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Description
CD38 signaling in T cells is initiated within a subset of membrane rafts containing Lck and the CD3-zeta subunit of the T cell antigen receptor
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The results are not directly comparable because the peptides are not equivalent products
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In conclusion, IA DDSs have the potential to enhance the penetration of drugs into the cartilage extracellular matrix, facilitating the sustained release of the potential peptides in vivo
Metabolic receptors may also be targeted
