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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Detalles Bibliográficos
Autores principales: Berg, Kelly A., Patwardhan, Amol M., Akopian, Armen N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763638/
https://www.ncbi.nlm.nih.gov/pubmed/24281378
http://dx.doi.org/10.3390/ph5030249

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763638/
https://www.ncbi.nlm.nih.gov/pubmed/24281378
http://dx.doi.org/10.3390/ph5030249

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