phosphorylethanolamine has been researched along with Brittle Bone Disease in 1 studies
phosphorylethanolamine: RN given refers to parent cpd; structure
O-phosphoethanolamine : The ethanolamine mono-ester of phosphoric acid, and a metabolite of phospholipid metabolism. This phosphomonoester shows strong structural similarity to the inhibitory neurotransmitter GABA, and is decreased in post-mortem Alzheimer's disease brain.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Infantile hypophosphatasia is a rare inborn error of metabolism in which the expression of the liver/kidney/bone locus of the alkaline phosphatase gene is defective." | 1.27 | Isoenzymes of alkaline phosphatase in infantile hypophosphatasia. ( Milne, JK; Mohyuddin, F; Mueller, HD; Stinson, RA, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Mueller, HD | 1 |
| Stinson, RA | 1 |
| Mohyuddin, F | 1 |
| Milne, JK | 1 |
1 other study available for phosphorylethanolamine and Brittle Bone Disease
| Article | Year |
|---|---|
Isoenzymes of alkaline phosphatase in infantile hypophosphatasia.
Topics: Adult; Alkaline Phosphatase; Bone and Bones; Ethanolamines; Female; Humans; Hypophosphatasia; Infant | 1983 |