mannose has been researched along with Ganglioside Storage Diseases in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yamashita, K | 1 |
| Distler, J; Hieber, V; Jourdian, GW; Myerowitz, R; Schmickel, RD | 2 |
| Fournet, B; Herlant-Peers, MC; Montreul, J; Strecker, G | 1 |
| Ng Kin Kin, NM; Wolfe, LS | 1 |
| Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI | 1 |
| Elleder, M | 1 |
| Van Hoof, F | 1 |
3 review(s) available for mannose and Ganglioside Storage Diseases
| Article | Year |
|---|---|
[Metabolic disorders of glycoproteins in congenital glycosidase deficiencies].
Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Chromatography, Paper; Fucose; G(M1) Ganglioside; Gangliosidoses; Glucosidases; Glycoproteins; Humans; Lactose Intolerance; Mannose; Mucolipidoses; Mucopolysaccharidoses; Neuraminidase; Oligosaccharides; Sandhoff Disease | 1984 |
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 |
Mucopolysaccharidoses and mucolipidoses.
Topics: beta-Galactosidase; Cells, Cultured; Child, Preschool; Chondroitin Sulfates; Female; Fucose; Gangliosidoses; Genetic Carrier Screening; Hexosyltransferases; Humans; Iduronidase; Liver; Lysosomes; Mannose; Mucolipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis III; Mucopolysaccharidosis IV; Mucopolysaccharidosis VI | 1974 |
5 other study(ies) available for mannose and Ganglioside Storage Diseases
| Article | Year |
|---|---|
Selective noncompetitive assimilation of bovine testicular beta-galactosidase and bovine liver beta-glucuronidase by generalized gangliosidosis fibroblasts.
Topics: Animals; beta-Galactosidase; Cattle; Fibroblasts; Galactosidases; Gangliosidoses; Glucuronidase; Humans; In Vitro Techniques; Kinetics; Liver; Male; Mannose; Organ Specificity; Skin; Species Specificity; Testis | 1980 |
Structure of seven oligosaccharides excreted in the urine of a patient with Sandhoff's disease (GM2 gangliosidosis-variant O).
Topics: Acetylglucosamine; Gangliosidoses; Humans; Magnetic Resonance Spectroscopy; Mannose; Molecular Conformation; Oligosaccharides | 1977 |
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 |
The role of glycosidically bound mannose in the assimilation of beta-galactosidase by generalized gangliosidosis fibroblasts.
Topics: Animals; Aspergillus niger; Binding Sites; Biological Transport; Cattle; Chromatography, Affinity; Concanavalin A; Fibroblasts; Galactosidases; Gangliosidoses; Glucosamine; Glucuronidase; Humans; Liver; Male; Mannose; Mannosidases; Mannosides; Plant Lectins; Plants; Protein Binding; Skin; Testis | 1976 |
Lectin histochemical study of lipopigments with special regard to neuronal ceroid-lipofuscinosis. Results with concanavalin A.
Topics: Adolescent; Adult; Animals; Ceroid; Child; Child, Preschool; Concanavalin A; Gangliosidoses; Humans; Lipofuscin; Mannose; Mucopolysaccharidoses; Neuronal Ceroid-Lipofuscinoses; Neurons; Olivary Nucleus; Pigments, Biological; Staining and Labeling | 1989 |