conspectus of researchon copper metabolism and requirements

2054 KARL E. MASON
plasmiti with cytocuprein. Biochim. Biophys.
Acta 328, 351-358.
490. Markowitz, H., Cartwright, G. E. & Wintrobe,
M. M. (1959) Studies on copper
metabolism. XXVII. Isolation and properties
of erythrocyte cuproprotein ( erythrocuprein).
J. Biol. Chem. 234, 40-45.
491. Markowitz, H., Gubler, C. J., Mahoney, J. P.
Cartwright, G. E. & Wintrobe, M. M.
(1955) Studies on copper metabolism. XIV.
Copper, ceruloplasmin and oxidase activity
in sera of normal human subjects, pregnant
women, and patients with infection, hepatolenticular
degeneration and the nephrotic
syndrome. J. Clin. Invest. 34, 1498-1508.
492. Markowitz, H., Shields, G. S., Klassen, W.
H., Cartwright, G. E. & Wintrobe, M. M.
( 1961 ) Spectrophotometric determination
of total erythrocyte copper. Anal. Chem. 33,
1594-1598.
493. Marston, H. R. ( 1952 ) Cobalt, copper and
molybdenum in the nutrition of animals and
plants. Physiol. Rev. 32, 62-111.
494. Masi, M., Paolucci, P., Vecchi, V. & Vivarelli,
F. ( 1975 ) La ceruloplasminemia nel
bambino normale. Minerva Pediat. 27, 1175-
1180.
495. Matsuda, I. (1978) Screening for Wilson's
disease. Lancet 1, 562.
496. Matsuda, I., Pearson, T. & Holtzman, N. A.
( 1974 ) Determination of apoceruloplasmin
by radioimmunoas^ay in nutritional copper
deficiency, Menkes' kinky hair syndrome, Wil
son's disease, and umbilical cord blood.
Pediat. Res. 8, 821-824.
497. Matter, B. J., Pederson, J., Psimenos, G. &
Lindeman, R. D. (1969) Lethal copper
intoxication in hemodialysis. Trans. Soc.
Artif. Intern. Organs 15, 309-315.
498. Matthews, W. B. (1954) The absorption
and excretion of radiocopper in hepatolenticular
degeneration (Wilson's disease).
J. Neurol. Neurosurg. Psychiat. 17, 242-246.
499. Matthews, W. B., Milne, M. D. & Bell, M.
( 1952 ) The metabolic disorder in hepatolenticular
degeneration. Quart. J. Med. 21,
425-446.
500. McCord, J. M. & Fridovich, I. (1969)
Superoxide dismutase. An enzymic function
for erythrocuprein (hemocuprein). J. Biol.
Chem. 244, 6049-6055.
501. McCord, J. M. & Fridovich, I. (1970) The
utility of Superoxide dismutase in studying
free radical reactions. II. The mechanism of
the mediation of cytochrome c reduction by
a variety of electron carriers. J. Biol. Chem.
245, 1374-1377.
502. McCosker, P. J. (1961) Paraphenylenediamine
oxidase activity and copper-levels in
mammalian plasmas. Nature 190, 887-889.
503. McCullars, G. M., O'Reilly, S. & Brennan,
M. (1977) Pigment binding of copper in
human bile. Clin. Chim. Acta 74, 33-38.
504. McDermott, J. A., Huber, C. T., Osaki, S.
& Frieden, E. (1968) Role of iron in the
oxidase activity of ceruloplasmin. Biochem.
Biophys. Acta 151, 541-557.
505. McEwen, C. M., Jr. (1965) Human
plasma monoamine oxidase. 1. Purification
and identification. J. Biol. Chem. 240, 2003-
2010.
506. McEwen, C. M., Jr. & Harrison, D. C.
( 1965 ) Abnormalities of serum monoamine
oxidase in chronic congestive heart failure.
J. Lab. Clin. Med. 65, 546-559.
507. McHargue, J. S. (1926) Further evidence
that small quantities of copper, manganese
and zinc are factors in the metabolism of
animals. Am. J. Physiol. 77, 245-255.
508. Mclntyre, N., Clink, H. M., Levi, A. J.,
Cummings, J. N. & Sherlock, S. (1967)
Hemolytic anemia in Wilson's disease. New
Engl. J. Med. 276, 439-444.
509. McKenzie, J. M. (1974) Tissue concen
tration of cadmium, zinc and copper from
autopsy samples. N.Z. Med. J. 79, 1016-
1019.
510. McKenzie, J. M., Guthrie, B. E. & Prior,
I. A. M. (1978) Zinc and copper status
of Polynesian residents in the Tokelau
Islands. Am. J. Clin. Nutr. 31, 422-428.
511. McKenzie, J. M., Van Rij, A. M., Robinson,
M. F. & Guthrie, B. E. (1976) Trace ele
ment balance studies during total parenteral
nutrition. In: Trace Substances in Environ
mental Health, X. University of Missouri,
Columbia.
512. McMullen, W. (1971) Copper contami
nation in soft drinks from bottle pourers.
Health Bulletin (Scotland) 29, 94-96.
513. Menkes, J. H., Alter, M., Steigleder, G. K.,
Weakley, D. R. & Sung, J. H. (1962) A
sex-linked recessive disorder with retarda
tion of growth, peculiar hair, and focal
cerebral and cerebellar degeneration. Pedi
atrics 29, 764-779.
514. Mertz, W. (1972) Human requirements:
basic and optimal. Ann. N.Y. Acad. Sci. 199,
191-201.
515. Mertz, W. (1976) Defining trace element
deficiencies and toxicities in man. In: Molyb
denum in the Environment. The Biology of
Molybdenum. (Chapell, W. R. & Peterson,
K. K., eds.), vol. I, pp. 267-286, Marcel
Dekker, New York.
516. Meyer, R. J. & Zalusky, R. (1977) The
mechanisms of hemolysis in Wilson's disease:
study of a case and review of the literature.
Mt. Sinai J. Med. 44, 530-538.
517. Miller, R. F. & Engel, R. W. (1960) In
terrelations of copper, molybdenum and sul
fate sulfur in nutrition. Federation Proc.
19, 666-677.
518. Mills, C. F. (1974) Trace-element inter
actions: effects of dietary composition on
the development of imbalance and toxicity.
In: Trace Element Metabolism in Animals—
2 (Hoekstra, W. G., Suttie, J. W., Ganther,
H. E. & Mertz, W., eds.), pp. 79-90, Uni
versity Park Press, Baltimore.
519. Mills, E. S. (1924) Hemochromatosis
with special reference to its frequency and
to its occurrence in women. Arch. Intern.
Med. 34, 292-300.
Downloaded from
jn.nutrition.org
by guest on February 27, 2013