Plasmid-free CRISPR/Cas9 genome editing in Plasmodium falciparum confirms mutations conferring resistance to the dihydroisoquinolone clinical candidate SJ733.
Genetic manipulation of the deadly malaria parasite Plasmodium falciparum remains challenging, but the rise of CRISPR/Cas9-based genome editing tools is increasing the feasibility of altering this parasite's genome in order to study its biology. Of particular interest is the investigation of dr...
Main Authors: | Emily D Crawford, Jenai Quan, Jeremy A Horst, Daniel Ebert, Wesley Wu, Joseph L DeRisi |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2017-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC5439709?pdf=render |
Similar Items
-
Selecting an anti-malarial clinical candidate from two potent dihydroisoquinolones
by: Yizhe Chen, et al.
Published: (2021-02-01) -
Plate-based transfection and culturing technique for genetic manipulation of <it>Plasmodium falciparum</it>
by: Caro Florence, et al.
Published: (2012-01-01) -
Chemical rescue of malaria parasites lacking an apicoplast defines organelle function in blood-stage Plasmodium falciparum.
by: Ellen Yeh, et al.
Published: (2011-08-01) -
The transcriptome of the intraerythrocytic developmental cycle of Plasmodium falciparum.
by: Zbynek Bozdech, et al.
Published: (2003-10-01) -
Genome-wide regulatory dynamics of translation in the Plasmodium falciparum asexual blood stages
by: Florence Caro, et al.
Published: (2014-12-01)