glycine has been researched along with Peutz-Jeghers Syndrome in 1 studies
Peutz-Jeghers Syndrome: A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 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 |
|---|---|
| Entius, MM | 1 |
| Westerman, AM | 1 |
| Giardiello, FM | 1 |
| van Velthuysen, ML | 1 |
| Polak, MM | 1 |
| Slebos, RJ | 1 |
| Wilson, JH | 1 |
| Hamilton, SR | 1 |
| Offerhaus, GJ | 1 |
1 other study available for glycine and Peutz-Jeghers Syndrome
| Article | Year |
|---|---|
Peutz-Jeghers polyps, dysplasia, and K-ras codon 12 mutations.
Topics: Autoradiography; Codon; Genes, ras; Glycine; Humans; Peutz-Jeghers Syndrome; Point Mutation; Polymer | 1997 |