A multistep damage recognition mechanism for global genomic nucleotide excision repair - Wikidata - awgldk - TriplyDB

A multistep damage recognition mechanism for global genomic nucleotide excision repair

A multistep damage recognition mechanism for global genomic nucleotide excision repair

http://www.wikidata.org/entity/Q28359842

about

Epigenetic changes of DNA repair genes in cancer INO80 chromatin remodeling complex promotes the removal of UV lesions by the nucleotide excision repair pathway Centrin 2 stimulates nucleotide excision repair by interacting with xeroderma pigmentosum group C protein.Sequential binding of UV DNA damage binding factor and degradation of the p48 subunit as early events after UV irradiation.Xeroderma pigmentosum group C protein interacts physically and functionally with thymine DNA glycosylase Global genome repair is required to activate KIN17, a UVC-responsive gene involved in DNA replication.Differential role of basal keratinocytes in UV-induced immunosuppression and skin cancer A novel regulation mechanism of DNA repair by damage-induced and RAD23-dependent stabilization of xeroderma pigmentosum group C protein Human XPC-hHR23B interacts with XPA-RPA in the recognition of triplex-directed psoralen DNA interstrand crosslinks.DNA repair factor XPC is modified by SUMO-1 and ubiquitin following UV irradiation Melanocortin 1 Receptor: Structure, Function, and Regulation Global-genome Nucleotide Excision Repair Controlled by Ubiquitin/Sumo Modifiers Nucleotide Excision Repair and Vitamin D--Relevance for Skin Cancer Therapy Xeroderma pigmentosum group C sensor: unprecedented recognition strategy and tight spatiotemporal regulation Nucleotide excision repair in eukaryotes Recognition of Damaged DNA for Nucleotide Excision Repair: A Correlated Motion Mechanism with a Mismatched cis-syn Thymine Dimer Lesion.Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD Structure and stability of DNA containing an aristolactam II-dA lesion: implications for the NER recognition of bulky adducts Base-displaced intercalation of the 2-amino-3-methylimidazo[4,5-f]quinolone N2-dG adduct in the NarI DNA recognition sequence Saccharomyces cerevisiae Cmr1 protein preferentially binds to UV-damaged DNA in vitro.Twist-open mechanism of DNA damage recognition by the Rad4/XPC nucleotide excision repair complex Transcriptional and Posttranslational Regulation of Nucleotide Excision Repair: The Guardian of the Genome against Ultraviolet Radiation XPC: Going where no DNA damage sensor has gone before DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae Nucleotide excision repair efficiencies of bulky carcinogen-DNA adducts are governed by a balance between stabilizing and destabilizing interactions The human DNA repair factor XPC-HR23B distinguishes stereoisomeric benzo[a]pyrenyl-DNA lesions Differential nucleotide excision repair susceptibility of bulky DNA adducts in different sequence contexts: hierarchies of recognition signals Two-stage dynamic DNA quality check by xeroderma pigmentosum group C protein.Structural basis for the recognition of diastereomeric 5',8-cyclo-2'-deoxypurine lesions by the human nucleotide excision repair system Chromatin restoration following nucleotide excision repair involves the incorporation of ubiquitinated H2A at damaged genomic sites.Xeroderma pigmentosum group A protein loads as a separate factor onto DNA lesions.Recognition and repair of the cyclobutane thymine dimer, a major cause of skin cancers, by the human excision nuclease.DDB accumulates at DNA damage sites immediately after UV irradiation and directly stimulates nucleotide excision repair.Molecular anatomy of the human excision nuclease assembled at sites of DNA damage.Biochemical analysis of the damage recognition process in nucleotide excision repair.NMR study on the interaction between RPA and DNA decamer containing cis-syn cyclobutane pyrimidine dimer in the presence of XPA: implication for damage verification and strand-specific dual incision in nucleotide excision repair.Recruitment of DNA damage checkpoint proteins to damage in transcribed and nontranscribed sequences.Initiation of DNA repair mediated by a stalled RNA polymerase IIO.Recognition of oxidized thymine base on the single-stranded DNA by replication protein A.The involvement of ataxia-telangiectasia mutated protein activation in nucleotide excision repair-facilitated cell survival with cisplatin treatment.

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A multistep damage recognition mechanism for global genomic nucleotide excision repair

http://www.wikidata.org/entity/Q28359842

description

2001 nî lūn-bûn

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2001 թուականի Մարտին հրատարակուած գիտական յօդուած

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2001 թվականի մարտին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年论文

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name

A multistep damage recognition mechanism for global genomic nucleotide excision repair

@ast

A multistep damage recognition mechanism for global genomic nucleotide excision repair

@en

A multistep damage recognition mechanism for global genomic nucleotide excision repair

@nl

type

label

A multistep damage recognition mechanism for global genomic nucleotide excision repair

@ast

A multistep damage recognition mechanism for global genomic nucleotide excision repair

@en

A multistep damage recognition mechanism for global genomic nucleotide excision repair

@nl

prefLabel

A multistep damage recognition mechanism for global genomic nucleotide excision repair

@ast

A multistep damage recognition mechanism for global genomic nucleotide excision repair

@en

A multistep damage recognition mechanism for global genomic nucleotide excision repair

@nl

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Genes & Development

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A multistep damage recognition mechanism for global genomic nucleotide excision repair

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C Masutani

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F Hanaoka

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K Sugasawa

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S Iwai

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T Okamoto

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Y Shimizu

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P2860

The xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA

Stable binding of human XPC complex to irradiated DNA confers strong discrimination for damaged sites

Two human homologs of Rad23 are functionally interchangeable in complex formation and stimulation of XPC repair activity

Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23

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

RPA involvement in the damage-recognition and incision steps of nucleotide excision repair

DNA repair defect in xeroderma pigmentosum group C and complementing factor from HeLa cells

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

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

Human DNA repair excision nuclease. Analysis of the roles of the subunits involved in dual incisions by using anti-XPG and anti-ERCC1 antibodies

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507-21

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1173802

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10.1101/GAD.866301

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5

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15

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12094287

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11238373

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312644

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