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Chemistry (Weinheim an Der Bergstrasse, Germany)|February 24, 2015
Access to new endoperoxide derivatives by electrochemical oxidation of substituted 3-azabicyclo[4.1.0]hept-4-enesFrédérick Nuter, Abdou Khadre Djily Dimé, Cheng Chen, et al.
The FEBS Journal|March 19, 2013
Antimalarial screening via large-scale purification of Plasmodium falciparum Ca2+-ATPase 6 and in vitro studiesStéphanie David-Bosne, Isabelle Florent, Anne-Marie Lund-Winther, et al.
Frontiers in Microbiology|February 24, 2018
Bile-Salt-Hydrolases from the Probiotic Strain Lactobacillus johnsonii La1 Mediate Anti-giardial Activity in Vitro and in VivoThibault Allain, Soraya Chaouch, Myriam Thomas, et al.
Frontiers in Microbiology|February 24, 2018
Bile Salt Hydrolase Activities: A Novel Target to Screen Anti-Giardia Lactobacilli?Thibault Allain, Soraya Chaouch, Myriam Thomas, et al.
Frontiers in Microbiology|October 13, 2016
Deconjugated Bile Salts Produced by Extracellular Bile-Salt Hydrolase-Like Activities from the Probiotic Lactobacillus johnsonii La1 Inhibit Giardia duodenalis In vitro GrowthMarie-Agnès Travers, Cissé Sow, Séverine Zirah, et al.
Parasites & Vectors|December 6, 2025
Impact of Lactobacillus johnsonii CNCM I-4884 on canine giardiasis: a probiotic-based approachBruno Polack, Myriam Thomas, Alejandra Wu-Chuang, et al.
Malaria Journal|January 4, 2026
Natural triterpenic phenolic esters target PfA-M17 in Plasmodium falciparumLúcia Mamede, Gabriel W Rangel, Marjorie Schmitt, et al.
European Journal of Microbiology & Immunology|December 17, 2016
Comparative Antibody Responses Against three Antimalarial Vaccine Candidate Antigens from Urban and Rural Exposed Individuals in GabonRoméo-Karl Imboumy-Limoukou, Sandrine Lydie Oyegue-Liabagui, Stella Ndidi, et al.
BMC Genomics|May 21, 2009
A Plasmodium falciparum FcB1-schizont-EST collection providing clues to schizont specific gene structure and polymorphismIsabelle Florent, Betina M Porcel, Elodie Guillaume, et al.
Molecules (Basel, Switzerland)|October 14, 2018
Aminobenzosuberone Scaffold as a Modular Chemical Tool for the Inhibition of Therapeutically Relevant M1 AminopeptidasesEmmanuel Salomon, Marjorie Schmitt, Anil Kumar Marapaka, et al.
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