acetylgalactosamine has been researched along with Lysosomal Enzyme Disorders in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Real, FX; Ulloa, F | 1 |
| Garboczi, DN; Garman, SC; Hannick, L; Zhu, A | 1 |
2 other study(ies) available for acetylgalactosamine and Lysosomal Enzyme Disorders
| Article | Year |
|---|---|
Benzyl-N-acetyl-alpha-D-galactosaminide induces a storage disease-like phenotype by perturbing the endocytic pathway.
Topics: Acetylgalactosamine; Benzyl Compounds; Cytoplasmic Vesicles; Endocytosis; HT29 Cells; Humans; In Vitro Techniques; Integrin beta1; Lysosomal Storage Diseases; Membrane Glycoproteins; Mucin-1; N-Acetylneuraminic Acid; Phenotype; Protein Transport; Sialic Acid Storage Disease; Transport Vesicles | 2003 |
The 1.9 A structure of alpha-N-acetylgalactosaminidase: molecular basis of glycosidase deficiency diseases.
Topics: Acetylgalactosamine; alpha-N-Acetylgalactosaminidase; Amino Acid Sequence; Animals; Binding Sites; Catalysis; Chickens; Crystallography, X-Ray; Dimerization; Hexosaminidases; Humans; Ligands; Lysosomal Storage Diseases; Lysosomes; Models, Molecular; Molecular Sequence Data; Molecular Structure; Mutation; Protein Structure, Secondary; Protein Structure, Tertiary; Sequence Alignment | 2002 |