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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-284344
- DOI to cite this document:
- 10.5283/epub.28434
Abstract
The investigation of the (patho)physiological role of the histamine H4 receptor (H4R) and its validation as a possible drug target in translational animal models are compromised by distinct species-dependent discrepancies regarding potencies and receptor subtype selectivities of the pharmacological tools. Such differences were extremely pronounced in case of proximal readouts, e. g. [32P]GTPase ...
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