about
Biophysics of malarial parasite exit from infected erythrocytesDiscovery of potent small-molecule inhibitors of multidrug-resistant Plasmodium falciparum using a novel miniaturized high-throughput luciferase-based assayThe malaria parasite progressively dismantles the host erythrocyte cytoskeleton for efficient egressSmall molecule targeting malaria merozoite surface protein-1 (MSP-1) prevents host invasion of divergent plasmodial species.Single-cell evaluation of red blood cell bio-mechanical and nano-structural alterations upon chemically induced oxidative stressSynthesis and in vitro evaluation of hydrazinyl phthalazines against malaria parasite, Plasmodium falciparum.Apicomplexan parasites co-opt host calpains to facilitate their escape from infected cells.A portable image-based cytometer for rapid malaria detection and quantification.Reversible host cell remodeling underpins deformability changes in malaria parasite sexual blood stages.Unambiguous determination of Plasmodium vivax reticulocyte invasion by flow cytometry.Development of bestatin-based activity-based probes for metallo-aminopeptidases.High-Content Screening of MMV Pathogen Box for Plasmodium falciparum Digestive Vacuole Disrupting Molecules Reveals Valuable Starting Points for Drug Discovery.Quantitative mass spectrometry of human reticulocytes reveal proteome-wide modifications during maturation.Synthesis, characterization and in vitro evaluation of novel enantiomerically-pure sulphonamide antimalarials.Targeted Phenotypic Screening in Plasmodium falciparum and Toxoplasma gondii Reveals Novel Modes of Action of Medicines for Malaria Venture Malaria Box Molecules.P. falciparum RH5-Basigin interaction induces changes in the cytoskeleton of the host RBC.Cytoskeleton Remodeling Induces Membrane Stiffness and Stability Changes of Maturing Reticulocytes.Febrile Temperature Elevates the Expression of Phosphatidylserine on Plasmodium falciparum (FCR3CSA) Infected Red Blood Cell Surface Leading to Increased CytoadhesionA reference document on Permissible Limits for solvents and buffers during in vitro antimalarial screeningErratum for Subramanian et al., "Targeted Phenotypic Screening in and Reveals Novel Modes of Action of Medicines for Malaria Venture Malaria Box Molecules"Evaluation of ferrocenyl phosphines as potent antimalarials targeting the digestive vacuole function of Plasmodium falciparum
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P50
description
researcher
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wetenschapper
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հետազոտող
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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RCD
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Raj
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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Rajesh Chandramohanadas
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P106
P31
P496
0000-0002-8760-0396