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William P. Clarke

Researcher at University of Texas Health Science Center at San Antonio

Publications -  84
Citations -  5101

William P. Clarke is an academic researcher from University of Texas Health Science Center at San Antonio. The author has contributed to research in topics: Receptor & Agonist. The author has an hindex of 36, co-authored 79 publications receiving 4817 citations. Previous affiliations of William P. Clarke include University of Texas at Austin & Northeastern University.

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Functional Selectivity and Classical Concepts of Quantitative Pharmacology

TL;DR: Besides the heuristically interesting nature of functional selectivity, there is a clear impact on drug discovery, because this mechanism raises the possibility of selecting or designing novel ligands that differentially activate only a subset of functions of a single receptor, thereby optimizing therapeutic action.
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Effector pathway-dependent relative efficacy at serotonin type 2a and 2c receptors : evidence for agonist-directed trafficking of receptor stimulus

TL;DR: Concentration-response curves to 5-HT2C agonists were fit well by a three-state model of receptor activation, suggesting that two active receptor states may be sufficient to explain pathway-dependent agonist efficacy.
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Constitutive Activity of the Serotonin2C Receptor Inhibits In Vivo Dopamine Release in the Rat Striatum and Nucleus Accumbens

TL;DR: First in vivo evidence that constitutive activity of the 5-HT2C receptor tonically inhibits mesencephalic DA neurons is provided and underscores the need for a better understanding of the pathophysiological role of constitutive receptor activity.
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Bradykinin-Induced Functional Competence and Trafficking of the δ-Opioid Receptor in Trigeminal Nociceptors

TL;DR: It is suggested that exposure to certain inflammatory mediators rapidly alters the signaling properties and neuronal localization of DOR, possibly contributing to peripheral opioid analgesia.
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RNA-editing of the 5-HT(2C) receptor alters agonist-receptor-effector coupling specificity.

TL;DR: An important role for the second intracellular loop in transmitting agonist‐specific information to signalling molecules is suggested in transmitting receptor stimulus to transducer molecules.