Receptor and Channel Heteromers as Pain Targets
Recent discoveries indicate that many G-protein coupled receptors (GPCRs) and channels involved in pain modulation are able to form receptor heteromers. Receptor and channel heteromers often display distinct signaling characteristics, pharmacological properties and physiological function in comparis...
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Format: | Book |
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MDPI AG,
2012-02-01T00:00:00Z.
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Call Number: |
A1234.567 |
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Copy 1 | Available |