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A high-efficiency microfluidic device for size-selective trapping and sorting

Lab on a chip, 2014-07, Vol.14 (14), p.2480-2490

2014

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Adaptation of Translational Machinery in Malaria Parasites to Accommodate Translation of Poly-Adenosine Stretches Throughout Its Life Cycle

Frontiers in microbiology, 2019-12, Vol.10, p.2823-2823

2019

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Plasmodium falciparum translational machinery condones polyadenosine repeats

eLife, 2020-05, Vol.9

2020

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Poly-basic peptides and polymers as new drug candidates against Plasmodium falciparum

Malaria journal, 2024-08, Vol.23 (1), p.227-18, Article 227

2024

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Imaging and identification of waterborne parasites using a chip-scale microscope

PloS one, 2014-02, Vol.9 (2), p.e89712-e89712

2014

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Association of the receptor for activated C-kinase 1 with ribosomes in Plasmodium falciparum

The Journal of biological chemistry, 2022-06, Vol.298 (6), p.101954-101954, Article 101954

2022

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Anilinoquinoline based inhibitors of trypanosomatid proliferation

PLoS neglected tropical diseases, 2018-11, Vol.12 (11), p.e0006834-e0006834

2018

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Replication attempt: "Effect of BMAP-28 antimicrobial peptides on Leishmania major promastigote and amastigote growth: role of leishmanolysin in parasite survival"

PloS one, 2014-12, Vol.9 (12), p.e114614-e114614

2014

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Wide field-of-view Talbot grid-based microscopy for multicolor fluorescence imaging

Optics express, 2013-06, Vol.21 (12), p.14555-14565

2013

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Protozoan Parasite Growth Inhibitors Discovered by Cross-Screening Yield Potent Scaffolds for Lead Discovery

Journal of medicinal chemistry, 2015-07, Vol.58 (14), p.5522-5537

2015

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Discovery and Optimization of a Compound Series Active against Trypanosoma cruzi, the Causative Agent of Chagas Disease

Journal of medicinal chemistry, 2020-03, Vol.63 (6), p.3066-3089

2020

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A high-efficiency microfluidic device for size-selective trapping and sortingElectronic supplementary information (ESI) available. See DOI: 10.1039/c4lc00219a

2014-06

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Antitrypanosomal Lead Discovery: Identification of a Ligand-Efficient Inhibitor of Trypanosoma cruzi CYP51 and Parasite Growth

Journal of medicinal chemistry, 2013-03, Vol.56 (6), p.2556-2567

2013

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Optimization of physicochemical properties for 4-anilinoquinazoline inhibitors of trypanosome proliferation

European journal of medicinal chemistry, 2017-12, Vol.141, p.446-459

2017

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Protein Synthesis Adaptation to the Au-Rich Transcriptome of Plasmodium Falciparum

Erath, Jessey Lee

2020

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Small-molecule xenomycins inhibit all stages of the Plasmodium life cycle

Antimicrobial agents and chemotherapy, 2015-03, Vol.59 (3), p.1427-1434

2015

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Scaffold and Parasite Hopping: Discovery of New Protozoal Proliferation Inhibitors

ACS medicinal chemistry letters, 2020-03, Vol.11 (3), p.249-257

2020

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Corrigendum to “Optimization of physicochemical properties for 4-Anilinoquinazoline inhibitors of trypanosome proliferation” [Eur. J. Med. Chem. 141 (2017) 446–459]

European journal of medicinal chemistry, 2018-05, Vol.152, p.515-515

2018

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Repurposing human Aurora kinase inhibitors as leads for anti-protozoan drug discovery

MedChemComm, 2014-05, Vol.5 (5), p.655-658

2014

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Antiparasitic Lead Discovery: Toward Optimization of a Chemotype with Activity Against Multiple Protozoan Parasites

ACS medicinal chemistry letters, 2017-03, Vol.8 (3), p.350-354

2017

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Series of Alkynyl-Substituted Thienopyrimidines as Inhibitors of Protozoan Parasite Proliferation

ACS medicinal chemistry letters, 2018-10, Vol.9 (10), p.996-1001

2018

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EVALUATION OF AROMATIC 6-SUBSTITUTED THIENOPYRIMIDINES AS SCAFFOLDS AGAINST PARASITES THAT CAUSE TRYPANOSOMIASIS, LEISHMANIASIS, AND MALARIA

MedChemComm, 2015-02, Vol.6 (2), p.339-346

2015

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Identification of “Preferred” Human Kinase Inhibitors for Sleeping Sickness Lead Discovery. Are Some Kinases Better than Others for Inhibitor Repurposing?

ACS infectious diseases, 2016-03, Vol.2 (3), p.180-186

2016

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Evaluation of aromatic 6-substituted thienopyrimidines as scaffolds against parasites that cause trypanosomiasis, leishmaniasis, and malariaElectronic supplementary information (ESI) available: Synthetic preparations, assay details, in vitro ADME data, and additional malaria screening data are described in the ESI. See DOI: 10.1039/c4md00441h

2015-02

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Replication Attempt: "Effect of BMAP-28 Antimicrobial Peptides on Leishmania Major Promastigote and Amastigote Growth: Role of Leishmanolysin in Parasite Survival": e114614

PloS one, 2014-12, Vol.9 (12)

2014

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A high-efficiency microfluidic device for size-selective trapping and sorting

Adaptation of Translational Machinery in Malaria Parasites to Accommodate Translation of Poly-Adenosine Stretches Throughout Its Life Cycle

Plasmodium falciparum translational machinery condones polyadenosine repeats

Poly-basic peptides and polymers as new drug candidates against Plasmodium falciparum

Imaging and identification of waterborne parasites using a chip-scale microscope

Association of the receptor for activated C-kinase 1 with ribosomes in Plasmodium falciparum

Anilinoquinoline based inhibitors of trypanosomatid proliferation

Replication attempt: "Effect of BMAP-28 antimicrobial peptides on Leishmania major promastigote and amastigote growth: role of leishmanolysin in parasite survival"

Wide field-of-view Talbot grid-based microscopy for multicolor fluorescence imaging

Protozoan Parasite Growth Inhibitors Discovered by Cross-Screening Yield Potent Scaffolds for Lead Discovery

Discovery and Optimization of a Compound Series Active against Trypanosoma cruzi, the Causative Agent of Chagas Disease

A high-efficiency microfluidic device for size-selective trapping and sortingElectronic supplementary information (ESI) available. See DOI: 10.1039/c4lc00219a

Antitrypanosomal Lead Discovery: Identification of a Ligand-Efficient Inhibitor of Trypanosoma cruzi CYP51 and Parasite Growth

Optimization of physicochemical properties for 4-anilinoquinazoline inhibitors of trypanosome proliferation

Protein Synthesis Adaptation to the Au-Rich Transcriptome of Plasmodium Falciparum

Small-molecule xenomycins inhibit all stages of the Plasmodium life cycle

Scaffold and Parasite Hopping: Discovery of New Protozoal Proliferation Inhibitors

Corrigendum to “Optimization of physicochemical properties for 4-Anilinoquinazoline inhibitors of trypanosome proliferation” [Eur. J. Med. Chem. 141 (2017) 446–459]

Repurposing human Aurora kinase inhibitors as leads for anti-protozoan drug discovery

Antiparasitic Lead Discovery: Toward Optimization of a Chemotype with Activity Against Multiple Protozoan Parasites

Series of Alkynyl-Substituted Thienopyrimidines as Inhibitors of Protozoan Parasite Proliferation

EVALUATION OF AROMATIC 6-SUBSTITUTED THIENOPYRIMIDINES AS SCAFFOLDS AGAINST PARASITES THAT CAUSE TRYPANOSOMIASIS, LEISHMANIASIS, AND MALARIA

Identification of “Preferred” Human Kinase Inhibitors for Sleeping Sickness Lead Discovery. Are Some Kinases Better than Others for Inhibitor Repurposing?

Replication Attempt: "Effect of BMAP-28 Antimicrobial Peptides on Leishmania Major Promastigote and Amastigote Growth: Role of Leishmanolysin in Parasite Survival": e114614

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