So far, N. benthamiana has been successfully explored as a model for expression of therapeutic proteins, such as antibodies [20].
It is also relevant that the effects human diets have on mouse liver transcriptomes can be used as a model for expression differences between humans and chimpanzees [ 79].
The ability of two AD mediators, TNF-α, a pro-inflammatory cytokine, and Aβ1−40 to induce the expression of CAP37 was tested using primary human cortical neurons (HCN-1A) as a model for induced expression.
The serotonin transporter (SERT) was chosen as a model MP for expression studies, as it has been shown to be a difficult to express MP that is toxic to cells when overexpression is attempted.
One may raise a concern about the use of fibroblasts as a model because the expression pattern of this molecule has been thought to be restricted within leukocytes.
The genome sequence of B. microti will serve as a model for differential expression analysis and complementation studies.
Using leptin/FSP27 double deficient mice as a model system, the expression of BAT-selective genes and regulatory factors was analyzed under the conditions of FSP27 deficiency and obesity.
We test this model for consistency with known genetic influences on MET, BC, PC and cancer, and find that there is significant evidence supporting the use of this network as a model of gene expression influences on MET, as well as BC and PC, and more generally in cancer.
In the absence of a sequenced genome, a well annotated reference transcriptome of the bald notothen will serve as a model of gene expression in the coldest and harshest of all polar marine environments, useful for future comparative studies of cold adaptation and thermal responses in polar teleosts and ectotherms.
This output shows that abs * p1 is currently defined as the source model expression.
We chose miR-122, an abundantly expressed miRNA, as a model for inducible shRNA expression.
