Disruption of Rosetting in Plasmodium falciparum Malaria with Chemically Modified Heparin and Low Molecular Weight Derivatives Possessing Reduced Anticoagulant and Other Serine Protease Inhibition Activities-Reference-Cited by-同舟云学术

Disruption of Rosetting in Plasmodium falciparum Malaria with Chemically Modified Heparin and Low Molecular Weight Derivatives Possessing Reduced Anticoagulant and Other Serine Protease Inhibition Activities

Published:2008-02-09 Issue:5 Volume:51 Page:1453-1458
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Skidmore Mark A.¹,Dumax-Vorzet Audrey F.¹,Guimond Scott E.¹,Rudd Timothy R.¹,Edwards Elizabeth A.¹,Turnbull Jeremy E.¹,Craig Alister G.¹,Yates Edwin A.¹

Affiliation:

1. School of Biological Sciences, The University of Liverpool, Crown Street, Liverpool, L69 7ZB, England, School of Medicine, The University of Manchester, Oxford Road, Manchester, M13 9PT, England, and Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA, England

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm701337t

Reference28 articles.

1. Malaria Parasites Can Develop Stable Resistance to Artemisinin but Lack Mutations in Candidate Genes atp6 (Encoding the Sarcoplasmic and Endoplasmic Reticulum Ca 2+ ATPase), tctp , mdr1 , and cg10

2. Resistance of Plasmodium falciparum field isolates to in-vitro artemether and point mutations of the SERCA-type PfATPase6

3. Plasmodium falciparum rosetting is associated with malaria severity in Kenya

4. Identification of Plasmodium falciparum Erythrocyte Membrane Protein 1 (PfEMP1) as the Rosetting Ligand of the Malaria Parasite P. falciparum

5. P. falciparum rosetting mediated by a parasite-variant erythrocyte membrane protein and complement-receptor 1

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