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Richard A. Miller,
M.D., Ph.D.
Miller's research work centers on problems in the genetics and cell biology of aging in mice. Special interests include: • analysis of genes and diets that increase life span in mice • studies of treatments that repair immune function in old age • relationship of cell stress resistance to extended life span in dwarf mice • biomarkers of aging rate Additional details may be found at the following URL: http://www-personal.umich.edu/~millerr/RAM_home_page.htm Recent Publications: Miller, R. A. 2002. Extending life: scientific prospects and political obstacles. Milbank Quarterly 80:155 – 174. Murakami, S., A. Salmon, and R. A. Miller. 2003. Multiplex stress resistance in cells from long-lived dwarf mice. FASEB Journal express article 10.1096/fj.02-1092fje. FASEB Journal 17: 1565-1566. Garcia, G. G., and R. A. Miller. 2003. Age-related defects in CD4+ T cell activation reversed by glycoprotein endopeptidase. European Journal of Immunology 33:3464 - 3472. Miller, R. A., J. M. Harper, A. Galecki, and D. T. Burke. 2002. Big mice die young: early-life body weight predicts longevity in genetically heterogeneous mice. Aging Cell 1: 22 - 29. Miller, R. A., Y. Chang, A. T. Galecki, K. Al-Regaiey, J. J. Kopchick, and
A. Bartke. 2002. Gene expression patterns in calorically restricted mice: partial
overlap with long-lived mutant mice. Molecular Endocrinology 16:2657-2666. |
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