Identification of Candidate Active Site Residues in Lysosomal β-Hexosaminidase A-Reference-Cited by-同舟云学术

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Identification of Candidate Active Site Residues in Lysosomal β-Hexosaminidase A

Published:1997-01 Issue:2 Volume:272 Page:814-820
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Fernandes Maria J.G.,Yew Sandy,Leclerc Daniel,Henrissat Bernard,Vorgias Constantin E.,Gravel Roy A.,Hechtman Peter,Kaplan Feige

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference45 articles.

1. 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.

2. Gene encoding the human beta-hexosaminidase beta chain: extensive homology of intron placement in the alpha- and beta-chain genes.

3. Liberation of N-acetylglucosamine-6-sulfate by human beta-N-acetylhexosaminidase A.

4. Evidence for two different active sites on human beta-hexosaminidase A. Interaction of GM2 activator protein with beta-hexosaminidase A.

5. Mapping of the gene coding for the human GM2activator protein to chromosome 5

Cited by 46 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Human Recombinant Lysosomal β-Hexosaminidase A produced in P.pastoris efficiently reduced GM2 ganglioside accumulation in Tay- Sachs Disease;2024-07-12

2. Silencing of B4Galnt1 Gene Prevents GM2 Accumulation in Tay-Sachs Cells;Advances in Cell and Gene Therapy;2024-03-26

3. Induction of Exocytosis Rescues Lysosomal GM2 Accumulation in Tay-Sachs Disease;Advances in Cell and Gene Therapy;2024-03-19

4. Lithium treatment rescues dysfunctional autophagy in the cell models of Tay-Sachs disease;Molecular Genetics and Metabolism;2024-03

5. Biochemical and mutational analyses of HEXA in a cohort of Egyptian patients with infantile Tay-Sachs disease. Expansion of the mutation spectrum;Orphanet Journal of Rare Diseases;2023-03-13

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