Sentence examples for demonstrating the developmental from inspiring English sources

Three decades of in vivo enhancer studies in mouse have laid the groundwork for the current understanding of mammalian enhancers, demonstrating the developmental and tissue-specific activity of enhancers and illuminating general features of enhancer evolution and function.

We have extended the pathway-controlled DNA self-assembly approach, demonstrating the developmental growth of a well-defined three-dimensional wireframe DNA tetrahedron, formed from metastable reactants conditionally in the presence of a single-stranded trigger and through a kinetically programmed pathway.

Our work in generating CAG::mRFP1 transgenic ES cells and mice demonstrates the developmental neutrality of mRFP1 in an organismal context.

We chose to use the ex vivo xenograft model to demonstrate the developmental regulation of innate immune response genes for several reasons.

In summary, we describe the use of transient transgenic RNAi knockdown to demonstrate the developmental consequences of a loss of function mutation.

Comparing the mean peak current amplitude across early postnatal weeks demonstrates the developmental upregulation of nicotinic excitation in male and female layer VI neurons as illustrated in Figure 1B.

Our work demonstrates the developmental neutrality of mRFP1, the first true monomeric RFP, in ES cells and mice.

This recognition of critical windows of vulnerability not only demonstrates the developmental basis of disease but also that the timing, as well as the dose, makes the poison.

By integrating temporal with spatial control, here we demonstrate the "developmental" self-assembly of a DNA tetrahedron, where a prescriptive molecular program orchestrates the kinetic pathways by which DNA molecules isothermally self-assemble into a well-defined three-dimensional wireframe geometry.

One typical example demonstrating the relationship between the developmental role and tumor suppressive function of p53 is the functional interaction between Brca1 and p53.

These tumors also demonstrate the wide developmental potential of hESCs, with the presence of derivatives of all embryonic germ layers.