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DNA Repair and Transcriptional Effects of Mutations in TFIIH in Drosophila Development
Mutations in XPB and XPD TFIIH helicases have been related with three hereditary human disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. The dual role of TFIIH in DNA repair and transcription makes it difficult to discern which of the mutant TFIIH phenotypes is due to def...
Gorde:
| Egile Nagusiak: | , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
The American Society for Cell Biology
2002
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC124156/ https://ncbi.nlm.nih.gov/pubmed/12221129 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E02-02-0087 |
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