Transcription Factor TFIIH
"Transcription Factor TFIIH" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A general transcription factor that is involved in basal GENETIC TRANSCRIPTION and NUCLEOTIDE EXCISION REPAIR. It consists of nine subunits including ATP-DEPENDENT DNA HELICASES; CYCLIN H; and XERODERMA PIGMENTOSUM GROUP D PROTEIN.
| Descriptor ID |
D051758
|
| MeSH Number(s) |
D12.776.260.775.875.875 D12.776.930.930.875.875
|
| Concept/Terms |
Transcription Factor TFIIH- Transcription Factor TFIIH
- TFIIH, Transcription Factor
- BTF2 Transcription Factor
- Transcription Factor, BTF2
- Transcription Factor BTF2
- BTF2, Transcription Factor
- Transcription Factor IIH
- Basic Transcription Factor 2
- TFIIH Transcription Factor
- Transcription Factor, TFIIH
|
Below are MeSH descriptors whose meaning is more general than "Transcription Factor TFIIH".
Below are MeSH descriptors whose meaning is more specific than "Transcription Factor TFIIH".
This graph shows the total number of publications written about "Transcription Factor TFIIH" by people in this website by year, and whether "Transcription Factor TFIIH" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 0 | 1 | 1 |
| 2007 | 0 | 1 | 1 |
| 2013 | 0 | 1 | 1 |
| 2015 | 0 | 1 | 1 |
| 2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Transcription Factor TFIIH" by people in Profiles.
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Genetic variant in DNA repair gene GTF2H4 is associated with lung cancer risk: a large-scale analysis of six published GWAS datasets in the TRICL consortium. Carcinogenesis. 2016 09; 37(9):888-896.
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Real-time observation of the initiation of RNA polymerase II transcription. Nature. 2015 Sep 10; 525(7568):274-7.
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Autophagy maturation associated with CD38-mediated regulation of lysosome function in mouse glomerular podocytes. J Cell Mol Med. 2013 Dec; 17(12):1598-607.
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Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells. Proc Natl Acad Sci U S A. 2013 Jan 15; 110(3):E212-20.
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New insights into the combined Cockayne/xeroderma pigmentosum complex: human XPG protein can function in transcription factor stability. Mol Cell. 2007 Apr 27; 26(2):162-4.
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Impairment of alveolar macrophage transcription in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2007 Jun 01; 175(11):1151-7.
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Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage. Mol Cell Biol. 2004 Dec; 24(24):10670-80.
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Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome. Mol Cell Biol. 2001 Apr; 21(7):2281-91.
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TFIIH with inactive XPD helicase functions in transcription initiation but is defective in DNA repair. J Biol Chem. 2000 Feb 11; 275(6):4258-66.
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Nucleotide excision repair of DNA with recombinant human proteins: definition of the minimal set of factors, active forms of TFIIH, and modulation by CAK. Genes Dev. 2000 Feb 01; 14(3):349-59.