mannose has been researched along with Glycogen Storage Disease Type II in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Huy, NX; Jung, JW; Kim, HB; Kim, NS; Van Giap, D; Yang, MS | 1 |
| Basile, I; Caillaud, C; Charbonné, HV; Da Silva, A; Daurat, M; El Cheikh, K; Garcia, M; Gary-Bobo, M; Godefroy, A; Maynadier, M; Morère, A; Sacconi, S; Schoser, B | 1 |
| Kroos, M; Oude Elferink, RP; Reuser, AJ; Tager, JM | 1 |
3 other study(ies) available for mannose and Glycogen Storage Disease Type II
| Article | Year |
|---|---|
Production of recombinant human acid α-glucosidase with high-mannose glycans in gnt1 rice for the treatment of Pompe disease.
Topics: alpha-Glucosidases; Enzyme Replacement Therapy; Glycogen Storage Disease Type II; Glycosylation; Humans; Mannose; Oryza; Plants, Genetically Modified; Recombinant Proteins | 2017 |
Mannose 6-phosphonate labelling: A key for processing the therapeutic enzyme in Pompe disease.
Topics: Adult; Animals; Cells, Cultured; Disease Models, Animal; Glycogen Storage Disease Type II; Humans; Lysosomes; Mannose; Mice; Muscle, Skeletal; Myoblasts; Organophosphonates | 2019 |
Defects in synthesis, phosphorylation, and maturation of acid alpha-glucosidase in glycogenosis type II.
Topics: Adolescent; Adult; alpha-Glucosidases; beta-N-Acetylhexosaminidases; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Glucan 1,4-alpha-Glucosidase; Glucosidases; Glycogen Storage Disease; Glycogen Storage Disease Type II; Hexosaminidases; Humans; Infant; Leucine; Male; Mannose; Phosphates; Phosphorylation | 1985 |