Differential human nucleotide excision repair of paired and mispaired cisplatin-DNA adducts. - Wikidata - awgldk - TriplyDB

Differential human nucleotide excision repair of paired and mispaired cisplatin-DNA adducts.

Differential human nucleotide excision repair of paired and mispaired cisplatin-DNA adducts.

http://www.wikidata.org/entity/Q34625375

about

MutS homologue hMSH5: role in cisplatin-induced DNA damage response 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 Inhibition of double-strand break non-homologous end-joining by cisplatin adducts in human cell extracts MSH2 missense mutations alter cisplatin cytotoxicity and promote cisplatin-induced genome instability Conformation, protein recognition and repair of DNA interstrand and intrastrand cross-links of antitumor trans-[PtCl2(NH3)(thiazole)].Circulating HMGB1 and RAGE as Clinical Biomarkers in Malignant and Autoimmune Diseases A multistep damage recognition mechanism for global genomic nucleotide excision repair Aberrant mobility phenomena of the DNA repair protein XPA Replication protein A (RPA) binding to duplex cisplatin-damaged DNA is mediated through the generation of single-stranded DNA.Recognition of nonhybridizing base pairs during nucleotide excision repair of DNA Stopped-flow kinetic analysis of replication protein A-binding DNA: damage recognition and affinity for single-stranded DNA reveal differential contributions of k(on) and k(off) rate constants.Photocrosslinking locates a binding site for the large subunit of human replication protein A to the damaged strand of cisplatin-modified DNA The XPA-binding domain of ERCC1 is required for nucleotide excision repair but not other DNA repair pathways.Binding and repair of mismatched DNA mediated by Rhp14, the fission yeast homologue of human XPA.Psoralen interstrand cross-link repair is specifically altered by an adjacent triple-stranded structure HMGB1: roles in base excision repair and related function.Biological properties of single chemical-DNA adducts: a twenty year perspective Effects of geometric isomerism and anions on the kinetics and mechanism of the stepwise formation of long-range DNA interstrand cross-links by dinuclear platinum antitumor complexes.Hepatitis B virus X protein impedes the DNA repair via its association with transcription factor, TFIIH The DNA damage response kinases DNA-dependent protein kinase (DNA-PK) and ataxia telangiectasia mutated (ATM) Are stimulated by bulky adduct-containing DNA.Transcription inhibition by platinum-DNA cross-links in live mammalian cells.Differential effects of cisplatin and MNNG on dna mutants of Escherichia coli.Determination of hypersensitivity to genotoxic agents among Escherichia coli single gene knockout mutants Repair of cisplatin-induced DNA interstrand crosslinks by a replication-independent pathway involving transcription-coupled repair and translesion synthesis Selective recognition of a cisplatin-DNA adduct by human mismatch repair proteins.Oxaliplatin induces different cellular and molecular chemoresistance patterns in colorectal cancer cell lines of identical origins Molecular mechanisms of resistance and toxicity associated with platinating agents.Molecular mechanisms of xeroderma pigmentosum (XP) proteins.Cisplatin damage: are DNA repair proteins saviors or traitors to the cell?Bipartite substrate discrimination by human nucleotide excision repair Base pair conformation-dependent excision of benzo[a]pyrene diol epoxide-guanine adducts by human nucleotide excision repair enzymes.Physical interaction between components of DNA mismatch repair and nucleotide excision repair Epistatic role of base excision repair and mismatch repair pathways in mediating cisplatin cytotoxicity Human HMGB1 directly facilitates interactions between nucleotide excision repair proteins on triplex-directed psoralen interstrand crosslinks Removal of misincorporated ribonucleotides from prokaryotic genomes: an unexpected role for nucleotide excision repair Preparation of mammalian expression vectors incorporating site-specifically platinated-DNA lesions.MutS inhibits RecA-mediated strand exchange with platinated DNA substrates DNA-protein cross-linking by trans-[PtCl(2)(E-iminoether)(2)]. A concept for activation of the trans geometry in platinum antitumor complexes Binding discrimination of MutS to a set of lesions and compound lesions (base damage and mismatch) reveals its potential role as a cisplatin-damaged DNA sensing protein.Human JC virus small tumour antigen inhibits nucleotide excision repair and sensitises cells to DNA-damaging agents.

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Differential human nucleotide excision repair of paired and mispaired cisplatin-DNA adducts.

http://www.wikidata.org/entity/Q34625375

description

1997 nî lūn-bûn

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1997 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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1997 թվականի փետրվարին հրատարակված գիտական հոդված

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1997年の論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年论文

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name

Differential human nucleotide ...... spaired cisplatin-DNA adducts.

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Differential human nucleotide ...... spaired cisplatin-DNA adducts.

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Differential human nucleotide ...... spaired cisplatin-DNA adducts.

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Differential human nucleotide ...... spaired cisplatin-DNA adducts.

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Differential human nucleotide ...... spaired cisplatin-DNA adducts.

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Differential human nucleotide ...... spaired cisplatin-DNA adducts.

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Differential human nucleotide ...... spaired cisplatin-DNA adducts.

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Differential human nucleotide ...... spaired cisplatin-DNA adducts.

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Nucleic Acids Research

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Differential human nucleotide ...... spaired cisplatin-DNA adducts.

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Karran P

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Moggs JG

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Szymkowski DE

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Yamada M

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P2860

XPG endonuclease makes the 3' incision in human DNA nucleotide excision repair

A 3' --> 5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription

Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease

Isolation and characterization of human cDNA clones encoding a high mobility group box protein that recognizes structural distortions to DNA caused by binding of the anticancer agent cisplatin

Isolation of cDNAs encoding a human protein that binds selectively to DNA modified by the anticancer drug cis-diamminedichloroplatinum(II)

Structure and isomerization of an intrastrand cisplatin-cross-linked octamer DNA duplex by NMR analysis

Crystal structure of double-stranded DNA containing the major adduct of the anticancer drug cisplatin

The solution structure of a DNA duplex containing the cis-Pt(NH3)2[d(-GTG-)-N7(G),N7(G)] adduct, as determined with high-field NMR and molecular mechanics/dynamics

Proliferating cell nuclear antigen is required for DNA excision repair

Transcription-coupled repair deficiency and mutations in human mismatch repair genes

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480-491

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scholarly article

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10.1093/NAR/25.3.480

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3

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Richard Dean Wood

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274409510

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9016585

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146461

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