Our study shows that selecting
the appropriate cell line, growing the cells as 3 - D aggregates and infecting them when they are fully differentiated is key for successful in vitro cell culturing of human noroviruses.»
Researchers would need to choose
an appropriate cell line to act as a host and then gradually swap out large chunks of its genome with the synthetic DNA.
Not exact matches
NeuroStemcell is focused on the identification and systematic comparison of progenitor
cell lines with the most favourable characteristics for mesDA and striatal GABAergic neuronal differentiation, generated either directly from human embryonic stem (ES)
cells, from Neural Stem (NS)
cells derived from ES
cells or fetal brain, from induced Pluripotent Stem (iPS)
cells or from in vitro short - term expanded neural progenitors from ventral midbrain grown as neurospheres (VMN, Ventral Midbrain Neurospheres) 4, and perform rigorous and systematic testing of the most prominent candidate
cells in
appropriate animals models.
Investigators using 129 substrains for targeted mutagenesis should be careful in the selection of the
appropriate 129 substrain to match the embryonic stem
cell line.
The donor luciferase enzyme can be expressed on the N - terminus of the receptor of interest in an
appropriate transfected
cell line.
They also nourish the gut
lining and ensure
appropriate production of immune
cells, helping to maintain balance in the immune system and prevent autoimmune disease.
Thus, some of the
cell lines approved for research under the Bush restrictions might actually not be approved under the Obama guidelines because they may not have been obtained with the
appropriate level of prior informed consent of the donor, a moral constraint on science that apparently did not concern President Bush.