Membrane transport proteins as therapeutic targets in malaria

Author:

Desai Sanjay A.1,Rayavara Kempaiah1,Sharma Paresh2,Syed Sayeed K.1,Nguitragool Wang3,Nina Praveen Balabaskaran4

Affiliation:

1. The Laboratory of Malaria and Vector Research; National Institute of Allergy and Infectious Diseases, National Institutes of Health; Rockville MD USA

2. National Institute of Animal Biotechnology; Hyderabad India

3. Department of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine; Mahidol University; Bangkok Thailand

4. PSG Institute of Medical Sciences and Research; Coimbatore India

Publisher

John Wiley & Sons, Inc.

Reference103 articles.

1. High-resolution autoradiography of malarial parasites treated with 3H-chloroquine;Aikawa;The American Journal of Pathology,1972

2. Plasmodium falciparum likely encodes the principal anion channel on infected human erythrocytes;Alkhalil;Blood,2004

3. Babesia and plasmodia increase host erythrocyte permeability through distinct mechanisms;Alkhalil;Cellular Microbiology,2007

4. The global pipeline of new medicines for the control and elimination of malaria;Anthony;Malaria Journal,2012

5. Limited genetic diversity of the Plasmodium falciparum aquaglyceroporin gene;Bahamontes-Rosa;Molecular and Biochemical Parasitology,2007

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