(2-(trimethylammonium)ethyl)methanethiosulfonate has been researched along with picrotoxin in 3 studies
Studies ((2-(trimethylammonium)ethyl)methanethiosulfonate) | Trials ((2-(trimethylammonium)ethyl)methanethiosulfonate) | Recent Studies (post-2010) ((2-(trimethylammonium)ethyl)methanethiosulfonate) | Studies (picrotoxin) | Trials (picrotoxin) | Recent Studies (post-2010) (picrotoxin) |
---|---|---|---|---|---|
143 | 0 | 17 | 4,135 | 6 | 406 |
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 |
---|---|
Haddrill, JL; Lynch, JW; Shan, Q | 2 |
Hawthorne, R; Lynch, JW | 1 |
3 other study(ies) available for (2-(trimethylammonium)ethyl)methanethiosulfonate and picrotoxin
Article | Year |
---|---|
A single beta subunit M2 domain residue controls the picrotoxin sensitivity of alphabeta heteromeric glycine receptor chloride channels.
Topics: Allosteric Regulation; Amino Acid Substitution; Binding Sites; Binding, Competitive; Cell Line; Chloride Channels; Dose-Response Relationship, Drug; Glycine; Humans; Kidney; Mesylates; Mutagenesis, Site-Directed; Picrotoxin; Protein Structure, Tertiary; Protein Subunits; Receptors, Glycine; Sequence Homology, Amino Acid; Sulfhydryl Reagents | 2001 |
Comparative surface accessibility of a pore-lining threonine residue (T6') in the glycine and GABA(A) receptors.
Topics: Amino Acid Sequence; Animals; Cell Line; Copper; Cysteine; Disulfides; Dithiothreitol; Ethyl Methanesulfonate; GABA Antagonists; Glycine; Humans; Indicators and Reagents; Mesylates; Molecular Sequence Data; Mutation; Oocytes; Patch-Clamp Techniques; Phenanthrolines; Picrotoxin; Protein Subunits; Rats; Receptors, GABA-A; Receptors, Glycine; Sequence Alignment; Statistics as Topic; Sulfhydryl Reagents; Threonine; Xenopus laevis | 2002 |
A picrotoxin-specific conformational change in the glycine receptor M2-M3 loop.
Topics: Allosteric Site; Cyclopentanes; Cysteine; Dimerization; Diterpenes; DNA, Complementary; Dose-Response Relationship, Drug; Electrophysiology; Furans; Ginkgolides; Glycine; Humans; Inhibitory Concentration 50; Kinetics; Mesylates; Mutagenesis, Site-Directed; Mutation; Picrotoxin; Protein Binding; Protein Conformation; Protein Structure, Secondary; Protein Structure, Tertiary; Receptors, Glycine; Time Factors | 2005 |