asparagine has been researched along with Degenerative Diseases, Central Nervous System in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (11.11) | 29.6817 |
| 2010's | 4 (44.44) | 24.3611 |
| 2020's | 4 (44.44) | 2.80 |
| Authors | Studies |
|---|---|
| Cheng, G; Cui, S; Dong, Y; Du, K; Li, H; Li, Y; Liu, L; Ren, C; Wang, H; Wang, J; Xia, L; Xu, Y; Yang, B; Zhang, X; Zhu, C | 1 |
| Rodin, S; Saei, AA; Wang, J; Zhang, X; Zubarev, RA | 1 |
| Bloom, LB; Chang, MC; Collins Ruff, K; Franz, DN; Kilberg, MS; McKenna, R; Merritt, ME; Qian, Z; Staklinski, SJ; Yu, F | 1 |
| Jana, B; Manna, RN; Onuchic, JN | 1 |
| Arslan, F; Barmada, SJ; Kanneganti, V; Liebman, SW; Park, SK; Purushothaman, P; Verma, SC | 1 |
| Cascarina, SM; Machihara, S; Paul, KR; Ross, ED | 1 |
| Akram, N; Chen, C; Ding, X; Luo, SZ; Xue, S | 1 |
| Boeve, BF; Dickson, DW; Dugger, BN; Fredrickson, P; Kaplan, J; Lin, SC; Spector, AR; Strongosky, A; Uitti, RJ; Wszolek, ZK | 1 |
| Hirano, T; Maeda, Y; Ohmori, H; Uchida, Y; Uchino, M; Uyama, E; Yamashita, S; Yonemura, K | 1 |
1 review(s) available for asparagine and Degenerative Diseases, Central Nervous System
| 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 |
8 other study(ies) available for asparagine and Degenerative Diseases, Central Nervous System
| Article | Year |
|---|---|
An intractable epilepsy phenotype of ASNS novel mutation in two patients with asparagine synthetase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Asparagine; Aspartate-Ammonia Ligase; Drug Resistant Epilepsy; Humans; Intellectual Disability; Microcephaly; Mutation; Neurodegenerative Diseases; Phenotype | 2022 |
First Experimental Evidence for Reversibility of Ammonia Loss from Asparagine.
Topics: Ammonia; Asparagine; Humans; Neurodegenerative Diseases; Proteins | 2022 |
Cellular and molecular characterization of two novel asparagine synthetase gene mutations linked to asparagine synthetase deficiency.
Topics: Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Asparagine; Aspartate-Ammonia Ligase; Atrophy; Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor; Child; HEK293 Cells; Humans; Intellectual Disability; Microcephaly; Mutation; Neurodegenerative Diseases | 2022 |
Road-blocker HSP disease mutation disrupts pre-organization for ATP hydrolysis in kinesin through a second sphere control.
Topics: Adenosine Triphosphate; Asparagine; Humans; Hydrolysis; Kinesins; Microtubules; Mutation; Neurodegenerative Diseases; Spastic Paraplegia, Hereditary; Tubulin | 2023 |
Overexpression of a conserved HSP40 chaperone reduces toxicity of several neurodegenerative disease proteins.
Topics: Animals; Asparagine; DNA-Binding Proteins; Glutamine; HEK293 Cells; HSP40 Heat-Shock Proteins; Humans; Neurodegenerative Diseases; Neurons; Peptides; Prions; Protein Aggregates; RNA-Binding Protein FUS; Ubiquitin; Yeasts | 2018 |
Sequence features governing aggregation or degradation of prion-like proteins.
Topics: Amino Acid Sequence; Asparagine; Glutamine; Heterogeneous-Nuclear Ribonucleoprotein Group A-B; Humans; Neurodegenerative Diseases; Peptide Termination Factors; Prions; Protein Aggregation, Pathological; Protein Domains; Proteolysis; Saccharomyces cerevisiae Proteins | 2018 |
Anatomy of disturbed sleep in pallido-ponto-nigral degeneration.
Topics: Actigraphy; Adult; Asparagine; Female; Genetic Testing; Globus Pallidus; Humans; Lysine; Male; Middle Aged; Mutation; Neurodegenerative Diseases; Neurofibrillary Tangles; Polysomnography; Pons; Severity of Illness Index; Sleep Wake Disorders; Substantia Nigra; tau Proteins; Tyrosine 3-Monooxygenase; Young Adult | 2011 |
Pantothenate kinase-associated neurodegeneration initially presenting as postural tremor alone in a Japanese family with homozygous N245S substitutions in the pantothenate kinase gene.
Topics: Acanthocytes; Adult; Anticonvulsants; Asian People; Asparagine; Basal Ganglia; Brain Mapping; Clonazepam; DNA Mutational Analysis; Family Health; Female; Homozygote; Humans; Magnetic Resonance Imaging; Mutation; Neurodegenerative Diseases; Phosphotransferases (Alcohol Group Acceptor); Propanolamines; Serine; Staining and Labeling; Tremor | 2004 |