Evidence for an Accessory Pathway of Galactose Metabolism in Mammalian Liver
Author:
Affiliation:
1. Department of Medicine, Harvard Medical School and Medical Service, Massachusetts General Hospital, Boston
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference14 articles.
1. Galactosemia, a congenital defect in a nucleotide transferase
2. Congenital Galactosemia, a Single Enzymatic Block in Galactose Metabolism
3. Townsend, E. P., Pediatrics 7: 760 (1951).
4. Studies on Metabolism of Carbon-14-Labeled Galactose in a Galactosemic Individual
5. Dutton, G. L., Biochem. J. (London) 57: 275 (1954).
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1. Uridine Diphosphate Glucose Pyrophosphorylase;Journal of Biological Chemistry;1970-05
2. Human Hepatic Uridine Diphosphate Galactose Pyrophosphorylase;Journal of Biological Chemistry;1969-02
3. Mammalian Galactose Dehydrogenase;Journal of Biological Chemistry;1966-12
4. Developmental Aspects and Some Characteristics of Mammalian Galactose 1-Phosphate Uridyltransferase;Journal of Biological Chemistry;1966-09
5. Mammalian Galactokinase;Journal of Biological Chemistry;1965-06
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