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Cockayne syndrome group B protein has novel strand annealing and exchange activities
Cockayne syndrome (CS) is a rare inherited human genetic disorder characterized by UV sensitivity, severe neurological abnormalities and prageroid symptoms. The CS complementation group B (CSB) protein is involved in UV-induced transcription coupled repair (TCR), base excision repair and general tra...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2006
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1331990/ https://ncbi.nlm.nih.gov/pubmed/16410611 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkj410 |
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