cytosine has been researched along with Hypophosphatasia in 2 studies
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 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zhu, T | 1 |
| Gan, YH | 1 |
| Liu, H | 1 |
| Watanabe, H | 1 |
| Hashimoto-Uoshima, M | 1 |
| Goseki-Sone, M | 1 |
| Orimo, H | 1 |
| Ishikawa, I | 1 |
2 other studies available for cytosine and Hypophosphatasia
| Article | Year |
|---|---|
Functional evaluation of mutations in the tissue-nonspecific alkaline phosphatase gene.
Topics: Adenine; Alkaline Phosphatase; Alleles; Calcification, Physiologic; Cell Culture Techniques; Cell Li | 2012 |
A novel point mutation (C571T) in the tissue-non-specific alkaline phosphatase gene in a case of adult-type hypophosphatasia.
Topics: Alanine; Alkaline Phosphatase; Alleles; Alveolar Bone Loss; Chromosomes, Human, Pair 1; Cytosine; Et | 2001 |