Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/50701
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dc.contributor.authorS. Moonchaien_US
dc.contributor.authorY. Lenburyen_US
dc.contributor.authorW. Triampoen_US
dc.date.accessioned2018-09-04T04:44:29Z-
dc.date.available2018-09-04T04:44:29Z-
dc.date.issued2010-12-01en_US
dc.identifier.issn17924863en_US
dc.identifier.other2-s2.0-79958719755en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79958719755&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/50701-
dc.description.abstractCellular automata simulation approach has become well known as a useful technique to investigate complex biomedical systems in situations where traditional methodologies are difficult or too costly to employ. So far, relatively simple cellular automata models have been proposed to simulate the dynamics of HIV infection in human. Most cellular automata models only considered viral proliferation in the lymph node. However, most clinical indications of AIDS progression are based on blood data, because these data are most easily obtained. Since viral population circulates between lymph node and plasma, viral load in the two compartments are important for the description of HIV infection dynamics. We present here cellular automata simulations of a two-compartment model of HIV proliferation with delay.en_US
dc.subjectComputer Scienceen_US
dc.titleMultiple latticed cellular automata: HIV dynamics in coupled lymph node and peripheral blood compartmentsen_US
dc.typeConference Proceedingen_US
article.title.sourcetitleInternational Conference on Applied Computer Science - Proceedingsen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsSouth Carolina Commission on Higher Educationen_US
Appears in Collections:CMUL: Journal Articles

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