Human placental N-acetyl-β-d-hexosaminidase isozymes
- 1 July 1978
- journal article
- research article
- Published by Elsevier in Archives of Biochemistry and Biophysics
- Vol. 189 (1) , 37-43
- https://doi.org/10.1016/0003-9861(78)90111-x
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Sandhoff Disease: Defective Glycosaminoglycan Catabolism in Cultured Fibroblasts and Its Correction by β‐N‐AcetylhexosaminidaseEuropean Journal of Biochemistry, 1974
- Oligosaccharides accumulating in the liver from a patient with GM2-gangliosidosis variant 0 (Sandhoff-Jatzkewitz disease)Biochemical and Biophysical Research Communications, 1974
- Hydrolysis of Tay-Sachs Ganglioside by β-Hexosaminidase A of Human Liver and UrinePublished by Elsevier ,1973
- Studies on the substrate specificity of hexosaminidase A and B from liverArchives of Biochemistry and Biophysics, 1972
- Anreicherung und Charakterisierung zweier Formen der menschlichen N-Acetyl-β-D-hexosaminidaseHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1971
- Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase ComponentScience, 1969
- N-Acetyl-β-glucosaminidases in human spleenBiochemical Journal, 1968
- Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organsLife Sciences, 1968
- Isolation of β-N-Acetylhexosaminidase, β-N-Acetylglucosaminidase, and β-N-Acetylgalactosaminidase from Calf Brain*Biochemistry, 1967
- The gangliosidesJournal of Lipid Research, 1964