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With the experience gained in producing ICs with HBsAg and influenza HA and their respective antibodies, appropriate ratios and methodologies for the manufacture of ICs can be standardized to fulfill the regulatory requirements for clinical application
[DOI] [PMC free article] [PubMed] [Google Scholar] 6.Lepetsos P., Papavassiliou A.G
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Researchers considering extended protocols should be aware that this safety gap exists and should monitor for unexpected effects in tissues where NNMT has normal physiological functions
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