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Allosteric modulation, the activation or modulation of a receptor through a site distinct from the endogenous ligand binding site, had been successfully exploited for class A and class C GPCRs but was largely unexplored for class B receptors

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However, patients in APOLLO were more likely to have high-risk cytogenetics, defined as presence of del(17p), t(14;16), or t(4;14), although cutoff levels were not reported

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