methyl mannoside, (alpha-d)-isomer has been researched along with Cherry Red Spot Myoclonus Syndrome in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (75.00) | 18.7374 |
1990's | 1 (25.00) | 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 |
---|---|
Ben-Yoseph, Y; Chen, TH; Mitchell, DA; Shih, LY; Wei, JT; Yager, RM | 1 |
Alcouloumre, M; Drotar, AM; Herman, S; Little, L; Miller, AL; Robertson, R; Yeh, RY | 1 |
Honey, NK; Little, LE; Miller, AL; Mueller, OT; Shows, TB | 1 |
Ben-Yoseph, Y; Elwell, DG; Melançon, SB; Mitchell, DA; Nadler, HL; Pack, BA; Potier, M | 1 |
4 other study(ies) available for methyl mannoside, (alpha-d)-isomer and Cherry Red Spot Myoclonus Syndrome
Article | Year |
---|---|
Mucolipidoses II and III variants with normal N-acetylglucosamine 1-phosphotransferase activity toward alpha-methylmannoside are due to nonallelic mutations.
Topics: Alleles; alpha-L-Fucosidase; Cells, Cultured; Fibroblasts; Galactosidases; Glucosidases; Golgi Apparatus; Humans; Lysosomes; Mannosidases; Methylmannosides; Mucolipidoses; Mutation; Phosphorylation; Phosphotransferases; Transferases (Other Substituted Phosphate Groups) | 1992 |
Properties of N-acetylglucosamine 1-phosphotransferase from human lymphoblasts.
Topics: Cell Line; Chromatography, Agarose; Fibroblasts; Humans; Hydrolases; Intracellular Fluid; Kinetics; Lymphocytes; Lysosomes; Methylmannosides; Mucolipidoses; Phosphorylation; Phosphotransferases; Subcellular Fractions; Transferases (Other Substituted Phosphate Groups) | 1987 |
Heterogeneity of N-acetylglucosamine 1-phosphotransferase within mucolipidosis III.
Topics: beta-N-Acetylhexosaminidases; Cell Line; Genetic Complementation Test; Hexosaminidases; Humans; Kinetics; Methylmannosides; Mucolipidoses; Phosphorylation; Phosphotransferases; Placenta; Sucrose; Temperature; Transferases (Other Substituted Phosphate Groups) | 1986 |
Characterization of the mutant N-acetylglucosaminylphosphotransferase in I-cell disease and pseudo-Hurler polydystrophy: complementation analysis and kinetic studies.
Topics: Cells, Cultured; Fibroblasts; Glycoside Hydrolases; Golgi Apparatus; Humans; Hybrid Cells; Kinetics; Methylmannosides; Mucolipidoses; Mutation; Phosphotransferases; Skin; Transferases (Other Substituted Phosphate Groups); Uridine Diphosphate N-Acetylglucosamine | 1986 |