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dc.contributor.authorCrispim, Marcell-
dc.date.accessioned2023-09-18T04:27:40Z-
dc.date.available2023-09-18T04:27:40Z-
dc.date.issued2023-
dc.identifier.otherOER000002316vi
dc.identifier.urihttp://dlib.hust.edu.vn/handle/HUST/23158-
dc.description.abstractPlasmodium falciparum causes the most severe form of human malaria, a parasitic disease with a high global burden. In 2021, the World Health Organization reported an estimated 247 million cases of malaria and 619,000 malaria-related deaths, with the majority occurring among children and pregnant women in Sub-Saharan Africa. In 2021, 96% of all malaria-related deaths occurred in this region. Resistance to current antimalarial drugs is a significant challenge for malaria control, leading to increased morbidity and mortality (WHO, 2022). Therefore, the identification and development of novel antimalarial therapies are urgently needed.vi
dc.description.urihttps://www.biorxiv.org/content/10.1101/2023.07.17.549440v1.full.pdf+htmlvi
dc.formatPDFvi
dc.language.isoenvi
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Vietnam*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/vn/*
dc.subjectký sinh trùngvi
dc.subjectsốt rétvi
dc.subjectPrenolvi
dc.subjectgeranylgeraniolvi
dc.subjectsinh tổng hợpvi
dc.subjectprenylation proteinvi
dc.subject.lccRA644vi
dc.titleBeyond the MEP Pathway: a novel kinase required for prenol utilization by malaria parasitesvi
dc.typeJournal Articlevi
dc.description.noteCC-BY-4.0vi
Appears in Collections:OER - Kỹ thuật hóa học; Công nghệ sinh học - Thực phẩm; Công nghệ môi trường

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