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Differential stem cell aging kinetics in Hutchinson-Gilford progeria syndrome and Werner syndrome
Hutchinson-Gilford progeria syndrome (HGPS) and Werner syndrome (WS) are two of the best characterized human progeroid syndromes. HGPS is caused by a point mutation in lamin A (LMNA) gene, resulting in the production of a truncated protein product—progerin. WS is caused by mutations in WRN gene, enc...
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| Publicat a: | Protein Cell |
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| Autors principals: | , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Higher Education Press
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5876188/ https://ncbi.nlm.nih.gov/pubmed/29476423 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13238-018-0517-8 |
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