1 tly signals through GSK3beta, a regulator of axogenesis.

2 haPS1, alphaPS2, and betaPS during embryonic axogenesis.

3 pression seems to coincide with the onset of axogenesis.

4 in or AICAR, potent AMPK activators, inhibit axogenesis and axon growth in an AMPK-dependent manner.

5           The cellular mechanisms underlying axogenesis and dendritogenesis are not completely unders

6                         This unusual mode of axogenesis and dendritogenesis from neuroepithelial-like

7 cytoskeletal proteins that are essential for axogenesis and maintenance of neuron shape in the nervou

8  during the periods of cell differentiation, axogenesis and synaptogenesis.

9 unctional c-jun allele was not essential for axogenesis, because ganglion cells in retinal grafts fro

10  that AP-2 has important roles in functional axogenesis by proper extension of axon as well as the fo

11  two molecules secreted by optic nerve glia, axogenesis factor-1 (AF-1) and AF-2, along with ciliary

12                    In contrast to long-range axogenesis, generation and maintenance of pyramidal neur

13                        Growth factor-induced axogenesis in RGCs was accompanied by many of the molecu

14 key regulators of fasciculation and targeted axogenesis in the mouse neocortex.

15     (2) The retinal neuroepithelium prior to axogenesis is nonpermissive for neurite outgrowth.

16  At the developmental stage corresponding to axogenesis, overexpression of P60 decreases the total nu

17      By the time primary motoneurons undergo axogenesis, specific subtypes express islet1, whereas ot

18 hibit the establishment of neuronal polarity/axogenesis under energy stress conditions, whereas brain