1-anilino-8-naphthalenesulfonate has been researched along with Amyloid Neuropathies in 2 studies
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.
Amyloid Neuropathies: Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Lashuel, HA | 1 |
Wurth, C | 1 |
Woo, L | 1 |
Kelly, JW | 1 |
Quintas, A | 1 |
Saraiva, MJ | 1 |
Brito, RM | 1 |
2 other studies available for 1-anilino-8-naphthalenesulfonate and Amyloid Neuropathies
Article | Year |
---|---|
The most pathogenic transthyretin variant, L55P, forms amyloid fibrils under acidic conditions and protofilaments under physiological conditions.
Topics: Amyloid; Amyloid Neuropathies; Anilino Naphthalenesulfonates; Electrophoresis, Polyacrylamide Gel; H | 1999 |
The tetrameric protein transthyretin dissociates to a non-native monomer in solution. A novel model for amyloidogenesis.
Topics: Amyloid; Amyloid Neuropathies; Anilino Naphthalenesulfonates; Chromatography, Gel; Guanidine; Humans | 1999 |