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Yeast RAD2, a homolog of human XPG, plays a key role in the regulation of the cell cycle and actin dynamics
Mutations in the human XPG gene cause Cockayne syndrome (CS) and xeroderma pigmentosum (XP). Transcription defects have been suggested as the fundamental cause of CS; however, defining CS as a transcription syndrome is inconclusive. In particular, the function of XPG in transcription has not been cl...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Company of Biologists
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892158/ https://www.ncbi.nlm.nih.gov/pubmed/24326185 http://dx.doi.org/10.1242/bio.20136403 |