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In summary, while GLP-1R expression is not ubiquitous across all cancers, tumor types with high receptor levels benefit significantly from nanoparticle-enabled imaging and therapy

Researchers who need to replicate the foundational incretin literature, establish single-receptor baselines for comparative studies, or specifically study GLP-1R mechanisms without the additional variables introduced by dual or triple agonism will find GLP-1(Sema) is still the correct compound for those protocols

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