Sentence examples for define the consequences of from inspiring English sources

To molecularly define the consequences of BRDT inhibition by JQ1, we performed genome-wide expression analysis of males treated with 50 mg/kg JQ1 daily for 6 weeks (6 12 weeks of age).

A significant development that facilitated the appreciation of the physiological importance of PTEN has been the generation of sophisticated animal models to define the consequences of the loss of function of this phosphatase [ 9].

To further define the consequences of astrocytes on GSCs, gene expression profiles were generated from NSC11 and GBAM1 cells grown alone (monoculture) and compared to those generated 48 h after the initiation of coculture with astrocytes.

Further studies are required to define the consequences of the inappropriate use of reporting recommendations in clinical and epidemiological research, in particular the use of these checklists as an instrument to assess the methodological quality of studies.

Moreover, additional studies are needed to define the consequences of ABCD3 overexpression in AA prostate tumors; however due to the intrinsic role of ABCD3 in fatty acid beta oxidation, this would imply that ABCD3 could have a role in enhanced growth in both BPH and malignant cells.

Thus, to define the consequence of the genetic switch to cyclin D1b on retinal phenotypes, expression of individual cyclin D1 isoforms was initially characterized in whole-eye lysates.

Collectively, these data are the first to define the consequence of cyclin D1b expression on normal cellular function, present evidence for cyclin D1b as an oncogene, and provide pre-clinical evidence of effective methods to thwart growth of cells dependent upon this oncogenic variant.

As such, a large body of work has focused on defining the consequences of psychostimulant use on dopamine signaling in the striatum as it relates to addictive behaviors.

Studies in this yeast have also defined the consequences of several mutations in isoform-1 of the ADP/ATP translocase [adenine nucleotide transporter isoform 1 (ANT1)] that have been associated with various diseases, including autosomal dominant PEO and hypertrophic cardiomyopathy (Kaukonen et al., 2000; Liu and Chen, 2013).

Additional experiments are required to determine whether decreased STIP1 contributes to ASD-like phenotypes by decreasing chaperone capacity in the developing brain, by impairing prion protein signaling, or through some other mechanism, and to define fully the consequences of disturbed STIP1 activity in ASD.

In this context, the proteins and domains that recognize histone modifications, named "effectors" or "readers", are thought to define the functional consequences of many classes of modifications by transducing molecular events at chromatin into biological outcomes.