| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/EMBOJ/16.5.1093 |
| P8608 | Fatcat ID | release_hhrjrf7xbrbmzc77zjwuiqwhuq |
| P932 | PMC publication ID | 1169708 |
| P698 | PubMed publication ID | 9118947 |
| P5875 | ResearchGate publication ID | 14099272 |
| P50 | author | Jan Hoeijmakers | Q15820773 |
| P2093 | author name string | Egly JM | |
| Gomez DM | |||
| Lutz Y | |||
| Marinoni JC | |||
| Miniou P | |||
| Roy R | |||
| Seroz T | |||
| Vermeulen W | |||
| Weeda G | |||
| P2860 | cites work | In vitro assembly of a functional human CDK7-cyclin H complex requires MAT1, a novel 36 kDa RING finger protein | Q24310168 |
| p44 and p34 subunits of the BTF2/TFIIH transcription factor have homologies with SSL1, a yeast protein involved in DNA repair | Q24315493 | ||
| Cloning, expression and subcellular localization of the human homolog of p40MO15 catalytic subunit of cdk-activating kinase | Q24324537 | ||
| MAT1, cdk7 and cyclin H form a kinase complex which is UV light-sensitive upon association with TFIIH | Q24563127 | ||
| The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor | Q24595611 | ||
| Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome | Q24672295 | ||
| Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3 | Q24673129 | ||
| Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes | Q27860600 | ||
| CpG islands in vertebrate genomes | Q27861045 | ||
| The yeast TFB1 and SSL1 genes, which encode subunits of transcription factor IIH, are required for nucleotide excision repair and RNA polymerase II transcription | Q27934367 | ||
| Relationship of CDK-activating kinase and RNA polymerase II CTD kinase TFIIH/TFIIK | Q28243206 | ||
| A novel cyclin associates with MO15/CDK7 to form the CDK-activating kinase | Q28247022 | ||
| Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II | Q28251866 | ||
| Localization of the xeroderma pigmentosum group B-correcting gene ERCC3 to human chromosome 2q21 | Q28307621 | ||
| Identification and characterization of a spinal muscular atrophy-determining gene | Q29547495 | ||
| Mapping of single-copy DNA sequences on human chromosomes by in situ hybridization with biotinylated probes: enhancement of detection sensitivity by intensified-fluorescence digital-imaging microscopy | Q33831874 | ||
| Cloning of the 62-kilodalton component of basic transcription factor BTF2. | Q34338584 | ||
| Genes encoding general initiation factors for RNA polymerase II transcription are dispersed in the human genome | Q34339774 | ||
| Human xeroderma pigmentosum group D gene encodes a DNA helicase | Q34358690 | ||
| MAT1 ('menage à trois') a new RING finger protein subunit stabilizing cyclin H-cdk7 complexes in starfish and Xenopus CAK. | Q37623860 | ||
| Repair synthesis by human cell extracts in DNA damaged by cis- and trans-diamminedichloroplatinum(II). | Q40538207 | ||
| A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy. | Q40540731 | ||
| DNA repair and transcription | Q41044019 | ||
| Cyclin-dependent kinase 7: at the cross-roads of transcription, DNA repair and cell cycle control? | Q41066914 | ||
| TFIIH: a key component in multiple DNA transactions | Q41099885 | ||
| Three Unusual Repair Deficiencies Associated with Transcription Factor BTF2(TFIIH): Evidence for the Existence of a Transcription Syndrome | Q41506150 | ||
| The DNA-dependent ATPase activity associated with the class II basic transcription factor BTF2/TFIIH. | Q42475790 | ||
| The MO15 cell cycle kinase is associated with the TFIIH transcription-DNA repair factor | Q42494377 | ||
| Subunits of yeast RNA polymerase II transcription factor TFIIH encoded by the CCL1 gene. | Q46027437 | ||
| Putative nuclear localization signals (NLS) in protein transcription factors | Q46347791 | ||
| Regional Localization of the XRCC4 Human Radiation Repair Gene | Q55064541 | ||
| Genomic structure of the human TATA-box-binding protein (TBP) | Q63707022 | ||
| Purification and interaction properties of the human RNA polymerase B(II) general transcription factor BTF2 | Q68041082 | ||
| Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19 | Q69362984 | ||
| DNA repair. Engagement with transcription | Q70683866 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA repair | Q210538 |
| General transcription factor IIH subunit 4 | Q21122192 | ||
| P304 | page(s) | 1093-1102 | |
| P577 | publication date | 1997-03-01 | |
| P1433 | published in | The EMBO Journal | Q1278554 |
| P1476 | title | Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH | |
| P478 | volume | 16 |
| Q28140055 | Activation of p53 or loss of the Cockayne syndrome group B repair protein causes metaphase fragility of human U1, U2, and 5S genes |
| Q39578554 | Adenovirus type 12-induced fragility of the human RNU2 locus requires p53 function. |
| Q41066042 | Affinity purification of human DNA repair/transcription factor TFIIH using epitope-tagged xeroderma pigmentosum B protein |
| Q39808790 | Cell cycle arrest and apoptosis provoked by UV radiation-induced DNA damage are transcriptionally highly divergent responses |
| Q39745562 | DNA damage and toxicogenomic analyses of hydrogen sulfide in human intestinal epithelial FHs 74 Int cells. |
| Q36881305 | DNA damage recognition by XPA protein promotes efficient recruitment of transcription factor II H. |
| Q48235478 | Deletion analysis in Turkish patients with spinal muscular atrophy |
| Q41059665 | Dynamics of the Extended String-Like Interaction of TFIIE with the p62 Subunit of TFIIH |
| Q27938329 | Genes for Tfb2, Tfb3, and Tfb4 subunits of yeast transcription/repair factor IIH. Homology to human cyclin-dependent kinase activating kinase and IIH subunits |
| Q36070191 | Genetic variants in DNA repair genes as potential predictive markers for oxaliplatin chemotherapy in colorectal cancer |
| Q32060809 | Genomic organization and promoter characterization of the mouse and human genes encoding p62 subunit of the transcription/DNA repair factor TFIIH. |
| Q73794909 | Human DNA repair genes |
| Q33536382 | Human DNA repair systems: an overview |
| Q24290465 | Human pre-mRNA cleavage factor II(m) contains homologs of yeast proteins and bridges two other cleavage factors |
| Q74326166 | Immunoaffinity purification of the human multisubunit transcription factor IIH |
| Q33890541 | Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH. |
| Q36226849 | Nucleotide excision repair |
| Q38835268 | Nucleotide excision repair and response and survival to chemotherapy in colorectal cancer patients |
| Q37700587 | Phosphorylation of XPB helicase regulates TFIIH nucleotide excision repair activity |
| Q28285490 | RNA polymerase II elongation complexes containing the Cockayne syndrome group B protein interact with a molecular complex containing the transcription factor IIH components xeroderma pigmentosum B and p62 |
| Q24644162 | Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes |
| Q50432469 | Ronin influences the DNA damage response in pluripotent stem cells. |
| Q27653533 | Structural basis for group A trichothiodystrophy |
| Q28142934 | Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder |
| Q24532143 | Substrate specificity of the cdk-activating kinase (CAK) is altered upon association with TFIIH |
| Q28581872 | TATA-Binding protein-interacting protein 120, TIP120, stimulates three classes of eukaryotic transcription via a unique mechanism |
| Q42521245 | TFIIH controls developmentally-regulated cell cycle progression as a holocomplex |
| Q28188877 | TFIIH inhibits CDK9 phosphorylation during human immunodeficiency virus type 1 transcription |
| Q40901956 | TFIIH with inactive XPD helicase functions in transcription initiation but is defective in DNA repair. |
| Q34286016 | The 14th Datta Lecture. TFIIH: from transcription to clinic |
| Q33887586 | The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex |
| Q33671306 | The RNA polymerase II general transcription factors: past, present, and future. |
| Q24336424 | The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor |
| Q52319133 | The essential and multi-functional TFIIH complex. |
| Q40982662 | The hematopoietic transcription factor SCL binds the p44 subunit of TFIIH. |
| Q35211264 | The molecular mechanism of mitotic inhibition of TFIIH is mediated by phosphorylation of CDK7. |
| Q33601019 | Transcription factor IIH: a key player in the cellular response to DNA damage |
| Q30661634 | 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 |
| Q33945643 | UVB induces a genome-wide acting negative regulatory mechanism that operates at the level of transcription initiation in human cells |
| Q24290089 | XAB2, a novel tetratricopeptide repeat protein involved in transcription-coupled DNA repair and transcription |
| Q50335569 | p52 Mediates XPB function within the transcription/repair factor TFIIH. |
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