Active arginine residues in beta-hexosaminidase. Identification through studies of the B1 variant of Tay-Sachs disease
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference38 articles.
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2. Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease.
3. Gene encoding the human beta-hexosaminidase beta chain: extensive homology of intron placement in the alpha- and beta-chain genes.
4. Evidence for two different active sites on human beta-hexosaminidase A. Interaction of GM2 activator protein with beta-hexosaminidase A.
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1. Comparison of HCMV IE and EF-1 Promoters for the Stable Expression of β-Subunit of Hexosaminidase in CHO Cell Lines;Biochemical Genetics;2006-04-28
2. Assessing the severity of the small inframe deletion mutation in the α-subunit of β-hexosaminidase A found in the Turkish population by reproducing it in the more stable β-subunit;Journal of Inherited Metabolic Disease;2004-11
3. An inversion of 25 base pairs causes feline G M2 gangliosidosis variant 0;Experimental Neurology;2004-05
4. Molecular cloning and sequence analysis of an ascidian egg beta-N-acetylhexosaminidase with a potential role in fertilization;Development, Growth and Differentiation;2003-06
5. Characterization of two Turkish β-hexosaminidase mutations causing Tay–Sachs disease;Brain and Development;2003-04
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