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dc.contributor.authorCox-Singh, J
dc.contributor.authorMahayet, S
dc.contributor.authorAbdullah, MS
dc.contributor.authorSingh, B
dc.date.accessioned2013-06-19T09:16:13Z
dc.date.available2013-06-19T09:16:13Z
dc.date.issued1997-12
dc.identifier.citationInt J Parasitol. 1997 Dec;27(12):1575-7en
dc.identifier.urihttp://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/9467744
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/36187
dc.description.abstractMalaria remains a disease of underdeveloped and remote regions of the world. The application of polymerase chain reaction (PCR) technology to malaria epidemiology has the potential for increasing our knowledge and understanding of this disease. In order to study malaria in all geographical locations it is important that specimen collection and DNA extraction for PCR be kept simple. Here we report a method for extracting DNA from dried blood spots on filter paper which is capable of detecting one Plasmodium falciparum and two Plasmodium vivax parasites/microliter of whole blood by nested PCR without compromising the simplicity of specimen collection or DNA extraction.en
dc.language.isoenen
dc.publisherUniversity of Nairobien
dc.subjectmalaria; PCR; field epidemiology; Plasmodiumen
dc.titleIncreased sensitivity of malaria detection by nested polymerase chain reaction using simple sampling and DNA extractionen
dc.typeArticleen
local.publisherSchool of medicine,University of Nairobien
local.publisherSchool of Medical Sciences, University of Science Malaysiaen


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