Page last updated: 2024-10-26

erythrosine and Fragile X Syndrome

erythrosine has been researched along with Fragile X Syndrome in 1 studies

Fluoresceins: A family of spiro(isobenzofuran-1(3H),9'-(9H)xanthen)-3-one derivatives. These are used as dyes, as indicators for various metals, and as fluorescent labels in immunoassays.

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

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
Boyd, VL1
Moody, KI1
Karger, AE1
Livak, KJ1
Zon, G1
Burns, JW1

Other Studies

1 other study available for erythrosine and Fragile X Syndrome

ArticleYear
Methylation-dependent fragment separation: direct detection of DNA methylation by capillary electrophoresis of PCR products from bisulfite-converted genomic DNA.
    Analytical biochemistry, 2006, Jul-15, Volume: 354, Issue:2

    Topics: Base Sequence; DNA; DNA Methylation; DNA Primers; Electrophoresis, Capillary; Female; Fluoresceins;

2006