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Studies with plant alpha-galactosidases
1976The two molecular forms, I and II, of [alpha]-galactosidase from immature, mature (resting) and germinated vicia faba seeds have been studied. The enzymes have been purified by a multistage procedure and, in particular, the effect these stages have upon the relative isoenzyme levels has been investigated.
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Structure-function relationships in alpha-galactosidase A.
Acta paediatrica (Oslo, Norway : 1992), 2007With recent interest in the molecular mechanisms responsible for Fabry disease, the number of known mutations in the GLA gene which encodes alpha-galactosidase A has expanded considerably. Combining a large database of Fabry disease-causing mutations with the recently determined crystal structure of human alpha-galactosidase A allows for a new ...
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A case of Fabry disease (alpha-galactosidase A deficiency).
The Journal of the Kentucky Medical Association, 1994Fabry disease is a rare lipid storage disorder, often silent until adulthood. We report the case of a rural, primary care patient whose initial presentation was that of progressive weakness from anemia. The anemia was determined to be of renal origin, and led to a diagnosis of Fabry disease.
W C, Thornbury, P, Aaron
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The nature of Vicia faba alpha-galactosidases
1983Two molecular forms I and II (separable by gel filtration) from mature Vicia faba seeds have been studied. The extractability of the enzymes and the in vitro conversion of the low MW form, II, to the larger oligomer, I has been examined over a range of salt concentrations.
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Alpha-galactosidase a from human placenta
Biochimica et Biophysica Acta (BBA) - Enzymology, 1977Jary S. Mayes, Ernest Beutler
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