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Author Details
Full Name
Madeline R Luth
Affiliation
University of California San Diego
ORCID
Career Start Year
2017
Papers
24
H Index
11
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37995692
Antiplasmodial peptaibols act through membrane directed mechanisms.
Cell Chem Biol
2024
36919909
Human Polo-like Kinase Inhibitors as Antiplasmodials.
ACS Infect Dis
2023
37546892
Reaction hijacking inhibition of <i>Plasmodium falciparum</i> asparagine tRNA synthetase.
Res Sq
2023
37737220
Diverse evolutionary pathways challenge the use of collateral sensitivity as a strategy to suppress resistance.
Elife
2023
37197802
Advances in malaria pharmacology and the online guide to MALARIA PHARMACOLOGY: IUPHAR review 38.
Br J Pharmacol
2023
36888694
Cytoplasmic isoleucyl tRNA synthetase as an attractive multistage antimalarial drug target.
Sci Transl Med
2023
34348113
Chemogenomics identifies acetyl-coenzyme A synthetase as a target for malaria treatment and prevention.
Cell Chem Biol
2022
35653481
Reaction hijacking of tyrosine tRNA synthetase as a new whole-of-life-cycle antimalarial strategy.
Science
2022
36260689
The anticancer human mTOR inhibitor sapanisertib potently inhibits multiple <i>Plasmodium</i> kinases and life cycle stages.
Sci Transl Med
2022
36008486
Elucidating the path to Plasmodium prolyl-tRNA synthetase inhibitors that overcome halofuginone resistance.
Nat Commun
2022
35149760
Adaptive laboratory evolution in S. cerevisiae highlights role of transcription factors in fungal xenobiotic resistance.
Commun Biol
2022
34460304
The Novel bis-1,2,4-Triazine MIPS-0004373 Demonstrates Rapid and Potent Activity against All Blood Stages of the Malaria Parasite.
Antimicrob Agents Chemother
2021
33715347
PfMFR3: A Multidrug-Resistant Modulator in <i>Plasmodium falciparum</i>.
ACS Infect Dis
2021
32286267
Pan-active imidazolopiperazine antimalarials target the Plasmodium falciparum intracellular secretory pathway.
Nat Commun
2020
32078764
Probing the Open Global Health Chemical Diversity Library for Multistage-Active Starting Points for Next-Generation Antimalarials.
ACS Infect Dis
2020
33064992
SnapShot: Antimalarial Drugs.
Cell
2020
31170268
Covalent Plasmodium falciparum-selective proteasome inhibitors exhibit a low propensity for generating resistance in vitro and synergize with multiple antimalarial agents.
PLoS Pathog
2019
31806760
Evolution of resistance in vitro reveals mechanisms of artemisinin activity in <i>Toxoplasma gondii</i>.
Proc Natl Acad Sci U S A
2019
31801884
In vitro selection predicts malaria parasite resistance to dihydroorotate dehydrogenase inhibitors in a mouse infection model.
Sci Transl Med
2019
29451780
Using in Vitro Evolution and Whole Genome Analysis To Discover Next Generation Targets for Antimalarial Drug Discovery.
ACS Infect Dis
2018
30523084
Open-source discovery of chemical leads for next-generation chemoprotective antimalarials.
Science
2018
30373366
Target Validation and Identification of Novel Boronate Inhibitors of the Plasmodium falciparum Proteasome.
J Med Chem
2018
27889151
Efficacy of post-harvest rinsing and bleach disinfection of E. coli O157:H7 on spinach leaf surfaces.
Food Microbiol
2017
29284029
CYP51 is an essential drug target for the treatment of primary amoebic meningoencephalitis (PAM).
PLoS Negl Trop Dis
2017
1 - 24 of 24
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