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Meanwhile, it has been shown that surface morphology can affect the blood compatibility of the polymers.
Furthermore, it has been shown that surface functionalization improves the biocompatibility of SiO2-NP [10, 11].
It has been shown that surface exposed hydrophobic residues can enhance the thermal stability of a given protein by serving as molecular "clips" or "staples" that prevent water penetration [20].
It has been shown that surface expression of human CD83 upon DC maturation is partially mediated by the transport of intracellular stored CD83 protein to the plasma membrane [24], [25].
It has been shown that surface BCR expression is mandatory for mature B cell survival, since conditional ablation of BCR expression subsequent to the establishment of steady-state B cell numbers, resulted in rapid death of most peripheral B cells [27].
It has been shown that surface exposure of CRT, secretion of ATP and passive release of HMGB1 are required for the activation of potent anti-cancer immunity.
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It is shown that surface preparation has a significant effect on both fracture energy release rate and rate of crack propagation which can be accelerated by exposure.
Further it is shown that surface form is maintained over a two year storage period under ambient conditions.
It is shown that surface diffusion contributes significantly to the overall intraparticle mass transfer.
It was shown that surface crystallization differs drastically from bulk crystallization due to the possible surface reconstruction.
It is shown that surface reaction-controlled dissolution of crystals in a solvent or solution is very unlikely.
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CEO of Professional Science Editing for Scientists @ prosciediting.com