lysine has been researched along with ALS - Amyotrophic Lateral Sclerosis in 25 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (4.00) | 18.7374 |
| 1990's | 5 (20.00) | 18.2507 |
| 2000's | 10 (40.00) | 29.6817 |
| 2010's | 6 (24.00) | 24.3611 |
| 2020's | 3 (12.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kang, YS; Latif, S | 1 |
| Buratti, E; Elsässer, SJ; Feederle, R; Garcia Morato, J; Gloeckner, CJ; Hans, F; Kahle, PJ; Neumann, M; Skodras, AA; von Zweydorf, F | 1 |
| Arenas, A; Barnett, KR; Chen, J; Gal, J; Kasarskis, EJ; Kuang, L; Zhu, H | 1 |
| Chen, S; Chen, Z; Cui, F; Huang, X; Li, Y; Ling, L; Ren, Y; Sun, B; Yang, F | 1 |
| Cohen, TJ; Hwang, AW; Lee, VM; Restrepo, CR; Trojanowski, JQ; Yuan, CX | 1 |
| Ball, LE; Comte-Walters, S; Harlan, BA; Neely, BA; Pehar, M; Sharma, DR; Vargas, MR | 1 |
| Gourie-Devi, M; Kukreti, R; Ramachandran, S; Taneja, B; Taneja, V; Vats, A; Verma, M | 1 |
| Kamishina, H; Kato, S; Kobatake, Y; Kohyama, M; Maeda, S; Sakai, H; Sasaki, J; Tsukui, T; Urushitani, M; Yamato, O | 1 |
| Baas, F; Bourque, PR; Diekstra, FP; Hennekam, EA; Lindhout, D; Ophoff, RA; Schelhaas, HJ; Strengman, E; van den Berg, LH; van Es, MA; Veldink, JH | 1 |
| Gordon, T; Hegedus, J; Jones, KE | 1 |
| Ashley, J; Bilgicer, B; Borchelt, DR; Hentz, M; Mowery, RA; Ramirez, AJ; Shaw, BF; Shi, Y; Slunt-Brown, H | 1 |
| Kikuchi, S; Makita, Z; Ogata, A; Shinpo, K; Takeuchi, M; Tashiro, K; Tsuji, S | 1 |
| Boehm, BO; Kaufmann, E; Kientsch-Engel, R; Ludolph, AC; Sperfeld, A; Süssmuth, SD; Tumani, H | 1 |
| Horiuchi, S; Kawaguchi, M; Kobayashi, M; Shibata, N | 1 |
| Hanemann, CO; Krause, BJ; Ludolph, AC; Meyer, T; Münch, C; Reske, S; Rosenbohm, A; Sedlmeier, R; Sperfeld, AD; Stumm, G; Uttner, I | 1 |
| Beck, M; Sendtner, M; Toyka, KV | 1 |
| Gralla, EB; Nishida, CR; Valentine, JS | 1 |
| Gamonet, F; Lauquin, GJ | 1 |
| Barnéoud, P; Curet, O | 1 |
| Asayama, K; Hirano, A; Horiuchi, S; Kato, S; Kobayashi, M; Komori, T; Nagai, R; Shibata, N; Umahara, T | 1 |
| Asayama, K; Hirano, A; Horiuchi, S; Kato, M; Kato, S; Nakano, I; Nakashima, K; Ohama, E; Saito, M; Shibata, N | 1 |
| Fujii, J; Kikuchi, S; Moriwaka, F; Ogata, A; Shinpo, K; Taniguchi, N; Tashiro, K | 1 |
| Asayama, K; Hirano, A; Horiuchi, S; Jono, T; Kato, S; Kobayashi, M; Miyata, S; Nagai, R; Sasaki, S; Shibata, N | 1 |
| Cleveland, DW; Hirano, A; Horiuchi, S; Kato, M; Kato, S; Liu, J; Nagai, R; Nakano, I; Nakashima, K; Ohama, E; Shibata, N; Takikawa, M | 1 |
| Bunch, LD; Poser, CM | 1 |
25 other study(ies) available for lysine and ALS - Amyotrophic Lateral Sclerosis
| Article | Year |
|---|---|
Differences of Transport Activity of Arginine and Regulation on Neuronal Nitric Oxide Synthase and Oxidative Stress in Amyotrophic Lateral Sclerosis Model Cell Lines.
Topics: Amino Acid Transport Systems, Basic; Amyotrophic Lateral Sclerosis; Animals; Arginine; Cell Line; Gene Expression Regulation; Humans; Hydrogen Peroxide; Lysine; Mice; Motor Neurons; Nitric Oxide Synthase Type I; Oxidative Stress; Spinal Cord; Superoxide Dismutase-1 | 2021 |
Sirtuin-1 sensitive lysine-136 acetylation drives phase separation and pathological aggregation of TDP-43.
Topics: Acetylation; Amyotrophic Lateral Sclerosis; DNA-Binding Proteins; Humans; Lysine; Protein Aggregation, Pathological; Protein Processing, Post-Translational; RNA; Sirtuin 1 | 2022 |
Lysine acetylation regulates the RNA binding, subcellular localization and inclusion formation of FUS.
Topics: Acetylation; Adult; Amyotrophic Lateral Sclerosis; beta Karyopherins; Female; Frontotemporal Dementia; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Lysine; Male; Middle Aged; Nuclear Localization Signals; Protein Domains; RNA-Binding Protein FUS; RNA-Binding Proteins; Sirtuins; Young Adult | 2020 |
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 |
An acetylation switch controls TDP-43 function and aggregation propensity.
Topics: Acetylation; Amyotrophic Lateral Sclerosis; Cloning, Molecular; DNA Primers; DNA-Binding Proteins; Frontotemporal Lobar Degeneration; Humans; Immunohistochemistry; Immunoprecipitation; Lysine; Mass Spectrometry; Mutagenesis, Site-Directed; Oxidative Stress; Protein Aggregation, Pathological; Recombinant Proteins; Reverse Transcriptase Polymerase Chain Reaction; RNA, Small Interfering; Spinal Cord | 2015 |
Changes in Protein Expression and Lysine Acetylation Induced by Decreased Glutathione Levels in Astrocytes.
Topics: Acetylation; Amyotrophic Lateral Sclerosis; Animals; Astrocytes; Disease Models, Animal; Gene Expression Regulation; Glutamate-Cysteine Ligase; Glutathione; Humans; Lysine; Mice; Mice, Knockout; Neurons; Protein Biosynthesis; Protein Processing, Post-Translational; Proteomics; Reactive Oxygen Species | 2016 |
Identification of L84F mutation with a novel nucleotide change c.255G > T in the superoxide dismutase gene in a North Indian family with amyotrophic lateral sclerosis.
Topics: Aged; Amyotrophic Lateral Sclerosis; DNA-Binding Proteins; Family Health; Female; Genetic Testing; Genotype; Humans; India; Lysine; Male; Middle Aged; Models, Molecular; Phenylalanine; Polymorphism, Single Nucleotide; Superoxide Dismutase-1 | 2016 |
Localization of a mutant SOD1 protein in E40K-heterozygous dogs: Implications for non-cell-autonomous pathogenesis of degenerative myelopathy.
Topics: Amyotrophic Lateral Sclerosis; Animals; Antibodies; Calcium-Binding Proteins; Disease Models, Animal; DNA-Binding Proteins; Dogs; Gene Expression Regulation; Glial Fibrillary Acidic Protein; Glutamic Acid; HEK293 Cells; Humans; Immunoprecipitation; Lysine; Microfilament Proteins; Mutation; Spinal Cord; Superoxide Dismutase-1; Transfection | 2017 |
A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation.
Topics: Aged; Amino Acid Sequence; Amino Acid Substitution; Amyotrophic Lateral Sclerosis; Base Sequence; Dementia; Female; Heterozygote; Humans; Isoleucine; Lysine; Male; Middle Aged; Mutation; Pedigree; Ribonuclease, Pancreatic | 2009 |
Development and use of the incremental twitch subtraction MUNE method in mice.
Topics: Action Potentials; Alanine; Amyotrophic Lateral Sclerosis; Animals; Biophysics; Electric Stimulation; Electromyography; Isometric Contraction; Lysine; Male; Mice; Mice, Transgenic; Motor Neurons; Muscle, Skeletal; Mutation; Superoxide Dismutase; Superoxide Dismutase-1; Time Factors | 2009 |
Abnormal SDS-PAGE migration of cytosolic proteins can identify domains and mechanisms that control surfactant binding.
Topics: Acetylation; Amino Acid Substitution; Amyotrophic Lateral Sclerosis; Animals; Electrophoresis, Polyacrylamide Gel; Humans; Lysine; Mice; Motion; Mutant Proteins; Protein Binding; Protein Processing, Post-Translational; Protein Structure, Tertiary; Superoxide Dismutase; Superoxide Dismutase-1; Surface-Active Agents | 2012 |
Detection of N epsilon-(carboxymethyl)lysine (CML) and non-CML advanced glycation end-products in the anterior horn of amyotrophic lateral sclerosis spinal cord.
Topics: Aged; Amyotrophic Lateral Sclerosis; Autopsy; Axons; Female; Glycation End Products, Advanced; Humans; Immunohistochemistry; Lysine; Male; Middle Aged; Neurons; Spinal Cord | 2002 |
The advanced glycation end-product N epsilon-(carboxymethyl)lysine level is elevated in cerebrospinal fluid of patients with amyotrophic lateral sclerosis.
Topics: Adult; Aged; Amyotrophic Lateral Sclerosis; Female; Glycation End Products, Advanced; Humans; Lysine; Male; Middle Aged; Statistics, Nonparametric | 2004 |
Glyoxal inactivates glutamate transporter-1 in cultured rat astrocytes.
Topics: Amino Acid Transport System X-AG; Amyotrophic Lateral Sclerosis; Animals; Animals, Newborn; Astrocytes; Cells, Cultured; Chromatography, High Pressure Liquid; Glutamic Acid; Glyoxal; Immunoblotting; Immunohistochemistry; Lysine; Rats | 2005 |
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.
Topics: Amyotrophic Lateral Sclerosis; Arginine; Dementia; DNA Mutational Analysis; Dynactin Complex; Family Health; Female; Humans; Lysine; Magnetic Resonance Imaging; Male; Microtubule-Associated Proteins; Middle Aged; Mutation | 2005 |
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 |
Characterization of three yeast copper-zinc superoxide dismutase mutants analogous to those coded for in familial amyotrophic lateral sclerosis.
Topics: Alanine; Amino Acid Sequence; Amyotrophic Lateral Sclerosis; Arginine; Edetic Acid; Glycine; Humans; Kinetics; Lysine; Mutagenesis; Paraquat; Point Mutation; Saccharomyces cerevisiae; Spectrophotometry; Superoxide Dismutase | 1994 |
The Saccharomyces cerevisiae LYS7 gene is involved in oxidative stress protection.
Topics: Alleles; Amino Acid Sequence; Amyotrophic Lateral Sclerosis; Copper; Cytosol; Fungal Proteins; Humans; Isoenzymes; Lysine; Methionine; Mitochondria; Molecular Chaperones; Molecular Sequence Data; Oxidative Stress; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Superoxide Dismutase; Superoxides | 1998 |
Beneficial effects of lysine acetylsalicylate, a soluble salt of aspirin, on motor performance in a transgenic model of amyotrophic lateral sclerosis.
Topics: Amyotrophic Lateral Sclerosis; Animals; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Body Weight; Brain; Humans; Lysine; Male; Mice; Mice, Transgenic; Motor Activity; Muscle, Skeletal; Mutation; Postural Balance; Reflex; Salicylates; Solubility; Superoxide Dismutase | 1999 |
Advanced glycation endproducts are deposited in neuronal hyaline inclusions: a study on familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation.
Topics: Adult; Aged; Aged, 80 and over; Amyotrophic Lateral Sclerosis; Antibodies; Female; Glycation End Products, Advanced; Humans; Hyalin; Immunohistochemistry; Inclusion Bodies; Lysine; Male; Microscopy, Immunoelectron; Middle Aged; Motor Neurons; Neurofilament Proteins; Spinal Cord; Superoxide Dismutase; Superoxide Dismutase-1; Ubiquitins | 1999 |
Astrocytic hyaline inclusions contain advanced glycation endproducts in familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation: immunohistochemical and immunoelectron microscopical analyses.
Topics: Adult; Aged; Amyotrophic Lateral Sclerosis; Astrocytes; Cytoplasmic Granules; Female; Glycation End Products, Advanced; Humans; Hyalin; Immunohistochemistry; Inclusion Bodies; Lewy Bodies; Lysine; Male; Microscopy, Immunoelectron; Middle Aged; Mutation; Neurofibrils; Neurons; Superoxide Dismutase; Superoxide Dismutase-1; Ubiquitins | 1999 |
Detection of an Amadori product, 1-hexitol-lysine, in the anterior horn of the amyotrophic lateral sclerosis and spinobulbar muscular atrophy spinal cord: evidence for early involvement of glycation in motoneuron diseases.
Topics: Amyotrophic Lateral Sclerosis; Atrophy; Axons; Glycosylation; Humans; Lysine; Muscular Disorders, Atrophic; Neurons; Spinal Cord; Time Factors | 2000 |
Nonoxidative protein glycation is implicated in familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation.
Topics: 8-Hydroxy-2'-Deoxyguanosine; Acrolein; Adult; Aged; Aldehydes; Amyotrophic Lateral Sclerosis; Arginine; Deoxyguanosine; Glycosylation; Humans; Imidazoles; Lipid Peroxidation; Lysine; Male; Middle Aged; Motor Neurons; Oxidative Stress; Spinal Cord; Superoxide Dismutase | 2000 |
Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation.
Topics: Adult; Aged; Aged, 80 and over; Amyotrophic Lateral Sclerosis; Animals; Arginine; Female; Glycation End Products, Advanced; Histocytochemistry; Humans; Immunohistochemistry; Inclusion Bodies; Lysine; Male; Mice; Mice, Transgenic; Microscopy, Electron; Microscopy, Immunoelectron; Middle Aged; Mutation; Norleucine; Pyrroles; Superoxide Dismutase; Superoxide Dismutase-1 | 2000 |
Serum amino acid studies in amyotrophic lateral sclerosis. II. Results of metrecal arginine lysine tolerance tests in US caucasians and Guam Chamorros.
Topics: Adolescent; Adult; Amino Acids; Amyotrophic Lateral Sclerosis; Arginine; Blood Chemical Analysis; Chromatography; Humans; Lysine; Male; Middle Aged; Pacific Islands; United States; White People | 1966 |