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1 be important for rapid, compartment-specific dendritic remodeling.
2 1) signaling in stress-evoked spine loss and dendritic remodeling.
3 stinctive activity-dependent critical period dendritic remodeling.
4 o-mediated signaling is sufficient to induce dendritic remodeling.
5 of Ca(2+) spikes may influence postembryonic dendritic remodeling.
6 o show normal synaptic responses and undergo dendritic remodeling.
7  control by eIF4G2 couples activity to local dendritic remodeling.
8 cessarily detrimental and may play a role in dendritic remodeling after neuronal injury.
9            Neuronal reconstructions indicate dendritic remodeling after training, which may represent
10                      This study explores the dendritic remodeling and development of Drosophila moton
11                               TBI-associated dendritic remodeling and myelin alterations, however, re
12 BA(A) receptor system may also contribute to dendritic remodeling and other stress-related changes in
13 dent stress and depression models have found dendritic remodeling and synaptic spines reduction in co
14 ssion in hSOD1(G93A) HMs revealed precocious dendritic remodeling, and behavioral assays revealed tra
15  hyperglycemia and prevention of hippocampal dendritic remodeling, and therefore, provides an effecti
16 s; spontaneous activity-dependent axonal and dendritic remodeling; and sensory-evoked plasticity driv
17 These increases were followed by a period of dendritic remodeling during which the values for all mea
18 tigation was to improve our understanding of dendritic remodeling exhibited by second-order gustatory
19   These results suggest that Purkinje neuron dendritic remodeling in ataxia is an adaptive response t
20 tress may thus involve neuropeptide-mediated dendritic remodeling in BLA principal neurons.
21 ip between prolonged ERK phosphorylation and dendritic remodeling in D1-primed rats.
22 ctional consequence of neurotrophin-mediated dendritic remodeling in developing neurons.
23 f neurogenesis in the dentate gyrus (DG) and dendritic remodeling in the cornu ammonis (CA), particul
24 res the current literature on stress-induced dendritic remodeling in the mPFC, with particular focus
25 tudy provides the first direct evidence that dendritic remodeling in the prefrontal cortex may underl
26       Larval Ca(2+) currents are absent when dendritic remodeling is most dramatic but increase marke
27  GLT-1 protein levels in the subregion where dendritic remodeling is most prominent, namely the CA3 r
28 or both of these neurotrophins in axonal and dendritic remodeling known to accompany the formation of
29            In cortical cultures, as in vivo, dendritic remodeling leads to an apparent transformation
30                            Activity-prompted dendritic remodeling leads to calcium-influx-dependent a
31 chanism through which repeated stress causes dendritic remodeling of CA3 pyramidal neurons.
32                                              Dendritic remodeling of medium spiny neurons induced by
33 e in mediating depression-like behaviors via dendritic remodeling of NAc D1-MSNs and may prove a usef
34 , suggesting a role for Ng in maturation and dendritic remodeling of tufted cells.
35 microtubule-associated protein-2 may reflect dendritic remodeling related to contextual memory storag
36  the molecular mechanisms that underlie this dendritic remodeling remain obscure.
37 s emerge as novel mediators of BDNF-mediated dendritic remodeling through the activation of a slowly
38 ressant tianeptine, which blocks CRS-induced dendritic remodeling, to modulate CRS-mediated changes i
39                                    Moreover, dendritic remodeling was evident during maturation of ne