mannose has been researched along with Lipidoses in 16 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 16 (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 |
---|---|
Hultberg, B; Sjöblad, S | 1 |
Ng Kin Kin, NM; Wolfe, LS | 1 |
Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI | 1 |
Creagan, RP; Darlington, GJ; Gilbert, F; Kucherlapati, R; Murnane, MJ; Ruddle, FH | 1 |
Brady, RO; Kolodny, EH; Tallman, JF | 1 |
Ockerman, PA | 1 |
Brown, B; Brunngraber, EG; Haberland, C; Witting, LA | 1 |
Robinson, D | 1 |
Touster, O | 1 |
Hultbery, B; Ockerman, PA | 1 |
Brady, RO; Tallman, JF | 1 |
Aro, A; Brown, BD; Brunngraber, EG | 1 |
Lalley, PA; Rattazzi, MC; Shows, TB | 1 |
Hultberg, B; Nordén, NE; Ockerman, PA | 1 |
Montreuil, J; Strecker, G | 1 |
Brady, RO; Kanfer, JN; Kolodny, EH; Quirk, JM | 1 |
3 review(s) available for mannose and Lipidoses
Article | Year |
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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 |
13 other study(ies) available for mannose and Lipidoses
Article | Year |
---|---|
Lysosomal enzymes in medium from cultured skin fibroblasts from normal individuals and patients with lysosomal diseases.
Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fabry Disease; Fibroblasts; Humans; In Vitro Techniques; Lipidoses; Lysosomes; Mannose; Metabolism, Inborn Errors; Mucolipidoses; Mucopolysaccharidosis I; Skin | 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 |
Tay-Sachs' and Sandhoff's diseases: the assignment of genes for hexosaminidase A and B to individual human chromosomes.
Topics: Animals; Carbohydrate Epimerases; Cell Line; Chromosome Mapping; Chromosomes, Human, 4-5; Clone Cells; Female; Genes; Genetic Linkage; Hexosaminidases; Humans; Hybrid Cells; Lipidoses; Male; Mannose; Mice; Pyruvate Kinase | 1975 |
The preparation of Tay-Sachs ganglioside specifically labeled in either the N-acetylneuraminosyl or N-acetylgalactosaminyl portion of the molecule.
Topics: Animals; Brain; Galactosamine; Galactosidases; Gangliosides; Hexosamines; Humans; Isotope Labeling; Lipidoses; Liver; Mannose; Methods; Neuraminidase; Rats; Sialic Acids; Tritium; Vibrio cholerae | 1975 |
Diseases of glycoprotein storage.
Topics: Brain; Carbohydrate Metabolism, Inborn Errors; Glucosamine; Glycosaminoglycans; Glycoside Hydrolases; Humans; Lipidoses; Liver; Mannose; Mucopolysaccharidoses | 1969 |
Glycoproteins in Tay-sachs disease: isolation and carbohydrate composition of glycopeptides.
Topics: Brain; Brain Stem; Cerebellum; Cerebral Cortex; Child; Chromatography, Paper; Electrophoresis; Female; Galactose; Gangliosides; Glucose; Glycopeptides; Glycoproteins; Glycosaminoglycans; Hexosaminidases; Humans; Infant; Lipidoses; Mannose; Peptides | 1972 |
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 |
The catabolism of Tay-Sachs ganglioside in rat brain lysosomes.
Topics: Acetates; Animals; Brain; Carbon Isotopes; Chromatography, Thin Layer; Cytosol; Gangliosides; Hexosamines; Hexosaminidases; Hydrogen-Ion Concentration; Kinetics; Lipid Metabolism; Lipidoses; Lysosomes; Male; Mannose; Neuraminidase; Rats; Subcellular Fractions; Surface-Active Agents; Tritium | 1972 |
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 |
Proceedings: Synteny relationships of beta-D-N-acetylhexosaminidase A and B in somatic cell hybrids.
Topics: Animals; Carbohydrate Epimerases; Chromosome Mapping; Chromosomes, Human, 6-12 and X; Clone Cells; Hexosaminidases; Humans; Hybrid Cells; Isoenzymes; Lipidoses; Lysosomes; Mannose; Mice | 1974 |
Isoenzymes of four acid hydrolases in human kidney and urine.
Topics: Chromatography, Gel; Glucosidases; Glucuronidase; Glycoside Hydrolases; Hexosaminidases; Humans; Isoelectric Focusing; Isoenzymes; Kidney; Lipidoses; Mannose | 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 |
Preparation of radioactive Tay-Sachs ganglioside labeled in the sialic acid moiety.
Topics: Animals; Brain; Chemical Phenomena; Chemistry; Chromatography, Thin Layer; Dialysis; Galactosidases; Gangliosides; Hexosamines; Humans; Lipidoses; Liver; Mannose; Methods; Neuraminic Acids; Neuraminidase; Rats; Tritium; Vibrio | 1970 |