Data from: Evidence of functional divergence in MSP7 paralogous proteins: a molecular-evolutionary and phylogenetic analysis

负责人：

关键词：

P. berghei;P. vinckei;Functional Divergence;P. cynomolgi;P. chabaudi;episodic positive selection;P. vivax;P. knowlesi;Plasmodium;P. coatneyi;P. falciparum;P. gallinaceum;P. reichenowi;P. yoelii;multigene family;msp7;P. inui

DOI：

doi:10.5061/dryad.3qk84

摘要：

that some paralogous proteins have diverged functionally. Conclusions: Even though msp7 has mainly evolved in line with a birth-and-death evolution

Data from: Blood meal-induced inhibition of vector-borne disease by transgenic microbiota

负责人：

关键词：

Anopheles stephensi;Plasmodium berghei;Asaia bogorensis;vector;malaria;mosquito;paratransgenesis

DOI：

doi:10.5061/dryad.s85j284

摘要：

Anopheles stephensi was engineered to produce an antiplasmodial effector causing the mosquito to become refractory to Plasmodium berghei. The midgut symbiont Asaia

Data from: Costs of crowding for the transmission potential in malaria parasites

负责人：

关键词：

Plasmodium berghei;life history strategies;Virulence;vector borne disease;fitness costs;programmed cell death;disease transmission;Density Dependence

DOI：

doi:10.5061/dryad.44jf2

摘要：

of rodent malaria (Plasmodium berghei) infections in Anopheles stephensi mosquitoes under different environmental conditions, we show that parasites exper

Antimalarial activity, toxicity, pharmacokinetics and metabolic drug interaction of Plumbago Indica linn.

负责人：

Kesara Na-Bangchang, Advisor

关键词：

Plumbagin Antimalarial Plasmodium falciparum Plasmodium berghei Permeability Transport Efflux transporters Caco-2 cell P-glycoprotein Pharmacokinetics

DOI：

doi:10.14457/tu.the.2015.159

摘要：

(270-490) nM, respectively. In vivo antimalarial activity was investigated in Plasmodium berghei infected mouse model. Chloroquine exhibited the mos