Results 61 to 70 of about 3,298 (171)
Unveiling Antimalarial Drug Resistance: The Role of CRISPR‐Cas Technologies in Malaria Research
Background Malaria, caused by Plasmodium parasites, remains a global health burden, with drug resistance threatening control efforts. CRISPR‐Cas technologies, particularly CRISPR‐Cas9, have transformed malaria research by enabling precise genetic manipulations to study antimalarial resistance mechanisms, develop novel therapeutics and enhance ...
Reuben Samson Dangana +3 more
wiley +1 more source
Heterologous Expression and ATPase Activity of Mutant versus Wild Type PfMDR1 Protein†
Mutation of the P. falciparum chloroquine resistance transporter (PfCRT) causes resistance to chloroquine (CQ) and other antimalarial drugs. Mutation and/or overexpression of one of the multidrug resistance protein homologues found in this malarial ...
Linda E. Amoah (2491204) +2 more
core +1 more source
Mutations in Pfcrt and Pfmdr1.
Mutations in Pfcrt and Pfmdr1.
Inke Lubis (6475796) +13 more
core +1 more source
Background: Artemisinin-based combination therapies (ACTs) are the global mainstay treatment of uncomplicated Plasmodium falciparum infections. PfMDR1 and PfCRT are two transmembrane transporters, associated with sensitivity to several antimalarials ...
A. Björkman (6249143) +7 more
core +1 more source
Background: Due to the widespread resistance of Plasmodium falciparum to chloroquine drug, artemisinin-based combination therapy (ACT) has been recommended as the first-line treatment. This study aims to evaluate the extent of chloroquine resistance in P.
Hiasindh Ashmi Antony +3 more
doaj +1 more source
Malaria remains a major global health problem, with uneven progress and the greatest disease burden clustered in sub‐Saharan Africa. Antimalarial drug resistance continues to undermine malaria control efforts, with widespread resistance reported in Plasmodium falciparum, including reduced susceptibility to artemisinin‐based combination therapies (ACTs).
Stephen Mwangi Njoroge +8 more
wiley +1 more source
Ein neuer Malariawirkstoff hemmt die Proteinsynthese von Plasmodium falciparum
Die Verbindung 31 stellt einen vielversprechenden Ansatz für die Entwicklung eines Malariawirkstoffs mit einem starken Wirkungsprofil dar (PfNF54 IC50 ± s.d. = 3,9 ± 0,4 nM). Sie hat einen neuartigen Wirkmechanismus, indem sie an zytosolische Ribosomen‐Untereinheiten bindet und dadurch die Proteinsynthese im Parasiten hemmt.
Patricia Bravo +16 more
wiley +1 more source
Molecular surveillance of drug resistance markers through time provides crucial information on genomic adaptations, especially in parasite populations exposed to changing drug pressures.
John Okombo +4 more
doaj +1 more source
Background Artemisinin resistance is present in the Greater Mekong region and poses a significant threat for current anti-malarial treatment guidelines in Bangladesh.
Mohammad Shafiul Alam +9 more
doaj +1 more source
Background In 2002, Zambia withdrew chloroquine as first-line treatment for Plasmodium falciparum malaria due to increased treatment failure and worldwide spread of chloroquine resistance.
Mwenda C. Mulenga +6 more
doaj +1 more source

