serine has been researched along with Corneal Dystrophies in 2 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yellore, VS | 1 |
| Khan, MA | 1 |
| Bourla, N | 1 |
| Rayner, SA | 1 |
| Chen, MC | 1 |
| Sonmez, B | 1 |
| Momi, RS | 1 |
| Sampat, KM | 1 |
| Gorin, MB | 1 |
| Aldave, AJ | 1 |
| Takács, L | 1 |
| Losonczy, G | 1 |
| Matesz, K | 1 |
| Balogh, I | 1 |
| Sohajda, Z | 1 |
| Tóth, K | 1 |
| Fazakas, F | 1 |
| Vereb, G | 1 |
| Berta, A | 1 |
2 other studies available for serine and Corneal Dystrophies
| Article | Year |
|---|---|
Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.
Topics: Amino Acid Substitution; Asparagine; Corneal Dystrophies, Hereditary; Dimethylallyltranstransferase; | 2007 |
TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.
Topics: Amino Acid Substitution; Amyloidosis; Base Sequence; Cornea; Corneal Dystrophies, Hereditary; Extrac | 2007 |