In vivo destabilization and functional defects of the xeroderma pigmentosum C protein caused by a pathogenic missense mutation
about
Structural basis of UV DNA-damage recognition by the DDB1-DDB2 complexA DNA repair complex functions as an Oct4/Sox2 coactivator in embryonic stem cellsTwo-stage dynamic DNA quality check by xeroderma pigmentosum group C protein.DGCR8 Mediates Repair of UV-Induced DNA Damage Independently of RNA Processing.In vitro functional effects of XPC gene rare variants from bladder cancer patients.The C/A polymorphism in intron 11 of the XPC gene plays a crucial role in the modulation of an individual's susceptibility to sporadic colorectal cancer.Regulation of nucleotide excision repair by UV-DDB: prioritization of damage recognition to internucleosomal DNAFunctional regulation of the DNA damage-recognition factor DDB2 by ubiquitination and interaction with xeroderma pigmentosum group C protein.Functional and mechanistic studies of XPC DNA-repair complex as transcriptional coactivator in embryonic stem cells.Potential risk of esophageal squamous cell carcinoma due to nucleotide excision repair XPA and XPC gene variants and their interaction among themselves and with environmental factors.Architecture of the human XPC DNA repair and stem cell coactivator complex.Xeroderma pigmentosum-variant patients from America, Europe, and Asia.XPC Lys939Gln polymorphism, smoking and risk of sporadic colorectal cancer among MalaysiansDissection of the molecular defects caused by pathogenic mutations in the DNA repair factor XPC.XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptomsXeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis-Cacchione Syndrome and a Novel XPC Mutation.Xeroderma 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.Regulation of DNA demethylation by the XPC DNA repair complex in somatic and pluripotent stem cells.ASH1L histone methyltransferase regulates the handoff between damage recognition factors in global-genome nucleotide excision repair.An association between XPC Lys939Gln polymorphism and the risk of bladder cancer: a meta-analysis.
P2860
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P2860
In vivo destabilization and functional defects of the xeroderma pigmentosum C protein caused by a pathogenic missense mutation
description
2007 nî lūn-bûn
@nan
2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
In vivo destabilization and fu ...... a pathogenic missense mutation
@ast
In vivo destabilization and fu ...... a pathogenic missense mutation
@en
In vivo destabilization and fu ...... pathogenic missense mutation.
@nl
type
label
In vivo destabilization and fu ...... a pathogenic missense mutation
@ast
In vivo destabilization and fu ...... a pathogenic missense mutation
@en
In vivo destabilization and fu ...... pathogenic missense mutation.
@nl
prefLabel
In vivo destabilization and fu ...... a pathogenic missense mutation
@ast
In vivo destabilization and fu ...... a pathogenic missense mutation
@en
In vivo destabilization and fu ...... pathogenic missense mutation.
@nl
P2093
P2860
P356
P1476
In vivo destabilization and fu ...... a pathogenic missense mutation
@en
P2093
Donata Orioli
Eriko Watanabe
Fumio Hanaoka
Gentaro Yasuda
Kaoru Sugasawa
Miria Stefanini
Ryotaro Nishi
Shigenori Iwai
Toshio Mori
P2860
P304
P356
10.1128/MCB.02166-06
P407
P577
2007-08-06T00:00:00Z