Page last updated: 2024-10-22

amlexanox and Cockayne-Touraine Disease

amlexanox has been researched along with Cockayne-Touraine Disease in 1 studies

amlexanox: SRA-A antagonist;structure given in first source
amlexanox : A pyridochromene-derived monocarboxylic acid having an amino substituent at the 2-position, an oxo substituent at the 5-position and an isopropyl substituent at the 7-position.

Research Excerpts

ExcerptRelevanceReference
"Recessive dystrophic epidermolysis bullosa (RDEB) is a rare monogenic blistering disorder caused by the lack of functional type VII collagen, leading to skin fragility and subsequent trauma-induced separation of the epidermis from the underlying dermis."2.55Amlexanox Enhances Premature Termination Codon Read-Through in COL7A1 and Expression of Full Length Type VII Collagen: Potential Therapy for Recessive Dystrophic Epidermolysis Bullosa. ( Atanasova, VS; Bruckner-Tuderman, L; Chen, M; Gruber, C; Has, C; Jiang, Q; McGrath, JA; Piñón Hofbauer, J; Prisco, M; South, AP; Uitto, J, 2017)

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
Atanasova, VS1
Jiang, Q1
Prisco, M1
Gruber, C1
Piñón Hofbauer, J1
Chen, M1
Has, C1
Bruckner-Tuderman, L1
McGrath, JA1
Uitto, J1
South, AP1

Reviews

1 review available for amlexanox and Cockayne-Touraine Disease

ArticleYear
Amlexanox Enhances Premature Termination Codon Read-Through in COL7A1 and Expression of Full Length Type VII Collagen: Potential Therapy for Recessive Dystrophic Epidermolysis Bullosa.
    The Journal of investigative dermatology, 2017, Volume: 137, Issue:9

    Topics: Aminopyridines; Codon, Nonsense; Collagen Type VII; Epidermolysis Bullosa Dystrophica; Female; Gene

2017