A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches
about
Characterization of a mammalian homolog of the Escherichia coli MutY mismatch repair proteinMechanism of human methyl-directed DNA methyltransferase and the fidelity of cytosine methylationEfficient removal of uracil from G.U mispairs by the mismatch-specific thymine DNA glycosylase from HeLa cellsIsolation of cDNAs encoding a human protein that binds selectively to DNA modified by the anticancer drug cis-diamminedichloroplatinum(II)Postreplicative mismatch repair.Role of DNA mismatch repair and p53 in signaling induction of apoptosis by alkylating agents.Mismatch-specific thymine DNA glycosylase and DNA polymerase beta mediate the correction of G.T mispairs in nuclear extracts from human cells.DNA mismatch repair in Xenopus egg extracts: repair efficiency and DNA repair synthesis for all single base-pair mismatches.Error removal in microchip-synthesized DNA using immobilized MutS.Functional analysis of human MutSalpha and MutSbeta complexes in yeastDNA-substrate sequence specificity of human G:T mismatch repair activity.A mismatch recognition defect in colon carcinoma confers DNA microsatellite instability and a mutator phenotype.Base mismatch-specific endonuclease activity in extracts from Saccharomyces cerevisiae.Identification of two mismatch-binding activities in protein extracts of Schizosaccharomyces pombe.An ultraviolet light-damaged DNA recognition protein absent in xeroderma pigmentosum group E cells binds selectively to pyrimidine (6-4) pyrimidone photoproductsCytosine methylation in CTF and Sp1 recognition sites of an HSV tk promoter: effects on transcription in vivo and on factor binding in vitro.Self-destruction and tolerance in resistance of mammalian cells to alkylation damage.Tolerance of human MSH2+/- lymphoblastoid cells to the methylating agent temozolomide.MSH6- or PMS2-deficiency causes re-replication in DT40 B cells, but it has little effect on immunoglobulin gene conversion or on repair of AID-generated uracils.A constitutive damage-specific DNA-binding protein is synthesized at higher levels in UV-irradiated primate cellsDual daughter strand incision is processive and increases the efficiency of DNA mismatch repair.Mismatch repair in Xenopus egg extracts: DNA strand breaks act as signals rather than excision points.Human cells contain protein specifically binding to a single 1,N6-ethenoadenine in a DNA fragment.Asymmetric recognition of DNA local distortion. Structure-based functional studies of eukaryotic Msh2-Msh6.A damage-recognition protein which binds to DNA containing interstrand cross-links is absent or defective in Fanconi anemia, complementation group A, cells.Enzymatic repair of 5-formyluracil. II. Mismatch formation between 5-formyluracil and guanine during dna replication and its recognition by two proteins involved in base excision repair (AlkA) and mismatch repair (MutS).Identification of the protein components of mismatch binding complexes in human cells using a gel-shift assay.hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSalphaThe ubiquitous nuclear protein, NHP1, binds with high affinity to different sequences of the chicken vitellogenin II gene.hMSH2-independent DNA mismatch recognition by human proteins.Potentiation of temozolomide and BCNU cytotoxicity by O(6)-benzylguanine: a comparative study in vitro.Phylogenetic evidence of a role for 5-hydroxymethyluracil-DNA glycosylase in the maintenance of 5-methylcytosine in DNA.Identification of hMutLbeta, a heterodimer of hMLH1 and hPMS1.A mammalian cell line deficient in activity of the DNA repair enzyme 5-hydroxymethyluracil-DNA glycosylase is resistant to the toxic effects of the thymidine analog 5-hydroxymethyl-2'-deoxyuridine.Recognition of DNA alterations by the mismatch repair systemReplication errors: cha(lle)nging the genome.Fibroblast growth factor-1 stimulation of quiescent NIH 3T3 cells increases G/T mismatch-binding protein expression.Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classification.Mismatch recognition and DNA-dependent stimulation of the ATPase activity of hMutSalpha is abolished by a single mutation in the hMSH6 subunit.YB-1 disrupts mismatch repair complex formation, interferes with MutSα recruitment on mismatch and inhibits mismatch repair through interacting with PCNA.
P2860
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P2860
A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches
description
1988 nî lūn-bûn
@nan
1988 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches
@ast
A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches
@en
type
label
A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches
@ast
A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches
@en
prefLabel
A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches
@ast
A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches
@en
P2093
P2860
P356
P1476
A human 200-kDa protein binds selectively to DNA fragments containing G.T mismatches
@en
P2093
P2860
P304
P356
10.1073/PNAS.85.23.8860
P407
P577
1988-12-01T00:00:00Z