Progression of Plasmodium berghei through Anopheles stephensi is density-dependent. - Test2 - elhamkhani - TriplyDB

Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

http://www.wikidata.org/entity/Q33312856

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Activation of Akt signaling reduces the prevalence and intensity of malaria parasite infection and lifespan in Anopheles stephensi mosquitoes An antibody against an Anopheles albimanus midgut myosin reduces Plasmodium berghei oocyst development Climate, environmental and socio-economic change: weighing up the balance in vector-borne disease transmission MAPK ERK signaling regulates the TGF-beta1-dependent mosquito response to Plasmodium falciparum Existing Infection Facilitates Establishment and Density of Malaria Parasites in Their Mosquito Vector Pivotal and distinct role for Plasmodium actin capping protein alpha during blood infection of the malaria parasite Vital role for the Plasmodium actin capping protein (CP) beta-subunit in motility of malaria sporozoites Rodent malaria-resistant strains of the mosquito, Anopheles gambiae, have slower population growth than -susceptible strains.Immune resistance and tolerance strategies in malaria vector and non-vector mosquitoes Insecticide control of vector-borne diseases: when is insecticide resistance a problem?Suppressive effect of azithromycin on Plasmodium berghei mosquito stage development and apicoplast replication Site-specific integration and expression of an anti-malarial gene in transgenic Anopheles gambiae significantly reduces Plasmodium infections.Analysis of two novel midgut-specific promoters driving transgene expression in Anopheles stephensi mosquitoes.Developing transmission-blocking strategies for malaria control.Injury and immune response: applying the danger theory to mosquitoes Population biology of malaria within the mosquito: density-dependent processes and potential implications for transmission-blocking interventions.Enterobacter-activated mosquito immune responses to Plasmodium involve activation of SRPN6 in Anopheles stephensi.Chemotherapy, within-host ecology and the fitness of drug-resistant malaria parasites Density-dependent effects on the weight of female Ascaris lumbricoides infections of humans and its impact on patterns of egg production.Comparative susceptibility of different biological forms of Anopheles stephensi to Plasmodium berghei ANKA strain.Killer bee molecules: antimicrobial peptides as effector molecules to target sporogonic stages of Plasmodium Modulation of malaria infection in Anopheles gambiae mosquitoes exposed to natural midgut bacteria.Investigating the evolution of apoptosis in malaria parasites: the importance of ecology.Modelling the impact of vector control interventions on Anopheles gambiae population dynamics.An overview of malaria transmission from the perspective of Amazon Anopheles vectors.Infection intensity-dependent responses of Anopheles gambiae to the African malaria parasite Plasmodium falciparum.Insecticide resistance and malaria transmission: infection rate and oocyst burden in Culex pipiens mosquitoes infected with Plasmodium relictum.Evolution of the Transmission-Blocking Vaccine Candidates Pvs28 and Pvs25 in Plasmodium vivax: Geographic Differentiation and Evidence of Positive Selection Probability of Transmission of Malaria from Mosquito to Human Is Regulated by Mosquito Parasite Density in Naïve and Vaccinated Hosts Mosquito transmission of the rodent malaria parasite Plasmodium chabaudi.The effects of ingested mammalian blood factors on vector arthropod immunity and physiology Insecticide resistance alleles affect vector competence of Anopheles gambiae s.s. for Plasmodium falciparum field isolates.Predicting mosquito infection from Plasmodium falciparum gametocyte density and estimating the reservoir of infection.The role of models in translating within-host dynamics to parasite evolution Costs of crowding for the transmission of malaria parasites Marked biological differences between insecticide resistant and susceptible strains of Anopheles funestus infected with the murine parasite Plasmodium berghei.Plasmodium development in the mosquito: biology bottlenecks and opportunities for mathematical modeling.Interactions between Asaia, Plasmodium and Anopheles: new insights into mosquito symbiosis and implications in malaria symbiotic control.A computational lens for sexual-stage transmission, reproduction, fitness and kinetics in Plasmodium falciparum Anopheles mortality is both age- and Plasmodium-density dependent: implications for malaria transmission.

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Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

http://www.wikidata.org/entity/Q33312856

description

2007 nî lūn-bûn

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2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

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Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

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Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

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Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

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Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

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Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

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Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

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Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

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Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

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JOURNAL.PPAT.0030195

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Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

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Adrian V Hill

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Emma J Dawes

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Geoff A Butcher

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Jacqui Mendoza

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Joanna Waldock

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Laura Andrews

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Olivia Finney

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Robert E Sinden

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Yasmene Alavi

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P2860

Feeding behaviour and sporozoite ejection by infected Anopheles stephensi

Host genotype by parasite genotype interactions underlying the resistance of anopheline mosquitoes to Plasmodium falciparum

Intravital observation of Plasmodium berghei sporozoite infection of the liver

High heterogeneity in the number of Plasmodium falciparum gametocytes in the bloodmeal of mosquitoes fed on the same host.

Anopheles gambiae immune responses to human and rodent Plasmodium parasite species.

Quantitative dynamics of Plasmodium yoelii sporozoite transmission by infected anopheline mosquitoes

Interaction between host complement and mosquito-midgut-stage Plasmodium berghei.

Genome expression analysis of Anopheles gambiae: responses to injury, bacterial challenge, and malaria infection

Infectivity of Plasmodium vivax and P. falciparum to Anopheles tessellatus; relationship between oocyst and sporozoite development.

Immune response of Anopheles gambiae to the early sporogonic stages of the human malaria parasite Plasmodium falciparum.

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e195

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10.1371/JOURNAL.PPAT.0030195

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12

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María-Gloria Basáñez

Sarah Catherine Gilbert

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2007-12-01T00:00:00Z

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5683730

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18166078

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Anopheles stephensi

Plasmodium berghei

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2156095

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