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Recurrent noncoding mutations in skin cancers: UV damage susceptibility or repair inhibition as primary driver?
Somatic mutations arising in human skin cancers are heterogeneously distributed across the genome, meaning that certain genomic regions (e.g., heterochromatin or transcription factor binding sites) have much higher mutation densities than others. Regional variations in mutation rates are typically n...
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| Vydáno v: | Bioessays |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6571124/ https://ncbi.nlm.nih.gov/pubmed/30801747 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bies.201800152 |
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