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Salivary glands during Plasmodium berghei infection
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2020-04-07
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Additional file 1 of Human plasma plasminogen internalization route in Plasmodium falciparum-infected erythrocytes
Additional file 1: Table S1. List of all proteins detected in immunoprecipitation followed by mass spectrometry analyses, with number of peptides (unique and total) and the sum intensity of any given
Figshare2020-08-27 更新60
Comparing transcrional changes in Plasmodium yoelii infected to uninfected primary hepatocytes. Comparing transcrional changes in Plasmodium yoelii infected to uninfected primary hepatocytes
GFP expressing Plasmodium yoelii (Py-GFP) infected, or naïve cultured primary hepatocytes were FACS sorted and re-suspended in TRIzol and RNA purified with RNAeasy kit (Qiagen).RNA was assessed for pu
NIAID Data Ecosystem40
DataSheet1_Absence of PEXEL-Dependent Protein Export in Plasmodium Liver Stages Cannot Be Restored by Gain of the HSP101 Protein Translocon ATPase.pdf
Host cell remodeling is critical for successful Plasmodium replication inside erythrocytes and achieved by targeted export of parasite-encoded proteins. In contrast, during liver infection the malaria
NIAID Data Ecosystem30
Highly Dynamic Host Actin Reorganization around Developing Plasmodium Inside Hepatocytes
Plasmodium sporozoites are transmitted by Anopheles mosquitoes and infect hepatocytes, where a single sporozoite replicates into thousands of merozoites inside a parasitophorous vacuole. The nature of
NIAID Data Ecosystem50
Plasmodium sporozoites require the protein B9 to invade hepatocytes
Here we report that the B9 protein, a member of the 6-cysteine domain protein family, is secreted from sporozoite micronemes and is required for productive invasion of hepatocytes.
NIAID Data Ecosystem30
