valine has been researched along with Fragile X 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 | 1 (33.33) | 29.6817 |
2010's | 2 (66.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bostrom, CA; Chiu, C; Chiu, J; Christie, BR; Eadie, BD; Fontaine, CJ; Ghilan, M; Hryciw, BN; Meconi, A; Sawchuk, S; Truesdell, A; Truesdell, E; Wortman, RC; Yau, SY | 1 |
Arvio, M; Castrén, ML; Louhivuori, V; Oksanen, V; Paunio, T; Soronen, P | 1 |
Ferrando, T; Genovés, J; Martorell, L; Molero, M; Naudó, M; Poo, P; Tondo, M | 1 |
3 other study(ies) available for valine and Fragile X Syndrome
Article | Year |
---|---|
Impaired bidirectional NMDA receptor dependent synaptic plasticity in the dentate gyrus of adult female Fmr1 heterozygous knockout mice.
Topics: Animals; Dentate Gyrus; Disease Models, Animal; Estrous Cycle; Female; Fragile X Mental Retardation Protein; Fragile X Syndrome; Genotype; Glycine; Hindlimb Suspension; Male; Memory; Mice; Mice, Inbred C57BL; Mice, Transgenic; Neuronal Plasticity; Receptors, N-Methyl-D-Aspartate; Spatial Behavior; Swimming; Valine | 2016 |
The Val66Met polymorphism in the BDNF gene is associated with epilepsy in fragile X syndrome.
Topics: Adolescent; Adult; Aged; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Epilepsy; Finland; Fragile X Syndrome; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Valine; Young Adult | 2009 |
Predisposition to epilepsy in fragile X syndrome: does the Val66Met polymorphism in the BDNF gene play a role?
Topics: Adolescent; Adult; Aged; Brain-Derived Neurotrophic Factor; Child; Child, Preschool; DNA Mutational Analysis; Epilepsy; Female; Fragile X Syndrome; Genetic Predisposition to Disease; Humans; Infant; Male; Methionine; Middle Aged; Polymorphism, Genetic; Valine; Young Adult | 2011 |