threonine has been researched along with Rett Syndrome in 3 studies
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 | 2 (66.67) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Chen, L; Cheng, J; Du, R; Duan, X; Fan, M; Li, Y; Wu, H; Wu, Y; Zhao, Z; Zhu, Q | 1 |
Bao, X; Downs, J; Leonard, H; Williams, S; Wong, K | 1 |
Bird, AP; Cohen, S; Ebert, DH; Ekiert, R; Gabel, HW; Greenberg, ME; Hu, LS; Kastan, NR; Lyst, MJ; Navarro, AJ; Robinson, ND | 1 |
3 other study(ies) available for threonine and Rett Syndrome
Article | Year |
---|---|
Loss of O-GlcNAcylation on MeCP2 at Threonine 203 Leads to Neurodevelopmental Disorders.
Topics: Animals; Humans; Methyl-CpG-Binding Protein 2; Mice; Neurodevelopmental Disorders; Rett Syndrome; Synaptic Transmission; Threonine | 2022 |
Using a large international sample to investigate epilepsy in Rett syndrome.
Topics: Adolescent; Adult; Age Factors; Age of Onset; Anticonvulsants; Arginine; Child; Child, Preschool; Cysteine; Epilepsy; Female; Gene Deletion; Genotype; Humans; Infant; Internationality; Methionine; Methyl-CpG-Binding Protein 2; Middle Aged; Mutation; Odds Ratio; Phenotype; Polymorphism, Single Nucleotide; Rett Syndrome; Sampling Studies; Severity of Illness Index; Threonine | 2013 |
Activity-dependent phosphorylation of MeCP2 threonine 308 regulates interaction with NCoR.
Topics: Animals; Cells, Cultured; Co-Repressor Proteins; Humans; Methyl-CpG-Binding Protein 2; Mice; Mutation; Neurons; Phosphorylation; Rett Syndrome; Threonine; Transcription, Genetic | 2013 |