Resistance to therapy in mature palmerston north mice treated with cyclophosphamide or hydrocortisone sodium succinate
dc.contributor.author | Walker, Sara Ellen | en_US |
dc.contributor.author | Schnitzer, Bertram | en_US |
dc.date.accessioned | 2006-04-28T16:22:24Z | |
dc.date.available | 2006-04-28T16:22:24Z | |
dc.date.issued | 1980-05 | en_US |
dc.identifier.citation | Walker, Sara Ellen; Schnitzer, Bertram (1980)."Resistance to therapy in mature palmerston north mice treated with cyclophosphamide or hydrocortisone sodium succinate." Arthritis & Rheumatism 23(5): 539-544. <http://hdl.handle.net/2027.42/37745> | en_US |
dc.identifier.issn | 0004-3591 | en_US |
dc.identifier.issn | 1529-0131 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/37745 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6966498&dopt=citation | en_US |
dc.description.abstract | Inbred Palmerston North (PN) mice are a newly reconized model of systemic lupus erythematosus.In this study PN mice with established autoimmune disease were treated until death with cyclophosphamide (8 mg/kg/day) or hydrocortisone (10 mg/kg/day). These doses had previously been found to prevent or suppress disease in another lupus model, the NZB/NZW mouse. In the PN strain, autoantibodies, severity of glomerulo-nephritis, and longevity were not influenced by treatment. Furthermore, the incidence of neoplasms was not increased in PN mice receiving prolonged therapy with immunosuppressive drugs. Unlike NZB/NZW mice, PN mice were resistant to the effects of cyclophomide and hydrocortisone. | en_US |
dc.format.extent | 555225 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | John Wiley & Sons, Inc. | en_US |
dc.subject.other | Life and Medical Sciences | en_US |
dc.subject.other | Rheumatology | en_US |
dc.title | Resistance to therapy in mature palmerston north mice treated with cyclophosphamide or hydrocortisone sodium succinate | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Geriatrics | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | University of Michigan Medical School, Ann Arbor, Michigan. ; R4633 Kresge I Research Building, 1405 East Ann Street,. Ann Arbor MI 48109 | en_US |
dc.contributor.affiliationum | University of Michigan Medical School, Ann Arbor, Michigan. | en_US |
dc.identifier.pmid | 6966498 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/37745/1/1780230504_ftp.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1002/art.1780230504 | en_US |
dc.identifier.source | Arthritis & Rheumatism | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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