コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ts from DB6 bipolar cells via a sparse outer axonal arbor.
2 ate of growth of the developing dopaminergic axonal arbor.
3 ely distributed throughout a highly branched axonal arbor.
4 aintain successful AP propagation across the axonal arbor.
5 sualization and reconstruction of long-range axonal arbors.
6 orded interneurons had similar dendritic and axonal arbors.
7 single neurons based on their dendritic and axonal arbors.
8 ced the density and thickness of sympathetic axonal arbors.
9 to construct lamina-restricted dendritic and axonal arbors.
10 ing cells, which have separate dendritic and axonal arbors.
11 nearly normal topography but fail to refine axonal arbors.
12 r loss of innervation, resulting in enlarged axonal arbors.
13 circuits are characterized by layer-specific axonal arbors.
14 learly not achieved by maintenance of static axonal arbors.
15 during embryogenesis involves redirection of axonal arbors.
16 r axons and tracked morphological changes in axonal arbors across hours in vivo in neonatal mice.
17 Both CaP and MiP ultimately formed normal axonal arbors after muscle pioneer ablation, showing tha
18 scending axons had a relatively sparse local axonal arbor and projected at least to layer II and some
19 lterations (decreased areas of dendritic and axonal arbors and decreased density of cells and synapse
20 od enabled us to reconstruct up to 5-cm-long axonal arbors and directly monitor axonal conduction acr
21 at interneurons varying in the span of their axonal arbors and hence in the potential regulation of d
22 a unique opportunity to reconstruct complete axonal arbors and identify all the postsynaptic targets.
23 h the segregation of sensory and sympathetic axonal arbors and suggests a role for target-derived NGF
26 o modulate the elaboration and refinement of axonal arbors and to participate in the establishment of
29 the development of cone bipolar cells whose axonal arbors at maturity synapse onto ganglion cell den
30 entially affect neurons with long or complex axonal arbors but the cellular and molecular bases for n
31 ing not only the morphological maturation of axonal arbors, but also their stabilization, by a mechan
32 to influence the morphological maturation of axonal arbors by directly influencing the stability of d
34 se in which activity-dependent plasticity of axonal arbors combined with their competition for collic
37 ers had finer caliber axons and the terminal axonal arbors covered a larger area than the correspondi
38 (2) a more extended, often sparsely branched axonal arbor derived from multiple thin axons emitted fr
40 age, thereby allowing a time-course study of axonal arbor development and synapse formation in single
41 cell remained constant, suggesting that the axonal arbor did not increase as a function of target av
46 ons was determined by reconstructing labeled axonal arbors from transgenic mice expressing yellow flu
49 tic fields of principal neurons and afferent axonal arbors has been proposed as the anatomical substr
50 ld bipolar cell in rabbit retina has a broad axonal arbor in layer 5 of the inner plexiform layer and
51 may shape the structure and function of the axonal arbor in mature sensory neurons in the main olfac
52 y morphological analysis of the dopaminergic axonal arbor in single aggregates containing between 0 a
56 P-recipient layer 4Cbeta neurons have dense axonal arbors in both blobs and interblobs but not layer
57 dual APs propagating along millimeter-length axonal arbors in cortical cultures with hundreds of micr
60 ng mice; cells in superficial layer 2/3 lack axonal arbors in layer 4, and cells close to the layer 4
61 Layer 2/3 pyramids in A1 have substantial axonal arbors in layer 4, and photostimulation demonstra
63 visual cortex, which in the adult have dense axonal arbors in layers 2/3 and 5 and not in layer 4.
64 ariations in gross morphological features of axonal arbors in the central nervous system can be assoc
65 12 subtypes defined dendritically, however, axonal arbors in the contralateral SC showed considerabl
67 ned by dendritic morphology have stereotyped axonal arbors in their main central target, the superior
69 d densely immunoreactive dendritic and local axonal arbors is greatest laterally, particularly in str
70 trated that in these mice, the complexity of axonal arbors is reduced, while the area covered by TCA
71 tal day (P) 14 and P18 the initial growth of axonal arbors lacks specificity for layers 2/3 and 5 and
76 rrent seizures in infancy, the dendritic and axonal arbors of biocytin-filled hippocampal pyramidal c
79 actions play a prominent role in shaping the axonal arbors of geniculocortical fibers and the arbors
80 reconstruct the complete dendritic and local axonal arbors of identified corticogeniculate neurons in
83 was also associated with alterations in the axonal arbors of inhibitory neurons, which underwent a p
84 aused by a lower connection probability; the axonal arbors of L4 cells were spatially diffuse in L2/3
85 s hypothesis by following the development of axonal arbors of layer 2/3 pyramidal neurons in ferret v
87 We describe a method to map the location of axonal arbors of many individual neurons simultaneously
90 power of this approach by reconstructing the axonal arbors of multiple neurons in the motor cortex ac
95 ls of deep cells forming columns and broader axonal arbors of superficial cells serving to distribute
96 beit at a lower than normal density, and the axonal arbors of these interneurons were organized into
99 features of olfactory receptor neuron (ORN) axonal arbors on postnatal days 0, 3, 6, 9, 12, and 21.
100 bursts of action potentials reliably invade axonal arbors over a range of developmental ages (postna
101 onal morphology, especially the shape of the axonal arbor, provides an essential descriptor of cell t
103 Furthermore, the normal development of ChC axonal arbors requires proper levels of activity in subc
104 ursting rhythms during the period when their axonal arbors segregate to occupy spatially distinct reg
107 case with respect to dopamine concentration, axonal arbor size per cell remained constant in the face
108 Previous studies have demonstrated that axonal arbors specific for the four main cortical layers
109 ckout mice, layer 2/3 pyramidal neurons form axonal arbors specifically in layers 2/3 and 5, avoiding
111 ptic properties to dynamics in dendritic and axonal arbor structure over hours or days of imaging.
112 ated layer 4B, whereas class I neurons whose axonal arbors target parvocellular (P) recipient layer 4
113 ex, and, in mature animals, these cells have axonal arbors that are highly specific for layer 4 and t
114 vidual neurons in V1 of mature macaques have axonal arbors that are highly specific for these sublaye
115 ividual pyramidal neurons form intracortical axonal arbors that are specific for particular cortical
116 vealed that individual cells have widespread axonal arbors that extend over nearly the full length of
117 ng complete neuronal morphologies, including axonal arbors that span substantial portions of the brai
118 ain is reflected in the dynamic sculpting of axonal arbors that takes place as connections between CN
119 y must be maintained by active remodeling of axonal arbors to adapt to the changes in overall size of
120 incubated for 5-7 d to allow initial, local axonal arbors to form in the absence of extrinsic influe
121 o interneurons with predominantly horizontal axonal arbors, using dual somatic recordings in prefront
123 Detailed visualization of dendritic and axonal arbors was obtained by silver-gold enhancement of
125 and extent of action potential invasion into axonal arbors, we have used two-photon excitation laser
127 al neurons within the areas traversed by its axonal arbor, with pockets of very high innervation dens