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For these experiments we used embryonic multipotent NSC cultures derived from mid-gestation rat embryonic cortex and expanded as monolayers in FGF2 [9], [10] [15], [15].
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We tried the same thing with fruit flies and then with rat embryonic neurons.
We studied the differentiation properties of isolated rat embryonic postmigratory CNCCs, expressing p75 neurotrophin receptor (p75NTR).
To focus on the possible roles of α1-adrenergic receptors (α1-ARs) in rat embryonic implantation.
Here, we compared NSCs derived from the spinal cord and embryonic cortex.
Cultures of rat (embryonic day 18, E18) cortical neurons were prepared as previously described [56], [57].
Here, we demonstrated the efficiency of the approach using rat embryonic pancreases.
Expression of Gli3 was higher in ICTEV model rat embryonic hindlimbs compared to normal control rat embryonic hindlimbs (Fig. 3).
We next examined the dynamics of polarity of Lrp12/Mig13a-positive Lrp12/Mig13a-positivel/rl embryonic cortex.
Neurons from embryonic cortex of mice were isolated and cultured as described previously [ 25].
Primary neurons from embryonic cortex at E13.5 were cultured as described previously.
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