fucose has been researched along with Congenital Mesodermal Dysmorphodystrophy in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Apte, SS; Berardinelli, SJ; Haltiwanger, RS; Hubmacher, D; Reinhardt, DP; Schneider, M; Takeuchi, H; Willard, B | 1 |
1 other study(ies) available for fucose and Congenital Mesodermal Dysmorphodystrophy
| Article | Year |
|---|---|
Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye disease.
Topics: ADAMTS Proteins; Animals; Cells, Cultured; Fibrillin-1; Fibrillin-2; Fucose; Furin; HEK293 Cells; Humans; Mice; Microfibrils; Protein Binding; Protein Processing, Post-Translational; Rats; Weill-Marchesani Syndrome | 2017 |