galactose has been researched along with Lysosomal Enzyme Disorders in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 3 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Benjamin, ER; Boyd, RE; Khanna, R; Lee, G; Rybczynski, P; Valenzano, KJ; Wustman, BA | 1 |
| Suzuki, Y | 1 |
| Nishimura, Y | 1 |
| Kotani, M; Sakuraba, H; Yamada, H | 1 |
| Bruggink, C; Deelder, AM; Froissart, R; Piraud, M; Poorthuis, BJ; Wuhrer, M | 1 |
| EDGAR, GW | 1 |
2 review(s) available for galactose and Lysosomal Enzyme Disorders
| Article | Year |
|---|---|
Pharmacological chaperones as therapeutics for lysosomal storage diseases.
Topics: Cell Line; Glycolipids; Humans; Lysosomal Storage Diseases; Molecular Chaperones; Structure-Activity Relationship | 2013 |
[The world of galactose and glucose: pathogenesis and therapy of lysosomal diseases].
Topics: Administration, Oral; Animals; Fabry Disease; Galactose; Galactosidases; Gangliosidosis, GM1; Glucose; Glucosidases; Humans; Leukodystrophy, Globoid Cell; Lysosomal Storage Diseases; Molecular Chaperones; Molecular Targeted Therapy; Pathology, Molecular; Proteostasis Deficiencies | 2014 |
4 other study(ies) available for galactose and Lysosomal Enzyme Disorders
| Article | Year |
|---|---|
Gem-diamine 1-N-iminosugars as versatile glycomimetics: synthesis, biological activity and therapeutic potential.
Topics: Animals; Antineoplastic Agents; Enzyme Inhibitors; Galactose; Glucose; Humans; Imino Pyranoses; Indicators and Reagents; Influenza, Human; Lysosomal Storage Diseases; Mice; Neoplasm Metastasis; Structure-Activity Relationship | 2009 |
Cytochemical and biochemical detection of intracellularly accumulated sialyl glycoconjugates in sialidosis and galactosialidosis fibroblasts with Macckia amurensis.
Topics: Blotting, Western; Cells, Cultured; Clinical Laboratory Techniques; Fibroblasts; Galactose; Glycoconjugates; Humans; Lysosomal Storage Diseases; Maackia; Mucolipidoses; N-Acetylneuraminic Acid; Plant Lectins; Staining and Labeling | 2004 |
Glycan profiling of urine, amniotic fluid and ascitic fluid from galactosialidosis patients reveals novel oligosaccharides with reducing end hexose and aldohexonic acid residues.
Topics: Amniotic Fluid; Ascitic Fluid; beta-Galactosidase; Carbohydrate Sequence; Cathepsin A; Chromatography, Ion Exchange; Fetus; Glycoside Hydrolases; Glycosphingolipids; Hexoses; Humans; Infant; Infant, Newborn; Lysosomal Storage Diseases; Mass Spectrometry; Molecular Sequence Data; Neuraminidase; Oligosaccharides; Oligosaccharides, Branched-Chain; Sugar Acids; Urine | 2010 |
[Biochemical approach to types of lipoidosis and leukodystrophy].
Topics: Brain; Brain Diseases; Hexoses; Humans; Lipid Metabolism; Lipidoses; Lysosomal Storage Diseases; Phospholipids | 1955 |