serine has been researched along with Genetic Diseases, X-Chromosome Linked in 3 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 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Li, Q | 1 |
| Chen, M | 1 |
| Liu, K | 1 |
| Lin, X | 1 |
| Chui, D | 1 |
| Vore, AP | 1 |
| Chang, EH | 1 |
| Hoppe, JE | 1 |
| Butler, MG | 1 |
| Forrester, S | 1 |
| Schneider, MC | 1 |
| Smith, LL | 1 |
| Burke, DW | 1 |
| Campbell, CA | 1 |
| Smith, RJ | 1 |
| Short, KM | 1 |
| Hopwood, B | 1 |
| Yi, Z | 1 |
| Cox, TC | 1 |
3 other studies available for serine and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Vocal cord paresis and probable X-linked Charcot-Marie-Tooth disease with novel GJB1 mutation.
Topics: Adolescent; Adult; Aged; Arginine; Charcot-Marie-Tooth Disease; China; Connexins; Female; Gap Juncti | 2010 |
Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness.
Topics: Chromosome Deletion; Chromosome Segregation; Deafness; Female; Genetic Diseases, X-Linked; Humans; L | 2005 |
MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders.
Topics: Amino Acid Motifs; Binding Sites; Dimerization; Genetic Diseases, X-Linked; Humans; Ligases; Microtu | 2002 |