Krex2 is not essential for either procyclic or bloodstream form trypanosoma brucei

PLoS ONE

Volumn 7, Issue 3, 2012, Pages

  Carnes, Jason ^a   Ernst, Nancy ^a   Wickham, Carey ^a   Panicucci, Brian ^a   Stuart, Kenneth ^a,b  

^a SEATTLE BIOMEDICAL RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EXONUCLEASE; KREX2 EXONUCLEASE; PROTOZOAL RNA; UNCLASSIFIED DRUG; MESSENGER RNA; PROTOZOAL PROTEIN;

ALLELE; ANIMAL CELL; ARTICLE; CELL MUTANT; CELL VIABILITY; CONTROLLED STUDY; ENZYME ACTIVITY; GENE; GENE DELETION; HOMOLOGOUS RECOMBINATION; IN VITRO STUDY; IN VIVO STUDY; KREX2 GENE; LIFE CYCLE STAGE; NONHUMAN; NULL CELL; POLYMERASE CHAIN REACTION; RNA EDITING; TRYPANOSOMA BRUCEI; ANIMAL; DRUG ANTAGONISM; GENE SILENCING; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; MOUSE; PHYSIOLOGY; RNA INTERFERENCE;

HEXAPODA; TRYPANOSOMA BRUCEI;

ANIMALS; EXONUCLEASES; GENE DELETION; GENE KNOCKDOWN TECHNIQUES; GENES, PROTOZOAN; MICE; PROTOZOAN PROTEINS; RNA EDITING; RNA INTERFERENCE; RNA, MESSENGER; RNA, PROTOZOAN; TRYPANOSOMA BRUCEI BRUCEI;

EID: 84858211340     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0033405     Document Type: Article

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