PIP(2) activates KCNQ channels, and its hydrolysis underlies receptor-mediated inhibition of M currents. [electronic resource]
Producer: 20030501Description: 963-75 p. digitalISSN:- 0896-6273
- Androstadienes -- pharmacology
- Animals
- Bradykinin -- pharmacology
- CHO Cells
- Cells, Cultured
- Cricetinae
- Electric Conductivity
- Enzyme Inhibitors -- pharmacology
- Female
- Hydrolysis
- KCNQ2 Potassium Channel
- KCNQ3 Potassium Channel
- Microscopy, Confocal
- Mutation
- Neurons -- physiology
- Patch-Clamp Techniques
- Phosphatidylinositol 4,5-Diphosphate -- metabolism
- Phosphoinositide-3 Kinase Inhibitors
- Potassium Channels -- genetics
- Potassium Channels, Voltage-Gated
- Rats
- Rats, Sprague-Dawley
- Receptor, Muscarinic M1
- Receptors, Muscarinic -- physiology
- Recombinant Proteins
- Second Messenger Systems
- Signal Transduction
- Superior Cervical Ganglion -- cytology
- Tetraethylammonium -- pharmacology
- Transfection
- Wortmannin
- Xenopus laevis
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
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