p53 modulation of TFIIH–associated nucleotide excision repair activity

scientific article published on June 1, 1995

p53 modulation of TFIIH–associated nucleotide excision repair activity is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1011936703
P356DOI10.1038/NG0695-188
P953full work available online athttps://repub.eur.nl/pub/54884/REPUB_54884_OA.pdf
http://www.nature.com/articles/ng0695-188
http://www.nature.com/articles/ng0695-188.pdf
P698PubMed publication ID7663514
P5875ResearchGate publication ID15534672

P50authorJean-Marc EglyQ3167372
Michele K. EvansQ55426351
Vincent MoncollinQ62669679
Laurent SchaefferQ88523164
P2093author name stringZ. Wang
R. Roy
X. W. Wang
H. Yeh
J. M. Egly
E. C. Freidberg
B. G. Taffe
P2860cites workCancer ResearchQ326097
Wild-type p53 binds to the TATA-binding protein and represses transcriptionQ24300991
A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndromeQ24306514
p44 and p34 subunits of the BTF2/TFIIH transcription factor have homologies with SSL1, a yeast protein involved in DNA repairQ24315493
DNA helicase activity of SV40 large tumor antigenQ24531720
Specific association between the human DNA repair proteins XPA and ERCC1Q24563058
The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factorQ24595611
Binding of basal transcription factor TFIIH to the acidic activation domains of VP16 and p53Q24609153
The gadd and MyD genes define a novel set of mammalian genes encoding acidic proteins that synergistically suppress cell growthQ24613548
Analysis of the accuracy and implications of simple methods for predicting the secondary structure of globular proteinsQ27860987
WAF1, a potential mediator of p53 tumor suppressionQ27861121
ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genesQ28213725
Prediction of protein conformationQ28240456
Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase IIQ28251866
p53 transcriptional activation mediated by coactivators TAFII40 and TAFII60Q28304820
Mice with DNA repair gene (ERCC-1) deficiency have elevated levels of p53, liver nuclear abnormalities and die before weaningQ28587990
Allosteric activation of latent p53 tetramersQ28623087
Transcription factors IIE and IIH and ATP hydrolysis direct promoter clearance by RNA polymerase IIQ28646845
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumoursQ29547697
The p21 inhibitor of cyclin-dependent kinases controls DNA replication by interaction with PCNAQ29615251
A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasiaQ29615437
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasmsQ29618586
DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factorQ29619833
Wild-type p53 induces apoptosis of myeloid leukaemic cells that is inhibited by interleukin-6Q29622924
Analysis of a protein-binding domain of p53Q33292314
The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.Q33640104
Defective Repair Replication of DNA in Xeroderma PigmentosumQ34054000
Cloning of the 62-kilodalton component of basic transcription factor BTF2.Q34338584
p53 binds single-stranded DNA ends and catalyzes DNA renaturation and strand transfer.Q34972350
Hepatitis B virus X protein inhibits p53 sequence-specific DNA binding, transcriptional activity, and association with transcription factor ERCC3Q35101216
DNA excision-repair defect of xeroderma pigmentosum prevents removal of a class of oxygen free radical-induced base lesionsQ36407505
Endogenous p53 protein generated from wild-type alternatively spliced p53 RNA in mouse epidermal cellsQ36647653
Cloning and expression of the cDNA for E6-AP, a protein that mediates the interaction of the human papillomavirus E6 oncoprotein with p53.Q36660357
Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair geneQ36767352
Inhibition of DNA replication factor RPA by p53.Q36768122
Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair functionQ38307435
Regulation of the specific DNA binding function of p53Q38324290
Alternatively spliced forms in the carboxy-terminal domain of the p53 protein regulate its ability to promote annealing of complementary single strands of nucleic acidsQ40021667
Mammalian membrane-bound adenylyl cyclasesQ40565005
p53-catalyzed annealing of complementary single-stranded nucleic acidsQ40873109
Transfected mutant p53 gene increases X-ray-induced cell killing and mutation in human fibroblasts immortalized with 4-nitroquinoline 1-oxide but does not induce neoplastic transformation of the cellsQ41358143
Differential induction of transcriptionally active p53 following UV or ionizing radiation: defects in chromosome instability syndromes?Q41513765
Gain of function mutations in p53.Q41557652
Different cytotoxic and mutagenic responses induced by X-rays in two human lymphoblastoid cell lines derived from a single donorQ41564882
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndromeQ41816411
Wild-type p53 restores cell cycle control and inhibits gene amplification in cells with mutant p53 alleles.Q43918911
The murine p53 protein blocks replication of SV40 DNA in vitro by inhibiting the initiation functions of SV40 large T antigenQ46840212
Mouse p53 inhibits SV40 origin-dependent DNA replicationQ46905586
Localization of p53, retinoblastoma and host replication proteins at sites of viral replication in herpes-infected cellsQ59057697
A new superfamily of replicative proteinsQ59069349
Altered cell cycle arrest and gene amplification potential accompany loss of wild-type p53Q67521108
Xeroderma pigmentosum complementation group H falls into complementation group DQ68016717
Anti-oncogene product p53 binds DNA helicaseQ72798169
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectDNA repairQ210538
tumor protein p53Q283350
ERCC excision repair 2, TFIIH core complex helicase subunitQ426168
ERCC excision repair 3, TFIIH core complex helicase subunitQ426194
TFII transcription factorsQ78125363
P304page(s)188-95
P577publication date1995-06-01
P1433published inNature GeneticsQ976454
P1476titlep53 modulation of TFIIH-associated nucleotide excision repair activity
p53 modulation of TFIIH–associated nucleotide excision repair activity
P478volume10