Differential stem cell aging kinetics in Hutchinson-Gilford progeria syndrome and Werner syndrome
Abstract 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...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , , , , , , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Oxford University Press
2018-02-01
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| Cyfres: | Protein & Cell |
| Pynciau: | |
| Mynediad Ar-lein: | http://link.springer.com/article/10.1007/s13238-018-0517-8 |
| Tagiau: |
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
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