ライフサイエンスコーパス: aspiny

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1 Aspiny (8%) and sparsely spiny multipolar (5%) CR+ neuro

2 and their dendritic processes were commonly aspiny and sometimes highly beaded.

3 Qualitatively, aspiny and spiny neurons in both species appeared morpho

4 er than [Ca2+]i from this source on the main aspiny apical shaft.

5 iking cells anatomically fully recovered had aspiny, beaded dendrites.

6 ells were identified in the striatum: small, aspiny, bipolar cells with varicose dendrites and larger

7 ing morphological features of both spiny and aspiny cells, many of which contained GABA.

8 The aspiny cells, which were more prevalent, corresponded mo

9 at m2-positive neurons corresponded to large aspiny cholinergic interneurons and ultrastructurally, t

10 Large aspiny cholinergic interneurons provide the sole source

11 e cytoplasm of isolated medium-large somata, aspiny dendrites and axon terminals.

12 permeable to calcium and are concentrated on aspiny dendrites of interneurons, which lack obvious phy

13 maging that activation of single synapses on aspiny dendrites of neocortical fast spiking (FS) intern

14 Because aspiny dendrites throughout the CNS express CP-AMPA rece

15 onal perikarya are relatively large, possess aspiny dendrites, and are rich in the pallidal neuron/st

16 ll-sized spiny ITCcs, L-ITCcs possess thick, aspiny dendrites, have highly branched, long-range axona

17 s induced by diffusible second messengers in aspiny dendrites, we examined diffusion of Ca(2+) and sm

18 lly spiny, which contrasts with their adult, aspiny equivalents.

19 LTP occurs in aspiny feed-forward interneurons and propagates to pyram

20 ng the dendrites and on the soma of normally aspiny hippocampal interneurons.

21 y, estrogen receptors have been localized to aspiny inhibitory hippocampal interneurons, indicating t

22 NGFI-B did not colocalize with striatal aspiny interneurons expressing choline acetyl transferas

23 een systematically investigated, these large aspiny interneurons may serve an important integrative f

24 tes characteristic of large and medium-sized aspiny interneurons, expressed SPR immunoreactivity.

25 SP and/or inhibitory neurotransmitters onto aspiny interneurons, some of which are cholinergic.

26 istics of either spiny projection neurons or aspiny interneurons.

27 striatal neurons, the large and medium-sized aspiny interneurons.

28 Kal7 are low in the dendrites of hippocampal aspiny interneurons.

29 ter transient global ischemia, whereas large aspiny (LA) neurons remain intact.

30 e categorized as medium spiny-like and large aspiny-like based on a combination of their activity aut

31 However, firing rates of large aspiny-like neurons were faster in both hemispheres of t

32 er of a second morphological type, the large aspiny neuron, did not differ following either adolescen

33 : (1) NT and D2 receptors are colocalized in aspiny neurons and dendrites, (2) NT may produce a direc

34 elative resistance of large and medium-sized aspiny neurons and the patch compartments to degeneratio

35 s of the substantia nigra, cholinergic large aspiny neurons of the striatum, and GABAergic and cholin

36 in vivo, we found clusters of both spiny and aspiny neurons surrounding the electroporated neuron in

37 Large cells corresponding to aspiny neurons were less frequently stained.

38 monly seen within the cytoplasm of spiny and aspiny neurons, many of which also expressed MOR.

39 -unidentifiable excitatory shaft synapses in aspiny neurons, such as parvalbumin-positive interneuron

40 membranes and nearby endosomal organelles in aspiny neurons.

41 re a heterogeneous group of medium spiny and aspiny neurons.

42 highly indented nuclei, a characteristic of aspiny neurons.

43 et has distinctive traits, including largely aspiny projection neurons that directly innervate the th

44 Aspiny stellate neurons were the last to appear.

45 es, presumably arising from spiny as well as aspiny-type somata, which also contained CB1R immunoreac

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