Nucleolar localization of the Werner syndrome protein in human cells
Werner Syndrome (WS) is a human genetic disorder with many features of premature aging. The gene defective in WS (WRN) has been cloned and encodes a protein homologous to several helicases, including Escherichia coli RecQ, the human Bloom syndrome protein (BLM), and Saccharomyces cerevisiae Sgs1p. T...
Na minha lista:
| Publicado no: | Proc Natl Acad Sci U S A |
|---|---|
| Principais autores: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
1998
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC22674/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9618508/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.95.12.6887 |
| Tags: |
Sem tags, seja o primeiro a adicionar uma tag!
|