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J

John Okombo

Harvard University
H指数:24
被引数:1,727

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Identification of genetic markers of quinine partial resistance in Plasmodium falciparum

鉴定恶性疟原虫中奎宁部分耐药性的遗传标记

2026-07-060
OAAI
Plasmodium falciparum HSP90 inhibitors show divergent resistance despite a shared ATP-binding site

恶性疟原虫HSP90抑制剂表现出差异性耐药性,尽管具有共同的ATP结合位点

2026-07-010
PRE
Collateral hypersensitivity between ZY19489 and piperaquine neutralizes PfCRT-mediated drug efflux and Plasmodium falciparum resistance

ZY19489与哌喹之间的交叉高敏性中和了PfCRT介导的药物外排和恶性疟原虫抗性

2026-04-010
OAAI
Plasmodium falciparum protein kinase 6 and hemozoin formation are inhibited by a type II human kinase inhibitor exhibiting antimalarial activity

Plasmodium falciparum蛋白激酶6和血红素晶体的形成被一种具有抗疟疾活性的II型人源激酶抑制剂所抑制

2025-07-070
PRE
Inhibitors of malaria parasite cyclic nucleotide phosphodiesterases block asexual blood-stage development and mosquito transmission
2024-12-060
OAAI
A novel 4-aminoquinoline chemotype with multistage antimalarial activity and lack of cross-resistance with PfCRT and PfMDR1 mutants

一种具有多阶段抗疟活性且与PfCRT和PfMDR1突变体缺乏交叉抗性的新型4-氨基喹啉化学型

2024-10-290
OAAI
Additional PfCRT mutations driven by selective pressure for improved fitness can result in the loss of piperaquine resistance and altered Plasmodium falciparum physiology
MBIO
IF4.7
2024-01-163
OAAI
Advances in malaria pharmacology and the online guide to MALARIA PHARMACOLOGY: IUPHAR review 38
2023-06-108
OAAI
Generation of a mutator parasite to drive resistome discovery in Plasmodium falciparum
2023-05-2715
OAAI
Cytoplasmic isoleucyl tRNA synthetase as an attractive multistage antimalarial drug target
2023-03-0811
OA
The Plasmodium falciparum ABC transporter ABCI3 confers parasite strain-dependent pleiotropic antimalarial drug resistance
2022-05-0118
OAAI
Prioritization of Molecular Targets for Antimalarial Drug Discovery

优先考虑抗疟药物发现的分子靶标

2021-09-1551
OAAI
Novel Antimalarial Tetrazoles and Amides Active against the Hemoglobin Degradation Pathway in Plasmodium falciparum
2021-02-2315
OA
Identification of 2,4-Disubstituted Imidazopyridines as Hemozoin Formation Inhibitors with Fast-Killing Kinetics and In Vivo Efficacy in the Plasmodium falciparum NSG Mouse Model (vol 63, pg 13013, 2020)
2021-01-280
PREAI
Identification of 2,4-Disubstituted Imidazopyridines as Hemozoin Formation Inhibitors with Fast-Killing Kinetics and In Vivo Efficacy in the Plasmodium falciparum NSG Mouse Model
2020-10-2613
OAAI