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Substitution of a mutant α(2a)-adrenergic receptor via “hit and run” gene targeting reveals the role of this subtype in sedative, analgesic, and anesthetic-sparing responses in vivo

Norepinephrine contributes to antinociceptive, sedative, and sympatholytic responses in vivo, and α(2) adrenergic receptor (α(2)AR) agonists are used clinically to mimic these effects. Lack of subtype-specific agonists has prevented elucidation of the role that each α(2)AR subtype (α(2A), α(2B), and...

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Autors principals: Lakhlani, Parul P., MacMillan, Leigh B., Guo, Tian Zhi, McCool, Brian A., Lovinger, David M., Maze, Mervyn, Limbird, Lee E.
Format: Artigo
Idioma:Inglês
Publicat: The National Academy of Sciences of the USA 1997
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC23306/
https://ncbi.nlm.nih.gov/pubmed/9275232
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