thymine has been researched along with Hypophosphatasia in 5 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)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Hypophosphatasia is caused by mutations of the tissue-non-specific alkaline phosphatase (TNSALP) gene with deficiency of dentin structure." | 1.36 | Genetic etiology and dental pulp cell deficiency of hypophosphatasia. ( Gan, Y; Ge, L; Lei, H; Li, J; Liu, H; Zhu, T, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 4 (80.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zhu, T | 2 |
| Gan, YH | 1 |
| Liu, H | 2 |
| Foster, BL | 1 |
| Sheen, CR | 1 |
| Hatch, NE | 1 |
| Liu, J | 1 |
| Cory, E | 1 |
| Narisawa, S | 1 |
| Kiffer-Moreira, T | 1 |
| Sah, RL | 1 |
| Whyte, MP | 1 |
| Somerman, MJ | 1 |
| Millán, JL | 1 |
| Wei, KW | 1 |
| Xuan, K | 1 |
| Liu, YL | 1 |
| Fang, J | 1 |
| Ji, K | 1 |
| Wang, X | 1 |
| Jin, Y | 1 |
| Watanabe, S | 1 |
| Watanabe, K | 1 |
| Ojihara, T | 1 |
| Li, J | 1 |
| Lei, H | 1 |
| Gan, Y | 1 |
| Ge, L | 1 |
| Watanabe, H | 1 |
| Hashimoto-Uoshima, M | 1 |
| Goseki-Sone, M | 1 |
| Orimo, H | 1 |
| Ishikawa, I | 1 |
5 other studies available for thymine 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 |
Periodontal Defects in the A116T Knock-in Murine Model of Odontohypophosphatasia.
Topics: Adenine; Alkaline Phosphatase; Alveolar Process; Animals; Biomechanical Phenomena; Bone Density; Bon | 2015 |
Clinical, pathological and genetic evaluations of Chinese patients with autosomal-dominant hypophosphatasia.
Topics: Adenine; Adult; Aged; Alkaline Phosphatase; Child; China; Dental Cementum; Dentin; Exons; Female; Ge | 2010 |
Genetic etiology and dental pulp cell deficiency of hypophosphatasia.
Topics: Adenine; Alkaline Phosphatase; Cells, Cultured; Child; Child, Preschool; Dental Cementum; Dental Ena | 2010 |
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 |