pubmed-article:21235533 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C1006305 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C0567416 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C0205462 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C0007009 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C0014072 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C0220912 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C1708528 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C0220913 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:21235533 | lifeskim:mentions | umls-concept:C0533932 | lld:lifeskim |
pubmed-article:21235533 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:21235533 | pubmed:dateCreated | 2011-2-9 | lld:pubmed |
pubmed-article:21235533 | pubmed:abstractText | We have evaluated the effects of the carbon monoxide-releasing molecule CORM-A1 [Na(2) (BH(3) CO(2) ); ALF421] on the development of relapsing-remitting experimental allergic encephalomyelitis (EAE) in SJL mice, an established model of multiple sclerosis (MS). The data show that the prolonged prophylactic administration of CORM-A1 improves the clinical and histopathological signs of EAE, as shown by a reduced cumulative score, shorter duration and a lower cumulative incidence of the disease as well as milder inflammatory infiltrations of the spinal cords. This study suggests that the use of CORM-A1 might represent a novel therapeutic strategy for the treatment of multiple sclerosis. | lld:pubmed |
pubmed-article:21235533 | pubmed:language | eng | lld:pubmed |
pubmed-article:21235533 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21235533 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:21235533 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21235533 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21235533 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21235533 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21235533 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21235533 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21235533 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21235533 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21235533 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21235533 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:21235533 | pubmed:month | Mar | lld:pubmed |
pubmed-article:21235533 | pubmed:issn | 1365-2249 | lld:pubmed |
pubmed-article:21235533 | pubmed:author | pubmed-author:NicolettiFF | lld:pubmed |
pubmed-article:21235533 | pubmed:author | pubmed-author:MotterliniRR | lld:pubmed |
pubmed-article:21235533 | pubmed:author | pubmed-author:Di MarcoRR | lld:pubmed |
pubmed-article:21235533 | pubmed:author | pubmed-author:MagroGG | lld:pubmed |
pubmed-article:21235533 | pubmed:author | pubmed-author:QuattrocchiCC | lld:pubmed |
pubmed-article:21235533 | pubmed:author | pubmed-author:ManganoKK | lld:pubmed |
pubmed-article:21235533 | pubmed:author | pubmed-author:FagonePP | lld:pubmed |
pubmed-article:21235533 | pubmed:author | pubmed-author:PenachoNN | lld:pubmed |
pubmed-article:21235533 | pubmed:author | pubmed-author:RomaoC CCC | lld:pubmed |
pubmed-article:21235533 | pubmed:copyrightInfo | © 2011 The Authors. Clinical and Experimental Immunology © 2011 British Society for Immunology. | lld:pubmed |
pubmed-article:21235533 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:21235533 | pubmed:volume | 163 | lld:pubmed |
pubmed-article:21235533 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:21235533 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:21235533 | pubmed:pagination | 368-74 | lld:pubmed |
pubmed-article:21235533 | pubmed:dateRevised | 2011-8-26 | lld:pubmed |
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pubmed-article:21235533 | pubmed:meshHeading | pubmed-meshheading:21235533... | lld:pubmed |
pubmed-article:21235533 | pubmed:year | 2011 | lld:pubmed |
pubmed-article:21235533 | pubmed:articleTitle | Prevention of clinical and histological signs of proteolipid protein (PLP)-induced experimental allergic encephalomyelitis (EAE) in mice by the water-soluble carbon monoxide-releasing molecule (CORM)-A1. | lld:pubmed |
pubmed-article:21235533 | pubmed:affiliation | Department of Biomedical Sciences, School of Medicine, University of Catania, Italy. | lld:pubmed |
pubmed-article:21235533 | pubmed:publicationType | Journal Article | lld:pubmed |