Page last updated: 2024-11-03

propidium and Fragile X Syndrome

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

Propidium: Quaternary ammonium analog of ethidium; an intercalating dye with a specific affinity to certain forms of DNA and, used as diiodide, to separate them in density gradients; also forms fluorescent complexes with cholinesterase which it inhibits.

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's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Green, KM1
Sheth, UJ1
Flores, BN1
Wright, SE1
Sutter, AB1
Kearse, MG1
Barmada, SJ1
Ivanova, MI1
Todd, PK1

Other Studies

1 other study available for propidium and Fragile X Syndrome

ArticleYear
High-throughput screening yields several small-molecule inhibitors of repeat-associated non-AUG translation.
    The Journal of biological chemistry, 2019, 12-06, Volume: 294, Issue:49

    Topics: Amyotrophic Lateral Sclerosis; Animals; Ataxia; Azepines; Cells, Cultured; Circular Dichroism; DNA R

2019