scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1011936703 |
P356 | DOI | 10.1038/NG0695-188 |
P953 | full work available online at | https://repub.eur.nl/pub/54884/REPUB_54884_OA.pdf |
http://www.nature.com/articles/ng0695-188 | ||
http://www.nature.com/articles/ng0695-188.pdf | ||
P698 | PubMed publication ID | 7663514 |
P5875 | ResearchGate publication ID | 15534672 |
P50 | author | Jean-Marc Egly | Q3167372 |
Michele K. Evans | Q55426351 | ||
Vincent Moncollin | Q62669679 | ||
Laurent Schaeffer | Q88523164 | ||
P2093 | author name string | Z. Wang | |
R. Roy | |||
X. W. Wang | |||
H. Yeh | |||
J. M. Egly | |||
E. C. Freidberg | |||
B. G. Taffe | |||
P2860 | cites work | Cancer Research | Q326097 |
Wild-type p53 binds to the TATA-binding protein and represses transcription | Q24300991 | ||
A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome | Q24306514 | ||
p44 and p34 subunits of the BTF2/TFIIH transcription factor have homologies with SSL1, a yeast protein involved in DNA repair | Q24315493 | ||
DNA helicase activity of SV40 large tumor antigen | Q24531720 | ||
Specific association between the human DNA repair proteins XPA and ERCC1 | Q24563058 | ||
The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor | Q24595611 | ||
Binding of basal transcription factor TFIIH to the acidic activation domains of VP16 and p53 | Q24609153 | ||
The gadd and MyD genes define a novel set of mammalian genes encoding acidic proteins that synergistically suppress cell growth | Q24613548 | ||
Analysis of the accuracy and implications of simple methods for predicting the secondary structure of globular proteins | Q27860987 | ||
WAF1, a potential mediator of p53 tumor suppression | Q27861121 | ||
ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes | Q28213725 | ||
Prediction of protein conformation | Q28240456 | ||
Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II | Q28251866 | ||
p53 transcriptional activation mediated by coactivators TAFII40 and TAFII60 | Q28304820 | ||
Mice with DNA repair gene (ERCC-1) deficiency have elevated levels of p53, liver nuclear abnormalities and die before weaning | Q28587990 | ||
Allosteric activation of latent p53 tetramers | Q28623087 | ||
Transcription factors IIE and IIH and ATP hydrolysis direct promoter clearance by RNA polymerase II | Q28646845 | ||
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours | Q29547697 | ||
The p21 inhibitor of cyclin-dependent kinases controls DNA replication by interaction with PCNA | Q29615251 | ||
A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia | Q29615437 | ||
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms | Q29618586 | ||
DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor | Q29619833 | ||
Wild-type p53 induces apoptosis of myeloid leukaemic cells that is inhibited by interleukin-6 | Q29622924 | ||
Analysis of a protein-binding domain of p53 | Q33292314 | ||
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 Pigmentosum | Q34054000 | ||
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 ERCC3 | Q35101216 | ||
DNA excision-repair defect of xeroderma pigmentosum prevents removal of a class of oxygen free radical-induced base lesions | Q36407505 | ||
Endogenous p53 protein generated from wild-type alternatively spliced p53 RNA in mouse epidermal cells | Q36647653 | ||
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 gene | Q36767352 | ||
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 function | Q38307435 | ||
Regulation of the specific DNA binding function of p53 | Q38324290 | ||
Alternatively spliced forms in the carboxy-terminal domain of the p53 protein regulate its ability to promote annealing of complementary single strands of nucleic acids | Q40021667 | ||
Mammalian membrane-bound adenylyl cyclases | Q40565005 | ||
p53-catalyzed annealing of complementary single-stranded nucleic acids | Q40873109 | ||
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 cells | Q41358143 | ||
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 donor | Q41564882 | ||
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome | Q41816411 | ||
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 antigen | Q46840212 | ||
Mouse p53 inhibits SV40 origin-dependent DNA replication | Q46905586 | ||
Localization of p53, retinoblastoma and host replication proteins at sites of viral replication in herpes-infected cells | Q59057697 | ||
A new superfamily of replicative proteins | Q59069349 | ||
Altered cell cycle arrest and gene amplification potential accompany loss of wild-type p53 | Q67521108 | ||
Xeroderma pigmentosum complementation group H falls into complementation group D | Q68016717 | ||
Anti-oncogene product p53 binds DNA helicase | Q72798169 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | DNA repair | Q210538 |
tumor protein p53 | Q283350 | ||
ERCC excision repair 2, TFIIH core complex helicase subunit | Q426168 | ||
ERCC excision repair 3, TFIIH core complex helicase subunit | Q426194 | ||
TFII transcription factors | Q78125363 | ||
P304 | page(s) | 188-95 | |
P577 | publication date | 1995-06-01 | |
P1433 | published in | Nature Genetics | Q976454 |
P1476 | title | p53 modulation of TFIIH-associated nucleotide excision repair activity | |
p53 modulation of TFIIH–associated nucleotide excision repair activity | |||
P478 | volume | 10 |