serine has been researched along with Spinal Muscular Atrophies of Childhood 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.
Spinal Muscular Atrophies of Childhood: A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)
| 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 |
|---|---|
| Kotani, T | 1 |
| Sutomo, R | 1 |
| Sasongko, TH | 1 |
| Sadewa, AH | 1 |
| Minato, T | 1 |
| Fujii, E | 1 |
| Endo, S | 1 |
| Lee, MJ | 1 |
| Ayaki, H | 1 |
| Harada, Y | 1 |
| Matsuo, M | 1 |
| Nishio, H | 1 |
1 other study available for serine and Spinal Muscular Atrophies of Childhood
| Article | Year |
|---|---|
A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins.
Topics: Amino Acid Substitution; Child; Child, Preschool; Chromatography, High Pressure Liquid; Chromosomal | 2007 |