戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 apoptosis or selectively degenerate only the axon (pruning).
2 as excess LGI1 accelerates, retinogeniculate axon pruning.
3 f GABA in regulating synapse elimination and axon pruning.
4 in MB gamma neurons is sufficient to inhibit axon pruning.
5 CNS as a negative regulator of developmental axon pruning.
6  of the developing nervous system undergoing axon pruning.
7 ubunits (SMC1 and SA) as being essential for axon pruning.
8 ecdysone receptor EcR-B1, a key regulator of axon pruning.
9 equently pruned-a process called stereotyped axon pruning.
10  of Ecdysone Receptor-B1, a key initiator of axon pruning.
11 ds are fated for removal in a process called axon pruning.
12 nation, which is associated with stereotyped axon pruning.
13 sms are likely employed for various forms of axon pruning.
14 al link between observed cellular events and axon pruning.
15 moval of axon fragments during developmental axon pruning.
16 ) or proteasome subunits in MB neurons block axon pruning.
17 out the cellular and molecular mechanisms of axon pruning.
18 naturally occurring cell death and selective axon pruning.
19 ion of the microtubule cytoskeleton precedes axon pruning.
20 ir processes, suggesting that OPCs engage in axon pruning.
21 (S) also disrupted naturally occurring local axon pruning and axon degeneration in spontaneously dyin
22 binds to the DR6 death receptor and mediates axon pruning and degeneration under trophic factor withd
23 l a previously unknown pathway that controls axon pruning and elucidate the biochemical mechanism by
24  et al. define a safeguard against apoptotic axon pruning and illustrate that Siah3 represses Parkin-
25                 This is because of extensive axon pruning and local axon terminal growth during early
26                                              Axon pruning and synapse elimination promote neural conn
27 ghts into the molecular events that underlie axon pruning and underscore the diversity of refinement
28 )-dependent pathway regulating developmental axon pruning, and in a pruning pathway operating during
29 ng axon degeneration during apoptosis versus axon pruning are distinct.
30       The signaling events that regulate IPT axon pruning are not known.
31                    beta2Chn is necessary for axon pruning both in vitro and in vivo, but it is dispen
32 istically, naturally occurring developmental axon pruning by degeneration and injury-induced axon deg
33                                              Axon pruning by degeneration remodels exuberant axonal c
34                Plum promotes MB gamma neuron axon pruning by regulating the expression of Ecdysone Re
35 e analyze ultrastructural changes underlying axon pruning by using a genetically encoded electron mic
36 uding neuronal migration, axonal elongation, axon pruning, dendrite morphogenesis, and synaptic matur
37 he chemorepellent Sema3F is required for IPT axon pruning, dendritic spine remodeling, and repulsion
38                                              Axon pruning during development is essential for proper
39      Our findings suggest that some forms of axon pruning during development may share similarities w
40 trates a mechanistic conservation between MB axon pruning during metamorphosis and the refinement of
41 ila mushroom body (MB) gamma neurons undergo axon pruning during metamorphosis through a process of l
42 c role of the ubiquitin-proteasome system in axon pruning; for example, loss-of-function mutations of
43 eta2Chn/Rac1 signaling axis distinguishes DG axon pruning from the effects of Sema3F on repulsion and
44                                              Axon pruning has recently been described in the simple n
45                                By inhibiting axon pruning in combination with the use of this EM mark
46 ut rather from rapid synapse elimination and axon pruning in the target olfactory glomerulus.
47 t microglia may play a role in developmental axon pruning in the thalamus by engulfing presynaptic re
48 lpha isoform, is essential for developmental axon pruning in vitro and in vivo.
49                                Developmental axon pruning is controlled by a careful balance of pro-
50 tailed time course analyses indicate that MB axon pruning is mediated by local degeneration rather th
51                                              Axon pruning is widely used for the refinement of neural
52                                Developmental axon pruning is widely used in constructing the nervous
53                                Developmental axon pruning is widely used to refine neural circuits.
54                                Developmental axon pruning of Drosophila memory center neurons occurs
55 osaic screen to identify mutations affecting axon pruning of Drosophila mushroom body gamma neurons.
56 Plum, that is cell autonomously required for axon pruning of mushroom body (MB) gamma neurons and for
57  Boule does not result in obvious defects in axon pruning or morphogenesis of MB neurons, suggesting
58 ripheral nervous system (PNS), developmental axon pruning relies on receptor-mediated extrinsic degen
59 eted intracellular point mutants showed that axon pruning requires tyrosine phosphorylation-dependent
60 omain of Grb4 is required and sufficient for axon pruning/retraction by mediating interactions with D
61 ons require both small-scale and large-scale axon pruning to generate precise adult connectivity, and
62  changes in MB gamma neurons at the onset of axon pruning, we use laser capture microdissection to is
63  mushroom-body neurons, it causes defects in axon pruning, whereas in cholinergic neurons it causes h