Further work using this cell line will help us to build dynamic models of TH signaling (Troncale et al., 2007).
The caveat scholasticus for using this cell and tissue type information in human is that although useful, this information is less complete compared with other species due to issues regarding tissue availability.
The sequence data generated by this study, including a searchable de novo genome assembly and annotated lists of mutated genes, will support future research using this cell line.
Using this cell architecture we present 2 and 3-input NAND gates showing their output response and error probabilities.
Using this cell library, we can easily expand circuit scale without the time-consuming dynamic simulations of whole circuits.
Using this cell we have examined the analytical properties of several recently developed fluorescent protein dyes chemically different from MDPF.
Using this cell type-independent approach, we could increase the expression of secreted and intracellular human proteins up to 200-fold.
Using this cell, we probe the local charging profiles of LiNi0.5Mn0.3Co0.2O2 ("NMC") particles during cycling and demonstrate the ability to achieve spatial maps of the Raman spectra.
By using this cell, the free movement of the phases is allowed and conditions for near-to-uniform electrical fields are met, thus allowing sound measurements of the effective conductivity of the dispersion to be made.
Using this cell and swopping of gases in binary systems H2-N2, H2-Ar, He-N2, He-Ar, expressureal presponseresponse curves were obtained for porous α-alumina pellets with mono- and bidisperse pore structures.
Some of the data obtained by the flotation method using this cell are in good agreement with data measured independently on the same minerals by the contact angles method.
