| scholarly article | Q13442814 |
| P356 | DOI | 10.1101/SQB.1994.059.01.036 |
| P953 | full work available at URL | https://syndication.highwire.org/content/doi/10.1101/SQB.1994.059.01.036 |
| P698 | PubMed publication ID | 7587084 |
| P50 | author | Laurent Schaeffer | Q88523164 |
| P2093 | author name string | G. Weeda | |
| A. R. Lehmann | |||
| C. F. Arlett | |||
| W. Vermeulen | |||
| N. G. Jaspers | |||
| E. Appeldoorn | |||
| A. Priestley | |||
| A. J. van Vuuren | |||
| M. Chipoulet | |||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA repair | Q210538 |
| TFII transcription factors | Q78125363 | ||
| P304 | page(s) | 317-329 | |
| P577 | publication date | 1994-01-01 | |
| P1433 | published in | Cold Spring Harbor Symposia on Quantitative Biology | Q15758412 |
| P1476 | title | Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome | |
| Three Unusual Repair Deficiencies Associated with Transcription Factor BTF2(TFIIH): Evidence for the Existence of a Transcription Syndrome | |||
| P478 | volume | 59 |
| Q24320802 | A 3' --> 5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription |
| Q28593147 | A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy |
| Q35238380 | A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy |
| Q28268795 | A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A |
| Q29014018 | A summary of mutations in the UV-sensitive disorders: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy |
| Q40606632 | A temperature-sensitive disorder in basal transcription and DNA repair in humans |
| Q41066042 | Affinity purification of human DNA repair/transcription factor TFIIH using epitope-tagged xeroderma pigmentosum B protein |
| Q92368881 | Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype |
| Q38336695 | Biochemical and biological characterization of wild-type and ATPase-deficient Cockayne syndrome B repair protein. |
| Q33601073 | Cancer from the outside, aging from the inside: mouse models to study the consequences of defective nucleotide excision repair |
| Q38339920 | Cisplatin- and UV-damaged DNA lure the basal transcription factor TFIID/TBP. |
| Q24315819 | Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH |
| Q24290499 | Cloning of a human homolog of the yeast nucleotide excision repair gene MMS19 and interaction with transcription repair factor TFIIH via the XPB and XPD helicases |
| Q24317053 | Cockayne syndrome group B protein enhances elongation by RNA polymerase II |
| Q24532391 | Cockayne syndrome: defective repair of transcription? |
| Q40826799 | Codominance associated with overexpression of certain XPD mutations |
| Q40427785 | DNA Repair: Nucleotide excision–repair in the test tube |
| Q41044019 | DNA repair and transcription |
| Q42513863 | Defective dendritic cell maturation in a child with nucleotide excision repair deficiency and CD4 lymphopenia. |
| Q28585729 | Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition |
| Q28302894 | Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G |
| Q35881437 | Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy |
| Q73377896 | Distinct roles for the helicases of TFIIH in transcript initiation and promoter escape |
| Q36690915 | Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage? |
| Q77407700 | From a DNA helicase to brittle hair |
| Q48784329 | From xeroderma pigmentosum to the biological clock contributions of Dirk Bootsma to human genetics |
| Q24683411 | Functional TFIIH is required for UV-induced translocation of CSA to the nuclear matrix |
| Q22008765 | Genomic organization and promoter characterization of two human UHS keratin genes |
| Q36935665 | Global regulation of promoter melting in naive lymphocytes |
| Q34330548 | Hot news: temperature-sensitive humans explain hereditary disease |
| Q34568150 | How nucleotide excision repair protects against cancer |
| Q28507519 | Hypermutation of immunoglobulin genes in memory B cells of DNA repair-deficient mice |
| Q35147361 | Identification and localization of a neuron-specific isoform of TAF1 in rat brain: implications for neuropathology of DYT3 dystonia |
| Q24563127 | MAT1, cdk7 and cyclin H form a kinase complex which is UV light-sensitive upon association with TFIIH |
| Q36888668 | Mechanism of open complex and dual incision formation by human nucleotide excision repair factors |
| Q27936483 | Molecular cloning and characterization of Saccharomyces cerevisiae RAD28, the yeast homolog of the human Cockayne syndrome A (CSA) gene |
| Q60585118 | Neurodegenerative disease and the repair of oxidatively damaged DNA |
| Q37308518 | Nucleic acid binding activity of human Cockayne syndrome B protein and identification of Ca(2+) as a novel metal cofactor |
| Q36541663 | Nucleotide excision repair and cancer |
| Q24609992 | Nucleotide excision repair of DNA with recombinant human proteins: definition of the minimal set of factors, active forms of TFIIH, and modulation by CAK |
| Q33601014 | Nucleotide excision repair: from E. coli to man. |
| Q28205658 | Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome |
| Q33333583 | Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy |
| Q36240837 | Photocarcinogenesis and inhibition of intercellular adhesion molecule 1 expression in cells of DNA-repair-defective individuals |
| Q52533287 | Rad26, the yeast homolog of the cockayne syndrome B gene product, counteracts inhibition of DNA repair due to RNA polymerase II transcription. |
| Q51841369 | Rapid switching of TFIIH between RNA polymerase I and II transcription and DNA repair in vivo. |
| Q35677795 | Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism |
| Q34012637 | Restoration of nucleotide excision repair in a helicase-deficient XPD mutant from intragenic suppression by a trichothiodystrophy mutation |
| Q40470920 | Restoring DNA repair capacity of cells from three distinct diseases by XPD gene-recombinant adenovirus. |
| Q24678938 | Retracted: A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function |
| Q31116972 | Scanning confocal fluorescence microscopy for single molecule analysis of nucleotide excision repair complexes |
| Q43029877 | Single-stranded DNA binding activity of XPBI, but not XPBII, from Sulfolobus tokodaii causes double-stranded DNA melting |
| Q33951430 | Slowly progressing nucleotide excision repair in trichothiodystrophy group A patient fibroblasts. |
| 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 |
| Q40901956 | TFIIH with inactive XPD helicase functions in transcription initiation but is defective in DNA repair. |
| Q34428876 | TTDA: big impact of a small protein |
| Q33887586 | The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex |
| Q24336424 | The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor |
| Q64387883 | The genetics of the hereditary xeroderma pigmentosum syndrome |
| Q33750326 | The molecular pathways of ultraviolet-induced carcinogenesis |
| Q36882150 | The role of Cockayne Syndrome group B (CSB) protein in base excision repair and aging. |
| Q33601019 | Transcription factor IIH: a key player in the cellular response to DNA damage |
| Q37353465 | Transcription syndromes and the role of RNA polymerase II general transcription factors in human disease |
| Q38332883 | Transcriptional profiles of unirradiated or UV-irradiated human cells expressing either the cancer-prone XPB/CS allele or the noncancer-prone XPB/TTD allele. |
| Q41928252 | Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissue |
| Q24291198 | Trichothiodystrophy, a transcription syndrome |
| Q77910521 | UV-induced mutations and skin cancer: how important is the link? |
| Q24605185 | UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells |
| Q35548058 | UVB-induced mutations in human key gatekeeper genes governing signalling pathways and consequences for skin tumourigenesis |
| Q33892830 | Variability in nucleotide excision repair and cancer risk: a review |
| Q36553351 | Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene. |
| Q30974742 | Xeroderma pigmentosum group A protein loads as a separate factor onto DNA lesions |
| Q42491460 | p44/SSL1, the regulatory subunit of the XPD/RAD3 helicase, plays a crucial role in the transcriptional activity of TFIIH. |
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