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Accordingly, the phenomena observed in vitro could be reproduced in purely deterministic biophysical model neurons.
We investigated if previously demonstrated inhibition of fluciclovine (18F) in vitro could be replicated in a PC3-Luc xenograft mouse model.
After coating of metallic biomaterials with a cross-linked collagen layer, an improved cellular response of human osteoblast-like cells (MG-63) in vitro could be recognized.
Every exon targeted in vitro could be removed from the dystrophin mRNA, although some exons are more efficiently excluded than others.
This review summarizes published information on clinical significance of ECM in cancer and examines whether effects of ECM on cell behaviour evidenced in vitro, could be supported by clinically based data acquired from analysis of tissue samples.
We discuss how the strategies used to engineer mature epithelial tissue models in vitro could be extrapolated to instruct the design of organotypic culture models that can recapitulate the structure of embryonic ectodermal tissues and enable the in vitro assessment of events critical to organ/tissue morphogenesis.
Therefore, the content of DNA released from DNA-PLA-PEG-NPs in vitro could be determined directly and calculated without adjustment.
T cell cytolytic activity in vitro could be maximized by administration of anti-PD-1 or anti-PD-L1 antibodies alone or in combination if applied prior to a round of T cell killing, but T cell inhibition could not be fully reversed by this blockade once the T cells had killed tumor.
Subsequently, [11C]erlotinib PET acquisitions of tumor-bearing mice were carried out in order to determine whether the differences between cell lines vis-à-vis erlotinib sensitivity in vitro could be translated into distinct patterns of [11C]erlotinib tumor uptake in vivo.
Virus-vector mediated gene transfer in vitro could be another option [26].
Thus, translation of AUG versus CUG-initiation codons in vitro could be distinguished by both edeine and bruceantin.
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