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Drosophila as a Model Organism to Understand the Effects during Development of TFIIH-Related Human Diseases
Human mutations in the transcription and nucleotide excision repair (NER) factor TFIIH are linked with three human syndromes: xeroderma pigmentosum (XP), trichothiodystrophy (TTD) and Cockayne syndrome (CS). In particular, different mutations in the XPB, XPD and p8 subunits of TFIIH may cause one or...
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| Gepubliceerd in: | Int J Mol Sci |
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| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
MDPI
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7013941/ https://ncbi.nlm.nih.gov/pubmed/31963603 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21020630 |
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