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Reddi, K. K. (1958). Biochim. biophy8. Acta, 28, 386. Roth, J. S. (1954). J. biol. Chem. 208, 181. Roth, J. S. (1956). Biochim. biophys. Acta, 21, 34. Roth, J. S. (1958a). J. biol. Chem. 231, 1085, 1097. Roth, J. S. (1958b). Arch. Biochem. Biophys. 74, 277. Smith, M., Moffatt, J. G. & Khorana, H. G. (1958). J. Amer. chem. Soc. 80, 6204. Speigelman, S. (1958). Recent Progress in Microbiology, p. 81. Ed. by Tunevall, G. Stockholm: Almqvist and Wiksell. Tissi6res, A., Watson, J. D., Schlessinger, D. & Holingworth, B. R. (1959). J. nwWle. Biol., 1, 221. Wade, H. E. (1960). Biochem. J. 77, 534. Wade, H. E. & Lovett, S. (1958). Biochem. J. 70, 697. Wade, H. E. & Morgan, D. M. (1954). Biochem. J. 56, 41. Wade, H. E. & Morgan, D. M. (1955). Biochem. J. 60, 264. Wade, H. E. & Morgan, D. M. (1957). Biochem. J. 65, 321. Wagman, J. & Trawick, W. R. (1958). In Microsomal Particles and Protein Synthesis, p. 11. Ed. by Roberts, R. B. Washington: Washington Academy of Sciences.

biochemical journal. cellular aspects

The metabolism of <i>Plasmodium berghei</i>, the malaria parasite of rodents. 2. An effect of mepacrine on the metabolism of glucose by the parasite separated from its host cell

The metabolism of Plasmodium berghei, the malaria parasite of rodents. 2. An effect of mepacrine on the metabolism of glucose by the parasite separated from its host cell