pubmed-article:15932636 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:15932636 | lifeskim:mentions | umls-concept:C0012191 | lld:lifeskim |
pubmed-article:15932636 | lifeskim:mentions | umls-concept:C0132555 | lld:lifeskim |
pubmed-article:15932636 | lifeskim:mentions | umls-concept:C0441655 | lld:lifeskim |
pubmed-article:15932636 | lifeskim:mentions | umls-concept:C0162615 | lld:lifeskim |
pubmed-article:15932636 | lifeskim:mentions | umls-concept:C1157325 | lld:lifeskim |
pubmed-article:15932636 | lifeskim:mentions | umls-concept:C0025980 | lld:lifeskim |
pubmed-article:15932636 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
pubmed-article:15932636 | lifeskim:mentions | umls-concept:C0851827 | lld:lifeskim |
pubmed-article:15932636 | lifeskim:mentions | umls-concept:C1701901 | lld:lifeskim |
pubmed-article:15932636 | pubmed:dateCreated | 2005-7-7 | lld:pubmed |
pubmed-article:15932636 | pubmed:abstractText | Diethylcarbamazine (DEC) has been used for many years in the treatment of human lymphatic filariasis. Its mode of action is not well understood, but it is known to interact with the arachidonic acid pathway. Here we have investigated the contribution of the nitric oxide and cyclooxygenase (COX) pathways to the activity of DEC against B. malayi microfilariae in mice. | lld:pubmed |
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pubmed-article:15932636 | pubmed:language | eng | lld:pubmed |
pubmed-article:15932636 | pubmed:status | PubMed-not-MEDLINE | lld:pubmed |
pubmed-article:15932636 | pubmed:author | pubmed-author:TaylorMark... | lld:pubmed |
pubmed-article:15932636 | pubmed:author | pubmed-author:PlantLeigh... | lld:pubmed |
pubmed-article:15932636 | pubmed:author | pubmed-author:McGarryHelen... | lld:pubmed |
pubmed-article:15932636 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:15932636 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:15932636 | pubmed:pagination | 4 | lld:pubmed |
pubmed-article:15932636 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
pubmed-article:15932636 | pubmed:articleTitle | Diethylcarbamazine activity against Brugia malayi microfilariae is dependent on inducible nitric-oxide synthase and the cyclooxygenase pathway. | lld:pubmed |
pubmed-article:15932636 | pubmed:affiliation | Filariasis Research Laboratory, Molecular and Biochemical Parasitology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK. hfcross@liverpool.ac.uk | lld:pubmed |
pubmed-article:15932636 | pubmed:publicationType | Journal Article | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15932636 | lld:pubmed |