Results 251 to 260 of about 261,281 (306)
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GALACTOSE STUDIES IN AN INFANT WITH IDIOPATHIC GALACTOSE INTOLERANCE
Pediatrics, 1948Galactose metabolism has been studied in a group of convalescent children and in one patient with galactosuria, hepatomegaly and splenomegaly, and cataracts. The galactose tolerance of the convalescent infants studied following intravenous injection of the sugar was similar to that observed in healthy adults.
L, GREENMAN, J C, RATHBUN
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Galactose-sensitive mutants of Salmonella I. Metabolism of galactose
Biochimica Et Biophysica Acta, 1961Abstract The metabolism of galactose was studied in peculiar mutants of Salmonella (M mutants) which (1) fail to produce acid from galactose and (2) undergo severe bacteriolysis when grown in the presence of galactose. The mutants were shown to have a specific hereditary defect in the enzyme UDPGal-4-epimerase, and to accumulate intracellularly ...
Hiroshi Nikaido
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Galactose toxicity in the chick: Oxidation of radioactive galactose
Biochimica et Biophysica Acta (BBA) - General Subjects, 1970Abstract Radioactive galactose has been shown to be converted to 14 CO 2 by both the intact chick and by various tissues in vitro . The pattern of 14 CO 2 liberation by the intact chick was not related to the sex of the chick nor to whether the 14 C was in C-1 or C-2 position. [1- 14 C]Glucose was metabolized to 14 CO 2 at a faster rate than [
H J, Wells, M, Gordon, S, Segal
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Galactose disorders: An overview
Journal of Inherited Metabolic Disease, 1990SummaryThere are three separate disorders of galactose metabolism of clinical importance. Galactokinase deficiency mainly causes cataracts which regress without complications providing a galactose‐free diet is started early enough. UDPgalactose‐4‐epimerase deficiency seems extremely rare.
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2002
The free radical-coupled copper catalytic motif has emerged as the unifying feature of a new family of enzymes, the radical copper oxidases. Their highly evolved active sites include a novel amino acid modification, the Tyr-Cys dimer, that forms spontaneously through self-processing of the protein during its maturation. The active site is remarkable in
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The free radical-coupled copper catalytic motif has emerged as the unifying feature of a new family of enzymes, the radical copper oxidases. Their highly evolved active sites include a novel amino acid modification, the Tyr-Cys dimer, that forms spontaneously through self-processing of the protein during its maturation. The active site is remarkable in
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Placenta, 1992
The galactose alpha 1-3 galactose (Gal alpha 1-3 Gal) residue is a carbohydrate widely distributed in many non-human mammals. Since Gal alpha 1-3 Gal residues are described on the cell surface of tumor cells, we have examined the possibility of their expression on human trophoblastic cells at different stages of placental implantation and in various ...
Y, Christiane +5 more
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The galactose alpha 1-3 galactose (Gal alpha 1-3 Gal) residue is a carbohydrate widely distributed in many non-human mammals. Since Gal alpha 1-3 Gal residues are described on the cell surface of tumor cells, we have examined the possibility of their expression on human trophoblastic cells at different stages of placental implantation and in various ...
Y, Christiane +5 more
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Glucose-galactose malabsorption
The Journal of Pediatrics, 1966This is the first report in the American literature of a patient with a deficiency of gastrointestinal absorption of glucose and galactose. The disease is characterized by severe, chronic, watery diarrhea starting soon after birth. Marked improvement occurs following the substitution of the offending sugars by fructose.
J F, Marks, J B, Norton, J S, Fordtran
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