scispace - formally typeset
E

Emily O. Kerr

Researcher at University of Washington

Publications -  14
Citations -  2850

Emily O. Kerr is an academic researcher from University of Washington. The author has contributed to research in topics: Saccharomyces cerevisiae & Calorie restriction. The author has an hindex of 11, co-authored 14 publications receiving 2640 citations.

Papers
More filters
Journal ArticleDOI

Regulation of Yeast Replicative Life Span by TOR and Sch9 in Response to Nutrients

TL;DR: It is proposed that the TOR and Sch9 kinases define a primary conduit through which excess nutrient intake limits longevity in yeast.
Journal ArticleDOI

Yeast Life Span Extension by Depletion of 60S Ribosomal Subunits Is Mediated by Gcn4

TL;DR: It is shown that a specific reduction of 60S ribosomal subunit levels slows aging in yeast, and genetic epistasis analyses suggest that dietary restriction, reduced 60S subunit abundance, and Gcn4 activation extend yeast life span by similar mechanisms.
Journal ArticleDOI

A Comprehensive Analysis of Replicative Lifespan in 4,698 Single-Gene Deletion Strains Uncovers Conserved Mechanisms of Aging.

TL;DR: A systematic analysis of yeast RLS in a set of 4,698 viable single-gene deletion strains demonstrated a significant conservation in longevity pathways between yeast and C. elegans, and mechanisms of aging identified, deletion of tRNA exporter LOS1 robustly extended lifespan.
Journal ArticleDOI

Quantitative evidence for conserved longevity pathways between divergent eukaryotic species

TL;DR: Findings indicate that the genetic component of life span determination is significantly conserved between divergent eukaryotic species, and suggest pathways that are likely to play a similar role in mammalian aging.
Journal ArticleDOI

Increased life span due to calorie restriction in respiratory-deficient yeast.

TL;DR: It is demonstrated that respiration is not required for the longevity benefits of CR in yeast, and shows that nicotinamide inhibits life span extension by CR through a Sir2-independent mechanism, and suggests that CR acts through a conserved, Sir2 -independent mechanism in both PSY316 and BY4742.