Abstract
Single gene mutations that extend lifespan have drastically changed ageing research because they offer potential answers to the questions of why and how we age. Mutations that lower activity of the insulin and insulin-like growth factor signalling (IIS) pathways extend the lifespan of worms, flies and mice. It is possible, therefore, to learn about human ageing from the conserved features of these long-lived models. Here, we summarise the available data in this light.
Original language | English |
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Pages (from-to) | 249-256 |
Number of pages | 8 |
Journal | Drug Discovery Today: Disease Models |
Volume | 2 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2005 |
Externally published | Yes |