glycine has been researched along with Gargoylism, Hunter Syndrome in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Mucopolysaccharidosis II (MPS II, Hunter syndrome; OMIM 309900) is an X-linked lysosomal storage disease caused by a deficiency in the enzyme iduronate-2-sulfatase (IDS), leading to accumulation of glycosaminoglycans (GAGs)." | 1.40 | A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome. ( Chang, MS; Chung, YK; Jin, DK; Kim, CH; Ko, AR; Kwun, Y; Lee, J; Lee, JY; Sohn, JM; Sohn, YB; Yook, YJ, 2014) |
| 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 |
|---|---|
| Chung, YK | 1 |
| Sohn, YB | 1 |
| Sohn, JM | 1 |
| Lee, J | 1 |
| Chang, MS | 1 |
| Kwun, Y | 1 |
| Kim, CH | 1 |
| Lee, JY | 1 |
| Yook, YJ | 1 |
| Ko, AR | 1 |
| Jin, DK | 1 |
1 other study available for glycine and Gargoylism, Hunter Syndrome
| Article | Year |
|---|---|
A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome.
Topics: Alanine; Animals; CHO Cells; Cricetinae; Cricetulus; Enzyme Replacement Therapy; Fibroblasts; Glycin | 2014 |