Dissecting the loci of low-level quinine resistance in malaria parasites. - Wikidata - wikimedia - TriplyDB

Dissecting the loci of low-level quinine resistance in malaria parasites.

Dissecting the loci of low-level quinine resistance in malaria parasites.

http://www.wikidata.org/entity/Q41914069

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Challenges of drug-resistant malaria Genome scanning of Amazonian Plasmodium falciparum shows subtelomeric instability and clindamycin-resistant parasites Plasmodium falciparum genome-wide scans for positive selection, recombination hot spots and resistance to antimalarial drugs Composite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii.The genetic map and comparative analysis with the physical map of Trypanosoma brucei Assessment of Plasmodium falciparum resistance to ferroquine (SSR97193) in field isolates and in W2 strain under pressure.Antimalarial drug resistance: An overview Antimalarial Drug Resistance: Literature Review and Activities and Findings of the ICEMR Network Plasmodium falciparum susceptibility to antimalarial drugs: global data issued from the Pasteur Institutes international network The interplay between drug resistance and fitness in malaria parasites Application of genomics to field investigations of malaria by the international centers of excellence for malaria research Global analysis of Plasmodium falciparum Na(+)/H(+) exchanger (pfnhe-1) allele polymorphism and its usefulness as a marker of in vitro resistance to quinine Disruption of a Plasmodium falciparum Multidrug Resistance-associated Protein (PfMRP) Alters Its Fitness and Transport of Antimalarial Drugs and Glutathione A HECT ubiquitin-protein ligase as a novel candidate gene for altered quinine and quinidine responses in Plasmodium falciparum PfCRT and its role in antimalarial drug resistance Probing the multifactorial basis of Plasmodium falciparum quinine resistance: Evidence for a strain-specific contribution of the sodium-proton exchanger PfNHE Plasmodium falciparum Na+/H+ Exchanger (pfnhe-1) Genetic Polymorphism in Indian Ocean Malaria-Endemic Areas Modulation of PF10_0355 (MSPDBL2) alters Plasmodium falciparum response to antimalarial drugs A genome wide association study of Plasmodium falciparum susceptibility to 22 antimalarial drugs in Kenya Characterization of drug resistance associated genetic polymorphisms among Plasmodium falciparum field isolates in Ujjain, Madhya Pradesh, India Advances in understanding the genetic basis of antimalarial drug resistance Regulatory hotspots in the malaria parasite genome dictate transcriptional variation Identification of a mutant PfCRT-mediated chloroquine tolerance phenotype in Plasmodium falciparum Functional characterization of the Plasmodium falciparum chloroquine-resistance transporter (PfCRT) in transformed Dictyostelium discoideum vesicles In vitro sensitivity of Plasmodium falciparum from China-Myanmar border area to major ACT drugs and polymorphisms in potential target genes A process similar to autophagy is associated with cytocidal chloroquine resistance in Plasmodium falciparum PfCRT and PfMDR1 modulate interactions of artemisinin derivatives and ion channel blockers Geographic patterns of Plasmodium falciparum drug resistance distinguished by differential responses to amodiaquine and chloroquine Drug resistance in eukaryotic microorganisms.A database of antimalarial drug resistance.World Antimalarial Resistance Network (WARN) III: molecular markers for drug resistant malaria.A major genetic locus in Trypanosoma brucei is a determinant of host pathology.High-throughput Plasmodium falciparum growth assay for malaria drug discovery.Eating at the table of another: metabolomics of host-parasite interactions.Diverse mutational pathways converge on saturable chloroquine transport via the malaria parasite's chloroquine resistance transporter In vitro sensitivities of Plasmodium falciparum to different antimalarial drugs in Uganda.Analysis of malaria parasite phenotypes using experimental genetic crosses of Plasmodium falciparum.Experimental evolution, genetic analysis and genome re-sequencing reveal the mutation conferring artemisinin resistance in an isogenic lineage of malaria parasites.Quantitative trait loci mapping reveals candidate pathways regulating cell cycle duration in Plasmodium falciparum.Quinine dimers are potent inhibitors of the Plasmodium falciparum chloroquine resistance transporter and are active against quinoline-resistant P. falciparum

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P2860

Dissecting the loci of low-level quinine resistance in malaria parasites.

http://www.wikidata.org/entity/Q41914069

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Dissecting the loci of low-level quinine resistance in malaria parasites.

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Dissecting the loci of low-level quinine resistance in malaria parasites.

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Dissecting the loci of low-level quinine resistance in malaria parasites.

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J.1365-2958.2004.04035.X

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Molecular Microbiology

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Dissecting the loci of low-level quinine resistance in malaria parasites.

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Bingbing Deng

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Deirdre A Joy

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Jianbing Mu

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Roland A Cooper

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Thomas E Wellems

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Severe falciparum malaria. World Health Organization, Communicable Diseases Cluster

Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique

In vivo and in vitro Plasmodium falciparum resistance to chloroquine, amodiaquine and quinine in the Brazilian Amazon.

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sodium/hydrogen exchanger