Trypanosoma brucei brucei: Endocytic recycling is important for mouse infectivity

Experimental Parasitology

Volumn 127, Issue 4, 2011, Pages 777-783

  Natesan, Senthil Kumar A ^a   Black, Alana ^c   Matthews, Keith R ^b   Mottram, Jeremy C ^c   Field, Mark C ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY OF EDINBURGH   (United Kingdom)

^c UNIVERSITY OF GLASGOW   (United Kingdom)

Author keywords

Endocytosis; Protein transport; Recycling; Trypanosome; Vesicle trafficking

Indexed keywords

CLATHRIN HEAVY CHAIN; RAB PROTEIN; RAB11 PROTEIN; RAB5 PROTEIN; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CELL CYCLE PROGRESSION; CELL PROLIFERATION; CELL VIABILITY; CONTROLLED STUDY; ENDOCYTOSIS; GROWTH RATE; HEMIZYGOTE; HOST PARASITE INTERACTION; IN VITRO STUDY; IN VIVO STUDY; MOUSE; NAGANA; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; TRYPANOSOMA BRUCEI; WILD TYPE;

ANIMALS; CLATHRIN HEAVY CHAINS; DISEASE MODELS, ANIMAL; ENDOCYTOSIS; GENE EXPRESSION REGULATION; GENE KNOCKOUT TECHNIQUES; MICE; MICE, INBRED ICR; PARASITEMIA; RAB GTP-BINDING PROTEINS; RAB5 GTP-BINDING PROTEINS; TRYPANOSOMA BRUCEI BRUCEI; TRYPANOSOMIASIS, AFRICAN;

MUS; TRYPANOSOMA BRUCEI; TRYPANOSOMA BRUCEI BRUCEI;

EID: 79952364099     PISSN: 00144894     EISSN: 10902449     Source Type: Journal    
DOI: 10.1016/j.exppara.2011.01.001     Document Type: Article

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