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In the mouse models studied here, we found that the majority of bacilli were indeed intracellular within macrophages through most of the infection.

Here we report that all circadian gene-mutant mouse models studied are cancer-prone and that hyperplastic growth of Per-mutant somatic cells is dependent upon extracellular mitogens.

A sublethal dose of γ-Radiation induced premature aging on the external appearance of all circadian gene-mutant mouse models studied and further increased incidence of tumor and hyperplasia as well as ulcerative dermatitis in Bmal1+/−, Per- and Cry-mutant mice (Fig. 1b, Table 1 and Fig. S1b).

Recently, Zimmermann and coworkers have described a pathway involving arginine metabolism in the context of allergic inflammation in mouse models studied using expression microarrays [ 3].

130, 139, 143, 144 Other mouse models studied to date include the mdx4CV mouse (nonsense mutation in exon 53 that requires removal of exons 52 and 53) 145 and the mdx52 mouse missing exon 52.

In particular, of the mouse models studied, the expression signature of the C3(1)Tag GEM model appears to most closely correlate to the human basal-like subtype [ 8].

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For instance, several mouse models studying Lactobacillus species of probiotics have demonstrated dampening of allergic lung responses [29], [30], [31], [32].

Although these are two artificial mouse models, studying their phenotype enhanced our understanding of the biology of IGF1 in tissues.

Thus, despite the apparent lack of gross FA symptoms in mouse models, studying them has allowed us to learn a great deal about the pathology of FA.

The LmnaDhe mouse model studied here exhibits physiological phenotypes similar to human progeria and related laminopathies characterized by lipodystrophy, cranial abnormalities, and skin defects [29].

The second mouse-model studied was BATIRKO mice under HFD for 16 weeks.

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