1-anilino-8-naphthalenesulfonate has been researched along with Amyotrophic Lateral Sclerosis in 6 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.
Amyotrophic Lateral Sclerosis: A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 3 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Del Poggetto, E | 1 |
| Chiti, F | 1 |
| Bemporad, F | 1 |
| McClure, M | 1 |
| Kim, E | 1 |
| Bickhart, D | 1 |
| Null, D | 1 |
| Cooper, T | 1 |
| Cole, J | 1 |
| Wiggans, G | 1 |
| Ajmone-Marsan, P | 1 |
| Colli, L | 1 |
| Santus, E | 1 |
| Liu, GE | 1 |
| Schroeder, S | 1 |
| Matukumalli, L | 1 |
| Van Tassell, C | 1 |
| Sonstegard, T | 1 |
| Vezzadini, P | 1 |
| Salomone, T | 1 |
| Addarii, F | 1 |
| Cristóvão, JS | 1 |
| Henriques, BJ | 1 |
| Gomes, CM | 1 |
| Tiwari, A | 1 |
| Liba, A | 1 |
| Sohn, SH | 1 |
| Seetharaman, SV | 1 |
| Bilsel, O | 1 |
| Matthews, CR | 1 |
| Hart, PJ | 1 |
| Valentine, JS | 1 |
| Hayward, LJ | 1 |
| Rakhit, R | 1 |
| Crow, JP | 1 |
| Lepock, JR | 1 |
| Kondejewski, LH | 1 |
| Cashman, NR | 1 |
| Chakrabartty, A | 1 |
6 other studies available for 1-anilino-8-naphthalenesulfonate and Amyotrophic Lateral Sclerosis
| Article | Year |
|---|---|
The Folding process of Human Profilin-1, a novel protein associated with familial amyotrophic lateral sclerosis.
Topics: Amyotrophic Lateral Sclerosis; Anilino Naphthalenesulfonates; Circular Dichroism; Escherichia coli; | 2015 |
Fine mapping for Weaver syndrome in Brown Swiss cattle and the identification of 41 concordant mutations across NRCAM, PNPLA8 and CTTNBP2.
Topics: Amyotrophic Lateral Sclerosis; Animals; Base Sequence; Cattle; Cattle Diseases; Cell Adhesion Molecu | 2013 |
[Study of pancreatic exocrine function in 10 cases of amyotrophic lateral sclerosis].
Topics: Adult; Aged; Amylases; Amyotrophic Lateral Sclerosis; Cholecystokinin; Female; Humans; Lipase; Male; | 1968 |
Biophysical and Spectroscopic Methods for Monitoring Protein Misfolding and Amyloid Aggregation.
Topics: Amyloidogenic Proteins; Amyotrophic Lateral Sclerosis; Anilino Naphthalenesulfonates; Benzothiazoles | 2019 |
Metal deficiency increases aberrant hydrophobicity of mutant superoxide dismutases that cause amyotrophic lateral sclerosis.
Topics: Amyotrophic Lateral Sclerosis; Anilino Naphthalenesulfonates; Disulfides; Electrophoresis; Holoenzym | 2009 |
Monomeric Cu,Zn-superoxide dismutase is a common misfolding intermediate in the oxidation models of sporadic and familial amyotrophic lateral sclerosis.
Topics: Amyotrophic Lateral Sclerosis; Anilino Naphthalenesulfonates; Calorimetry; Chromatography, Liquid; C | 2004 |