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Poly(I:C)-Encapsulating Nanoparticles Enhance Innate Immune Responses to the Tuberculosis Vaccine Bacille Calmette–Guérin (BCG) via Synergistic Activation of Innate Immune Receptors

https://doi.org/10.1021/acs.molpharmaceut.7b00795

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1521-4141(200204)32:4<994::aid-immu994>3.0.co;2-6openalex-snapshot

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