We investigated the impact of these changes on islets by examining a set of Swiss-Webster mice that had grown to weigh 42.0±1.0 g (n = 3) as compared to control mice that only grew to a mean weight of 29.1±0.9 g (n = 10, p<0.001 for differences in body weight).
By examining a wide range of networks from mouse, human and yeast, as well as multiple prediction methods and evaluation metrics, we provide evidence that this problem is pervasive and does not reflect the failings of any particular algorithm or data type.
Brains from four mice (three sections from each mouse) were analysed by examining an average of 10 fields per section.
Dr. Xu's innovation allowed them to find out by examining mouse genes on a vast scale.
We investigated the significance of this gene arrangement to TCRα LCR activity by examining transgenic mice bearing a construct where the LCR was flanked by two separate reporter genes.
By examining mouse embryos at multiple embryonic stages, we confirmed the Wnt7b is expressed by perichondrial cells undergoing Ihh-dependent ossification and that the expression is dependent on Ihh.
Here, by examining human and mouse expressed sequenced tags (EST) libraries, we ask whether cancer transcriptomes show any differences in transcript quality compared with normal tissues.
The biological roles of CS, DS, and HS chains in vivo have been revealed by examining knockout mice in addition to nematodes, fruit flies, and zebrafish [ 4, 8, 12– 12].
Now, Li et al. have identified a protein called Nur77 as an important regulator of NFATc1 by examining genetically engineered mice that lack Nur77.
We have addressed this question by examining mice genetically engineered to over- or underexpress neuregulin-1 (NRG1), a direct modulator of synaptic transmission.
