Molecular genetics evidence for the in vivo roles of the two major NADPH-dependent disulfide reductases in the malaria parasite

Journal of Biological Chemistry

Volumn 285, Issue 48, 2010, Pages 37388-37395

  Buchholz, Kathrin ^a,b,c,e   Putrianti, Elyzana D ^d   Rahlfs, Stefan ^a   Schirmer, R Heiner ^b   Becker, Katja ^b   Matuschewski, Kai ^a  

^a JUSTUS LIEBIG UNIVERSITY   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c UNIVERSITY OF HEIDELBERG   (Germany)

^d MAX PLANCK INSTITUTE FOR INFECTION BIOLOGY   (Germany)

^e HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DISULFIDE REDUCTASE; DRUG TARGETS; ELECTRON DONORS; EXTRACELLULAR; GENE TARGETING; GLUTATHIONE REDUCTASE; GLUTATHIONES; IN-VIVO; INTERVENTION STRATEGY; MALARIA PARASITE; MOLECULAR GENETICS; NETWORK-BASED; OXYGEN-RICH ENVIRONMENT; PARASITE-; PLASMODIUM PARASITES; THIOREDOXIN REDUCTASE; THIOREDOXINS;

BLOOD; GENETIC ENGINEERING; MOLECULAR BIOLOGY; OXYGEN;

ENZYME ACTIVITY;

GLUTATHIONE REDUCTASE; THIOREDOXIN REDUCTASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL PROLIFERATION; CONTROLLED STUDY; DISEASE CARRIER; ENZYME ACTIVITY; GENE EXPRESSION PROFILING; GENE TARGETING; GENOTYPE; HOST PARASITE INTERACTION; IN VIVO STUDY; MOLECULAR GENETICS; MOUSE; NONHUMAN; OXIDATIVE STRESS; PARASITE DEVELOPMENT; PARASITE SURVIVAL; PARASITE VIRULENCE; PLASMODIUM (LIFE CYCLE STAGE); PLASMODIUM BERGHEI; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; QUANTITATIVE ANALYSIS; RAT; REAL TIME POLYMERASE CHAIN REACTION; WILD TYPE;

ANIMALS; CELL PROLIFERATION; GENE SILENCING; GLUTATHIONE REDUCTASE; HUMANS; MALARIA; MICE; MICE, INBRED C57BL; NADP; PLASMODIUM BERGHEI; PROTOZOAN PROTEINS; RATS; RATS, SPRAGUE-DAWLEY; THIOREDOXIN-DISULFIDE REDUCTASE;

HEXAPODA; PLASMODIUM BERGHEI; PLASMODIUM PARASITES;

EID: 78549246255     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.123323     Document Type: Article

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