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1. Full Text Host Cell Invasion by Apicomplexan Parasites: Insights from the Co-Structure of AMA1 with a RON2 Peptide
by Michelle L. Tonkin and Magali Roques and Mauld H. Lamarque and Martine Pugnière and Dominique Douguet and Joanna Crawford and Maryse Lebrun and Martin J. Boulanger
Science, ISSN 0036-8075, 7/2011, Volume 333, Issue 6041, pp. 463 - 467
Apicomplexan parasites such as Toxoplasma gondii and Plasmodium species actively invade host cells through a moving junction (MJ) complex assembled at the... 
Receptors | Obligate parasites | REPORTS | Cell membranes | Parasitism | Parasites | Parasite hosts | APICAL MEMBRANE ANTIGEN-1 | COMPLEX | MULTIDISCIPLINARY SCIENCES | MOVING JUNCTION | TOXOPLASMA-GONDII | INHIBITORY ANTIBODY | ERYTHROCYTE | Antigens, Protozoan - immunology | Molecular Sequence Data | Toxoplasma - ultrastructure | Antigens, Protozoan - metabolism | Protozoan Proteins - metabolism | Toxoplasma - chemistry | Plasmodium falciparum - metabolism | Protozoan Proteins - chemistry | Antigens, Protozoan - genetics | Membrane Proteins - metabolism | Protein Interaction Domains and Motifs | Host-Parasite Interactions | Toxoplasma - metabolism | Antibodies, Monoclonal - immunology | Plasmodium falciparum - chemistry | Amino Acid Sequence | Peptide Fragments - metabolism | Antigens, Protozoan - chemistry | Protein Structure, Secondary | Antibodies, Protozoan - immunology | Models, Molecular | Membrane Proteins - immunology | Toxoplasma - pathogenicity | Peptide Fragments - chemistry | Membrane Proteins - chemistry | Mutagenesis | Hydrophobic and Hydrophilic Interactions | Plasmodium falciparum - pathogenicity | Protein Binding | Protein Conformation | Protozoan Proteins - immunology | Amino Acid Substitution | Physiological aspects | Cell receptors | Research | Peptides | Medicinal Chemistry | Life Sciences | Cheminformatics | Computer Science | Bioinformatics | Chemical Sciences | Pharmaceutical sciences
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2. Full Text The RON2-AMA1 interaction is a critical step in moving junction-dependent invasion by apicomplexan parasites
by Lamarque, Mauld and Besteiro, Sébastien and Papoin, Julien and Roques, Magali and Vulliez-Le Normand, Brigitte and Morlon-Guyot, Juliette and Dubremetz, Jean-François and Fauquenoy, Sylvain and Tomavo, Stanislas and Faber, Bart W and Kocken, Clemens H and Thomas, Alan W and Boulanger, Martin J and Bentley, Graham A and Lebrun, Maryse
PLoS Pathogens, ISSN 1553-7366, 2011, Volume 7, Issue 2, p. e1001276
Obligate intracellular Apicomplexa parasites share a unique invasion mechanism involving a tight interaction between the host cell and the parasite surfaces... 
APICAL MEMBRANE ANTIGEN-1 | HOST-CELLS | COMPLEX | MICROBIOLOGY | PLASMODIUM-FALCIPARUM APICAL-MEMBRANE-ANTIGEN-1 | ERYTHROCYTE INVASION | MALARIA VACCINE CANDIDATE | HIGH-LEVEL EXPRESSION | VIROLOGY | PROTEIN MIC3 | TOXOPLASMA-GONDII | MONOCLONAL-ANTIBODIES | PARASITOLOGY | Parasites - physiology | Protein Binding - genetics | Humans | Cercopithecus aethiops | Toxoplasma - physiology | Protozoan Proteins - genetics | Parasites - genetics | Virus Internalization | Apicomplexa - metabolism | Antigens, Protozoan - metabolism | Host-Parasite Interactions - genetics | Protozoan Proteins - metabolism | Membrane Proteins - physiology | Protein Interaction Domains and Motifs - genetics | Plasmodium falciparum - genetics | Conserved Sequence | Plasmodium falciparum - metabolism | Protozoan Proteins - chemistry | Antigens, Protozoan - genetics | Membrane Proteins - metabolism | Plasmodium falciparum - physiology | Toxoplasma - metabolism | Vero Cells | Antigens, Protozoan - chemistry | Host-Parasite Interactions - physiology | Membrane Proteins - genetics | Apicomplexa - physiology | Cells, Cultured | Models, Molecular | Apicomplexa - genetics | Connexins - metabolism | Animals | Toxoplasma - genetics | Parasites - metabolism | Models, Biological | Proteins | Parasites | Vaccines | Malaria | Experiments
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3. Full Text Mosaic VSGs and the Scale of Trypanosoma brucei Antigenic Variation
by Hall, James P. J and Wang, Huanhuan and David Barry, J
PLoS Pathogens, ISSN 1553-7366, 07/2013, Volume 9, Issue 7, p. e1003502
A main determinant of prolonged Trypanosoma brucei infection and transmission and success of the parasite is the interplay between host acquired immunity and... 
AFRICAN TRYPANOSOMES | INFECTIONS | MICROBIOLOGY | GENOME | VARIANT SURFACE GLYCOPROTEIN | SEGMENTAL GENE CONVERSION | TRANSMISSION | VIROLOGY | SEQUENCE | DIVERSITY | PARASITE | EXPRESSION | PARASITOLOGY | Membrane Glycoproteins - metabolism | Genes, Protozoan | Protozoan Proteins - genetics | Genetic Variation | RNA, Protozoan - blood | Antigens, Protozoan - metabolism | Protozoan Proteins - metabolism | Time Factors | Surface Properties | Female | Antigens, Protozoan - genetics | Organisms, Genetically Modified | Antibodies, Protozoan - analysis | Trypanosomiasis - parasitology | Antigenic Variation | Trypanosoma brucei brucei - metabolism | Trypanosoma brucei brucei - genetics | Trypanosomiasis - blood | Membrane Glycoproteins - genetics | RNA, Protozoan - metabolism | Trypanosomiasis - immunology | Animals | Pseudogenes | Mice | Mice, Inbred BALB C | Trypanosoma brucei brucei - immunology | Genetic variation | Physiological aspects | Host-parasite relationships | Genetic aspects | Research | Trypanosoma brucei | Health aspects | Archives & records | Genes | Cloning | Colleges & universities | Infections | Genomes | Parasites | Mass spectrometry | Immune system
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4. Full Text Apical membrane antigen 1: a malaria vaccine candidate in review
by Remarque, Edmond J and Faber, Bart W and Kocken, Clemens H.M and Thomas, Alan W
Trends in Parasitology, ISSN 1471-4922, 2007, Volume 24, Issue 2, pp. 74 - 84
Apical membrane antigen 1 (AMA1) is a micronemal protein of apicomplexan parasites that appears to be essential during the invasion of host cells. Immune... 
Infectious Disease | Gastroenterology and Hepatology | NATURAL IMMUNE-RESPONSES | DOMAIN-III | MEROZOITE SURFACE PROTEIN-1 | HIGH-LEVEL EXPRESSION | CHABAUDI MALARIA | INHIBITORY ANTIBODIES | ANTIBODY-RESPONSES | PLASMODIUM-FALCIPARUM MALARIA | PARASITOLOGY | BLOOD-STAGE VACCINE | ERYTHROCYTE INVASION | Antigens, Protozoan - immunology | Humans | Child, Preschool | Malaria - mortality | Molecular Sequence Data | Infant | Protozoan Proteins - genetics | Antigens, Protozoan - metabolism | Antibodies, Protozoan - blood | Protozoan Proteins - metabolism | Adult | Female | Protozoan Proteins - chemistry | Antigens, Protozoan - genetics | Membrane Proteins - metabolism | Child | Plasmodium - immunology | Amino Acid Sequence | Rabbits | Antigens, Protozoan - chemistry | Membrane Proteins - genetics | Malaria - immunology | Plasmodium - genetics | Plasmodium - metabolism | Models, Molecular | Membrane Proteins - immunology | Clinical Trials as Topic | Mice, Inbred Strains | Polymorphism, Genetic | Malaria - prevention & control | Animals | Malaria Vaccines - administration & dosage | Membrane Proteins - chemistry | Malaria - parasitology | Mice | Plasmodium - classification | Protozoan Proteins - immunology | Antigens | Vaccines | Malaria | Malaria vaccine | Analysis
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5. Full Text Structural and functional insight into how the Plasmodium falciparum VAR2CSA protein mediates binding to chondroitin sulfate A in placental malaria
by Clausen, Thomas M and Christoffersen, Stig and Dahlbäck, Madeleine and Langkilde, Annette Eva and Jensen, Kamilla E and Resende, Mafalda and Agerbæk, Mette Ø and Andersen, Daniel and Berisha, Besim and Ditlev, Sisse B and Pinto, Vera V and Nielsen, Morten A and Theander, Thor G and Larsen, Sine and Salanti, Ali
Journal of Biological Chemistry, ISSN 0021-9258, 07/2012, Volume 287, Issue 28, pp. 23332 - 23345
Malaria is a major global health problem. Pregnant women are susceptible to infection regardless of previously acquired immunity. Placental malaria is caused... 
ANTIBODIES | ADHESION | PREGNANCY-ASSOCIATED MALARIA | VACCINE CANDIDATE | SMALL-ANGLE SCATTERING | BIOCHEMISTRY & MOLECULAR BIOLOGY | INFECTED ERYTHROCYTES | IDENTIFICATION | DOMAINS | ADHERENCE | FAMILY | Antigens, Protozoan - immunology | Chondroitin Sulfates - metabolism | Rats, Wistar | Humans | Plasmodium falciparum - immunology | Protozoan Proteins - genetics | Antigens, Protozoan - metabolism | Protozoan Proteins - metabolism | Immune Sera - metabolism | X-Ray Diffraction | Malaria, Falciparum - metabolism | Female | Antigens, Protozoan - genetics | Host-Parasite Interactions | Plasmodium falciparum - physiology | Protein Structure, Tertiary | Recombinant Proteins - metabolism | Immune Sera - immunology | Immunization | Placenta - immunology | Models, Molecular | Pregnancy Complications, Parasitic | Rats | Recombinant Proteins - chemistry | Scattering, Small Angle | Binding Sites - genetics | Chondroitin Sulfates - chemistry | Placenta - metabolism | Pregnancy | Malaria, Falciparum - parasitology | Animals | Recombinant Proteins - immunology | Malaria, Falciparum - immunology | Protein Binding | Kinetics | Mutation | Placenta - parasitology | Chondroitin Sulfates - immunology | Protozoan Proteins - immunology | Molecular Bases of Disease | Vaccine Development | Placenta | Malaria | Placental Malaria | VAR2CSA | Protein Structure | PfEMP1
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6. Full Text P113 is a merozoite surface protein that binds the N terminus of Plasmodium falciparum RH5
by Galaway, Francis and Drought, Laura G and Fala, Maria and Cross, Nadia and Kemp, Alison C and Rayner, Julian C and Wright, Gavin J
Nature Communications, ISSN 2041-1723, 02/2017, Volume 8, Issue 1, p. 14333
Invasion of erythrocytes by Plasmodium falciparum merozoites is necessary for malaria pathogenesis and is therefore a primary target for vaccine development.... 
ANTIBODIES | PFRH5 | COMPLEX | MULTIDISCIPLINARY SCIENCES | VACCINE | MEMBRANES | CELL-SURFACE | ANTIGENS | IDENTIFICATION | BASIGIN | ERYTHROCYTE INVASION | Erythrocytes - immunology | Antigens, Protozoan - immunology | Antibodies, Protozoan - immunology | Humans | Plasmodium falciparum - immunology | Antigens, Protozoan - metabolism | Malaria, Falciparum - parasitology | Animals | Carrier Proteins - metabolism | Protozoan Proteins - metabolism | HEK293 Cells | Malaria Vaccines - immunology | Malaria, Falciparum - immunology | Malaria, Falciparum - metabolism | Protein Binding | Plasmodium falciparum - metabolism | Membrane Proteins - metabolism | Plasmodium falciparum - physiology | Erythrocytes - parasitology | Carrier Proteins - immunology | Antibodies, Protozoan - metabolism | Merozoites - metabolism
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7. Full Text A library of functional recombinant cell-surface and secreted p. Falciparum merozoite proteins
by Crosnier, Cécile and Wanaguru, Madushi and McDade, Brian and Osier, Faith H and Marsh, Kevin and Rayner, Julian C and Wright, Gavin J
Molecular and Cellular Proteomics, ISSN 1535-9476, 12/2013, Volume 12, Issue 12, pp. 3976 - 3986
Malaria, an infectious disease caused by parasites of the Plasmodium genus, is one of the world's major public health concerns causing up to a million deaths... 
HIGH-LEVEL | ENHANCED EXPRESSION | RTS,S/AS01 MALARIA VACCINE | ESCHERICHIA-COLI | BIOCHEMICAL RESEARCH METHODS | PARASITE PLASMODIUM-FALCIPARUM | MULTIGENE FAMILY | PHASE-3 TRIAL | INHIBITORY ANTIBODIES | HETEROLOGOUS EXPRESSION | ERYTHROCYTE INVASION | Proteome - genetics | Antigens, Protozoan - immunology | Immune Sera - chemistry | Humans | Merozoite Surface Protein 1 - genetics | Peptide Library | Plasmodium falciparum - immunology | Protozoan Proteins - genetics | Merozoite Surface Protein 1 - metabolism | Antigens, Protozoan - metabolism | Protozoan Proteins - metabolism | Plasmodium falciparum - genetics | Proteome - immunology | Cloning, Molecular | HEK293 Cells | Antigens, Surface - metabolism | Plasmodium falciparum - metabolism | Antigens, Protozoan - genetics | Membrane Proteins - metabolism | Carrier Proteins - immunology | Merozoites - metabolism | Merozoites - immunology | Recombinant Proteins - metabolism | Gene Expression | Membrane Proteins - genetics | Molecular Sequence Annotation | Antigens, Surface - genetics | Sialic Acids - metabolism | Membrane Proteins - immunology | Recombinant Proteins - genetics | Carrier Proteins - genetics | Carrier Proteins - metabolism | Recombinant Proteins - immunology | Merozoite Surface Protein 1 - immunology | Protein Binding | Erythrocytes - parasitology | Merozoites - chemistry | Antigens, Surface - immunology | Proteome - metabolism | Protozoan Proteins - immunology | Technological Innovation and Resources
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8. Full Text Revealing the Sequence and Resulting Cellular Morphology of Receptor-Ligand Interactions during Plasmodium falciparum Invasion of Erythrocytes
by Weiss, Greta E and Gilson, Paul R and Taechalertpaisarn, Tana and Tham, Wai-Hong and de Jong, Nienke W. M and Harvey, Katherine L and Fowkes, Freya J. I and Barlow, Paul N and Rayner, Julian C and Wright, Gavin J and Cowman, Alan F and Crabb, Brendan S
PLoS Pathogens, ISSN 1553-7366, 2015, Volume 11, Issue 2, p. e1004670
During blood stage Plasmodium falciparum infection, merozoites invade uninfected erythrocytes via a complex, multistep process involving a series of distinct... 
MOLECULAR-MECHANISM | COMPLEX | AMA1 | EVENTS | MICROBIOLOGY | INHIBITORY ANTIBODIES | MALARIA PARASITE INVASION | MEMBRANE ANTIGEN 1 | VIROLOGY | CALCIUM | BINDING | PARASITOLOGY | MEROZOITE SURFACE PROTEIN | Calcium - metabolism | Merozoites - pathology | Antigens, Protozoan - metabolism | Malaria, Falciparum - blood | Protozoan Proteins - metabolism | Cell Shape | Erythrocytes - pathology | Malaria, Falciparum - metabolism | Plasmodium falciparum - metabolism | Membrane Proteins - metabolism | Merozoites - metabolism | Rabbits | Host-Parasite Interactions - physiology | Signal Transduction | Cells, Cultured | Receptors, Cell Surface - metabolism | Malaria, Falciparum - parasitology | Animals | Carrier Proteins - metabolism | Erythrocytes - metabolism | Basigin - metabolism | Plasmodium falciparum - pathogenicity | Protein Binding | Ligands | Erythrocytes - parasitology | Medical research | Parasites | Vaccines | Malaria | Erythrocytes
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9. Full Text Transgenic Eimeria tenella as a vaccine vehicle: Expressing TgSAG1 elicits protective immunity against Toxoplasma gondii infections in chickens and mice
by Tang, Xinming and Yin, Guangwen and Qin, Mei and Tao, Geru and Suo, Jingxia and Liu, Xianyong and Suo, Xun
Scientific Reports, ISSN 2045-2322, 07/2016, Volume 6, Issue 1, p. 29379
The surface antigen 1 of Toxoplasma gondii (TgSAG1) is a major immunodominant antigen and is widely considered an ideal candidate for the development of an... 
RESPONSES | TRANSFECTION | COCCIDIOSIS | MULTIDISCIPLINARY SCIENCES | CONSTRUCTION | COMPARTMENTALIZATION | APICOMPLEXA | SPOROZOITES | CD8 T-CELLS | ANTIGEN | VECTOR | Toxoplasma - immunology | Antigens, Protozoan - immunology | Toxoplasmosis - immunology | Vaccination | Eimeria tenella - genetics | Cercopithecus aethiops | Protozoan Proteins - genetics | Antigens, Protozoan - metabolism | Protozoan Proteins - metabolism | Cloning, Molecular | Antigens, Protozoan - genetics | Toxoplasma - metabolism | Vero Cells | Disease Models, Animal | Protozoan Vaccines - immunology | Protozoan Vaccines - administration & dosage | Chickens - immunology | Animals | Toxoplasma - genetics | Toxoplasmosis - prevention & control | Eimeria tenella - immunology | Mice | Mice, Inbred BALB C | Protozoan Proteins - immunology | Antibodies, Protozoan - metabolism
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10. Full Text Elongation factor-1 α is a novel protein associated with host cell invasion and a potential protective antigen of Cryptosporidium parvum
by Matsubayashi, Makoto and Teramoto-Kimata, Isao and Uni, Shigehiko and Lillehoj, Hyun S and Matsuda, Haruo and Furuya, Masaru and Tani, Hiroyuki and Sasai, Kazumi
Journal of Biological Chemistry, ISSN 0021-9258, 11/2013, Volume 288, Issue 47, pp. 34111 - 34120
Background: Apicomplexan parasites, including Cryptosporidium, possess organelles associated with host cell invasion. Results: A chicken-derived monoclonal... 
Cell-penetrating Peptides | BIOCHEMISTRY & MOLECULAR BIOLOGY | SEA-URCHIN EGGS | Protozoan | SPOROZOITES | MONOCLONAL-ANTIBODY | BINDING PROTEIN | IDENTIFICATION | Electron Microscopy (EM) | EIMERIA | Western Blotting | Translation Elongation Factors | Cytoskeleton | ACTIN CYTOSKELETON | FACTOR 1A | TOXOPLASMA INVASION | Transcription Elongation Factors | FACTOR-I ALPHA | Antigens, Protozoan - immunology | Cryptosporidium parvum - pathogenicity | Male | Cryptosporidiosis - metabolism | Protozoan Proteins - genetics | Cryptosporidiosis - immunology | Sporozoites - immunology | Antigens, Protozoan - metabolism | Protozoan Proteins - metabolism | Peptide Elongation Factor 1 - immunology | Cryptosporidiosis - prevention & control | Antigens, Protozoan - genetics | Cell Membrane - metabolism | Peptide Elongation Factor 1 - genetics | Cryptosporidiosis - genetics | Protozoan Vaccines - immunology | Antibodies, Protozoan - immunology | Cryptosporidium parvum - immunology | Mice, SCID | Cryptosporidium parvum - metabolism | Animals | Sporozoites - metabolism | Cell Line, Tumor | Cell Membrane - immunology | Mice | Peptide Elongation Factor 1 - metabolism | Protozoan Proteins - immunology | Molecular Bases of Disease
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11. Full Text Plasmodium falciparum Expressing Domain Cassette 5 Type PfEMP1 (DC5-PfEMP1) Bind PECAM1
by Berger, Sanne S and Turner, Louise and Wang, Christian W and Petersen, Jens E. V and Kraft, Maria and Lusingu, John P. A and Mmbando, Bruno and Marquard, Andrea M and Bengtsson, Dominique B. A. C and Hviid, Lars and Nielsen, Morten A and Theander, Thor G and Lavstsen, Thomas
PLoS ONE, ISSN 1932-6203, 07/2013, Volume 8, Issue 7, p. e69117
Members of the Plasmodium falciparum Erythrocyte Membrane protein 1 (PfEMP1) family expressed on the surface of malaria-infected erythrocytes mediate binding... 
NATURALLY ACQUIRED-IMMUNITY | PREGNANCY-ASSOCIATED MALARIA | ERYTHROCYTE-MEMBRANE PROTEIN-1 | MULTIDISCIPLINARY SCIENCES | VARIANT SURFACE-ANTIGENS | VAR GENE-TRANSCRIPTION | CHONDROITIN SULFATE-A | ADHESION-INHIBITORY ANTIBODIES | NORTH-EASTERN TANZANIA | INFECTED ERYTHROCYTES | BRAIN ENDOTHELIAL-CELLS | Malaria, Falciparum - prevention & control | Antigens, Protozoan - immunology | Humans | Transcriptome | Plasmodium falciparum - immunology | Protozoan Proteins - genetics | Antigens, Protozoan - metabolism | Protozoan Proteins - metabolism | Immunoglobulin G - immunology | Platelet Endothelial Cell Adhesion Molecule-1 - metabolism | Plasmodium falciparum - genetics | Conserved Sequence | Malaria, Falciparum - metabolism | Plasmodium falciparum - metabolism | Protozoan Proteins - chemistry | Antigens, Protozoan - genetics | Protein Interaction Domains and Motifs | Antigens, Protozoan - chemistry | Antibodies, Protozoan - immunology | Endothelial Cells - metabolism | Gene Expression Regulation | Erythrocytes - metabolism | Malaria, Falciparum - immunology | Protein Binding | Erythrocytes - parasitology | Bone Marrow Cells - metabolism | Antibodies, Protozoan - metabolism | Cluster Analysis | Immunoglobulin G - metabolism | Viral antibodies | Plasmodium falciparum | Malaria | Antibodies | Hemoglobin | Development and progression | Children | Diseases | Genes | Erythrocytes | Parasites | Cell adhesion & migration | Proteins | Receptors | Immunology | Red blood cells | Erythrocyte membrane protein 1 | Lining (process) | Bone marrow | Cassettes | Binding | Vector-borne diseases | Medical research | Parasitology | Immunoglobulins | Mortality | Endothelial cells | Membrane proteins | Studies | Infectious diseases | Hospitals | Womens health | Chondroitin sulfate
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12. Full Text Targets of antibodies against Plasmodium falciparum-infected erythrocytes in malaria immunity
by Chan, Jo-Anne and Howell, Katherine B and Reiling, Linda and Ataide, Ricardo and Mackintosh, Claire L and Fowkes, Freya J. I and Petter, Michaela and Chesson, Joanne M and Langer, Christine and Warimwe, George M and Duffy, Michael F and Rogerson, Stephen J and Bull, Peter C and Cowman, Alan F and Marsh, Kevin and Beeson, James G
Journal of Clinical Investigation, ISSN 0021-9738, 09/2012, Volume 122, Issue 9, pp. 3227 - 3238
Plasmodium falciparum is the major cause of malaria globally and is transmitted by mosquitoes. During parasitic development, P. falciparum-infected... 
EXPRESSION PATTERNS | STEVOR PROTEINS | MEDICINE, RESEARCH & EXPERIMENTAL | ACQUIRED-IMMUNITY | CLINICAL MALARIA | VARIANT SURFACE-ANTIGENS | MEMBRANE PROTEIN-1 | VAR GENES | PREGNANT-WOMEN | RED-BLOOD-CELLS | INHIBITORY ANTIBODIES | Kenya - epidemiology | Humans | Middle Aged | Child, Preschool | Infant | Plasmodium falciparum - immunology | Protozoan Proteins - genetics | Endemic Diseases | Young Adult | Antigens, Protozoan - metabolism | Malaria, Falciparum - blood | Antibodies, Protozoan - blood | Protozoan Proteins - metabolism | Plasmodium falciparum - genetics | Malaria, Falciparum - epidemiology | Statistics, Nonparametric | Adult | Plasmodium falciparum - metabolism | Antigens, Protozoan - genetics | Organisms, Genetically Modified | Child | Promoter Regions, Genetic | Disease Resistance | Kaplan-Meier Estimate | Disease-Free Survival | Genetic Engineering | Adolescent | Malaria, Falciparum - immunology | Erythrocytes - parasitology | Phagocytosis | Antigen-antibody reactions | Care and treatment | Gene targeting | Malaria | Erythrocytes | Genetic aspects | Research
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