Article
Dietary Restriction Fails to Extend Lifespan of <i>Drosophila</i> Model of Werner Syndrome
2023-09-22
Abstract excerpt
Werner syndrome (WS) is a rare genetic disease in humans, caused by mutations in the WRN gene that encodes a protein containing helicase and exonuclease domains. WS is characterized by symptoms of accelerated aging in multiple tissues and organs, involving increased risk of cancer, heart failure, and metabolic dysfunction. These conditions ultimately lead to the premature mortality of patients with WS. In this st...
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Identifiers and source
- Literature Corpus work
- 689e2a86-122f-548e-b147-bb91d4575a29
- DOI
- 10.1101/2023.09.20.558691
