Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH
about
Dynamic interaction of TTDA with TFIIH is stabilized by nucleotide excision repair in living cellsDistinct regions of MAT1 regulate cdk7 kinase and TFIIH transcription activitiesXPD gene polymorphism and host characteristics in the association with cutaneous malignant melanoma riskConformational effects of a common codon 751 polymorphism on the C-terminal domain of the xeroderma pigmentosum D proteinA yeast four-hybrid system identifies Cdk-activating kinase as a regulator of the XPD helicase, a subunit of transcription factor IIHNucleotide excision repair of DNA with recombinant human proteins: definition of the minimal set of factors, active forms of TFIIH, and modulation by CAKSubunit architecture of general transcription factor TFIIHThe carboxy terminus of the small subunit of TFIIE regulates the transition from transcription initiation to elongation by RNA polymerase IIStimulation of the XPB ATP-dependent helicase by the beta subunit of TFIIEABCC5, ERCC2, XPA and XRCC1 transcript abundance levels correlate with cisplatin chemoresistance in non-small cell lung cancer cell linesPolymorphisms in human DNA repair genes and head and neck squamous cell carcinomaCrystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPDThe Structure of the TFIIH p34 Subunit Reveals a Von Willebrand Factor A Like FoldArchitecture of the RNA polymerase II preinitiation complex and mechanism of ATP-dependent promoter opening.Double-stranded DNA translocase activity of transcription factor TFIIH and the mechanism of RNA polymerase II open complex formation.Plasmodium falciparum XPD translocates in 5' to 3' direction, is expressed throughout the blood stages, and interacts with p44A meta-analysis of XPD/ERCC2 Lys751Gln polymorphism and melanoma susceptibilityEnzymatic activities and DNA substrate specificity of Mycobacterium tuberculosis DNA helicase XPBStructural insights into transcription initiation by RNA polymerase II.Transcriptional regulation of the TFIIH transcription repair components XPB and XPD by the hepatitis B virus x protein in liver cells and transgenic liver tissue.Architecture of the Human and Yeast General Transcription and DNA Repair Factor TFIIHOther proteins interacting with XP proteins.ERCC2, ERCC1 polymorphisms and haplotypes, cooking oil fume and lung adenocarcinoma risk in Chinese non-smoking femalesThe effect of XPD polymorphisms on digestive tract cancers risk: a meta-analysisBoth XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients.Phosphorylation of steroidogenic factor 1 is mediated by cyclin-dependent kinase 7Ten years of TFIIH.Dysregulation of the peroxisome proliferator-activated receptor target genes by XPD mutationsMutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH.Restoration of nucleotide excision repair in a helicase-deficient XPD mutant from intragenic suppression by a trichothiodystrophy mutationEctodermal dysplasias: not only 'skin' deep.Potentially functional polymorphisms in the ERCC2 gene and risk of esophageal squamous cell carcinoma in Chinese populations.On the traces of XPD: cell cycle matters - untangling the genotype-phenotype relationship of XPD mutationsStrand- and site-specific DNA lesion demarcation by the xeroderma pigmentosum group D helicase.Associations between XPD Asp312Asn polymorphism and risk of head and neck cancer: a meta-analysis based on 7,122 subjects.In TFIIH, XPD helicase is exclusively devoted to DNA repairPolymorphisms in the DNA repair gene ERCC2/XPD and breast cancer risk: a HapMap-based case-control study among Han Women in a Chinese less-developed areaThe 14th Datta Lecture. TFIIH: from transcription to clinic.Dynamic partnership between TFIIH, PGC-1α and SIRT1 is impaired in trichothiodystrophy.HCMV-infected cells maintain efficient nucleotide excision repair of the viral genome while abrogating repair of the host genome.
P2860
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P2860
Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH
description
1998 nî lūn-bûn
@nan
1998 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Mutations in the XPD helicase ...... D and the p44 subunit of TFIIH
@ast
Mutations in the XPD helicase ...... D and the p44 subunit of TFIIH
@en
Mutations in the XPD helicase ...... D and the p44 subunit of TFIIH
@nl
type
label
Mutations in the XPD helicase ...... D and the p44 subunit of TFIIH
@ast
Mutations in the XPD helicase ...... D and the p44 subunit of TFIIH
@en
Mutations in the XPD helicase ...... D and the p44 subunit of TFIIH
@nl
prefLabel
Mutations in the XPD helicase ...... D and the p44 subunit of TFIIH
@ast
Mutations in the XPD helicase ...... D and the p44 subunit of TFIIH
@en
Mutations in the XPD helicase ...... D and the p44 subunit of TFIIH
@nl
P2860
P50
P356
P1433
P1476
Mutations in the XPD helicase ...... D and the p44 subunit of TFIIH
@en
P2093
A M Pedrini
J C Marinoni
P2860
P2888
P356
10.1038/2491
P407
P577
1998-10-01T00:00:00Z