In vitro studies indicate that enhancing cell proliferation with growth factor exposure enhances plasmid DNA uptake and expression.
In summary, our in vitro studies indicate that the co-treatment of GNCs, PTT, and RT may be a promising approach for cancer therapy.
In vivo and in vitro studies indicate that the oxidation of LDL isolated from postmenopausal women was inhibited differently by various estrogens and other antioxidants.
Recent in vitro studies indicate that Wnt signaling plays key roles in regulating morphological events in FGF-induced fiber cell differentiation in the mammalian lens.
In vitro studies indicate that Salmonella/pCMV-hgp100 is efficiently scavenged by dendritic cells, resulting in the expression of the hgp100 transcription unit in the DC.
In conclusion, these in vitro studies indicate that it could be feasible to reach therapeutic levels by transdermal iontophoresis of pergolide.
Our in vitro studies indicate that the oxathiazine compounds have inhibitory activity on estrone sulfatase in MCF-7 human breast cancer cells.
Clinical data remain scarce for infections due to multidrug-resistant A. baumannii [139], although in vitro studies indicate that combining colistin with rifampicine, carbapenems or tigecycline may be effective to prevent the emergence of colistin-resistant mutants [109].
Perhaps more relevant to astrocyte-mediated effects of PACAP on synaptic activity, in vitro studies indicate that PACAP/PAC1 signaling increases glutamate uptake via induced expression of GLT-1/EAAT2, GLAST/EAAT1 and increases glutamine synthase (GS) [121].
The results obtained from the in vitro studies indicate that the cell adhesion, proliferation, and differentiation of the osteoblastic cells were accelerated on PLGA/nHA-I composite nanofiber scaffold as compared to PLGA/nHA composite and pristine PLGA nanofiber scaffolds.
Both in vivo and in vitro studies indicate low substrate specificity of the modification machinery, which has been explored for re-engineering of the structures of a number of members.
