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Cellular and Biochemical Changes in the Aging Mouse Immune System
dc.contributor.authorMiller, Richard A.en_US
dc.date.accessioned2010-06-01T21:58:32Z
dc.date.available2010-06-01T21:58:32Z
dc.date.issued1995-04en_US
dc.identifier.citationMiller, Richard A. (1995). "Cellular and Biochemical Changes in the Aging Mouse Immune System." Nutrition Reviews 53(4): S8-S17. <http://hdl.handle.net/2027.42/75006>en_US
dc.identifier.issn0029-6643en_US
dc.identifier.issn1753-4887en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/75006
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7644159&dopt=citationen_US
dc.format.extent829197 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights1995 International Life Sciences Instituteen_US
dc.titleCellular and Biochemical Changes in the Aging Mouse Immune Systemen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMedicine (General)en_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationuma Professor of Pathology and the Associate Director for Research at the Geriatric Center, University of Michigan, Ann Arbor, MI 48109, USA.en_US
dc.identifier.pmid7644159en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/75006/1/j.1753-4887.1995.tb01521.x.pdf
dc.identifier.doi10.1111/j.1753-4887.1995.tb01521.xen_US
dc.identifier.sourceNutrition Reviewsen_US
dc.identifier.citedreferenceFlurkey K, Stadecker M, Miller RA. Memory T lymphocyte hyporesponsiveness to non-cognate stimuli: a key factor in age-related immunodeficiency. Eur J Immunol 1992; 22: 931 – 5.en_US
dc.identifier.citedreferencePhilosophe B, Miller RA. Diminished calcium signal generation in subsets of T lymphocytes that predominate in old mice. J Gerontol 1992; 57: B87 – 93.en_US
dc.identifier.citedreferenceWitkowski JM, Li SP, Gorgas G, Miller RA. Extrusion of the P-glycoprotein substrate rhodamine–123 distinguishes CD4 memory T cell subsets that differ in IL-2 driven IL-4 production. J Immunol 1994; 153: 658 – 65.en_US
dc.identifier.citedreferenceMiller RA, Turke C, Ruger J, et al. Age-sensitive T cell phenotypes covary in genetically heterogeneous mice and predict early death from lymphoma. J Gerontol, in press.en_US
dc.identifier.citedreferenceLerner A, Yamada T, Miller RA. Pgp-1hi T lymphocytes accumulate with age in mice and respond poorly to concanavalin A. Eur J Immunol 1989; 19: 977 – 82.en_US
dc.identifier.citedreferenceMiller RA, Jacobson B, Weil G, Simon ER. Diminished calcium influx in lectin-stimulated T cells from old mice. J Cell Physiol 1987; 132: 337 – 42.en_US
dc.identifier.citedreferenceShi J, Miller RA. Tyrosine-specific protein phosphorylation in response to anti-CD3 antibody is diminished in old mice. J Gerontol 1992; 47: B147 – 53.en_US
dc.identifier.citedreferencePhilosophe B, Miller RA. T lymphocyte heterogeneity in old and young mice: functional defects in T cells selected for poor calcium signal generation. Eur J Immunol 1989; 19: 695 – 9.en_US
dc.identifier.citedreferenceShi J, Miller RA. Differential tyrosine-specific protein phosphorylation in mouse T lymphocyte subsets. Effect of age. J Immunol 1993; 151: 730 – 9.en_US
dc.identifier.citedreferenceWitkowski JM, Miller RA. Increased function of P-glycoprotein in T lymphocyte subsets of aging mice. J Immunol 1993; 150: 1296 – 306.en_US
dc.identifier.citedreferenceLi SP, Miller RA. Age-associated decline in IL-4 production by murine T lymphocytes in extended culture. Cell Immunol 1993; 151: 187 – 95.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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