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PLoS Pathogens, ISSN 1553-7366, 09/2017, Volume 13, Issue 9, p. e1006586
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2011, Volume 108, Issue 32, pp. 13275 - 13280
The commitment of Plasmodium merozoites to invade red blood cells (RBCs) is marked by the formation of a junction between the merozoite and the RBC and the... 
Apposition | Antigens | Malaria | Erythrocytes | Erythrocyte invasion | Parasitism | Cell membranes | Parasites | Merozoites | Vacuoles | Moving junction | AMA1-RON2 | APICAL MEMBRANE ANTIGEN-1 | PARASITOPHOROUS VACUOLE | APICOMPLEXAN PARASITES | MULTIDISCIPLINARY SCIENCES | malaria | moving junction | ERYTHROCYTE INVASION | MALARIA VACCINE CANDIDATE | ANONYMOUS PROTEIN | TOXOPLASMA-GONDII | INHIBITORY ANTIBODY | FALCIPARUM MEROZOITES | Conserved Sequence - genetics | Hydrophobic and Hydrophilic Interactions - drug effects | Molecular Sequence Data | Protein Transport - drug effects | Structure-Activity Relationship | Plasmodium falciparum - drug effects | Cytochalasin D - pharmacology | Fructose-Bisphosphate Aldolase - chemistry | Protozoan Proteins - metabolism | Protein Binding - drug effects | Merozoites - drug effects | Plasmodium falciparum - metabolism | Protozoan Proteins - chemistry | Cysteine - metabolism | Fructose-Bisphosphate Aldolase - metabolism | Binding Sites | Plasmodium falciparum - ultrastructure | Merozoites - metabolism | Amino Acid Sequence | Antibodies, Protozoan - immunology | Merozoites - ultrastructure | Erythrocytes - drug effects | Animals | Models, Biological | Plasmodium falciparum - pathogenicity | Erythrocytes - parasitology | Physiological aspects | Plasmodium | Genetic aspects | Research | Protein binding | Biological Sciences | AMA1–RON2
Journal Article
PLoS Pathogens, ISSN 1553-7366, 07/2017, Volume 13, Issue 7, p. e1006453
Egress of the malaria parasite Plasmodium falciparum from its host red blood cell is a rapid, highly regulated event that is essential for maintenance and... 
CYSTEINE PROTEASE | SUBTILISIN | PARASITOPHOROUS VACUOLE | CRE RECOMBINASE | MICROBIOLOGY | RELEASE | INVASION | MEROZOITE SURFACE PROTEIN-1 | ENZYME | VIROLOGY | SERINE | PARASITOLOGY | ANTIGEN | Cell Membrane - parasitology | Merozoites - physiology | Peptide Hydrolases - genetics | Humans | Erythrocytes - chemistry | Merozoites - genetics | Antigens, Protozoan - metabolism | Malaria, Falciparum - parasitology | Animals | Proteolysis | Plasmodium falciparum - genetics | Antigens, Protozoan - genetics | Merozoites - growth & development | Kinetics | Plasmodium falciparum - growth & development | Plasmodium falciparum - physiology | Erythrocytes - parasitology | Merozoites - chemistry | Peptide Hydrolases - metabolism | Plasmodium falciparum - chemistry | Plasmodium falciparum | Malaria | Proteases | Host-parasite relationships | Development and progression | Genetic aspects | Virulence (Microbiology) | Health aspects | Visualization | Cysteine | Membranes | Laboratories | Funding | Serine | Erythrocytes | Cysteine proteinase | Biochemistry | Egress | Parasites | Kinases | Blood | Parasitophorous vacuole | Proteins | Efficiency | Protease | Life cycle engineering | Complementation | Vector-borne diseases | Medical research | Enzymes | Blood cells | Rupture | Papain | Roles | Merozoites | Serine proteinase | Life cycles
Journal Article
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
Journal Article
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 10, p. e24886
Merozoite Surface Protein 1 is expressed on the surface of malaria merozoites and is important for invasion of the malaria parasite into erythrocytes.... 
IMMUNITY | RESPONSES | MEROZOITE SURFACE PROTEIN-1 | DENDRITIC CELLS | MECHANISM | CHABAUDI | MACROPHAGES | BIOLOGY | LYSOSOMAL STORAGE | ANTIBODY | PARASITE | Antigens, Protozoan - immunology | Spleen - immunology | Dendritic Cells - immunology | Spleen - drug effects | Plasmodium chabaudi - immunology | Protease Inhibitors - pharmacology | Chimera - immunology | Merozoite Surface Protein 1 - chemistry | Immunoglobulin G - immunology | Bone Marrow Cells - immunology | Merozoites - drug effects | Bone Marrow Cells - drug effects | Dendritic Cells - drug effects | Merozoites - immunology | Antibody Formation - immunology | Antigens, Protozoan - chemistry | Bone Marrow Cells - cytology | Parasitemia - immunology | Cathepsin D - deficiency | Malaria - immunology | Antigen Presentation - immunology | Cathepsin D - metabolism | Erythrocytes - drug effects | Spleen - parasitology | Phenotype | Animals | Histocompatibility Antigens Class II - immunology | Merozoite Surface Protein 1 - immunology | Antibody Formation - drug effects | Malaria - parasitology | Parasitemia - parasitology | Plasmodium chabaudi - drug effects | Antigen Presentation - drug effects | Mice | Erythrocytes - parasitology | Viral antibodies | Plasmodium falciparum | Enzymes | Malaria | Dendritic cells | Cathepsins | Antibodies | B cells | T cells | Recombinant proteins | Aspartic proteinases | Antigenic determinants | Peptides | Erythrocytes | Antigen processing | Infections | Lymphocytes T | Immunity | Merozoite surface protein 1 | Proteins | Red blood cells | Lymphocytes | Bone marrow | Cathepsin D | Immune system | Recombinant | Vector-borne diseases | Spleen | Antigen presentation | Medical research | CD11c antigen | Antigens | Parasitology | T cell receptors | Epitopes | Merozoites | CD4 antigen
Journal Article
Immunity, ISSN 1074-7613, 03/2015, Volume 42, Issue 3, pp. 580 - 590
Journal Article
Journal Article
Nature communications, ISSN 2041-1723, 04/2016, Volume 7, Issue 1, p. 11449
Blood-stage replication of the human malaria parasite Plasmodium falciparum occurs via schizogony, wherein daughter parasites are formed by a specialized... 
PLASMODIUM-FALCIPARUM MEROZOITES | HOST-CELL INVASION | ERYTHROCYTES | APICOMPLEXAN PARASITES | MULTIDISCIPLINARY SCIENCES | KINASE | GENE-EXPRESSION | TOXOPLASMA-GONDII | IDENTIFICATION | INNER MEMBRANE COMPLEX | MOTILITY
Journal Article
Journal Article