mannose has been researched along with Pigmentary Retinopathy in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (83.33) | 18.7374 |
| 1990's | 1 (16.67) | 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 |
|---|---|
| Frederick, JM; Hollyfield, JG; Tabor, GA; Ulshafer, RJ | 1 |
| Kaushal, S; Khorana, HG | 1 |
| Eriksson, O; Hultberg, B; Ockerman, PA | 1 |
| Bach, G; Cantz, M; Eisenberg, F; Neufeld, EF | 1 |
| Den Tandt, WR; Lassila, E; Philippart, M | 1 |
| Hultbery, B; Ockerman, PA | 1 |
6 other study(ies) available for mannose and Pigmentary Retinopathy
| Article | Year |
|---|---|
Metabolic studies on retinal tissue from a donor with a dominantly inherited chorioretinal degeneration resembling sectoral retinitis pigmentosa.
Topics: Aged; Amino Acids; Choroid; Culture Techniques; Female; Humans; Leucine; Mannose; Photoreceptor Cells; Retinal Degeneration; Retinitis Pigmentosa; Trichloroacetic Acid; Uridine; Uveal Diseases | 1984 |
Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa.
Topics: Amino Acid Sequence; Animals; Biological Transport; Cattle; Cell Line; Cell Membrane; Endoplasmic Reticulum; Gene Transfer Techniques; Glycosylation; Mannose; Molecular Sequence Data; Mutagenesis; Photochemistry; Point Mutation; Protein Folding; Protein Structure, Secondary; Retinaldehyde; Retinitis Pigmentosa; Rhodopsin; Structure-Activity Relationship | 1994 |
Enzyme patterns in tissues and body fluids in mucopolysaccharidoses.
Topics: Acid Phosphatase; Brain; Carbohydrate Metabolism, Inborn Errors; Chromatography, Gel; Fucose; Galactosidases; Glucosamine; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hot Temperature; Humans; Intellectual Disability; Kidney; Mannose; Molecular Weight; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Spleen | 1969 |
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase.
Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fibroblasts; Galactose; Glucosamine; Glucuronidase; Glycosaminoglycans; Glycosides; Humans; Iduronic Acid; Intellectual Disability; Mannose; Mucopolysaccharidosis II; Retinitis Pigmentosa; Skin; Sulfatases; Sulfur Isotopes; Sulfuric Acids; Tritium; Uronic Acids | 1973 |
Leroy's l-cell disease: markedly increased activity of plasma acid hydrolases.
Topics: Abnormalities, Multiple; Acid Phosphatase; Arabinose; Corneal Opacity; Cytoplasmic Granules; Fibroblasts; Galactosidases; Glucosidases; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Intellectual Disability; Mannose; Metabolism, Inborn Errors; Mucopolysaccharidoses; Phosphoric Diester Hydrolases; Retinitis Pigmentosa; Skin | 1974 |
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 |