Biochemical and structural domain analysis of xeroderma pigmentosum complementation group C protein.
about
Nucleotide excision repair is associated with the replisome and its efficiency depends on a direct interaction between XPA and PCNAGlobal-genome Nucleotide Excision Repair Controlled by Ubiquitin/Sumo ModifiersNucleotide Excision Repair and Vitamin D--Relevance for Skin Cancer TherapyRole of the XPA protein in the NER pathway: A perspective on the function of structural disorder in macromolecular assemblyXeroderma pigmentosum group C sensor: unprecedented recognition strategy and tight spatiotemporal regulationNucleotide excision repair in eukaryotesExposure of Human Lung Cells to Tobacco Smoke Condensate Inhibits the Nucleotide Excision Repair PathwayTwo-stage dynamic DNA quality check by xeroderma pigmentosum group C protein.Untangling the relationships between DNA repair pathways by silencing more than 20 DNA repair genes in human stable clones.A comprehensive haplotype analysis of the XPC genomic sequence reveals a cluster of genetic variants associated with sensitivity to tobacco-smoke mutagensIn vitro functional effects of XPC gene rare variants from bladder cancer patients.c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.XPA: A key scaffold for human nucleotide excision repair.DNA repair genes: alternative transcription and gene expression at the exon level in response to the DNA damaging agent, ionizing radiationFunctional and mechanistic studies of XPC DNA-repair complex as transcriptional coactivator in embryonic stem cells.Preclinical corrective gene transfer in xeroderma pigmentosum human skin stem cells.Architecture of the human XPC DNA repair and stem cell coactivator complex.Dissection of the molecular defects caused by pathogenic mutations in the DNA repair factor XPC.Xeroderma pigmentosum complementation group C protein (XPC) serves as a general sensor of damaged DNA.A human XPC protein interactome--a resourceXeroderma pigmentosum group C protein interacts with histones: regulation by acetylated states of histone H3.SUMOylation of xeroderma pigmentosum group C protein regulates DNA damage recognition during nucleotide excision repair.Molecular mechanism of global genome nucleotide excision repair.Paracrine regulation of melanocyte genomic stability: a focus on nucleotide excision repair.Comparative analysis of interaction of human and yeast DNA damage recognition complexes with damaged DNA in nucleotide excision repair.Regulation of DNA demethylation by the XPC DNA repair complex in somatic and pluripotent stem cells.Enhanced spontaneous DNA twisting/bending fluctuations unveiled by fluorescence lifetime distributions promote mismatch recognition by the Rad4 nucleotide excision repair complex.Chromatin remodeler CHD1 promotes XPC-to-TFIIH handover of nucleosomal UV lesions in nucleotide excision repair.Xeroderma pigmentosum: man deprived of his right to light.
P2860
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P2860
Biochemical and structural domain analysis of xeroderma pigmentosum complementation group C protein.
description
2006 nî lūn-bûn
@nan
2006 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Biochemical and structural dom ...... mplementation group C protein.
@ast
Biochemical and structural dom ...... mplementation group C protein.
@en
type
label
Biochemical and structural dom ...... mplementation group C protein.
@ast
Biochemical and structural dom ...... mplementation group C protein.
@en
prefLabel
Biochemical and structural dom ...... mplementation group C protein.
@ast
Biochemical and structural dom ...... mplementation group C protein.
@en
P2093
P2860
P356
P1433
P1476
Biochemical and structural dom ...... mplementation group C protein.
@en
P2093
Brian E Fuller
Christopher G Bunick
Ellen Fanning
Michael R Miller
Walter J Chazin
P2860
P304
14965-14979
P356
10.1021/BI061370O
P407
P577
2006-12-01T00:00:00Z