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Structure of the human dopamine D3 receptor in complex with a D2/D3 selective antagonist.
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Membrane protein crystallization from lipidic phases.
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Aqueous phase behavior of lipids with isoprenoid type hydrophobic chains.
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Crystallizing membrane proteins using lipidic mesophases.
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The 2.6 angstrom crystal structure of a human A2A adenosine receptor bound to an antagonist.
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High-resolution crystal structure of an engineered human beta2-adrenergic G protein-coupled receptor.
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