kojic acid has been researched along with Fragile X Syndrome in 1 studies
Fragile X Syndrome: A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. INTELLECTUAL DISABILITY occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226)
Excerpt | Relevance | Reference |
---|---|---|
"Fragile X syndrome is caused by the functional loss of the fragile X mental retardation 1 (FMR1) gene." | 1.35 | Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila. ( Bray, SM; Chang, S; He, C; Jin, P; Li, Z; Warren, ST; Zarnescu, DC, 2008) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chang, S | 1 |
Bray, SM | 1 |
Li, Z | 1 |
Zarnescu, DC | 1 |
He, C | 1 |
Jin, P | 1 |
Warren, ST | 1 |
1 other study available for kojic acid and Fragile X Syndrome
Article | Year |
---|---|
Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila.
Topics: Animals; Disease Models, Animal; Drosophila; Drosophila Proteins; Drug Evaluation, Preclinical; Fema | 2008 |