mannose has been researched along with Cherry Red Spot Myoclonus Syndrome in 15 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (60.00) | 18.7374 |
| 1990's | 1 (6.67) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (20.00) | 24.3611 |
| 2020's | 2 (13.33) | 2.80 |
| Authors | Studies |
|---|---|
| Bartenschlager, R; Bertozzi, CR; Blish, CA; Bogyo, M; Braulke, T; Carette, JE; Flynn, RA; Jabs, S; Klüssendorf, M; Mosen, PR; Nagamine, CM; Ooi, YS; Peters, CE; Puschnik, AS; Qiao, W; Richards, CM; Riley, NM; Rustagi, A; Schweizer, M; Shi, PY; Varanese, LD; Widen, JC; Winter, D; Xie, X; Zengel, JR | 1 |
| Jabs, S; Qiao, W; Richards, CM | 1 |
| Flanagan-Steet, H; Matheny, C; Parker, J; Petrey, A; Steet, R | 1 |
| Braulke, T; Encarnação, M; Kollmann, K; Lübke, T; Marschner, K; Müller-Loennies, S; Pohl, S; Poorthuis, BJ; Sakwa, I; Storch, S; Tiede, S | 1 |
| Barnes, J; Blanchard, F; Godard, A; Lim, JM; Steet, R; Wells, L | 1 |
| Yamashita, K | 1 |
| Hasilik, A; Von Figura, K | 1 |
| Federico, A; Guazzi, G | 1 |
| Ben-Yoseph, Y; DeFranco, CL; Hahn, LC; Nadler, HL | 1 |
| Kinnon, C; Kress, BC; Lewis, L; Miller, AL; Stein, R | 1 |
| Aula, P; Ekblom, P; Laurila, P; Nordling, S; Raivio, KO; Virtanen, I | 1 |
| DiCioccio, RA; Miller, AL | 1 |
| Hultberg, B; Sjöblad, S | 1 |
| Hultberg, B | 1 |
| Van Hoof, F | 1 |
4 review(s) available for mannose and Cherry Red Spot Myoclonus Syndrome
| Article | Year |
|---|---|
Mannose phosphorylation in health and disease.
Topics: Animals; Disease; Health; Humans; Mannose; Mucolipidoses; Phosphorylation; Transferases (Other Substituted Phosphate Groups) | 2010 |
[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 |
Urinary oligosaccharides in lysosomal and other metabolic disorders.
Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Chromatography, Thin Layer; Fucose; Glycogen Storage Disease; Humans; Mannose; Marfan Syndrome; Mass Screening; Metabolism, Inborn Errors; Mucolipidoses; Oligosaccharides; Osteogenesis Imperfecta; Sandhoff Disease; Tay-Sachs Disease | 1982 |
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 |
11 other study(ies) available for mannose and Cherry Red Spot Myoclonus Syndrome
| Article | Year |
|---|---|
The human disease gene LYSET is essential for lysosomal enzyme transport and viral infection.
Topics: Animals; Cathepsins; COVID-19; Humans; Lysosomes; Mannose; Mice; Mice, Knockout; Mucolipidoses; Proteins; Transferases (Other Substituted Phosphate Groups) | 2022 |
LYSET/TMEM251- a novel key component of the mannose 6-phosphate pathway.
Topics: Autophagy; Cations; Humans; Hydrolases; Lysosomes; Mannose; Mucolipidoses; Phosphotransferases; Receptor, IGF Type 2 | 2023 |
Enzyme-specific differences in mannose phosphorylation between GlcNAc-1-phosphotransferase αβ and γ subunit deficient zebrafish support cathepsin proteases as early mediators of mucolipidosis pathology.
Topics: Animals; Cathepsins; Glycoside Hydrolases; Hydrolases; Mannose; Mannosephosphates; Mucolipidoses; Mutation; Oocytes; Peptide Hydrolases; Phenotype; Phosphorylation; Transferases (Other Substituted Phosphate Groups); Zebrafish | 2016 |
Extensive mannose phosphorylation on leukemia inhibitory factor (LIF) controls its extracellular levels by multiple mechanisms.
Topics: Animals; Cell Differentiation; CHO Cells; Cricetinae; Cricetulus; Embryonic Stem Cells; Glycosylation; HeLa Cells; Humans; Leukemia Inhibitory Factor; Lysosomes; Mannose; Mannosephosphates; Mass Spectrometry; Mice; Mucolipidoses; Mutation; Protein Transport | 2011 |
Oligosaccharides in lysosomal enzymes. Distribution of high-mannose and complex oligosaccharides in cathepsin D and beta-hexosaminidase.
Topics: Acetylglucosaminidase; beta-N-Acetylhexosaminidases; Cathepsin D; Cathepsins; Cells, Cultured; Enzyme Precursors; Fibroblasts; Hexosaminidases; Humans; Lysosomes; Mannose; Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase; Molecular Weight; Mucolipidoses; Oligosaccharides; Phosphates; Phosphorylation | 1981 |
Deficient phosphorylation of mannose residues of mannan in fibroblasts of patients with mucolipidoses II and III.
Topics: Cells, Cultured; Electrophoresis, Paper; Fibroblasts; Glucose; Humans; Mannans; Mannose; Mucolipidoses; Phosphorylation; Polysaccharides; Skin | 1981 |
Effect of tunicamycin and cycloheximide on the secretion of acid hydrolases from I-cell cultured fibroblasts.
Topics: alpha-L-Fucosidase; Cells, Cultured; Cycloheximide; Fibroblasts; Glucosamine; Hexosaminidases; Humans; Leucine; Mannose; Mucolipidoses; Tunicamycin | 1980 |
Characterization of storage material in cultured fibroblasts by specific lectin binding in lysosomal storage diseases.
Topics: Carbohydrate Metabolism, Inborn Errors; Fibroblasts; Fluorescent Dyes; Fucose; Glucose; Histocytochemistry; Humans; Lectins; Lysosomes; Mannose; Mucolipidoses | 1980 |
Phosphorylation and subcellular location of alpha-L-fucosidase in lymphoid cells from patients with I-cell disease and pseudo-Hurler polydystrophy.
Topics: alpha-L-Fucosidase; Cells, Cultured; Humans; Lymphocytes; Mannose; Mannosephosphates; Mucolipidoses; Phosphorylation; Subcellular Fractions | 1993 |
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 |
Metabolism of mannose and fucose in cultured fibroblasts from patients with mannosidosis and mucolipidosis.
Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Chromatography, Gel; Chromatography, Paper; Electrophoresis; Fibroblasts; Fucose; Humans; Mannose; Mucolipidoses | 1979 |