Harvard Catalyst Profiles
Contact, publication, and social network information about Harvard faculty and fellows.
Open Source Software
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to
Targeted disruption of maebl in Plasmodium falciparum.
Type II fatty acid synthesis is essential only for malaria parasite late liver stage development.
Reticulocyte-binding protein homologue 1 is required for sialic acid-dependent invasion into human erythrocytes by Plasmodium falciparum.
Negative selection using yeast cytosine deaminase/uracil phosphoribosyl transferase in Plasmodium falciparum for targeted gene deletion by double crossover recombination.
Negative selection of Plasmodium falciparum reveals targeted gene deletion by double crossover recombination.
Disruption of the Plasmodium falciparum liver-stage antigen-1 locus causes a differentiation defect in late liver-stage parasites.
Gene deletion from Plasmodium falciparum using FLP and Cre recombinases: implications for applied site-specific recombination.
Analysis of structure and function of the giant protein Pf332 in Plasmodium falciparum.
Characterization of a conserved rhoptry-associated leucine zipper-like protein in the malaria parasite Plasmodium falciparum.
Preerythrocytic, live-attenuated Plasmodium falciparum vaccine candidates by design.
First-in-human evaluation of genetically attenuated Plasmodium falciparum sporozoites administered by bite of Anopheles mosquitoes to adult volunteers.
A next-generation genetically attenuated Plasmodium falciparum parasite created by triple gene deletion.