methionine has been researched along with Andersen Cardiodysrhythmic Periodic Paralysis 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 |
|---|---|
| Ma, D; Rogers, TB; Tang, XD; Welling, PA | 1 |
| Furukawa, T; Kurokawa, J; Miura, D; Nakamura, K; Ohe, T; Ouchida, M; Shimizu, K; Tani, Y | 1 |
2 other study(ies) available for methionine and Andersen Cardiodysrhythmic Periodic Paralysis
| Article | Year |
|---|---|
An andersen-Tawil syndrome mutation in Kir2.1 (V302M) alters the G-loop cytoplasmic K+ conduction pathway.
Topics: Amino Acid Substitution; Andersen Syndrome; Animals; Cell Line; Cell Membrane Permeability; Heart Conduction System; Humans; Hydrophobic and Hydrophilic Interactions; Ion Transport; Methionine; Mutation, Missense; Phosphatidylinositol 4,5-Diphosphate; Potassium; Potassium Channels, Inwardly Rectifying; Protein Structure, Secondary; Protein Structure, Tertiary; Rats; Rats, Sprague-Dawley; Structure-Activity Relationship; Valine; Xenopus laevis | 2007 |
T75M-KCNJ2 mutation causing Andersen-Tawil syndrome enhances inward rectification by changing Mg2+ sensitivity.
Topics: Adult; Andersen Syndrome; Base Sequence; Cell Line; Cell Membrane; DNA Mutational Analysis; Female; Genes, Dominant; Humans; Ion Channel Gating; Magnesium; Methionine; Molecular Sequence Data; Mutation; Potassium Channels, Inwardly Rectifying; Protein Transport; Spermine; Threonine | 2007 |