Page last updated: 2024-10-30

kojic acid and Fragile X Syndrome

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)

Research Excerpts

ExcerptRelevanceReference
"Fragile X syndrome is caused by the functional loss of the fragile X mental retardation 1 (FMR1) gene."1.35Identification 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)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chang, S1
Bray, SM1
Li, Z1
Zarnescu, DC1
He, C1
Jin, P1
Warren, ST1

Other Studies

1 other study available for kojic acid and Fragile X Syndrome

ArticleYear
Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila.
    Nature chemical biology, 2008, Volume: 4, Issue:4

    Topics: Animals; Disease Models, Animal; Drosophila; Drosophila Proteins; Drug Evaluation, Preclinical; Fema

2008