The xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA
about
Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosomeCentrosome protein centrin 2/caltractin 1 is part of the xeroderma pigmentosum group C complex that initiates global genome nucleotide excision repairTranslocation of Cockayne syndrome group A protein to the nuclear matrix: possible relevance to transcription-coupled DNA repairCentrin 2 stimulates nucleotide excision repair by interacting with xeroderma pigmentosum group C protein.Xeroderma pigmentosum group C protein interacts physically and functionally with thymine DNA glycosylaseGlobal genome repair is required to activate KIN17, a UVC-responsive gene involved in DNA replication.A novel regulation mechanism of DNA repair by damage-induced and RAD23-dependent stabilization of xeroderma pigmentosum group C proteinHuman XPC-hHR23B interacts with XPA-RPA in the recognition of triplex-directed psoralen DNA interstrand crosslinks.Global-genome Nucleotide Excision Repair Controlled by Ubiquitin/Sumo ModifiersXeroderma pigmentosum group C sensor: unprecedented recognition strategy and tight spatiotemporal regulationNucleotide excision repair in eukaryotesRecognition of Damaged DNA for Nucleotide Excision Repair: A Correlated Motion Mechanism with a Mismatched cis-syn Thymine Dimer Lesion.Structural and functional evidence that Rad4 competes with Rad2 for binding to the Tfb1 subunit of TFIIH in NERThe active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif.Mammalian nucleotide excision repair proteins and interstrand crosslink repairA multistep damage recognition mechanism for global genomic nucleotide excision repairDevelopmental defects and male sterility in mice lacking the ubiquitin-like DNA repair gene mHR23BTwo-stage dynamic DNA quality check by xeroderma pigmentosum group C protein.Erythropoietic defect associated with reduced cell proliferation in mice lacking the 26S proteasome shuttling factor Rad23b.Double-check probing of DNA bending and unwinding by XPA-RPA: an architectural function in DNA repair.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.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.Potentially functional variants in the core nucleotide excision repair genes predict survival in Japanese gastric cancer patients.Ordered conformational changes in damaged DNA induced by nucleotide excision repair factors.The protein shuffle. Sequential interactions among components of the human nucleotide excision repair pathway.Biochemical and structural domain analysis of xeroderma pigmentosum complementation group C protein.Sequence variations in DNA repair gene XPC is associated with lung cancer risk in a Chinese population: a case-control studyIn vivo destabilization and functional defects of the xeroderma pigmentosum C protein caused by a pathogenic missense mutationOther proteins interacting with XP proteins.Dissociation of CAK from core TFIIH reveals a functional link between XP-G/CS and the TFIIH disassembly state.Localization of xeroderma pigmentosum group A protein and replication protein A on damaged DNA in nucleotide excision repair.Stochastic and reversible assembly of a multiprotein DNA repair complex ensures accurate target site recognition and efficient repair.Slowly progressing nucleotide excision repair in trichothiodystrophy group A patient fibroblasts.The role of XPC: implications in cancer and oxidative DNA damageUSF-1 is critical for maintaining genome integrity in response to UV-induced DNA photolesions.XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase.Structure of the mouse peptide N-glycanase-HR23 complex suggests co-evolution of the endoplasmic reticulum-associated degradation and DNA repair pathways.
P2860
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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
description
2000 nî lūn-bûn
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2000 թուականի Մարտին հրատարակուած գիտական յօդուած
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2000年の論文
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2000年論文
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2000年論文
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name
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@ast
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@en
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@en-gb
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@nl
type
label
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@ast
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@en
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@en-gb
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@nl
prefLabel
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@ast
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@en
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@en-gb
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@nl
P2093
P2860
P3181
P356
P1476
The xeroderma pigmentosum grou ...... tion factor IIH to damaged DNA
@en
P2093
P2860
P304
P3181
P356
10.1074/JBC.275.13.9870
P407
P577
2000-03-31T00:00:00Z