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Studies on human N-acetyl-Beta-d-hexosaminidase C separated from neonatal brain.
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Purification and some properties of liver and brain beta-N-acetyl-hexosaminidase S.
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Juvenile Sandhoff disease: some properties of the residual hexosaminidase in cultured fibroblasts.
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N-acetyl-beta-D-hexosaminidase component A. Different forms in human tissues and fluids.
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Immunological properties of N-acetyl-beta-D-glucosaminidase of normal human liver and of GM2-gangliosidosis liver.
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Characterization and tissue distribution of N-acetyl hexosaminidase C: suggestive evidence for a separate hexosaminidase locus.
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[Isolation and some properties of N-acetyl-beta-D-hexosaminidase from Sarcoscipha coccinea].
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The separation of bovine brain beta-N-acetyl-D-hexosaminidases. Abnormal gel-filtration behaviour of beta-N-acetyl-D-glucosaminidase C.
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beta-Hexosaminidase isozymes in human colonic carcinoma.
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Beta-hexosaminidase activities and isoenzymes in normal human ovary and ovarian adenocarcinoma.
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Mammalian cells contain a second nucleocytoplasmic hexosaminidase.
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Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymograms.
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Enzyme activities and phospholipid storage patterns in brain and spleen samples from Niemann-Pick disease variants: a comparison of neuropathic and non-neuropathic forms.
J Inherit Metab Dis. 1986;9(1):59-71. doi: 10.1007/BF01813904.
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Glycosphingolipid hydrolases: properties and molecular genetics.
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The use of natural and artifical substrates in the prenatal diagnosis of Krabbe's disease.
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The multiple forms and kinetic properties of the N-acetyl-beta-D-hexosaminidases from colonic tumours and mucosa of rats treated with 1,2-dimethylhydrazine.
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Tay-Sachs disease: generalized absence of a beta-D-N-acetylhexosaminidase component.
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Deficient hexozaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs.
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A simple apparatus for rapid isoelectrofocusing of multiple samples on a micro scale.
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Electrophoretic separation of -N-acetylhexosaminidases of human and bovine brain and liver and of Tay-Sachs brain tissue.
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The demonstration of multiple heat stable forms of N-acetyl- -glucosaminidase in normal human serum.
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Separation and characterisation of N-acetyl- -glucosaminidases A and P from maternal serum.
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Differences between the N-acetyl hexosaminidase isozymes in serum and tissues.
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On the molecular basis of Sandhoff's disease.
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