phosphorylethanolamine has been researched along with Dental Enamel Hypoplasia 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.
Dental Enamel Hypoplasia: An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors.
Excerpt | Relevance | Reference |
---|---|---|
"A kindred with dominant hypophosphatasia resulting from an alanine to threonine substitution at position 99 of the alkaline phosphatase protein is described." | 3.70 | Characterization of a family with dominant hypophosphatasia. ( Hu, JC; Mornet, E; Plaetke, R; Simmer, JP; Sun, X; Thomas, HF; Zhang, C, 2000) |
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 |
---|---|
Hu, JC | 1 |
Plaetke, R | 1 |
Mornet, E | 1 |
Zhang, C | 1 |
Sun, X | 1 |
Thomas, HF | 1 |
Simmer, JP | 1 |
1 other study available for phosphorylethanolamine and Dental Enamel Hypoplasia
Article | Year |
---|---|
Characterization of a family with dominant hypophosphatasia.
Topics: Alanine; Alkaline Phosphatase; Amino Acid Substitution; Child; Dental Cementum; Dental Enamel Hypopl | 2000 |