mannose has been researched along with Gaucher Disease in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (41.67) | 18.7374 |
| 1990's | 2 (16.67) | 18.2507 |
| 2000's | 3 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 2 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Fujiyama, K; Kajiura, H; Misaki, R; Uthailak, N | 1 |
| Cadena-Nava, RD; Chauhan, K; Juárez-Moreno, K; Olivares-Medina, CN; Rodríguez-Hernández, AG; Vazquez-Duhalt, R; Villagrana-Escareño, MV | 1 |
| Edmunds, T; Ganesa, C; Huff, MR; Hughes, H; Kutzko, JP; Piepenhagen, PA; Qiu, H; Reczek, D; Van Patten, SM; Waire, J; Ward, PV | 1 |
| Aviezer, D; Bartfeld, D; Baum, G; Boldin-Adamsky, SA; Brill-Almon, E; Dym, O; Futerman, AH; Galili, G; Hashmueli, S; Shaaltiel, Y; Silman, I; Sussman, JL | 1 |
| Brady, RO; Murray, GJ; Oldfield, EH; Sanchez, OA; Zirzow, GC | 1 |
| Brady, RO; Kaneski, C; Murray, G; Sandhoff, K; Schueler, U | 1 |
| Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI | 1 |
| Barton, NW; Brady, RO; Howard, KD; Murray, GJ; Richards, SM | 1 |
| Robinson, D | 1 |
| Touster, O | 1 |
| Hultbery, B; Ockerman, PA | 1 |
| Friedman, RB; Kanfer, JN | 1 |
3 review(s) available for mannose and Gaucher Disease
| Article | Year |
|---|---|
Glycoprotein catabolism in brain tissue in the lysosomal enzyme deficiency diseases.
Topics: Adolescent; Binding Sites; Brain; Child; Concanavalin A; Fucose; Galactose; Gangliosidoses; Gaucher Disease; Glycoproteins; Hexosamines; Humans; Infant, Newborn; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Lysosomes; Mannose; Middle Aged; Protein Binding; Sialic Acids; Sphingolipidoses | 1976 |
Multiple forms of glycosidases in the normal and pathological states.
Topics: Carbohydrate Metabolism, Inborn Errors; Chondroitin; Chromatography, Gel; Diffuse Cerebral Sclerosis of Schilder; Fabry Disease; Fucose; Galactosidases; Gangliosides; Gaucher Disease; Glycogen Storage Disease; Glycolipids; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Infant; Isoenzymes; Lactose Intolerance; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Mucopolysaccharidoses | 1974 |
Some aspects of the cellular biochemistry of lysosomal and related glycosidases.
Topics: Animals; Carbohydrate Metabolism, Inborn Errors; Diffuse Cerebral Sclerosis of Schilder; Fucose; Galactosamine; Galactosidases; Gangliosides; Gaucher Disease; Glucosidases; Glucuronidase; Glycoside Hydrolases; Golgi Apparatus; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Isoenzymes; Leukodystrophy, Metachromatic; Lipidoses; Lysosomes; Mannose; Neuraminidase; Serine; Xylose | 1973 |
9 other study(ies) available for mannose and Gaucher Disease
| Article | Year |
|---|---|
Production of recombinant β-glucocerebrosidase in wild-type and glycoengineered transgenic Nicotiana benthamiana root cultures with different N-glycan profiles.
Topics: Gaucher Disease; Glucosylceramidase; Glycosylation; Mannose; Nicotiana; Plants, Genetically Modified; Polysaccharides; Recombinant Proteins | 2022 |
Targeted Enzymatic VLP-Nanoreactors with β-Glucocerebrosidase Activity as Potential Enzyme Replacement Therapy for Gaucher's Disease.
Topics: Enzyme Replacement Therapy; Gaucher Disease; Glucosylceramidase; Humans; Mannose; Nanotechnology | 2022 |
Effect of mannose chain length on targeting of glucocerebrosidase for enzyme replacement therapy of Gaucher disease.
Topics: Animals; CHO Cells; Cricetinae; Cricetulus; Drug Delivery Systems; Gaucher Disease; Gene Expression; Glucosylceramidase; Glycosylation; Humans; Lectins, C-Type; Mannose; Mannose Receptor; Mannose-Binding Lectin; Mannose-Binding Lectins; Mice; Mice, Knockout; Oligosaccharides; Polysaccharides; Protein Modification, Translational; Receptors, Cell Surface; Species Specificity | 2007 |
Production of glucocerebrosidase with terminal mannose glycans for enzyme replacement therapy of Gaucher's disease using a plant cell system.
Topics: Animals; Blotting, Western; Cells, Cultured; CHO Cells; Cricetinae; Cricetulus; Crystallography, X-Ray; Daucus carota; Drug Evaluation, Preclinical; Female; Gaucher Disease; Glucosylceramidase; Humans; Macrophages; Male; Mannose; Mice; Mice, Inbred ICR; Polysaccharides; Recombinant Proteins | 2007 |
Delivery, distribution, and neuronal uptake of exogenous mannose-terminal glucocerebrosidase in the intact rat brain.
Topics: Animals; Blood-Brain Barrier; Brain; Gaucher Disease; Glucosylceramidase; Immunohistochemistry; Mannose; Neurons; Rats; Rats, Sprague-Dawley; Tissue Distribution | 1999 |
Uptake of mannose-terminal glucocerebrosidase in cultured human cholinergic and dopaminergic neuron cell lines.
Topics: Acetylcholine; Biological Transport; Cell Differentiation; Cell Line; Cells, Cultured; Culture Media; Dopamine beta-Hydroxylase; Gaucher Disease; Glucosylceramidase; Humans; Kinetics; Mannose; Neurons | 2002 |
Gaucher's disease: lack of antibody response in 12 patients following repeated intravenous infusions of mannose terminal glucocerebrosidase.
Topics: Animals; Enzyme-Linked Immunosorbent Assay; Gaucher Disease; Glucosylceramidase; Humans; Immunoglobulins; Infusions, Intravenous; Mannose; Rabbits | 1991 |
Artificial substrates in the assay of acid glycosidases.
Topics: Chlorides; Chromatography, Gel; Enzyme Activation; Galactosidases; Gaucher Disease; Glucosidases; Glucuronidase; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Isoelectric Focusing; Lipidoses; Liver; Lysosomes; Macromolecular Substances; Mannose; Methods; Mucopolysaccharidoses; Osmolar Concentration; Retinitis Pigmentosa | 1972 |
Composition of sialoglycans isolated from Gaucher's spleen.
Topics: Adolescent; Arabinose; Chromatography, DEAE-Cellulose; Chromatography, Gas; Chromatography, Ion Exchange; Female; Fucose; Galactose; Gaucher Disease; Glucose; Glycopeptides; Hexosamines; Humans; Mannose; Neuraminic Acids; Spleen; Xylose | 1974 |