Skip to main content

. 1971 Jan;23(1):55–61.

Ganglioside GM2 storage diseases: hexosaminidase deficiencies in cultured fibroblasts.

S Okada, M L Veath, J Leroy, J S O'Brien

PMCID: PMC1706637 PMID: 5581981

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
Leroy J. G., Demars R. I. Mutant enzymatic and cytological phenotypes in cultured human fibroblasts. Science. 1967 Aug 18;157(3790):804–806. doi: 10.1126/science.157.3790.804. [DOI] [PubMed] [Google Scholar]
O'Brien J. S. Five gangliosidoses. Lancet. 1969 Oct 11;2(7624):805–805. doi: 10.1016/s0140-6736(69)90524-8. [DOI] [PubMed] [Google Scholar]
O'Brien J. S., Okada S., Chen A., Fillerup D. L. Tay-sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay. N Engl J Med. 1970 Jul 2;283(1):15–20. doi: 10.1056/NEJM197007022830104. [DOI] [PubMed] [Google Scholar]
Okada S., O'Brien J. S. Tay-Sachs disease: generalized absence of a beta-D-N-acetylhexosaminidase component. Science. 1969 Aug 15;165(3894):698–700. doi: 10.1126/science.165.3894.698. [DOI] [PubMed] [Google Scholar]
Sandhoff K. Variation of beta-N-acetylhexosaminidase-pattern in Tay-Sachs disease. FEBS Lett. 1969 Aug;4(4):351–354. doi: 10.1016/0014-5793(69)80274-7. [DOI] [PubMed] [Google Scholar]

ACTIONS

PDF (620.3 KB)

RESOURCES