Sentence examples for multiple mouse tissues from inspiring English sources
Mett10d is expressed in multiple mouse tissues, and its high degree of sequence conservation indicates that it may have essential functions in development or response to stress.
All antibodies were human specific and were exhaustively tested against multiple mouse tissues to confirm the species specificity and non cross-reactivity betweenon cross-reactivity
Rather than examining the effects of p53 germline deletion, we chose to somatically delete p53 in multiple mouse tissues at varying ages and at varying times before, during, and after a carcinogenic insult.
After determining that Spire1C mRNA was present in multiple mouse tissues, we examined its presence and conservation among species.
Additional studies with histopathological examination of multiple mouse tissues are needed to assess the potential side effects of this p53-activating approach.
To examine what biologically importantly entries are enriched in the mouse oocyte, we compared our dataset with a combined database of multiple mouse tissues as a reference.
Listed above are genes that are components of the p53 signaling pathway that show an age effect on expression in multiple mouse tissue-types.
To remedy this, we performed large-scale analyses of microarray hybridisations with male and female RNA from multiple somatic mouse tissues including kidney, liver, lung, eye, and two brain regions: the striatum and hippocampus.
Because every primary tissue contains different sets of transcription factors, chromatin remodelers, and, indeed, chromatin structures, the presence of a commonly bound set of genes that makes up the large majority of E2F4 binding targets in multiple human (or mouse) tissues suggests that this key member of the DREAM complex binds independently of the above factors.
Su and coworkers reported a gene expression atlas across multiple human and mouse tissues including several mouse brain regions (Su et al. 2004).
Methylation, specifically in the core and proximal promoter regions, negatively regulated the gene expression level across multiple human and mouse tissues and human cell lines.
