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Distribution of Antibodies Specific to the 19-kDa and 33-kDa Fragments of |
Sylvatrie-Danne Dinzouna-Boutamba, Sanghyun Lee, Ui-Han Son, Su-Min Song, Hye Soo Yun, So-Young Joo, Dongmi Kwak, Man Hee Rhee, Dong-Il Chung, Yeonchul Hong, Youn-Kyoung Goo |
Osong Public Health Res Perspect. 2016;7(4):213-219. Published online August 31, 2016 DOI: https://doi.org/10.1016/j.phrp.2016.05.006 |
Distribution of Antibodies Specific to the 19-kDa and 33-kDa Fragments of Plasmodium vivax Merozoite Surface Protein 1 in Two Pathogenic Strains Infecting Korean Vivax Malaria Patients IgG isotype to C-terminal 19�kDa of Plasmodium vivax merozoite surface protein 1 among subjects with different levels of exposure to malaria in Brazil Origin of Two Most Virulent Agents of Human Malaria: Plasmodium falciparum and Plasmodium vivax Naturally Acquired Antibody Responses to Plasmodium vivax and Plasmodium falciparum Merozoite Surface Protein 1 (MSP1) C-Terminal 19 kDa Domains in an Area of Unstable Malaria Transmission in Southeast Asia Merozoite surface protein-3α is a reliable marker for population genetic analysis of Plasmodium vivax Immunogenicity of a plasmid DNA vaccine encoding 42 kDa fragment of Plasmodium vivax merozoite surface protein-1 Plasmodium vivax merozoite surface proteins-3β and-3γ share structural similarities with P. vivax merozoite surface protein-3α and define a new gene family Exploring novel therapeutic strategies against vivax malaria through an integrated computational investigation to inhibit the merozoite surface protein−1 of Plasmodium vivax Antigenic malaria protein derived from Plasmodium falciparum, Plasmodium vivax, Plasmodium ovalae or Plasmodium malariae Genetic Diversity and Natural Selection in 42 kDa Region of Plasmodium vivax Merozoite Surface Protein-1 from China-Myanmar Endemic Border |