serine has been researched along with Rett Syndrome 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.
Rett Syndrome: An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Soto, D | 1 |
| Olivella, M | 1 |
| Grau, C | 1 |
| Armstrong, J | 1 |
| Alcon, C | 1 |
| Gasull, X | 1 |
| Santos-Gómez, A | 1 |
| Locubiche, S | 1 |
| Gómez de Salazar, M | 1 |
| García-Díaz, R | 1 |
| Gratacòs-Batlle, E | 1 |
| Ramos-Vicente, D | 1 |
| Chu-Van, E | 1 |
| Colsch, B | 1 |
| Fernández-Dueñas, V | 1 |
| Ciruela, F | 1 |
| Bayés, À | 1 |
| Sindreu, C | 1 |
| López-Sala, A | 1 |
| García-Cazorla, À | 1 |
| Altafaj, X | 1 |
| Sekiguchi, M | 1 |
| Katayama, S | 1 |
| Hatano, N | 1 |
| Shigeri, Y | 1 |
| Sueyoshi, N | 1 |
| Kameshita, I | 1 |
| Zhou, Z | 1 |
| Hong, EJ | 1 |
| Cohen, S | 1 |
| Zhao, WN | 1 |
| Ho, HY | 1 |
| Schmidt, L | 1 |
| Chen, WG | 1 |
| Lin, Y | 1 |
| Savner, E | 1 |
| Griffith, EC | 1 |
| Hu, L | 1 |
| Steen, JA | 1 |
| Weitz, CJ | 1 |
| Greenberg, ME | 1 |
3 other studies available for serine and Rett Syndrome
| Article | Year |
|---|---|
L-Serine dietary supplementation is associated with clinical improvement of loss-of-function
Topics: Animals; Brain Diseases; Child; Cognition; Dietary Supplements; Humans; Loss of Function Mutation; M | 2019 |
Identification of amphiphysin 1 as an endogenous substrate for CDKL5, a protein kinase associated with X-linked neurodevelopmental disorder.
Topics: Amino Acid Sequence; Animals; Brain; Isoelectric Focusing; Male; Mice; Molecular Sequence Data; Muta | 2013 |
Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation.
Topics: Animals; Brain; Brain-Derived Neurotrophic Factor; Calcium Signaling; Calcium-Calmodulin-Dependent P | 2006 |