Transcription Factor TFIID
"Transcription Factor TFIID" 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.
The major sequence-specific DNA-binding component involved in the activation of transcription of RNA POLYMERASE II. It was originally described as a complex of TATA-BOX BINDING PROTEIN and TATA-BINDING PROTEIN ASSOCIATED FACTORS. It is now know that TATA BOX BINDING PROTEIN-LIKE PROTEINS may take the place of TATA-box binding protein in the complex.
| Descriptor ID |
D035362
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| MeSH Number(s) |
D12.776.260.775.875.750 D12.776.930.930.875.750
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Transcription Factor TFIID".
Below are MeSH descriptors whose meaning is more specific than "Transcription Factor TFIID".
This graph shows the total number of publications written about "Transcription Factor TFIID" by people in this website by year, and whether "Transcription Factor TFIID" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Transcription Factor TFIID" by people in Profiles.
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Aneichyk T, Hendriks WT, Yadav R, Shin D, Gao D, Vaine CA, Collins RL, Domingo A, Currall B, Stortchevoi A, Multhaupt-Buell T, Penney EB, Cruz L, Dhakal J, Brand H, Hanscom C, Antolik C, Dy M, Ragavendran A, Underwood J, Cantsilieris S, Munson KM, Eichler EE, Acu?a P, Go C, Jamora RDG, Rosales RL, Church DM, Williams SR, Garcia S, Klein C, M?ller U, Wilhelmsen KC, Timmers HTM, Sapir Y, Wainger BJ, Henderson D, Ito N, Weisenfeld N, Jaffe D, Sharma N, Breakefield XO, Ozelius LJ, Bragg DC, Talkowski ME. Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly. Cell. 2018 02 22; 172(5):897-909.e21.
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Sediv? A, Smith CI, Asplund AC, Hadac J, Janda A, Zeman J, Hans?kov? H, Dvor?kov? L, Mr?zov? L, Velbri S, Koehler C, Roesch K, Sullivan KE, Futatani T, Ochs HD. Contiguous X-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes. J Clin Immunol. 2007 Nov; 27(6):640-6.