Phenotype screening for genetically determined age-onset disorders and increased longevity in ENU-mutagenized mice.
Publication/Presentation Date
3-1-2005
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.
Volume
27
Issue
1
First Page
75
Last Page
90
ISSN
0161-9152
Published In/Presented At
Johnson, D. K., Rinchik, E. M., Moustaid-Moussa, N., Miller, D. R., Williams, R. W., Michaud, E. J., Jablonski, M. M., Elberger, A., Hamre, K., Smeyne, R., Chesler, E., & Goldowitz, D. (2005). Phenotype screening for genetically determined age-onset disorders and increased longevity in ENU-mutagenized mice. Age (Dordrecht, Netherlands), 27(1), 75–90. https://doi.org/10.1007/s11357-005-4131-3
Disciplines
Business Administration, Management, and Operations | Health and Medical Administration | Management Sciences and Quantitative Methods
PubMedID
23598606
Department(s)
Administration and Leadership
Document Type
Article