Human XPA and RPA DNA repair proteins participate in specific recognition of triplex-induced helical distortions - Wikidata - wikimedia - TriplyDB

Human XPA and RPA DNA repair proteins participate in specific recognition of triplex-induced helical distortions

Human XPA and RPA DNA repair proteins participate in specific recognition of triplex-induced helical distortions

http://www.wikidata.org/entity/Q31049492

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Defining the function of xeroderma pigmentosum group F protein in psoralen interstrand cross-link-mediated DNA repair and mutagenesis gamma-H2AX formation in response to interstrand crosslinks requires XPF in human cells Mismatch repair participates in error-free processing of DNA interstrand crosslinks in human cells.Correction of a splice-site mutation in the beta-globin gene stimulated by triplex-forming peptide nucleic acids Human XPC-hHR23B interacts with XPA-RPA in the recognition of triplex-directed psoralen DNA interstrand crosslinks.Triplex-induced recombination and repair in the pyrimidine motif.Advances in mechanisms of genetic instability related to hereditary neurological diseases.Stm1p, a G4 quadruplex and purine motif triplex nucleic acid-binding protein, interacts with ribosomes and subtelomeric Y' DNA in Saccharomyces cerevisiae.Oligo/polynucleotide-based gene modification: strategies and therapeutic potential High mobility group protein B1 enhances DNA repair and chromatin modification after DNA damage Disruption of Higher Order DNA Structures in Friedreich's Ataxia (GAA)n Repeats by PNA or LNA Targeting In vivo correction of anaemia in β-thalassemic mice by γPNA-mediated gene editing with nanoparticle delivery DHX9 helicase is involved in preventing genomic instability induced by alternatively structured DNA in human cells Site-directed recombination via bifunctional PNA-DNA conjugates.Psoralen interstrand cross-link repair is specifically altered by an adjacent triple-stranded structure Human replication protein A melts a DNA triple helix structure in a potent and specific manner Inhibitory effects of Baicalin on ultraviolet B-induced photo-damage in keratinocyte cell line.Human MLH1 protein participates in genomic damage checkpoint signaling in response to DNA interstrand crosslinks, while MSH2 functions in DNA repair Mismatch repair and nucleotide excision repair proteins cooperate in the recognition of DNA interstrand crosslinks.Progressive GAA.TTC repeat expansion in human cell lines.Mutagenic repair of DNA interstrand crosslinks.Targeting and processing of site-specific DNA interstrand crosslinks.Triplex technology in studies of DNA damage, DNA repair, and mutagenesis Optimizing anti-gene oligonucleotide 'Zorro-LNA' for improved strand invasion into duplex DNA.UV-induced nuclear import of XPA is mediated by importin-α4 in an ATR-dependent manner Xeroderma pigmentosum: low prevalence of germline XPA mutations in a Brazilian XP population.HMGB1 interacts with XPA to facilitate the processing of DNA interstrand crosslinks in human cells.The DNA-polymerase-X family: controllers of DNA quality?Triplex structures induce DNA double strand breaks via replication fork collapse in NER deficient cells.Local delivery of gene-modifying triplex-forming molecules to the epidermis.Processing of triplex-directed psoralen DNA interstrand crosslinks by recombination mechanisms.The triple helix: 50 years later, the outcome.DNA triple helices: biological consequences and therapeutic potential.Efficient processing of TFO-directed psoralen DNA interstrand crosslinks by the UvrABC nuclease Systemic delivery of triplex-forming PNA and donor DNA by nanoparticles mediates site-specific genome editing of human hematopoietic cells in vivo.Human HMGB1 directly facilitates interactions between nucleotide excision repair proteins on triplex-directed psoralen interstrand crosslinks Repair of DNA lesions associated with triplex-forming oligonucleotides.DNA damage tolerance and a web of connections with DNA repair at Yale.Naturally occurring H-DNA-forming sequences are mutagenic in mammalian cells.Potential in vivo roles of nucleic acid triple-helices.

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P2860

Human XPA and RPA DNA repair proteins participate in specific recognition of triplex-induced helical distortions

http://www.wikidata.org/entity/Q31049492

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2002 nî lūn-bûn

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2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2002 թվականի ապրիլին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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Human XPA and RPA DNA repair p ...... ex-induced helical distortions

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Human XPA and RPA DNA repair p ...... ex-induced helical distortions

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Human XPA and RPA DNA repair p ...... ex-induced helical distortions

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Human XPA and RPA DNA repair p ...... ex-induced helical distortions

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Human XPA and RPA DNA repair p ...... ex-induced helical distortions

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Human XPA and RPA DNA repair p ...... ex-induced helical distortions

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Human XPA and RPA DNA repair p ...... ex-induced helical distortions

@en

P2093

Jesper Christensen

http://www.w3.org/2001/XMLSchema#string

Karen M Vasquez

http://www.w3.org/2001/XMLSchema#string

Lei Li

http://www.w3.org/2001/XMLSchema#string

Peter M Glazer

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Rick A Finch

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P2860

Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair

Structure of a triple helical DNA with a triplex-duplex junction

A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy

Replication protein A: a heterotrimeric, single-stranded DNA-binding protein required for eukaryotic DNA metabolism

A summary of mutations in the UV-sensitive disorders: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy

The causes of cancer: quantitative estimates of avoidable risks of cancer in the United States today

DNA excision repair

Recognition of nonhybridizing base pairs during nucleotide excision repair of DNA

Triplex-induced recombination in human cell-free extracts. Dependence on XPA and HsRad51.

Triple-helix formation induces recombination in mammalian cells via a nucleotide excision repair-dependent pathway.

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5848-5853

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10.1073/PNAS.082193799

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9

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99

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11396456

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11972036

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122865

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