STUDIES ON HUMAN LYSOSOMAL β-D-N-ACETYL HEXOSAMINIDASE AND ARYLSULFATASE ISOZYMES
Authors:
- 1 January 1975
- book chapter
- Published by Elsevier
- p. 439-468
Abstract
No abstract availableThis publication has 56 references indexed in Scilit:
- Genetic complementation after fusion of Tay-Sachs and Sandhoff cellsNature, 1974
- A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblastsBiochemical and Biophysical Research Communications, 1974
- Isolation and characterization of the major .beta.-N-acetyl-D-glucosaminidase from human plasmaBiochemistry, 1974
- Complementation Analysis of Maple Syrup Urine Disease in Heterokaryons derived from Cultured Human FibroblastsNature, 1973
- A correlation of intracellular cerebroside sulfatase activity in fibroblasts with latency in metachromatic leukodystrophyBiochemical and Biophysical Research Communications, 1971
- Lysosomal hydrolases: Conversion of acidic to basic forms by neuraminidaseFEBS Letters, 1971
- Tay‐sachs disease and related disorders: Fractionation of brain N‐acetyl‐β‐hexosaminidase on DEAE‐celluloseFEBS Letters, 1970
- Demonstration of an alteration of ganglioside metabolism in Tay-Sachs diseaseBiochemical and Biophysical Research Communications, 1969
- Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organsLife Sciences, 1968
- Purification and Properties of Neuraminidase from Vibrio choleraeJournal of General Microbiology, 1961