about
MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexesEvidence for involvement of HMGB1 protein in human DNA mismatch repairN-terminus of hMLH1 confers interaction of hMutLalpha and hMutLbeta with hMutSalphaSome Provocative Thoughts on Damage and Repair of DNA.Recognition and binding of mismatch repair proteins at an oncogenic hot spotDNA triplet repeat expansion and mismatch repairPostreplicative mismatch repair.Bcl-2 expression suppresses mismatch repair activity through inhibition of E2F transcriptional activityAffinity of mismatch-binding protein MutS for heteroduplexes containing different mismatchesPartial reconstitution of human DNA mismatch repair in vitro: characterization of the role of human replication protein ATransient mismatch repair gene transfection for functional analysis of genetic hMLH1 and hMSH2 variants.Structural maintenance of chromosomes (SMC) proteins: conserved molecular properties for multiple biological functions.Somatic hypermutation of immunoglobulin and non-immunoglobulin genes.Hypermutation in bacteria and other cellular systemsRequirement for Phe36 for DNA binding and mismatch repair by Escherichia coli MutS protein.Human DNA mismatch repair in vitro operates independently of methylation status at CpG sitesMitotic recombination in yeast: elements controlling its incidence.Suppression of genome instability by redundant S-phase checkpoint pathways in Saccharomyces cerevisiae.Clinical and molecular analysis of hereditary non-polyposis colorectal cancer in Chinese colorectal cancer patients.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.Role of MED1 (MBD4) Gene in DNA repair and human cancer.Functional interactions and signaling properties of mammalian DNA mismatch repair proteins.Somatic mutations at the trinucleotide repeats of androgen receptor gene in male hepatocellular carcinoma.The Saccharomyces cerevisiae DNA recombination and repair functions of the RAD52 epistasis group inhibit Ty1 transpositionRequirement for Msh6, but not for Swi4 (Msh3), in Msh2-dependent repair of base-base mismatches and mononucleotide loops in Schizosaccharomyces pombeControl of GT repeat stability in Schizosaccharomyces pombe by mismatch repair factorsNon-Hodgkin lymphoma risk and variants in genes controlling lymphocyte developmentMismatch repair protein expression in colorectal cancer.Soil microbiome responses to the short-term effects of Amazonian deforestation.Biochemical analysis of the human mismatch repair proteins hMutSα MSH2(G674A)-MSH6 and MSH2-MSH6(T1219D)Involvement of mismatch repair in the reciprocal control of motility and adherence of uropathogenic Escherichia coli.The RAD5-dependent postreplication repair pathway is important to suppress gross chromosomal rearrangementsDNA damage and repair in epithelium after allogeneic hematopoietic stem cell transplantationMismatch repair deficiencies transforming stem cells into cancer stem cells and therapeutic implications.Multiple populations of artemisinin-resistant Plasmodium falciparum in Cambodia.Identification of factors influencing strand bias in oligonucleotide-mediated recombination in Escherichia coli.Helicobacter pylori infection and expression of DNA mismatch repair proteins.Life without dUTPase.Asymmetric recognition of DNA local distortion. Structure-based functional studies of eukaryotic Msh2-Msh6.
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Replication errors: cha
@nl
Replication errors: cha(lle)nging the genome.
@en
type
label
Replication errors: cha
@nl
Replication errors: cha(lle)nging the genome.
@en
prefLabel
Replication errors: cha
@nl
Replication errors: cha(lle)nging the genome.
@en
P2860
P356
P1433
P1476
Replication errors: cha(lle)nging the genome.
@en
P2093
P2860
P304
P356
10.1093/EMBOJ/17.22.6427
P407
P577
1998-11-01T00:00:00Z