Ketonic metabolites of progesterone and 19-norprogesterone in rabbit urine.

نویسنده

  • G H THOMAS
چکیده

Bunyan, J., Green, J., Edwin, E. E. & Diplock, A. T. (1960). Biochem. J. 77, 47. Christensen, F., Dam, H., Gortner, R. A., jun. & S0ndergaard, E. (1956). Acta physiol. scand. 35, 215. Cowlishaw, B. (1961). Biochim. biophy8. Acta, 49, 583. Evans, J. D., Waldron, L. M., Oleksyshyn, N. L. & Riemenschneider, R. W. (1956). J. biol. Chem. 218, 255. Glavind, J. & Hartmann, S. (1951). Acta chem. 8cand. 5, 975. Goodman, D. S. (1957). Science, 123, 1296. Gordon, R. S. (1957). J. clin. Invest. 36, 810. Green, J., Marcinkiewicz, S. & Watt, P. R. (1955). J. Sci. Fd Agric. 6, 274. Hilditch, T. P. (1956). The Chemical Constitution of Natural Fats, p. 175. London: Chapman and Hall Ltd. Horwitt, M. K., Harvey, C. C., Duncan, G. D. & Wilson, W. G. (1956). Amer. J. clin. Nutr. 4, 408. Kenaston, C. B., Wilbur, K. M., Ottolenghi, A. & Bernheim, F. (1955). J. Amer. Oil Chem. Soc. 32, 33. Palmer, W. W. (1918). J. biol. Chem. 33, 119. Patton, S. & Kurtz, G. W. (1951). J. Dairy Sci. 34, 669. Ponder, E. (1948). Haemolysis and Related Phenomena, pp. 23, 329. London: J. and A. Churchill Ltd. Rose, C. S. & Gyorgy, P. (1952). Amer. J. Physiol. 168, 414. Saslaw, L. D. & Waravdekar, V. S. (1957). J. org. Chem. 22, 843. Swift, C. E. (1946). In Trans. 18t Josiah Macy, jun., Conf., Biological Antioxidant8, p. 16. Ed. by Mackenzie, C. G. Tappel, A. L. (1953). Fd Res. 18, 104. Tsen, C. C. & Collier, H. B. (1960). Canad. J. Biochem. Physiol. 38, 957. Waravdekar, V. S. & Saslaw, L. D. (1959). J. biol. Chem. 234, 1945. Warren, L. (1959). J. biol. Chem. 234, 1971. Weissbach, A. & Hurwitz, J. (1959). J. biol. Chem. 234, 705. Wilbur, K. M., Bernheim, F. & Shapiro, 0. W. (1949). Arch. Biochem. 24, 305.

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عنوان ژورنال:
  • The Biochemical journal

دوره 83  شماره 

صفحات  -

تاریخ انتشار 1962