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How ligands illuminate GPCR molecular pharmacology
G protein-coupled receptors (GPCRs), which are modulated by a variety of endogenous and synthetic ligands, represent the largest family of druggable targets in the human genome. Recent structural and molecular studies have both transformed and expanded classical concepts of receptor pharmacology and...
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| Foilsithe in: | Cell |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2017
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5560499/ https://ncbi.nlm.nih.gov/pubmed/28753422 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2017.07.009 |
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