phosphoserine has been researched along with Peutz-Jeghers Syndrome in 1 studies
Phosphoserine: The phosphoric acid ester of serine.
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 | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Sapkota, GP | 1 |
| Boudeau, J | 1 |
| Deak, M | 1 |
| Kieloch, A | 1 |
| Morrice, N | 1 |
| Alessi, DR | 1 |
1 other study available for phosphoserine and Peutz-Jeghers Syndrome
| Article | Year |
|---|---|
Identification and characterization of four novel phosphorylation sites (Ser31, Ser325, Thr336 and Thr366) on LKB1/STK11, the protein kinase mutated in Peutz-Jeghers cancer syndrome.
Topics: Amino Acid Sequence; AMP-Activated Protein Kinase Kinases; Animals; Cell Line; Drosophila; Embryo, M | 2002 |