phosphoserine has been researched along with Amyotrophic Lateral Sclerosis in 3 studies
Phosphoserine: The phosphoric acid ester of serine.
Amyotrophic Lateral Sclerosis: A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
| 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 |
|---|---|
| Inukai, Y | 1 |
| Nonaka, T | 2 |
| Arai, T | 2 |
| Yoshida, M | 1 |
| Hashizume, Y | 1 |
| Beach, TG | 1 |
| Buratti, E | 1 |
| Baralle, FE | 1 |
| Akiyama, H | 2 |
| Hisanaga, S | 1 |
| Hasegawa, M | 2 |
| Kametani, F | 1 |
| Suzuki, T | 1 |
| Dohmae, N | 1 |
| Pesaresi, MG | 1 |
| Amori, I | 1 |
| Giorgi, C | 1 |
| Ferri, A | 1 |
| Fiorenzo, P | 1 |
| Gabanella, F | 1 |
| Salvatore, AM | 1 |
| Giorgio, M | 1 |
| Pelicci, PG | 1 |
| Pinton, P | 1 |
| Carrì, MT | 1 |
| Cozzolino, M | 1 |
3 other studies available for phosphoserine and Amyotrophic Lateral Sclerosis
| Article | Year |
|---|---|
Abnormal phosphorylation of Ser409/410 of TDP-43 in FTLD-U and ALS.
Topics: Amyotrophic Lateral Sclerosis; Animals; Antibodies, Monoclonal; Brain; Dementia; DNA-Binding Protein | 2008 |
Identification of casein kinase-1 phosphorylation sites on TDP-43.
Topics: Amino Acid Sequence; Amyotrophic Lateral Sclerosis; Brain; Casein Kinase I; Dementia; DNA-Binding Pr | 2009 |
Mitochondrial redox signalling by p66Shc mediates ALS-like disease through Rac1 inactivation.
Topics: Amyotrophic Lateral Sclerosis; Animals; Apoptosis; Cytoprotection; Down-Regulation; Enzyme Activatio | 2011 |