serine has been researched along with Epilepsy Syndromes in 4 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 | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 4 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Adhikari, A | 1 |
| Buchanan, FKB | 1 |
| Fenton, TA | 1 |
| Cameron, DL | 1 |
| Halmai, JANM | 1 |
| Copping, NA | 1 |
| Fink, KD | 1 |
| Silverman, JL | 1 |
| Fuchs, C | 1 |
| Cosentino, L | 1 |
| Urbinati, C | 1 |
| Talamo, MC | 1 |
| Medici, G | 1 |
| Quattrini, MC | 1 |
| Mottolese, N | 1 |
| Pietraforte, D | 1 |
| Fuso, A | 1 |
| Ciani, E | 1 |
| De Filippis, B | 1 |
| Colarusso, A | 1 |
| Lauro, C | 1 |
| Calvanese, M | 1 |
| Parrilli, E | 1 |
| Tutino, ML | 1 |
| Pujol-Giménez, J | 1 |
| Mirzaa, G | 1 |
| Blue, EE | 1 |
| Albano, G | 1 |
| Miller, DE | 1 |
| Allworth, A | 1 |
| Bennett, JT | 1 |
| Byers, PH | 1 |
| Chanprasert, S | 1 |
| Chen, J | 1 |
| Doherty, D | 1 |
| Folta, AB | 1 |
| Gillentine, MA | 1 |
| Glass, I | 1 |
| Hing, A | 1 |
| Horike-Pyne, M | 1 |
| Leppig, KA | 1 |
| Parhin, A | 1 |
| Ranchalis, J | 1 |
| Raskind, WH | 1 |
| Rosenthal, EA | 1 |
| Schwarze, U | 1 |
| Sheppeard, S | 1 |
| Strohbehn, S | 1 |
| Sybert, VP | 1 |
| Timms, A | 1 |
| Wener, M | 1 |
| Bamshad, MJ | 1 |
| Hisama, FM | 1 |
| Jarvik, GP | 1 |
| Dipple, KM | 1 |
| Hediger, MA | 1 |
| Stergachis, AB | 1 |
4 other studies available for serine and Epilepsy Syndromes
| Article | Year |
|---|---|
Touchscreen cognitive deficits, hyperexcitability and hyperactivity in males and females using two models of Cdkl5 deficiency.
Topics: Animals; Cognition; Cyclin-Dependent Kinases; Epileptic Syndromes; Female; Humans; Male; Mice; Prote | 2022 |
Treatment with FRAX486 rescues neurobehavioral and metabolic alterations in a female mouse model of CDKL5 deficiency disorder.
Topics: Animals; Disease Models, Animal; Disks Large Homolog 4 Protein; Epileptic Syndromes; Female; Glucose | 2022 |
Active human full-length CDKL5 produced in the Antarctic bacterium Pseudoalteromonas haloplanktis TAC125.
Topics: Antarctic Regions; Cold Temperature; Epileptic Syndromes; Humans; Peptide Hydrolases; Protein Kinase | 2022 |
Dominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome.
Topics: Amino Acid Transport System ASC; Child; Epilepsy; Epileptic Syndromes; Heterozygote; Humans; Microce | 2023 |