review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0300-9084(99)80035-2 |
P698 | PubMed publication ID | 10214907 |
P2093 | author name string | Egly JM | |
Bergmann E | |||
Frit P | |||
P2860 | cites work | A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome | Q24306514 |
Cdk-activating kinase complex is a component of human transcription factor TFIIH | Q24306759 | ||
Isolation and characterization of two human transcription factor IIH (TFIIH)-related complexes: ERCC2/CAK and TFIIH | Q24309302 | ||
Human cyclin-dependent kinase-activating kinase exists in three distinct complexes | Q24309353 | ||
Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair | Q24312736 | ||
Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II | Q24314310 | ||
p44 and p34 subunits of the BTF2/TFIIH transcription factor have homologies with SSL1, a yeast protein involved in DNA repair | Q24315493 | ||
Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH | Q24315819 | ||
Cockayne syndrome group B protein enhances elongation by RNA polymerase II | Q24317053 | ||
Open complex formation around a lesion during nucleotide excision repair provides a structure for cleavage by human XPG protein | Q38348603 | ||
Reaction mechanism of human DNA repair excision nuclease | Q38359257 | ||
TATA binding protein discriminates between different lesions on DNA, resulting in a transcription decrease | Q39575189 | ||
Yeast RNA polymerase II transcription in vitro is inhibited in the presence of nucleotide excision repair: complementation of inhibition by Holo-TFIIH and requirement for RAD26. | Q39583863 | ||
RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair | Q39719255 | ||
Saccharomyces cerevisiae mms19 mutants are deficient in transcription-coupled and global nucleotide excision repair. | Q39721487 | ||
A three-step pathway of transcription initiation leading to promoter clearance at an activation RNA polymerase II promoter | Q40018556 | ||
The sensitivity of Cockayne's syndrome cells to DNA-damaging agents is not due to defective transcription-coupled repair of active genes | Q40019597 | ||
Dual requirement for the yeast MMS19 gene in DNA repair and RNA polymerase II transcription | Q40020418 | ||
The CDK7-cycH-p36 complex of transcription factor IIH phosphorylates p53, enhancing its sequence-specific DNA binding activity in vitro | Q40023550 | ||
An interaction between the Tfb1 and Ssl1 subunits of yeast TFIIH correlates with DNA repair activity | Q40393247 | ||
Phosphorylation of the C-terminal domain of RNA polymerase II. | Q40503251 | ||
Schizosaccharomyces pombe Mop1-Mcs2 is related to mammalian CAK. | Q40790211 | ||
The requirement for the basal transcription factor IIE is determined by the helical stability of promoter DNA. | Q40805836 | ||
The transcription-repair coupling factor CSA is required for efficient repair only during the elongation stages of RNA polymerase II transcription | Q41020602 | ||
Ultraviolet radiation-induced ubiquitination and proteasomal degradation of the large subunit of RNA polymerase II. Implications for transcription-coupled DNA repair | Q41056225 | ||
Relationships between DNA repair and transcription | Q41114776 | ||
Mammalian nucleotide excision repair and syndromes | Q41370274 | ||
Reconstitution of human DNA repair excision nuclease in a highly defined system | Q41370395 | ||
Three Unusual Repair Deficiencies Associated with Transcription Factor BTF2(TFIIH): Evidence for the Existence of a Transcription Syndrome | Q41506150 | ||
Nucleotide excision repair in mammalian cells | Q41593250 | ||
Regulation of CDK/cyclin complexes during the cell cycle | Q41639250 | ||
The p53 network | Q41673584 | ||
Multiple ATP-dependent steps in RNA polymerase II promoter melting and initiation | Q42172995 | ||
Is Cdk7/cyclin H/MAT1 the genuine cdk activating kinase in cycling Xenopus egg extracts? | Q42444931 | ||
The MO15 cell cycle kinase is associated with the TFIIH transcription-DNA repair factor | Q42494377 | ||
Promoter escape by RNA polymerase II. A role for an ATP cofactor in suppression of arrest by polymerase at promoter-proximal sites | Q42522949 | ||
SSL1, a suppressor of a HIS4 5'-UTR stem-loop mutation, is essential for translation initiation and affects UV resistance in yeast | Q44662542 | ||
Different forms of TFIIH for transcription and DNA repair: holo-TFIIH and a nucleotide excision repairosome | Q46391372 | ||
Alternative mechanisms of CAK assembly require an assembly factor or an activating kinase | Q46760600 | ||
Lethality in yeast of trichothiodystrophy (TTD) mutations in the human xeroderma pigmentosum group D gene. Implications for transcriptional defect in TTD. | Q52014722 | ||
DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall. | Q54455838 | ||
Structure and function of transcription-repair coupling factor. I. Structural domains and binding properties. | Q54615768 | ||
Molecular mechanism of transcription-repair coupling. | Q54659174 | ||
Transcription factor b (TFIIH) is required during nucleotide-excision repair in yeast | Q58318854 | ||
Genetic homogeneity between acute and chronic forms of spinal muscular atrophy | Q59092681 | ||
Specific interaction between the nonphosphorylated form of RNA polymerase II and the TATA-binding protein | Q68133927 | ||
The transcriptional elongation inhibitor 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole inhibits transcription factor IIH-associated protein kinase | Q71823410 | ||
Inhibition of Rad3 DNA helicase activity by DNA adducts and abasic sites: implications for the role of a DNA helicase in damage-specific incision of DNA | Q72941188 | ||
Cyclin-dependent kinase inhibitor p16INK4A inhibits phosphorylation of RNA polymerase II by general transcription factor TFIIH | Q74263600 | ||
Lack of transcription-coupled repair of acetylaminofluorene DNA adducts in human fibroblasts contrasts their efficient inhibition of transcription | Q74567408 | ||
Genes for Tfb2, Tfb3, and Tfb4 subunits of yeast transcription/repair factor IIH. Homology to human cyclin-dependent kinase activating kinase and IIH subunits | Q27938329 | ||
KIN28 encodes a C-terminal domain kinase that controls mRNA transcription in Saccharomyces cerevisiae but lacks cyclin-dependent kinase-activating kinase (CAK) activity | Q27938422 | ||
Reconstitution of TFIIH and requirement of its DNA helicase subunits, Rad3 and Rad25, in the incision step of nucleotide excision repair | Q27940170 | ||
Reconstitution of yeast nucleotide excision repair with purified Rad proteins, replication protein A, and transcription factor TFIIH. | Q27940221 | ||
ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes | Q28213725 | ||
The general transcription-repair factor TFIIH is recruited to the excision repair complex by the XPA protein independent of the TFIIE transcription factor | Q28235620 | ||
Association of Cdk-activating kinase subunits with transcription factor TFIIH | Q28236002 | ||
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 | ||
The guanylyltransferase domain of mammalian mRNA capping enzyme binds to the phosphorylated carboxyl-terminal domain of RNA polymerase II | Q28267712 | ||
A human RNA polymerase II complex associated with SRB and DNA-repair proteins | Q28276653 | ||
Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH | Q28285305 | ||
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 | Q28285490 | ||
Requirement for TFIIH kinase activity in transcription by RNA polymerase II | Q28289887 | ||
The general transcription factors of RNA polymerase II | Q28298663 | ||
The C-terminal domain of RNA polymerase II couples mRNA processing to transcription | Q28301744 | ||
A mammalian RNA polymerase II holoenzyme containing all components required for promoter-specific transcription initiation | Q28569992 | ||
The C-terminal domain of the largest subunit of RNA polymerase II interacts with a novel set of serine/arginine-rich proteins | Q28570708 | ||
5'-Capping enzymes are targeted to pre-mRNA by binding to the phosphorylated carboxy-terminal domain of RNA polymerase II | Q28623635 | ||
Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template | Q28628394 | ||
Recycling of the general transcription factors during RNA polymerase II transcription | Q28646829 | ||
Transcription factors IIE and IIH and ATP hydrolysis direct promoter clearance by RNA polymerase II | Q28646845 | ||
A role for TFIIH in controlling the activity of early RNA polymerase II elongation complexes | Q28646872 | ||
DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor | Q29619833 | ||
Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene | Q30054509 | ||
The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA. | Q33640104 | ||
Repression of TFIIH transcriptional activity and TFIIH-associated cdk7 kinase activity at mitosis | Q33772499 | ||
Regulation of CDK7 substrate specificity by MAT1 and TFIIH. | Q33886335 | ||
The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex | Q33887586 | ||
A kinase-deficient transcription factor TFIIH is functional in basal and activated transcription | Q34295542 | ||
An RNA polymerase II transcription factor has an associated DNA-dependent ATPase (dATPase) activity strongly stimulated by the TATA region of promoters | Q34306436 | ||
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions. | Q34419163 | ||
Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein | Q24317182 | ||
A 3' --> 5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription | Q24320802 | ||
ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3 | Q24321908 | ||
A serine/arginine-rich nuclear matrix cyclophilin interacts with the C-terminal domain of RNA polymerase II | Q24322515 | ||
The XPB and XPD DNA helicases are components of the p53-mediated apoptosis pathway | Q24336089 | ||
The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor | Q24336424 | ||
p53 modulation of TFIIH–associated nucleotide excision repair activity | Q24336880 | ||
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH | Q24336968 | ||
Substrate specificity of the cdk-activating kinase (CAK) is altered upon association with TFIIH | Q24532143 | ||
Cockayne syndrome: defective repair of transcription? | Q24532391 | ||
Three transitions in the RNA polymerase II transcription complex during initiation | Q24532893 | ||
Factors associated with the mammalian RNA polymerase II holoenzyme | Q24546284 | ||
TFIIH-mediated nucleotide excision repair and initiation of mRNA transcription in an optimized cell-free DNA repair and RNA transcription assay | Q24548165 | ||
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 | ||
mRNA capping enzyme is recruited to the transcription complex by phosphorylation of the RNA polymerase II carboxy-terminal domain | Q24602633 | ||
UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells | Q24605185 | ||
Binding of basal transcription factor TFIIH to the acidic activation domains of VP16 and p53 | Q24609153 | ||
p53 is phosphorylated by CDK7-cyclin H in a p36MAT1-dependent manner | Q24643993 | ||
Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes | Q24644162 | ||
Cell cycle analysis of the activity, subcellular localization, and subunit composition of human CAK (CDK-activating kinase) | Q24673102 | ||
RAD25 is a DNA helicase required for DNA repair and RNA polymerase II transcription | Q27930190 | ||
Civ1 (CAK in vivo), a novel Cdk-activating kinase | Q27930216 | ||
Nucleotide excision repair in yeast is mediated by sequential assembly of repair factors and not by a pre-assembled repairosome | Q27930912 | ||
The Cdk-activating kinase (CAK) from budding yeast. | Q27932735 | ||
The KIN28 gene is required both for RNA polymerase II mediated transcription and phosphorylation of the Rpb1p CTD. | Q27932917 | ||
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 | ||
A cyclin-dependent kinase-activating kinase (CAK) in budding yeast unrelated to vertebrate CAK. | Q27935027 | ||
Transcription factor TFIIH and DNA endonuclease Rad2 constitute yeast nucleotide excision repair factor 3: implications for nucleotide excision repair and Cockayne syndrome | Q27935884 | ||
RAD26, the yeast homolog of human Cockayne's syndrome group B gene, encodes a DNA-dependent ATPase | Q27936827 | ||
DNA repair deficiencies associated with mutations in genes encoding subunits of transcription initiation factor TFIIH in yeast | Q34594438 | ||
Reduced RNA polymerase II transcription in extracts of cockayne syndrome and xeroderma pigmentosum/Cockayne syndrome cells | Q34636040 | ||
Cdk7 is essential for mitosis and for in vivo Cdk-activating kinase activity. | Q35190030 | ||
The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA | Q35907237 | ||
Reduced RNA polymerase II transcription in intact and permeabilized Cockayne syndrome group B cells | Q36128504 | ||
A functional interaction between the carboxy-terminal domain of RNA polymerase II and pre-mRNA splicing | Q36254478 | ||
Splicing factors associate with hyperphosphorylated RNA polymerase II in the absence of pre-mRNA | Q36254517 | ||
Transitions in the coupling of transcription and nucleotide excision repair within RNA polymerase II-transcribed genes of Saccharomyces cerevisiae | Q36300531 | ||
Transcription-dependent redistribution of the large subunit of RNA polymerase II to discrete nuclear domains | Q36382489 | ||
TFIIH functions in regulating transcriptional elongation by RNA polymerase II in Xenopus oocytes | Q36560509 | ||
Mammalian DNA nucleotide excision repair reconstituted with purified protein components. | Q36697936 | ||
Sequence-specific and domain-specific DNA repair in xeroderma pigmentosum and Cockayne syndrome cells | Q36875627 | ||
DNA damage recognition by XPA protein promotes efficient recruitment of transcription factor II H. | Q36881305 | ||
Mechanism of open complex and dual incision formation by human nucleotide excision repair factors | Q36888668 | ||
Characterization of reaction intermediates of human excision repair nuclease. | Q36889922 | ||
RAD25 (SSL2), the yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential for viability | Q37323177 | ||
MAT1 ('menage à trois') a new RING finger protein subunit stabilizing cyclin H-cdk7 complexes in starfish and Xenopus CAK. | Q37623860 | ||
Identification of a cdk-activating kinase in fission yeast. | Q37626433 | ||
Escherichia coli mfd mutant deficient in "mutation frequency decline" lacks strand-specific repair: in vitro complementation with purified coupling factor | Q37653163 | ||
Yeast nucleotide excision repair proteins Rad2 and Rad4 interact with RNA polymerase II basal transcription factor b (TFIIH) | Q38307487 | ||
Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repair | Q38313225 | ||
Cisplatin- and UV-damaged DNA lure the basal transcription factor TFIID/TBP. | Q38339920 | ||
Rig2, a RING finger protein that interacts with the Kin28/Ccl1 CTD kinase in yeast | Q38343781 | ||
Model for XPC-independent transcription-coupled repair of pyrimidine dimers in humans | Q38347606 | ||
P433 | issue | 1-2 | |
P921 | main subject | DNA damage | Q5205747 |
P304 | page(s) | 27-38 | |
P577 | publication date | 1999-01-01 | |
P1433 | published in | Biochimie | Q2904035 |
P1476 | title | Transcription factor IIH: a key player in the cellular response to DNA damage | |
P478 | volume | 81 |