glucosamine has been researched along with Lipidoses in 15 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 14 (93.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (6.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Glen, RC; Lowe, R; Mitchell, JB | 1 |
Ng Kin Kin, NM; Wolfe, LS | 1 |
Dreyfus, JC; Poenaru, L; Svennerholm, L | 1 |
Bach, G; Cohen, MM; Kohn, G | 1 |
Ockerman, PA | 1 |
Beutler, E; Srivastava, SK | 1 |
Cantz, M; Kresse, H | 1 |
Fukushima, DK; Kolodny, EH; Tomasi, LG | 1 |
McGuire, EJ; Roseman, S; Schachter, H | 1 |
Aro, A; Brown, BD; Brunngraber, EG | 1 |
Okada, S; Sumi, K; Yabuuchi, H; Yutaka, T | 1 |
Montreuil, J; Strecker, G | 1 |
Den, H; Kaufman, B; Roseman, S | 1 |
Cotlier, E; Duwelius, A; O'Brien, JS; Okada, S; Tennant, L | 1 |
Burton, R; Handa, S; Howard, RE; Vietti, T | 1 |
15 other study(ies) available for glucosamine and Lipidoses
Article | Year |
---|---|
Predicting phospholipidosis using machine learning.
Topics: Animals; Artificial Intelligence; Databases, Factual; Drug Discovery; Humans; Lipidoses; Models, Biological; Phospholipids; Support Vector Machine | 2010 |
Storage and excretion of oligosaccharides and glycopeptides in the gangliosidoses.
Topics: Galactose; Gangliosidoses; Glucosamine; Glycopeptides; Humans; Infant; Lipidoses; Liver; Mannose; Molecular Conformation; Molecular Weight; Oligosaccharides | 1976 |
Absence of hexosaminidase A and B in a normal adult.
Topics: Aminoglycosides; Brain Chemistry; Child; Coumarins; Electrophoresis; Female; Gangliosides; Glucosamine; Heterozygote; Hexosaminidases; Hot Temperature; Humans; Hymecromone; Infant; Leukocytes; Lipidoses; Male; Mutation; Tritium | 1975 |
Abnormal ganglioside accumulation in cultured fibroblasts from patients with mucolipidosis IV.
Topics: Cells, Cultured; Fibroblasts; Gangliosides; Glucosamine; Humans; Lipidoses; Skin | 1975 |
Diseases of glycoprotein storage.
Topics: Brain; Carbohydrate Metabolism, Inborn Errors; Glucosamine; Glycosaminoglycans; Glycoside Hydrolases; Humans; Lipidoses; Liver; Mannose; Mucopolysaccharidoses | 1969 |
Studies on human beta-D-N-acetylhexosaminidases. 3. Biochemical genetics of Tay-Sachs and Sandhoff's diseases.
Topics: Acetates; Animals; Antigens; Chromosome Mapping; Coumarins; Electrophoresis; Enzyme Precursors; Female; Genes; Genetics, Medical; Glucosamine; Hexosaminidases; Humans; Immunodiffusion; Immunoelectrophoresis; Isoenzymes; Lipidoses; Liver; Macromolecular Substances; Models, Chemical; Molecular Biology; Placenta; Pregnancy; Rabbits | 1974 |
Sandhoff disease: defective glycosaminoglycan catabolism in cultured fibroblasts and its correction by beta-N-acetylhexosaminidase.
Topics: Biodegradation, Environmental; Carbon Radioisotopes; Cells, Cultured; Chemical Precipitation; Chromatography; Chromatography, Gel; Electrophoresis; Fibroblasts; Glucosamine; Glycosaminoglycans; Hexosaminidases; Humans; Isoelectric Focusing; Isoenzymes; Lipidoses; Mucopolysaccharidoses; Skin; Sulfur Radioisotopes | 1974 |
Steroid hexosaminidase activity in Tay-Sachs and Sandhoff-Jatzkewitz diseases.
Topics: Carbon Radioisotopes; Catalysis; Child, Preschool; Dehydroepiandrosterone; Galactosidases; Gangliosides; Glucosamine; Hexosaminidases; Humans; Infant; Kinetics; Lipidoses; Liver; Sphingolipidoses; Testosterone | 1974 |
Sialic acids. 13. A uridine diphosphate D-galactose: mucin galactosyltransferase from porcine submaxillary gland.
Topics: Acetates; Animals; Cadmium; Calcium Chloride; Carbon Isotopes; Chlorides; Chromatography, Paper; Clostridium perfringens; Enzyme Activation; Galactosamine; Galactose; Galactosidases; Gangliosides; Glucosamine; Glucose; Glycoproteins; Hexosaminidases; Hexosyltransferases; Hydrogen-Ion Concentration; Kinetics; Lipidoses; Manganese; Mathematics; Models, Structural; Mucins; Neuraminic Acids; Neuraminidase; Nucleoside Diphosphate Sugars; Oligosaccharides; Ovalbumin; Sheep; Submandibular Gland; Surface-Active Agents; Swine; Uracil Nucleotides; Zinc | 1971 |
Glycoproteins in brain tissue of the O-variant of GM2 gangliosidosis.
Topics: Acetamides; Brain; Brain Chemistry; Child, Preschool; Chromatography, Gel; Electrophoresis; Female; Fucose; Galactose; Gangliosides; Glucosamine; Glycoproteins; Hexosamines; Hexosaminidases; Humans; Lipidoses; Male; Mannose; Neuraminic Acids | 1974 |
Chromatographic study of serum hexosaminidase in normal and GM 2-gangliosidosis.
Topics: Chromatography, DEAE-Cellulose; Drug Stability; Female; Glucosamine; Heterozygote; Hexosaminidases; Hot Temperature; Humans; Lipidoses; Pregnancy | 1974 |
[Oligosaccharide excretion in a case of GM 2 gangliosidosis due to total N-acetylhexosaminidase deficiency].
Topics: Acetates; Carbohydrate Metabolism, Inborn Errors; Chemical Precipitation; Chromatography; Chromatography, Ion Exchange; Chromatography, Paper; Colorimetry; Ethanol; Fucose; Galactose; Gangliosides; Glucosamine; Glucose; Glycoproteins; Glycoside Hydrolases; Hexosamines; Hexosaminidases; Hexoses; Humans; Infant; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Monosaccharides; Neuraminic Acids; Oligosaccharides; Uronic Acids | 1971 |
Properties of some glycosyltransferases in embryonic chicken brain.
Topics: Aging; Albumins; Amniotic Fluid; Animals; Brain; Carbon Isotopes; Chick Embryo; Cytosine Nucleotides; Detergents; Galactose; Gangliosides; Glucosamine; Glycoproteins; Guinea Pigs; Humans; Lipidoses; Mucins; Neuraminic Acids; Neuraminidase; Oligosaccharides; Serine; Transferases; Uracil Nucleotides; Vitreous Body; Xylose | 1970 |
Effect of ascorbic acid on hexosaminidase activity.
Topics: Acetates; Ascorbic Acid; Chemical Phenomena; Chemistry; Coumarins; Glucosamine; Glycoside Hydrolases; Glycosides; Hexosamines; Humans; In Vitro Techniques; Infant; Lipidoses; Nitrophenols; Stimulation, Chemical | 1971 |
Incorporation of selected isotopes into lipids of humans with cerebral lipidoses: studies on D-glucosamine-1-14C.
Topics: Brain; Carbon Isotopes; Child; Child, Preschool; Female; Gangliosides; Glucosamine; Humans; Lipid Metabolism; Lipidoses; Niemann-Pick Diseases; Sphingomyelins | 1968 |