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1 nd their axons as a cohesive tract ("primary axon bundle").
2  out of primary astrocyte processes into the axon bundles.
3 cells with vertically oriented dendrites and axon bundles.
4 aveled across CSPG substrata as fasciculated axon bundles.
5 ina can be visualized as two heavily labeled axon bundles.
6 leukin-33 (Il33) and ensheath AT sympathetic axon bundles.
7  and mechanical properties of the navigating axon bundles.
8 ns, but is required for the stabilization of axon bundles.
9 tes enhance the later developmental event of axon bundling.
10 ed similar activation thresholds and reduced axon bundle activation in the central retina, but lower
11 G(beta), G(alphai1-3), and G(alphao)) in the axon bundles and an absence of labeling in the microvill
12 n axons situated at the perimeter of sensory axon bundles are found in close contact with neighboring
13                                              Axon bundles are found to have a larger distribution of
14 tangential sections through layer IVC, these axon bundles are regularly arranged.
15                                         When axon bundles are surrounded by complex heterogeneous tis
16  exist before thinning of peripapillary RNFL axon bundles begins.
17 t, AGalphao is localized along the flagellar axon bundle but is absent from chemosensory sensilla, wh
18                             Visualization of axon bundles by DiI application in formalin-fixed tissue
19 bundles, it is suggested that the myelinated axon bundles contain the efferent axons from the project
20 tingly, in EphB1 cKOVgat mice, the misguided axon bundles contained co-mingled striatal GABAergic and
21  nm isotropic resolution allowed identifying axon bundles, dendrites and synapses in mouse brain tiss
22 al mechanical mechanisms that lead to higher axon bundle density in gyri (ridges) compared to sulci (
23  cell (RGC) damage without investigating RGC axon bundles directly.
24 hyme cells and SGNs are important for proper axon bundling during development.
25 cted from the in vivo organization, PNS-like axon bundles elaborated by apical cocultures were longer
26      In some sections through an OP, a thick axon bundle emerging from the bottom of the pouch was vi
27 erve layer; however, focal stimulation of an axon bundle entering an individual glomerulus revealed t
28   Little is known about the structure of RGC axon bundles extending from individual RGC somas to the
29 s trajectory choice and promote ventromedial axon-bundle formation.
30        The extension and termination of this axon bundle in the central nervous system has not been e
31 ut or LRRK2 G2019S knockin, the dopaminergic axon bundle in the midbrain was significantly widened an
32 roscopy is introduced and applied to imaging axon bundles in a saline bath environment.
33 2+) transients in postganglionic sympathetic axon bundles in mouse vas deferens have been characteriz
34 normal axonal bundling and elongation within axon bundles in the nematode Caenorhabditis elegans.
35 omerular neuropil; glial processes ensheathe axon bundles in the nerve layer but likely contribute li
36 hing approximately one-quarter of all of the axon bundles in the nerve, and each glial tube contains
37                        G(alphao) labeled the axon bundles in the VNE and the somata of the vomeronasa
38 directly visualizing and analyzing mouse RGC axon bundles in vivo In this study, we validated vis-OCT
39 iving human brain, and at the level of whole axon bundles in white matter tracts.
40 nt Schwann cells could interdigitate between axon bundles, indicating that FAK signaling was not requ
41 xon bundles originate, the trajectory of the axon bundles into the neuropile, and the relationship of
42 ally quantify and track RGC damage at single axon bundle level in optic neuropathies.SIGNIFICANCE STA
43 tothermally induced spatial gradients at the axon bundle membrane interfaces with saline and surround
44  existing models fail to explain how growing axon bundles navigate the stress field within a folding
45 d development, IGLE density and longitudinal axon bundle number in the intestine of INT-BDNF(-/-) mic
46                                        Thus, axon bundles of lineages that are neighbors in the corte
47  new, laminin-rich BM, which advances around axon bundles of newly differentiated photoreceptors as t
48                  Vis-OCTF for monitoring RGC axon bundle organization has the potential to bring new
49 to directly quantify global and regional RGC axon bundle organizations in vivo as a new biomarker for
50 imary lineages in the brain cortex where the axon bundles originate, the trajectory of the axon bundl
51                    Simulations incorporating axon bundle reorientation and stress-induced growth reve
52 canned with a confocal microscope, and vagal axon bundles, single axons, putative mechanoreceptor pre
53                           LY and NB revealed axon bundles, somas and dendrites of GCs.
54 heir peripheral origin and relationship with axon bundles suggest that they share features with mamma
55 g ventral nerve cord produces defasciculated axon bundles that do not reach their targets.
56 those in neighboring modules, the individual axon bundles that emerge from each module would be expec
57 tiation sets in, neuroblast lineages produce axon bundles that initially form a scaffold of unbranche
58            We generated a map of the primary axon bundles that visualizes the location of the primary
59                Each lineage forms a cohesive axon bundle, the secondary axon tract (SAT).
60                                 Immature OSN axon bundles were enlarged and associated OECs increased
61                         By E6.0-E6.5, CTb-LI axon bundles were seen ipsilaterally in the TT.
62 n width, spacing and width of the associated axon bundles) were made in four regions of cortex (prima
63 (WT) mice and showed that the changes in RGC axon bundle width and thickness were location-dependent.
64 validated vis-OCTF's ability to quantify RGC axon bundles with an increased number of RGCs using mice
65 , the trajectories of these 39 area-specific axon bundles with good-to-excellent test-retest reproduc
66    We confirmed the presence of unmyelinated axon bundles within the P3 CC, but failed to detect any