Gene expression profiling in Werner syndrome closely resembles that of normal aging
Werner syndrome (WS) is a premature aging disorder, displaying defects in DNA replication, recombination, repair, and transcription. It has been hypothesized that several WS phenotypes are secondary consequences of aberrant gene expression and that a transcription defect may be crucial to the develo...
Uloženo v:
| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2003
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC218746/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/14527998/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.2130723100 |
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