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1 nd their axons as a cohesive tract ("primary axon bundle").
2 cells with vertically oriented dendrites and axon bundles.
3 aveled across CSPG substrata as fasciculated axon bundles.
4 ns, but is required for the stabilization of axon bundles.
5 ina can be visualized as two heavily labeled axon bundles.
6  out of primary astrocyte processes into the axon bundles.
7 G(beta), G(alphai1-3), and G(alphao)) in the axon bundles and an absence of labeling in the microvill
8 n axons situated at the perimeter of sensory axon bundles are found in close contact with neighboring
9 tangential sections through layer IVC, these axon bundles are regularly arranged.
10  exist before thinning of peripapillary RNFL axon bundles begins.
11 t, AGalphao is localized along the flagellar axon bundle but is absent from chemosensory sensilla, wh
12                             Visualization of axon bundles by DiI application in formalin-fixed tissue
13 bundles, it is suggested that the myelinated axon bundles contain the efferent axons from the project
14 cted from the in vivo organization, PNS-like axon bundles elaborated by apical cocultures were longer
15      In some sections through an OP, a thick axon bundle emerging from the bottom of the pouch was vi
16 erve layer; however, focal stimulation of an axon bundle entering an individual glomerulus revealed t
17 s trajectory choice and promote ventromedial axon-bundle formation.
18        The extension and termination of this axon bundle in the central nervous system has not been e
19 2+) transients in postganglionic sympathetic axon bundles in mouse vas deferens have been characteriz
20 normal axonal bundling and elongation within axon bundles in the nematode Caenorhabditis elegans.
21 omerular neuropil; glial processes ensheathe axon bundles in the nerve layer but likely contribute li
22 hing approximately one-quarter of all of the axon bundles in the nerve, and each glial tube contains
23                        G(alphao) labeled the axon bundles in the VNE and the somata of the vomeronasa
24 nt Schwann cells could interdigitate between axon bundles, indicating that FAK signaling was not requ
25 xon bundles originate, the trajectory of the axon bundles into the neuropile, and the relationship of
26 d development, IGLE density and longitudinal axon bundle number in the intestine of INT-BDNF(-/-) mic
27                                        Thus, axon bundles of lineages that are neighbors in the corte
28 imary lineages in the brain cortex where the axon bundles originate, the trajectory of the axon bundl
29 canned with a confocal microscope, and vagal axon bundles, single axons, putative mechanoreceptor pre
30                           LY and NB revealed axon bundles, somas and dendrites of GCs.
31 heir peripheral origin and relationship with axon bundles suggest that they share features with mamma
32 those in neighboring modules, the individual axon bundles that emerge from each module would be expec
33 tiation sets in, neuroblast lineages produce axon bundles that initially form a scaffold of unbranche
34            We generated a map of the primary axon bundles that visualizes the location of the primary
35                Each lineage forms a cohesive axon bundle, the secondary axon tract (SAT).
36                                 Immature OSN axon bundles were enlarged and associated OECs increased
37                         By E6.0-E6.5, CTb-LI axon bundles were seen ipsilaterally in the TT.
38 n width, spacing and width of the associated axon bundles) were made in four regions of cortex (prima
39    We confirmed the presence of unmyelinated axon bundles within the P3 CC, but failed to detect any

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