has been cited by the following article(s):
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[1]
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Identification of a Human Anti-Alpha-Toxin Monoclonal Antibody Against Staphylococcus aureus Infection
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Frontiers in …,
2021 |
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[2]
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Nouvelles méthodes électrochimiques pour le criblage d'inhibiteurs de transcétolases
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2018 |
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[3]
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Recent progress in the identification and development of anti-malarial agents using virtual screening based approaches
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Combinatorial chemistry & high throughput screening,
2015 |
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[4]
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Chemical and genetic validation of thiamine utilization as an antimalarial drug target
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Nature communications,
2013 |
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[5]
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Molecular Modelling and Docking Studies of Human Blood Coagulation Factor-XIIIA Protein
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SK Gunda, AM Madasu, P Kakarla, M Shaik - ijrpbsonline.com,
2013 |
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[6]
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Synthesis of hybrid 4-anilinoquinoline triazines as potent antimalarial agents, their in silico modeling and bioevaluation as Plasmodium falciparum transketolase and β-hematin inhibitors
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MedChemComm,
2012 |
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[7]
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Thiamin (vitamin B1) biosynthesis and regulation: a rich source of antimicrobial drug targets?
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International journal of biological sciences,
2011 |
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[1]
|
Identification of a Human Anti-Alpha-Toxin Monoclonal Antibody Against Staphylococcus aureus Infection
Frontiers in Microbiology,
2021
DOI:10.3389/fmicb.2021.692279
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[2]
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Innovative Electrochemical Screening Allows Transketolase Inhibitors to Be Identified
Analytical Chemistry,
2018
DOI:10.1021/acs.analchem.8b01752
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[3]
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Innovative Electrochemical Screening Allows Transketolase Inhibitors to Be Identified
Analytical Chemistry,
2018
DOI:10.1021/acs.analchem.8b01752
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[4]
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Chemical and genetic validation of thiamine utilization as an antimalarial drug target
Nature Communications,
2013
DOI:10.1038/ncomms3060
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[5]
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Chemical and genetic validation of thiamine utilization as an antimalarial drug target
Nature Communications,
2013
DOI:10.1038/ncomms3060
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[6]
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Synthesis of hybrid 4-anilinoquinoline triazines as potent antimalarial agents, their in silico modeling and bioevaluation as Plasmodium falciparumtransketolase and β-hematin inhibitors
Med. Chem. Commun.,
2012
DOI:10.1039/C1MD00188D
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