Pharmacology of Vanilloid Transient Receptor Potential Cation Channels
Article Properties
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LanguageEnglish
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DOI (url)
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Publication Date2009/03/18
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Journal
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Indian UGC (journal)
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Refrences184
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Citations281
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Joris Vriens
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Giovanni Appendino
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Bernd Nilius
Journal Categories
Medicine
Public aspects of medicine
Toxicology
Poisons
Medicine
Therapeutics
Pharmacology
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Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
| Tetrahydropyridine-4-carboxamides as novel, potent transient receptor potential vanilloid 1 (TRPV1) antagonists | Bioorganic & Medicinal Chemistry |
| 40 | 2008 |
| Structure–activity relationships of 1,4-dihydropyridines that act as enhancers of the vanilloid receptor 1 (TRPV1) | Bioorganic & Medicinal Chemistry |
| 22 | 2008 |
| α-Substituted N-(4-tert-butylbenzyl)-N′-[4-(methylsulfonylamino)benzyl]thiourea analogues as potent and stereospecific TRPV1 antagonists | Bioorganic & Medicinal Chemistry |
| 23 | 2007 |
| Cdk5: A New Player in Pain Signaling | Cell Cycle |
| 46 | 2006 |
| Proton Activation Does Not Alter Antagonist Interaction with the Capsaicin-Binding Pocket of TRPV1 | Molecular Pharmacology |
| 60 | 2005 |
Citations
Citations Analysis
The category
Science: Biology (General) 83
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Ca2+ Channels on the Move and was published in 2009. The most recent citation comes from a 2024 study titled Evaluation of histological and ultrastructural changes provoked by prenatal tramadol on postnatal cortical cerebellar neuronal development in rats: possible implication of Ki67, GFAP and MicroRNA-7/P53 signalling trajectories. This article reached its peak citation in 2015, with 36 citations. It has been cited in 188 different journals, 20% of which are open access. Among related journals, the International Journal of Molecular Sciences cited this research the most, with 8 citations. The chart below illustrates the annual citation trends for this article.