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Titlebook: Complex Carbohydrates of Nervous Tissue; Richard U. Margolis,Renée K. Margolis Book 1979 Plenum Press, New York 1979 adenosine.brain.carbo

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[Acetyl-CoA carboxylase] kinase,laminae and produce axons that ignore numerous incompatible neurons and eventually locate “target” cells at considerable distances from their cell body. These axons are then enveloped by a myelin sheath (derived from the plasma membrane of oligodendroglial cells of neuroectodermal origin) and surrou
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[Acetyl-CoA carboxylase] kinase,y granules and vesicles. These intracellular storage organelles, which are delimited by a single membrane, are endowed with the ability to discharge their content into the extracellular space by exocytosis. Since each secretory system is characterized by the specificity of its secretion products, th
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[Tyrosine 3-monooxygenase] kinase,cosidases. Numerous human neurological and neurovisceral storage diseases, known collectively as the lysosomal storage diseases, have been found to result from the inherited deficiency of any one of these glycosidases. Two groups of these disorders, namely, the inborn errors of glycoprotein cataboli
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Histochemistry and Cytochemistry of Glycoproteins and Glycosaminoglycans,and Gommi, 1965; Vaccari .., 1971), and there is evidence that the cholera toxin receptor involves a ganglioside (Cuatrecasas, 1973; Holmgren .., 1973; Van Heyningen W. E., .., 1971; Van Heyningen, S., 1974). The nicotinic acetylcholine receptor also contains carbohydrate (Meunier ., 1974; Raftery .
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