serine has been researched along with Autosomal Dominant Hereditary Spastic Paraplegia 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 | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Svenson, IK | 1 |
| Kloos, MT | 1 |
| Gaskell, PC | 1 |
| Nance, MA | 1 |
| Garbern, JY | 1 |
| Hisanaga, S | 1 |
| Pericak-Vance, MA | 1 |
| Ashley-Koch, AE | 1 |
| Marchuk, DA | 1 |
| McDermott, CJ | 1 |
| Burness, CE | 1 |
| Kirby, J | 1 |
| Cox, LE | 1 |
| Rao, DG | 1 |
| Hewamadduma, C | 1 |
| Sharrack, B | 1 |
| Hadjivassiliou, M | 1 |
| Chinnery, PF | 1 |
| Dalton, A | 1 |
| Shaw, PJ | 1 |
| Cho, HJ | 1 |
| Sung, DH | 1 |
| Ki, CS | 1 |
3 other studies available for serine and Autosomal Dominant Hereditary Spastic Paraplegia
| Article | Year |
|---|---|
Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations.
Topics: Adenosine Triphosphatases; Adolescent; Alternative Splicing; CDC2 Protein Kinase; Child; Child, Pres | 2004 |
Clinical features of hereditary spastic paraplegia due to spastin mutation.
Topics: Adenosine Triphosphatases; Adult; Aged; Cohort Studies; DNA Mutational Analysis; Exons; Female; Gene | 2006 |
Identification of de novo BSCL2 Ser90Leu mutation in a Korean family with Silver syndrome and distal hereditary motor neuropathy.
Topics: Adolescent; Adult; Amino Acid Substitution; DNA Mutational Analysis; Female; GTP-Binding Protein gam | 2007 |