Genetic complementation after fusion of Tay-Sachs and Sandhoff cells
- 1 August 1974
- journal article
- Published by Springer Nature in Nature
- Vol. 250 (5467), 580-582
- https://doi.org/10.1038/250580a0
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- On the molecular basis of Sandhoff's diseasePublished by Springer Nature ,1973
- Mucolipidosis III (Pseudo-Hurler Polydystrophy): Multiple Lysosomal Enzyme Abnormalities in Serum and Cultured Fibroblast CellsPediatric Research, 1973
- Complementation Analysis of Maple Syrup Urine Disease in Heterokaryons derived from Cultured Human FibroblastsNature, 1973
- Electrophoretic study of hexosaminidases. Hexosaminidase CClinica Chimica Acta; International Journal of Clinical Chemistry, 1973
- Genetic Heterogeneity of Xeroderma Pigmentosum demonstrated by Somatic Cell HybridizationNature New Biology, 1972
- TAY-SACHS DISEASE: INTERRELATION OF HEXOSAMINIDASES A AND BThe Lancet, 1972
- Lysosomal hydrolases: Conversion of acidic to basic forms by neuraminidaseFEBS Letters, 1971
- Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase ComponentScience, 1969
- Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organsLife Sciences, 1968
- Poliovirus Replication and Cytopathogenicity in Monolayer Hamster Cell Cultures Fused with Beta Propiolactone-Inactivated Sendai VirusExperimental Biology and Medicine, 1968