Article
Dietary restriction fails to extend lifespan of Drosophila model of Werner syndrome.
G3 (Bethesda, Md.) - 7 May 2024
Sember Eileen, Chennakesavula Ranga, Beard Breanna, Opoola Mubaraq, Hwangbo Dae-Sung
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...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
