How a Mutation that Slows Aging Can Also Disproportionately Extend End-of-Life Decrepitude

Cell Reports

Volumn 19, Issue 3, 2017, Pages 441-450

  Podshivalova, Katie ^a,b   Kerr, Rex A ^a,b   Kenyon, Cynthia ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b Calico Life Sciences LLC   (United States)

Author keywords

aging; daf 2; healthspan; IGF 1; lifespan; mortality; pathogenesis

Indexed keywords

GENTAMICIN; CAENORHABDITIS ELEGANS PROTEIN;

ADULT; AGED; AGING; ALLELE; ANIMAL EXPERIMENT; ANTIBACTERIAL ACTIVITY; ARTICLE; BACILLUS SUBTILIS; BACTERIAL COLONIZATION; CAENORHABDITIS ELEGANS; CONTROLLED STUDY; DAF 2 GENE; DEATH; GENE; GENE MUTATION; INFECTION RESISTANCE; JUVENILE ANIMAL; LIFE EXTENSION; MIDDLE AGED; MUTANT; NONHUMAN; PHENOTYPE; SURVIVAL; WILD TYPE; YOUNG ADULT; ANIMAL; BACTERIAL COUNT; ESCHERICHIA COLI; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; MICROBIOLOGY; MUTATION; PHYSIOLOGY; RISK FACTOR;

AGING; ANIMALS; CAENORHABDITIS ELEGANS; CAENORHABDITIS ELEGANS PROTEINS; COLONY COUNT, MICROBIAL; ESCHERICHIA COLI; MUTATION; RISK FACTORS;

EID: 85017619071     PISSN: None     EISSN: 22111247     Source Type: Journal    
DOI: 10.1016/j.celrep.2017.03.062     Document Type: Article

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