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dc.contributor.authorCupit, PM
dc.contributor.authorSteinauer, ML
dc.contributor.authorTonnessen, BW
dc.contributor.authorEric Agola, L
dc.contributor.authorKinuthia, JM
dc.contributor.authorMwangi, IN
dc.contributor.authorMutuku, MW
dc.contributor.authorMkoji, GM
dc.contributor.authorLoker, ES
dc.contributor.authorCunningham, C
dc.date.accessioned2013-10-11T09:20:49Z
dc.date.available2013-10-11T09:20:49Z
dc.date.issued2011
dc.identifier.citationInt J Parasitol. 2011 Oct;41(12):1249-52en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/21889508
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/57594
dc.description.abstractA vaccine against schistosomiasis would contribute significantly to reducing the 3-70 million disability-adjusted life years lost annually to the disease. Towards this end, inoculation with the large extracellular loop (EC-2) of Schistosoma mansoni tetraspanin-2 protein (Sm-TSP-2) has proved effective in reducing worm and egg burdens in S. mansoni-infected mice. The EC-2 loop of Schistosoma japonicum TSP-2, however, has been found to be highly polymorphic, perhaps diminishing the likelihood that this antigen can be used for vaccination against this species. Here, we examine polymorphism of the EC-2 of Sm-TSP-2 in genetically unique worms derived from six individuals from Kisumu, Kenya.en
dc.language.isoenen
dc.publisherElsevieren
dc.titlePolymorphism associated with the Schistosoma mansoni tetraspanin-2 gene.en
dc.typeArticleen
local.publisherCenter for Evolutionary and Theoretical Immunology, Department of Biology, University of New Mexico, Albuquerque, NM 87131, USA.en


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