lysine has been researched along with Apraxias in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bouchard, JP; Brais, B; Dicaire, MJ; Duquette, A; Gosselin, I; Labuda, D; Loisel, L; Marchand, L; Mathieu, J; McNabb-Baltar, J; Roddier, K; St-Denis, A | 1 |
Bieganowski, P; Brenner, C; Seidle, HF | 1 |
2 other study(ies) available for lysine and Apraxias
Article | Year |
---|---|
Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy.
Topics: Adult; Aged; alpha-Fetoproteins; Apraxias; Arginine; Ataxia; Chromosomes, Human, Pair 9; Cluster Analysis; DNA Helicases; DNA Mutational Analysis; Family Health; Female; Glutamic Acid; Humans; Leucine; Linkage Disequilibrium; Lysine; Male; Middle Aged; Multifunctional Enzymes; Mutation; Oculomotor Nerve Diseases; Quebec; RNA Helicases | 2005 |
Disease-associated mutations inactivate AMP-lysine hydrolase activity of Aprataxin.
Topics: Adenosine Monophosphate; Alleles; Apraxias; Ataxia; Binding Sites; Blotting, Western; Cations; DNA Damage; DNA-Binding Proteins; Electrophoresis, Polyacrylamide Gel; Escherichia coli; Eye Diseases; Humans; Hydrogen-Ion Concentration; Hydrolases; Kinetics; Lysine; Metals; Motor Neuron Disease; Mutagenesis, Site-Directed; Mutation; Nuclear Proteins; Phenotype; Plasmids; Protein Binding; Protein Structure, Tertiary; RNA, Messenger; Substrate Specificity; Syndrome; Temperature; Zinc Fingers | 2005 |