, 2012 ▸ ) and very recently highly significant progress with studies of the heteromeric human α4β2 nAChR (Morales-Perez et al. , 2016 ▸ ; Walsh et al. , 2018 ▸ ) and αβγ GABA A receptors (Laverty et al. , 2019 ▸ ; Masiulis et al. , 2019 ▸ ; Phulera et al. , 2018 ▸ ; Zhu et al. , 2018 ▸ ).
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Engineering a surrogate human heteromeric α/β glycine receptor orthosteric site exploiting the structural homology and stability of acetylcholine-binding protein.
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