical and functional interactions between Werner syndrome helicase and mismatch-repair initiation factors (Q24338232) (← links)
- The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2 (Q24596494) (← links)
- hMSH3 and hMSH6 interact with PCNA and colocalize with it to replication foci (Q24602221) (← links)
- Mechanism of mismatch recognition revealed by human MutSβ bound to unpaired DNA loops (Q24614021) (← links)
- Functional studies and homology modeling of Msh2-Msh3 predict that mispair recognition involves DNA bending and strand separation (Q24619622) (← links)
- Mismatch repair deficiency associated with overexpression of the MSH3 gene (Q24681589) (← links)
- Role of APC and DNA mismatch repair genes in the development of colorectal cancers (Q24806345) (← links)
- Activation of the DNA Damage Response by RNA Viruses (Q26769967) (← links)
- DNA triplet repeat expansion and mismatch repair (Q26996542) (← links)
- Causal link between microsatellite instability and hMRE11 dysfunction in human cancers (Q27026386) (← links)
- Functional studies on the candidate ATPase domains of Saccharomyces cerevisiae MutLalpha. (Q27929951) (← links)
- Conserved properties between functionally distinct MutS homologs in yeast (Q27931606) (← links)
- Genetic and biochemical analysis of Msh2p-Msh6p: role of ATP hydrolysis and Msh2p-Msh6p subunit interactions in mismatch base pair recognition. (Q27932001) (← links)
- Saccharomyces cerevisiae Msh2p and Msh6p ATPase activities are both required during mismatch repair (Q27932017) (← links)
- Enhancement of MSH2-MSH3-mediated mismatch recognition by the yeast MLH1-PMS1 complex (Q27932428) (← links)
- exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair (Q27935389) (← links)
- Separation-of-function mutations in Saccharomyces cerevisiae MSH2 that confer mismatch repair defects but do not affect nonhomologous-tail removal during recombination (Q27938377) (← links)
- Eukaryotic DNA mismatch repair (Q27939116) (← links)
- ATP-dependent assembly of a ternary complex consisting of a DNA mismatch and the yeast MSH2-MSH6 and MLH1-PMS1 protein complexes (Q27939412) (← links)
- Lessons from hereditary colorectal cancer (Q28131788) (← links)
- Identification of mismatch repair protein complexes in HeLa nuclear extracts and their interaction with heteroduplex DNA (Q28140727) (← links)
- Nuclear translocation of mismatch repair proteins MSH2 and MSH6 as a response of cells to alkylating agents (Q28144364) (← links)
- The human mismatch recognition complex hMSH2-hMSH6 functions as a novel molecular switch (Q28258968) (← links)
- Exonuclease 1-dependent and independent mismatch repair (Q28261787) (← links)
- Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2 (Q28277364) (← links)
- Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activities (Q28285134) (← links)
- MutS homologs in mammalian cells (Q28303186) (← links)
- The Eukaryotic Mismatch Recognition Complexes Track with the Replisome during DNA Synthesis (Q28551589) (← links)
- Elevated mutant frequencies and predominance of G:C to A:T transition mutations in Msh6(-/-) small intestinal epithelium (Q28592464) (← links)
- Mutation in the mismatch repair gene Msh6 causes cancer susceptibility (Q28592583) (← links)
- Mechanisms of human DNA repair: an update (Q28608973) (← links)
- The role of mismatched nucleotides in activating the hMSH2-hMSH6 molecular switch (Q28610649) (← links)
- Partial reconstitution of human DNA mismatch repair in vitro: characterization of the role of human replication protein A (Q28610670) (← links)
- DHFR/MSH3 amplification in methotrexate-resistant cells alters the hMutSalpha/hMutSbeta ratio and reduces the efficiency of base-base mismatch repair (Q28610848) (← links)
- Isolation of MutSbeta from human cells and comparison of the mismatch repair specificities of MutSbeta and MutSalpha (Q28610863) (← links)
- Genetic Instability Caused by Loss of MutS Homologue 3 in Human Colorectal Cancer (Q29395710) (← links)
- Role of DNA mismatch repair and p53 in signaling induction of apoptosis by alkylating agents. (Q30454407) (← links)
- Oligomerization of a MutS mismatch repair protein from Thermus aquaticus (Q30751633) (← links)
- The instability within: problems in current analyses of microsatellite instability (Q31833517) (← links)
- Mismatch Repair proteins are recruited to replicating DNA through interaction with Proliferating Cell Nuclear Antigen (PCNA) (Q33305049) (← links)
- Mutation rates of TGFBR2 and ACVR2 coding microsatellites in human cells with defective DNA mismatch repair (Q33378445) (← links)
- Genomic amplification of the human DHFR/MSH3 locus remodels mismatch recognition and repair activities (Q33724516) (← links)