serine has been researched along with Camurati-Engelmann Disease in 1 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Camurati-Engelmann disease (CED) is a rare sclerosing bone disorder in humans with autosomal dominant inheritance." | 1.46 | An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes. ( Fukumura, R; Furuichi, T; Gondo, Y; Ichimura, S; Ikegawa, S; Murata, T; Sasaki, S, 2017) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ichimura, S | 1 |
| Sasaki, S | 1 |
| Murata, T | 1 |
| Fukumura, R | 1 |
| Gondo, Y | 1 |
| Ikegawa, S | 1 |
| Furuichi, T | 1 |
1 other study available for serine and Camurati-Engelmann Disease
| Article | Year |
|---|---|
An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes.
Topics: Amino Acid Substitution; Animals; Camurati-Engelmann Syndrome; Cysteine; Ethylnitrosourea; Female; G | 2017 |