PfEMP1-DBL1 amino acid motifs in severe disease states of Plasmodium falciparum malaria-Reference-Cited by-同舟云学术

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PfEMP1-DBL1 amino acid motifs in severe disease states of Plasmodium falciparum malaria

Published:2007-09-25 Issue:40 Volume:104 Page:15835-15840
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Normark J.,Nilsson D.,Ribacke U.,Winter G.,Moll K.,Wheelock C. E.,Bayarugaba J.,Kironde F.,Egwang T. G.,Chen Q.,Andersson B.,Wahlgren M.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference38 articles.

1. Malaria Pathogenesis

2. Genome sequence of the human malaria parasite Plasmodium falciparum

3. Cloning the P. falciparum gene encoding PfEMP1, a malarial variant antigen and adherence receptor on the surface of parasitized human erythrocytes

4. Switches in expression of plasmodium falciparum var genes correlate with changes in antigenic and cytoadherent phenotypes of infected erythrocytes

5. The large diverse gene family var encodes proteins involved in cytoadherence and antigenic variation of plasmodium falciparum-infected erythrocytes

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1. Identification of novel PfEMP1 variants containing domain cassettes 11, 15 and 8 that mediate thePlasmodium falciparumvirulence-associated rosetting phenotype;2024-07-22

2. Genotyping var Gene DBL1α Domain of Severe and Non-severe Plasmodium falciparum Patients;Indian Journal of Microbiology;2024-02-06

3. Measuring changes inPlasmodium falciparumcensus population size in response to sequential malaria control interventions;2023-05-19

4. Neutral vs. non-neutral genetic footprints of Plasmodium falciparum multiclonal infections;PLOS Computational Biology;2023-01-03

5. Bayesian estimation of community size and overlap from random subsamples;PLOS Computational Biology;2022-09-19

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