tryptophan has been researched along with Alexander Disease in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ben-Sira, L; Blumkin, L; Edvardson, S; Henneke, M; Lerman-Sagie, T; Leshinsky-Silver, E; Lev, D; Nishri, D | 1 |
| Aoki, Y; Della Nave, R; Mascalchi, M; Matsubara, Y; Pastorelli, F; Salvi, F; Scaglione, C; Vella, A | 1 |
| Brenner, M; Der Perng, M; Gibbon, T; Li, R; Prescott, AR; Quinlan, RA; Su, M; Wen, SF | 1 |
3 other study(ies) available for tryptophan and Alexander Disease
| Article | Year |
|---|---|
Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorder.
Topics: Alexander Disease; Arginine; Child, Preschool; Exome; Female; Frontal Lobe; Glial Fibrillary Acidic Protein; High-Throughput Nucleotide Sequencing; Humans; Magnetic Resonance Imaging; Mitochondrial Diseases; Mutation; Tryptophan; White Matter | 2014 |
Adult Alexander's disease without leukoencephalopathy.
Topics: Aged; Alexander Disease; Arginine; Brain Diseases; Glial Fibrillary Acidic Protein; Humans; Magnetic Resonance Imaging; Male; Mutation; Tryptophan | 2005 |
The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27.
Topics: Alexander Disease; alpha-Crystallin B Chain; Amino Acid Substitution; Animals; Arginine; Cell Line, Tumor; Genes, Dominant; Glial Fibrillary Acidic Protein; Heat-Shock Proteins; HSP27 Heat-Shock Proteins; Humans; Mice; Molecular Chaperones; Mutation, Missense; Neoplasm Proteins; Signal Transduction; Tryptophan | 2006 |