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devices or arrangements, the optical operation of which ismodified by changing the optical properties of the medium of thedevices or arrangements for the control of the intensity,colour, phase, polarisation or direction of light, e.g.switching, gating, modulating or demodulating (17) 17
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Angewandte Chemie International Edition, ISSN 1433-7851, 02/2014, Volume 53, Issue 8, pp. 2235 - 2239
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2014, Volume 53, Issue 27, pp. 7079 - 7084
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 04/2015, Volume 58, Issue 7, pp. 3117 - 3130
Journal Article
Science, ISSN 0036-8075, 9/2010, Volume 329, Issue 5996, pp. 1175 - 1180
Recent reports of increased tolerance to artemisinin derivatives—the most recently adopted class of antimalarials— have prompted a need for new treatments. The... 
Malaria | Artemisinins | RESEARCH ARTICLES | Genomics | Adenosine triphosphatases | Antimalarials | Parasites | Inhibitory concentration 50 | Drug resistance | Dosage | Genetic mutation | VIVAX | MULTIDISCIPLINARY SCIENCES | PARASITE PLASMODIUM-FALCIPARUM | ERADICATION | CALCIUM-PUMP | DRUG-RESISTANCE | SARCOPLASMIC-RETICULUM | ANTIMALARIALS | IDENTIFICATION | CHLOROQUINE | ARTEMISININ | Parasitic Sensitivity Tests | Humans | Male | Plasmodium falciparum - drug effects | Indoles - administration & dosage | Plasmodium falciparum - genetics | Protein Synthesis Inhibitors - pharmacology | Mutant Proteins - antagonists & inhibitors | Antimalarials - pharmacokinetics | Adenosine Triphosphatases - metabolism | Models, Molecular | Rats | Spiro Compounds - pharmacokinetics | Adenosine Triphosphatases - antagonists & inhibitors | Antimalarials - administration & dosage | Malaria - parasitology | Adenosine Triphosphatases - genetics | Mice | Mutation | Erythrocytes - parasitology | Plasmodium berghei - drug effects | Plasmodium vivax - growth & development | Protein Synthesis Inhibitors - chemistry | Rats, Wistar | Spiro Compounds - administration & dosage | Genes, Protozoan | Protozoan Proteins - genetics | Protein Synthesis Inhibitors - administration & dosage | Protozoan Proteins - metabolism | Female | Indoles - pharmacology | Protozoan Proteins - chemistry | Drug Resistance | Spiro Compounds - chemistry | Cell Line | Plasmodium vivax - drug effects | Mutant Proteins - metabolism | Drug Discovery | Protozoan Proteins - biosynthesis | Antimalarials - pharmacology | Protein Synthesis Inhibitors - pharmacokinetics | Animals | Mutant Proteins - chemistry | Antimalarials - chemistry | Adenosine Triphosphatases - chemistry | Indoles - pharmacokinetics | Malaria - drug therapy | Plasmodium falciparum - growth & development | Indoles - chemistry | Spiro Compounds - pharmacology | Research | Pharmacology | Inhibitor drugs | Drug therapy | Protein synthesis | Drugs | Mutations | Nanomaterials | Encoding | Cations | Nanostructure | Ablation | Index Medicus
Journal Article
Solar Energy Materials and Solar Cells, ISSN 0927-0248, 2009, Volume 93, Issue 12, pp. 2088 - 2092
Journal Article
Nature, ISSN 0028-0836, 2013, Volume 504, Issue 7479, pp. 248 - 253
Achieving the goal of malaria elimination will depend on targeting Plasmodium pathways essential across all life stages. Here we identify a lipid kinase,... 
YEAST | TRANSMISSION | POTENT | VIVAX | PHOSPHATIDYLINOSITOL 4-PHOSPHATE | FALCIPARUM | MULTIDISCIPLINARY SCIENCES | DRUG DISCOVERY | KINASE | ZINC-FINGER NUCLEASES | SACCHAROMYCES-CEREVISIAE | Plasmodium - enzymology | Phosphatidylinositol Phosphates - metabolism | Humans | Male | rab GTP-Binding Proteins - genetics | Macaca mulatta | Plasmodium - drug effects | Hepatocytes - parasitology | 1-Phosphatidylinositol 4-Kinase - metabolism | Quinoxalines - pharmacology | Schizonts - cytology | Adenosine Triphosphate - metabolism | Plasmodium - growth & development | Female | Binding Sites | Fatty Acids - metabolism | Cytokinesis - drug effects | Imidazoles - metabolism | Life Cycle Stages - drug effects | Pyrazoles - pharmacology | 1-Phosphatidylinositol 4-Kinase - genetics | rab GTP-Binding Proteins - metabolism | 1-Phosphatidylinositol 4-Kinase - chemistry | Reproducibility of Results | Models, Molecular | 1-Phosphatidylinositol 4-Kinase - antagonists & inhibitors | Drug Resistance - drug effects | Imidazoles - pharmacology | Quinoxalines - metabolism | Pyrazoles - metabolism | Schizonts - drug effects | Drug Resistance - genetics | Animals | Models, Biological | Malaria - parasitology | Malaria - drug therapy | Plasmodium - classification | Plasma | Mosquitoes | Malaria | Licenses | Infections | Parasites | Kinases | Drug dosages | Index Medicus
Journal Article
Science, ISSN 0036-8075, 12/2011, Volume 334, Issue 6061, pp. 1372 - 1377
Most malaria drug development focuses on parasite stages detected in red blood cells, even though, to achieve eradication, next-generation drugs active against... 
Schizonts | Malaria | RESEARCH ARTICLES | Liver | Antimalarials | Infections | Parasites | Inhibitory concentration 50 | Scaffolds | Blood | Chemicals | INFECTIONS | FALCIPARUM | MULTIDISCIPLINARY SCIENCES | METHEMOGLOBINEMIA | RESISTANCE | MALARIA | TARGETS | MUTATIONS | Plasmodium berghei - physiology | Humans | Imidazoles - chemistry | Plasmodium - physiology | Piperazines - chemistry | Plasmodium falciparum - drug effects | Plasmodium - growth & development | Imidazoles - therapeutic use | Plasmodium falciparum - physiology | Antimalarials - pharmacokinetics | Antimalarials - therapeutic use | Imidazoles - pharmacology | Piperazines - therapeutic use | Random Allocation | Piperazines - pharmacology | Plasmodium berghei - cytology | Small Molecule Libraries | Malaria - parasitology | Cell Line, Tumor | Plasmodium berghei - growth & development | Mice | Mice, Inbred BALB C | Liver - parasitology | Erythrocytes - parasitology | Plasmodium berghei - drug effects | Plasmodium - cytology | Plasmodium falciparum - cytology | Plasmodium - drug effects | Imidazoles - pharmacokinetics | Plasmodium yoelii - growth & development | Protozoan Proteins - genetics | Sporozoites - growth & development | Protozoan Proteins - metabolism | Plasmodium yoelii - drug effects | Protozoan Proteins - chemistry | Molecular Structure | Piperazines - pharmacokinetics | Drug Evaluation, Preclinical | Sporozoites - drug effects | Drug Resistance | Plasmodium yoelii - physiology | Plasmodium yoelii - cytology | Drug Discovery | Antimalarials - pharmacology | Malaria - prevention & control | Animals | Antimalarials - chemistry | Polymorphism, Single Nucleotide | Malaria - drug therapy | Plasmodium falciparum - growth & development | Pharmaceutical research | Plasmodium | Care and treatment | Analysis | Research | Drug therapy | Index Medicus
Journal Article
SIAM Journal on Scientific Computing, ISSN 1064-8275, 2018, Volume 40, Issue 6, pp. A3928 - A3954
The bootstrap algebraic multigrid framework allows for the adaptive construction of algebraic multigrid methods in situations where geometric multigrid methods... 
Regression | Adaptivity | Preconditioning | Algebraic multigrid | Machine learning | INTERPOLATION | MATHEMATICS, APPLIED | adaptivity | regression | COMPATIBLE RELAXATION | algebraic multigrid | machine learning | preconditioning
Journal Article