D
Donald Robinson
Researcher at Queen Elizabeth College, Mauritius
Publications - 53
Citations - 2177
Donald Robinson is an academic researcher from Queen Elizabeth College, Mauritius. The author has contributed to research in topics: Mannosidosis & Hexosaminidases. The author has an hindex of 25, co-authored 53 publications receiving 2169 citations.
Papers
More filters
Journal ArticleDOI
N-Acetyl-β-glucosaminidases in human spleen
Donald Robinson,John L. Stirling +1 more
TL;DR: The N-acetyl-β-glucosaminidase of human spleen has been separated by gel electrophoresis into two components, an acidic form A and a basic form B, and evidence is presented to indicate that the A form contains a number of sialic acid residues.
Journal ArticleDOI
Separation and properties of β-galactosidase, β-glucosidase, β-glucuronidase and n-acetyl-β-glucosaminidase from rat kidney
TL;DR: DEAE-cellulose chromatography and filtration on Sephadex gels suggests that the β-glucosidase component is a small acidic molecule, of molecular weight approx.
Journal ArticleDOI
β-Galactosidase, β-glucosidase and N-acetyl-β-glucosaminidase in human kidney
TL;DR: The levels of N -acetyl- β -glucosaminidase, β-galactosidase and β-glucosaidase activity in normal human kidney were determined fluorimetrically as discussed by the authors.
Journal ArticleDOI
Human mannosidosis — The enzymic defect
TL;DR: Normal human liver α-mannosidase exists in at least 3 forms, separable by DEAE cellulose chromatography, and the A and B forms are most active at pH 4.4 while activity of form C is maximal at pH 6.0.
Journal ArticleDOI
Genetic heterogeneity in GM1-gangliosidosis.
Hans Galjaard,A. T. Hoogeveen,W. Keijzer,H.A. de Wit-Verbeek,Arnold J. J. Reuser,Mae Wan Ho,Donald Robinson +6 more
TL;DR: GM1-GANGLIOSIDOSIS is an inherited lysosomal storage disease which is due to a deficiency of the acid hydrolase GM1-β-galactosidase1 but no experimental evidence has been provided to support the hypotheses.