Sentence examples for specification regulatory from inspiring English sources

Pmar1 is expressed in micromeres and functions as a critical component of an endomesodermal specification regulatory network.

Differentiation and functional specification of these cells require specific regulatory elements promoting (Liu et al. 2003) or inhibiting (Liu et al. 2006) lineage-specific gene expression.

Therefore, induction of the pluripotent stem cells with lineage-specific regulatory signals, or small molecule inducers, is a prerequisite for effectively directing lineage specification for cell-based therapeutics.

The manuscript by Arvey et al. explores genetic and epigenetic variation in the lineage specification of regulatory T cells.

Thank you for sending your work entitled "Genetic and epigenetic variation in the lineage specification of regulatory T cells" for consideration at eLife.

The following dataset was generated: Arvey A, van der Veeken J, Plitas G, Rudensky AY, 2015, Genetic and epigenetic variation in the lineage specification of regulatory T cells, http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi acc=GSE73418, Publicly available at the Gene Expression Omnibus (Accession no: GSE73418).

In practice, however, the power pooling between transmission points is not possible, because total transmission power at the transmission point cannot be exceeded due to system specifications and regulatory issues.

Features of the Perc Test include simplicity, intuitive measurements (decline in water ponding depth, H, with time, t), and inclusion of PT criteria in most absorption field design specifications and regulatory codes.

The unified Perc CHWP methodology improves measurement of water transmission in absorption field investigations by providing: physically based PT values required by many design specifications and regulatory codes; Kfs values required for estimation of long-term water acceptance rates; and functionally linked PT Kfs data pairs that are accurate and based on rigorous borehole infiltration theory.

On the contrary, falsified medicines are those which do not meet the quality specifications of regulatory authority with deliberate intent.

The product specifications and regulatory guidance for TDS are a good start to determine a list of potential CQAs.