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Dvantages over traditional strategies in terms of safety, stability, ease ofDvantages over traditional strategies in terms of safety, stability, ease of manufacturing, and immunogenicity (Table 1). As DNAbased plasmid vaccines are non-live, non-replicating, non-spreading vaccines, there is a little or no risk of mutation or reversion to the virulent form as with viral vectors, therefore rais
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Dvantages over traditional strategies in terms of safety, stability, ease ofDvantages over traditional strategies in terms of safety, stability, ease of manufacturing, and immunogenicity (Table 1). As DNAbased plasmid vaccines are non-live, non-replicating, non-spreading vaccines, there is a little or no risk of mutation or reversion to the virulent form as with viral vectors, therefore rais
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Rvations made and the hypotheses stated earlier indicate that in the absence of SP-A there is a loss of regulatory control to appropriately modulate expression of DEF proteins in response to infection. Consistent with this postulate, a recent study with SP-A-/mice demonstrated that in response to low level intrapharyngeal LPS treatment (0.5 ng), significantly higher levels of MIP-2 were observed c
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Rvations made and the hypotheses stated earlier indicate that in the absence of SP-A there is a loss of regulatory control to appropriately modulate expression of DEF proteins in response to infection. Consistent with this postulate, a recent study with SP-A-/mice demonstrated that in response to low level intrapharyngeal LPS treatment (0.5 ng), significantly higher levels of MIP-2 were observed c
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Ibodies, primarily SC-1173 and SC9040 [160, 161]. AT1 receptors in the RVLM and NTS showed increased AT1 immunoreactivity, while AT2 receptors showed decreased immunoreactivity. Infusion of Ang II into the brain of rabbits to simulate a heart failure model increased AT1 receptor immunoreactivity in the RVLM [162]. Interestingly, viral transfection of AT2 receptors into the RVLM, which was document
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