4-nitrophenylphosphate has been researched along with Hypophosphatasia in 1 studies
nitrophenylphosphate: RN given refers to mono(4-nitrophenyl) ester of phosphoric acid
4-nitrophenyl phosphate : An aryl phosphate resulting from the mono-esterification of phosphoric acid with 4-nitrophenol.
Hypophosphatasia: A genetic metabolic disorder resulting from serum and bone alkaline phosphatase deficiency leading to hypercalcemia, ethanolamine phosphatemia, and ethanolamine phosphaturia. Clinical manifestations include severe skeletal defects resembling vitamin D-resistant rickets, failure of the calvarium to calcify, dyspnea, cyanosis, vomiting, constipation, renal calcinosis, failure to thrive, disorders of movement, beading of the costochondral junction, and rachitic bone changes. (From Dorland, 27th ed)
| 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 |
|---|---|
| Watanabe, H | 1 |
| Goseki-Sone, M | 1 |
| Orimo, H | 1 |
| Hamatani, R | 1 |
| Takinami, H | 1 |
| Ishikawa, I | 1 |
1 other study available for 4-nitrophenylphosphate and Hypophosphatasia
| Article | Year |
|---|---|
Function of mutant (G1144A) tissue-nonspecific ALP gene from hypophosphatasia.
Topics: Adult; Alkaline Phosphatase; Animals; Buffers; COS Cells; DNA, Complementary; Enzyme Activation; Gen | 2002 |