| Literature DB >> 23598606 |
Dabney K Johnson1, Eugene M Rinchik, Naima Moustaid-Moussa, Darla R Miller, Robert W Williams, Edward J Michaud, Monica M Jablonski, Andrea Elberger, Kristen Hamre, Richard Smeyne, Elissa Chesler, Daniel Goldowitz.
Abstract
With the goal of discovering genes that contribute to late-onset neurological and ocular disorders and also genes that extend the healthy life span in mammals, we are phenotyping mice carrying new mutations induced by the chemical N-ethyl-N-nitrosourea (ENU). The phenotyping plan includes basic behavioral, neurohistological, and vision testing in sibling cohorts of mice aged to 18 months, and then evaluation for markers of growth trajectory and stress response in these same cohorts aged up to 28 months. Statistical outliers are identified by comparison to test results of similar aged cohorts, and potential mutants are recovered for re-aging to confirm heritability of the phenotype.Entities:
Keywords: ENU mutations; age-onset; longevity; neurological disorders; phenotype-screening
Year: 2005 PMID: 23598606 PMCID: PMC3456097 DOI: 10.1007/s11357-005-4131-3
Source DB: PubMed Journal: Age (Dordr) ISSN: 0161-9152