Giudice, A. & Trounson, A. Genetic modification of human embryonic stem cells for derivation of target cells.
However, carry-over of infectious vector particles has been described to occur upon ex vivo transduction of target cells.
Micropatterning of target cells is highly desired for tissue engineering and cell biology.
Gene therapy is based on the genetic manipulation of target cells.
This suggests that HIV-1 acquisition risk is influenced more by the frequency of target cells than by the generalized level of immune activation.
Long-range axon guidance and topographic mapping mechanisms bring axons into spatial proximity of target cells and thus limit the number of potential synaptic partners.
As nonviral vectors, NPs can greatly enhance the transfection of target cells with pro-angiogenic genes with relatively fewer safety concern.
Using three different methods, we find that the availability of target cells and CD8\ T cells are important predictors of viral load dynamics.
Sastalla, I. et al. The Bacillus cereus Hbl and Nhe tripartite enterotoxin components assemble sequentially on the surface of target cells and are not interchangeable.
Krebs, P. et al. NK-cell-mediated killing of target cells triggers robust antigen-specific T-cell-mediated and humoresponsesnses.
In all cases H222 Sp gamma localized in the nucleus of target cells.
