Historical review: Negative efficacy and the constitutive activity of G-protein-coupled receptors
Trends in Pharmacological Sciences, ISSN: 0165-6147, Vol: 26, Issue: 12, Page: 618-624
2005
- 107Citations
- 92Captures
Metric Options: Counts1 Year3 YearSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations107
- Citation Indexes107
- 107
- CrossRef101
- Captures92
- Readers92
- 92
Review Description
The idea that a receptor can produce signalling without agonist intervention and that several antagonists can be ‘active’ in repressing such spontaneous activity is contained in the concept of ligand-induced conformational changes. Yet, this idea was neglected by pharmacologists for many years. In this article, we review the events that brought inverse agonism and constitutive activity to general attention and made this phenomenon a topic of current research. We also suggest a classification of antagonists based on the cooperativity that links their primary site of interaction with other functional domains of the receptor.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0165614705002750; http://dx.doi.org/10.1016/j.tips.2005.10.009; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=27744451411&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/16260046; https://linkinghub.elsevier.com/retrieve/pii/S0165614705002750; https://dx.doi.org/10.1016/j.tips.2005.10.009
Elsevier BV
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