arginine has been researched along with Alexander Disease in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 3 (50.00) | 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 |
| Goldman, JE; Hagemann, TL; McKhann, GM; Messing, A; Sosunov, AA; Tian, R; Wu, X | 1 |
| Austin, EV; Hagemann, TL; Jacka, EM; Johnson, DA; Johnson, JA; LaPash Daniels, CM; Messing, A; Rockney, DE | 1 |
| Asahina, N; Kanazawa, N; Okamoto, T; Saitoh, S; Sudo, A; Tsujino, S | 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 |
6 other study(ies) available for arginine 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 |
Alexander disease mutant glial fibrillary acidic protein compromises glutamate transport in astrocytes.
Topics: 8-Bromo Cyclic Adenosine Monophosphate; Alexander Disease; Animals; Arginine; Astrocytes; Cells, Cultured; Coculture Techniques; Cysteine; Excitatory Amino Acid Agonists; Excitatory Amino Acid Transporter 2; Flow Cytometry; Gene Expression Regulation; Glial Fibrillary Acidic Protein; Green Fluorescent Proteins; Hippocampus; Kainic Acid; Membrane Potentials; Mutation; Nerve Tissue Proteins; Neurons; Patch-Clamp Techniques; Rats; Transfection | 2010 |
Beneficial effects of Nrf2 overexpression in a mouse model of Alexander disease.
Topics: Age Factors; Alexander Disease; Alkaline Phosphatase; Animals; Arginine; Astrocytes; Body Weight; Brain; Chromatography, High Pressure Liquid; Disease Models, Animal; Enzyme-Linked Immunosorbent Assay; Female; Gene Expression Regulation; Glial Fibrillary Acidic Protein; Glutamate-Cysteine Ligase; Glutathione; GPI-Linked Proteins; Histidine; Humans; Isoenzymes; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mutation; Nerve Fibers; NF-E2-Related Factor 2; RNA, Messenger | 2012 |
An infantile-juvenile form of Alexander disease caused by a R79H mutation in GFAP.
Topics: Age of Onset; Alexander Disease; Arginine; Child; DNA Mutational Analysis; Glial Fibrillary Acidic Protein; Histidine; Humans; Magnetic Resonance Imaging; Male; Mutation | 2006 |
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 |