The pharmacology of mechanogated membrane ion channels

Keyphrases

• Fatty Acids 100%
• Pharmacology 100%
• Membrane Ion Channels 100%
• Channel Blocker 50%
• Mechanism of Action 50%
• Therapeutic Potential 50%
• Pathological Process 50%
• High Affinity 50%
• Acetylcholine Receptor (AChR) 50%
• Nerve 50%
• Cation Channel 50%
• High Specificity 50%
• Type-specific 50%
• Excitability 50%
• Vascular Tone Regulation 50%
• Voltage-gated Channels 50%
• Amiloride 50%
• Vascular Control 50%
• Mechanotransduction 50%
• Tetrodotoxin 50%
• Gentamicin 50%
• Voltage Dependence 50%
• Gadolinium 50%
• Functional Characterization 50%
• Physiological Stimuli 50%
• Venom 50%
• K+ Channels 50%
• Neuronal Network 50%
• Network Excitability 50%
• Structural Characterization 50%
• K Channels 50%
• Receptor Sites 50%
• Concentration Dependence 50%
• Potent Drugs 50%
• Fatty Acid Receptor 50%
• Chemical Influence 50%
• Low Susceptibility 50%
• Amphiphilic Compounds 50%
• Mechanosensory Cells 50%
• α-bungarotoxin 50%
• Non-sensory 50%

Neuroscience

• Ion Channel 100%
• Fatty Acids 100%
• Receptor 100%
• Excitability 66%
• Potassium Channel 66%
• Channel Blocker 33%
• Sodium Channel 33%
• Cholinergic Receptor 33%
• Tetrodotoxin 33%
• Gentamicin 33%
• Cation Channel 33%
• Mechanotransduction 33%
• Bungarotoxin 33%
• Amiloride 33%

Pharmacology, Toxicology and Pharmaceutical Science

• Fatty Acid 100%
• Receptor 100%
• Ion Channel 100%
• Potassium Channel 66%
• Sodium Channel 33%
• Amiloride 33%
• Cholinergic Receptor 33%
• Tetrodotoxin 33%
• Gentamicin 33%
• Channel Blocker 33%
• Gadolinium 33%
• Amphiphile 33%
• Cation Channel 33%
• Bungarotoxin 33%