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The authors evaluated the expression of conserved genes among vertebrates at different stages of development using a mouse model.
We evaluated the expression of these genes in different contexts.
We first evaluated the expression of pluripotency genes in C5E.
We first evaluated the expression of FLI1 in prostate cells.
This array evaluated the expression of 84 genes involved in cell-cell and cell-matrix interactions.
In companion studies, we evaluated the expression of several other cell surface activation markers.
We evaluated the expression of nitric oxide synthase (NOS), also known to metabolize l-arginine.
We evaluated the expression of pluripotency genes as well as of mesoderm induction and specification markers.
We next evaluated the expression of integrin α7B and dystroglycan in dy3K/δE3 muscles.
Immunohistochemical (IHC) analysis evaluated the expression of MLH1, MSH2, PMS2 and MSH6.
We thus evaluated the expression of these molecules in newborn olfactory interneurons by immunohistochemistry (Fig. 3).
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