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Publikováno v:
Medicinal Research Reviews
Medicinal Research Reviews, 40(2), 683-708
Medicinal Research Reviews, 40(2), 683-708
The function of G protein-coupled receptors (GPCRs) can be modulated by compounds that bind to other sites than the endogenous orthosteric binding site, so-called allosteric sites. Structure elucidation of a number of GPCRs has revealed the presence