asparagine has been researched along with Amyotrophic Lateral Sclerosis in 8 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (37.50) | 29.6817 |
2010's | 5 (62.50) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chen, S; Chen, Z; Cui, F; Huang, X; Li, Y; Ling, L; Ren, Y; Sun, B; Yang, F | 1 |
Akram, N; Chen, C; Ding, X; Luo, SZ; Xue, S | 1 |
Dai, B; Gu, J; Gui, X; He, J; He, L; Jiang, L; Li, D; Li, X; Li, Y; Liu, C; Liu, Z; Luo, F; Qin, Z; Shin, WS; Sun, B; Xie, M; Zhao, K; Zhao, M; Zhou, H | 1 |
Abdolvahabi, A; Cook, NP; Kohn, T; Marti, AA; Rhodes, NR; Shaw, BF; Shi, Y | 1 |
Baloh, RH; Bell, S; Diamond, MI; Fuentealba, RA; Shao, J; Udan, M; Wegorzewska, I; Weihl, CC | 1 |
Albo, F; Bernardi, G; Ferrari, F; Longone, P; Pascucci, T; Puglisi-Allegra, S; Spalloni, A; Zona, C | 1 |
Njajou, OT; Sinke, RJ; Sutedja, NA; Van den Berg, LH; Van der Linden, MW; Van der Schouw, YT; Van Duijn, CM; Van Vught, PW; Veldink, JH; Wokke, JH | 1 |
Beck, M; Sendtner, M; Toyka, KV | 1 |
1 review(s) available for asparagine and Amyotrophic Lateral Sclerosis
Article | Year |
---|---|
Fused in Sarcoma: Properties, Self-Assembly and Correlation with Neurodegenerative Diseases.
Topics: Amyotrophic Lateral Sclerosis; Asparagine; Frontotemporal Lobar Degeneration; GPI-Linked Proteins; Humans; Neurodegenerative Diseases; Peptides; Prions; Protein Aggregation, Pathological; Protein Domains; RNA-Binding Protein FUS | 2019 |
7 other study(ies) available for asparagine and Amyotrophic Lateral Sclerosis
Article | Year |
---|---|
A novel D90_K91insN mutation in exon 4 of the SOD1 gene caused familial amyotrophic lateral sclerosis in a Chinese pedigree.
Topics: Adult; Aged; Amyotrophic Lateral Sclerosis; Asparagine; Computational Biology; DNA Mutational Analysis; Exons; Humans; Lysine; Male; Middle Aged; Models, Molecular; Mutation; Pediatrics; Superoxide Dismutase-1 | 2018 |
Structural basis for reversible amyloids of hnRNPA1 elucidates their role in stress granule assembly.
Topics: Amyloid; Amyotrophic Lateral Sclerosis; Asparagine; Cytoplasmic Granules; HeLa Cells; Heterogeneous Nuclear Ribonucleoprotein A1; Humans; Microscopy, Electron, Transmission; Models, Molecular; Mutation; Recombinant Proteins; X-Ray Diffraction | 2019 |
Deamidation of asparagine to aspartate destabilizes Cu, Zn superoxide dismutase, accelerates fibrillization, and mirrors ALS-linked mutations.
Topics: Amyotrophic Lateral Sclerosis; Asparagine; Aspartic Acid; Humans; Models, Molecular; Molecular Structure; Mutation, Missense; Protein Stability; Superoxide Dismutase; Superoxide Dismutase-1; Temperature | 2013 |
Interaction with polyglutamine aggregates reveals a Q/N-rich domain in TDP-43.
Topics: Amyotrophic Lateral Sclerosis; Asparagine; Cell Line; Cell Nucleus; DNA-Binding Proteins; Glutamine; Humans; Multiprotein Complexes; Peptides; Protein Multimerization | 2010 |
Altered vulnerability to kainate excitotoxicity of transgenic-Cu/Zn SOD1 neurones.
Topics: Amyotrophic Lateral Sclerosis; Analysis of Variance; Animals; Asparagine; Calcium Channel Blockers; Cell Count; Cell Survival; Cells, Cultured; Cerebral Cortex; Cobalt; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Interactions; Embryo, Mammalian; Female; Glial Fibrillary Acidic Protein; Glutamic Acid; Immunohistochemistry; Kainic Acid; Male; Mice; Mice, Transgenic; Motor Neurons; Neurotoxins; Nifedipine; Phosphopyruvate Hydratase; Sodium Channel Blockers; Spinal Cord; Superoxide Dismutase; Tetrodotoxin; Time Factors | 2004 |
The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population.
Topics: Adult; Aged; Aged, 80 and over; Amyotrophic Lateral Sclerosis; Asparagine; Confidence Intervals; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Hemochromatosis Protein; Histidine; Histocompatibility Antigens Class I; Humans; Male; Membrane Proteins; Middle Aged; Mutation; Netherlands; Odds Ratio; Retrospective Studies | 2007 |
Novel SOD1 N86K mutation is associated with a severe phenotype in familial ALS.
Topics: Amyotrophic Lateral Sclerosis; Asparagine; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Humans; Lysine; Middle Aged; Mutation; Phenotype; Superoxide Dismutase; Superoxide Dismutase-1 | 2007 |