threonine has been researched along with Eulenburg Disease in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bouhours, M; Davoine, CS; Ferrer, X; Fontaine, B; Sternberg, D; Tabti, N; Willer, JC | 1 |
Abbruzzese, JL; Dice, MS; Fujimoto, E; Groome, JR; Ruben, PC; Wheeler, JT | 1 |
Alexander, GM; Boulos, PT; Heiman-Patterson, TD; Tahmoush, AJ | 1 |
3 other study(ies) available for threonine and Eulenburg Disease
Article | Year |
---|---|
Functional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humans.
Topics: Adult; Alanine; Amino Acid Substitution; Cell Line; Cold Temperature; Electrophysiology; Female; Humans; Kinetics; Muscle, Skeletal; Mutation, Missense; Myotonic Disorders; NAV1.4 Voltage-Gated Sodium Channel; Pedigree; Phenotype; Sodium Channels; Temperature; Threonine; Time Factors | 2004 |
Temperature-sensitive defects in paramyotonia congenita mutants R1448C and T1313M.
Topics: Animals; Arginine; Cold Temperature; Cysteine; Female; Humans; Ion Channel Gating; Methionine; Muscle Proteins; Mutagenesis, Site-Directed; Myotonic Disorders; NAV1.4 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Sodium Channels; Temperature; Threonine; Xenopus laevis | 2004 |
Patch clamp studies of the thr1313met mutant sodium channel causing paramyotonia congenita.
Topics: Adult; Cells, Cultured; Female; Humans; Ion Channel Gating; Methionine; Muscle Fibers, Skeletal; Muscle, Skeletal; Myotonic Disorders; Nuclear Family; Patch-Clamp Techniques; Point Mutation; Sodium Channels; Threonine | 2000 |