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1 and TTC-SOD-1 were distributed in a punctate perineuronal and intraneuronal pattern similar to that s
2                              STAT3 regulates perineuronal astrocytic process formation and re-express
3 the cortex, a subset of microglia (sometimes perineuronal) consists of cells that are probably phagoc
4 ast, the brain of the daughter revealed only perineuronal deposition of diffuse amyloid in cerebral c
5  astrocytes constitutes a major component of perineuronal extracellular matrix in the adult brain.
6   These included increases in the number and perineuronal location of CX3CR1-expressing microglia, de
7                Of particular interest is the perineuronal net (PN), an extracellular matrix component
8 etzincin proteases involved in reshaping the perineuronal net (PNN) and Mme encoding for Neprilysin,
9 zation leads to dynamic turnover of selected perineuronal net (PNN) components well beyond the normal
10 te proteoglycans (CSPGs) associated with the perineuronal net (PNN) is upregulated around the phrenic
11 g, are stored as the pattern of holes in the perineuronal net (PNN), a specialized ECM that envelops
12  wave induced cavitation collapse within the perineuronal net (PNN), which is the near-neuron domain
13 teoglycans (CSPGs) within the glial scar and perineuronal net creates a barrier to axonal regrowth an
14 sion exhibited by the Cat-315 CSPG and other perineuronal net CSPGs imparts a distinct molecular surf
15 ct a balance between the oxidative burden on perineuronal net degradation and the capacity of the sys
16  the integrity of PVIs and the extracellular perineuronal net enwrapping these interneurons.
17                                          The perineuronal net forms the extracellular matrix of many
18 at is restrictive, suggesting a role for the perineuronal net in this developmental transition.
19                                          The perineuronal net is first detected late in development,
20          The other link protein that shows a perineuronal net pattern in the DCN, Bral2, is upregulat
21 of parvalbumin interneurons, including their perineuronal net.
22 ons have also been shown to be ensheathed by perineuronal nets (PNN), extracellular matrix envelopes
23  as well as specific ECM structures, such as perineuronal nets (PNNs) and interstitial matrix, are di
24            Most PV neurons are surrounded by perineuronal nets (PNNs) and the density of PNNs, as det
25                                              Perineuronal nets (PNNs) are enigmatic structures compos
26                                              Perineuronal nets (PNNs) are extracellular matrix struct
27                                              Perineuronal nets (PNNs) are extracellular matrix struct
28                                              Perineuronal nets (PNNs) are extracellular matrix struct
29             Lattice-like structures known as perineuronal nets (PNNs) are key components of the extra
30                                              Perineuronal nets (PNNs) are specialized aggregates of t
31                                              Perineuronal nets (PNNs) are thought to play a major rol
32 radation of protective ECM structures called perineuronal nets (PNNs) around fast-spiking inhibitory
33                                              Perineuronal nets (PNNs) enwrapping PV+ cells are long-s
34        Emerging evidence suggests a role for perineuronal nets (PNNs) in learning and regulation of p
35 EMENT: Emerging evidence suggests a role for perineuronal nets (PNNs) in learning and regulation of p
36                           Here, we find that perineuronal nets (PNNs) on the surfaces of PV cells per
37 -rich extracellular matrix structures called perineuronal nets (PNNs) restrict plasticity and regener
38  the ECM condenses to superstructures called perineuronal nets (PNNs) that surround synapses.
39               Here, we present evidence that perineuronal nets (PNNs), a specialized extracellular ma
40                                    Recently, perineuronal nets (PNNs), extracellular matrix (ECM) str
41 ed structures of extracellular matrix called perineuronal nets (PNNs), which are integral to the main
42 component in extracellular structures called perineuronal nets (PNNs), which surround parvalbumin-exp
43 uch as the extracellular matrix structure of perineuronal nets (PNNs).
44 ing postnatal development, forming so-called perineuronal nets (PNNs).
45 on bubble collapse, on damage to the brain's perineuronal nets (PNNs).
46 ning for two types of extracellular markers--perineuronal nets (PNs) and perisomatic rings of termina
47                                              Perineuronal nets (PNs) are a specialized form of brain
48 nspicuous manifestation in the brain are the perineuronal nets (PNs) which surround somata and proxim
49 iated Wisteria floribunda agglutinin-labeled perineuronal nets (WFA/PNNs) are altered in SZ and BD, a
50                                 Although the perineuronal nets act as a protective shield, they are a
51 ectin histochemistry resulted in labeling of perineuronal nets and cells with clear glial morphology,
52 t rather may be extrasynaptically located in perineuronal nets and concerned with the modulation of n
53 jor component of the extracellular matrix of perineuronal nets and is highly enriched in the perisyna
54                                              Perineuronal nets and perisomatic rings of glutamatergic
55 ur knowledge of the presence of lecticans in perineuronal nets and their importance in regulating syn
56 lel, parvalbumin cells enwrapped with mature perineuronal nets are better protected than immature par
57                                              Perineuronal nets are composed of lecticans, a family of
58 chondroitin sulphate proteoglycan-containing perineuronal nets around many neurons.
59 e relationship between the robustness of the perineuronal nets around parvalbumin cells and the degre
60  in the extracellular space or aggregated as perineuronal nets around specific classes of neurons.
61 , the percentage of parvalbumin neurons with perineuronal nets correlated with song maturity.
62 hich is up-regulated in the visual cortex as perineuronal nets form during development and after dark
63 lular staining of brevican resembled that in perineuronal nets in which tenascin-R has been localized
64  total and parvalbumin-positive neurons with perineuronal nets increased with development.
65 on of chondroitin sulphate proteoglycan into perineuronal nets is therefore the key event in the cont
66                    We show that formation of perineuronal nets is triggered by neuronal production of
67 s of similar sizes, each antibody recognizes perineuronal nets on distinct but overlapping sets of ne
68         Transplantation was found to degrade perineuronal nets on endogenous inhibitory neurons and e
69 me of these "brakes" are structural, such as perineuronal nets or myelin, which inhibit neurite outgr
70                 Enzymatic degradation of the perineuronal nets renders mature parvalbumin cells and f
71                                              Perineuronal nets show a great degree of molecular heter
72                                              Perineuronal nets were also unaffected.
73                                              Perineuronal nets were reduced in the lateral nucleus of
74 xtracellular matrix pericellular aggregates (perineuronal nets) in the amygdala and entorhinal cortex
75 nthetic enzymes, vesicular GABA transporter, perineuronal nets, and enhanced GABA transmission among
76                                     Abnormal perineuronal nets, as observed in the postmortem patient
77  monkey amygdala, WFA histochemistry labeled perineuronal nets, but not glial cells.
78           Mice lacking Crtl1 have attenuated perineuronal nets, but the overall levels of chondroitin
79  an enzyme, chondroitinase ABC, that digests perineuronal nets, promoting axon sprouting.
80 these extracellular matrix glycoproteins are perineuronal nets, specialized lattice-like structures t
81 imbalance, we demonstrate that extracellular perineuronal nets, which constitute a specialized polyan
82                             We now show that perineuronal nets, which correlate with sensory critical
83 ess was accompanied by a significant loss of perineuronal nets, which normally enwrap mature fast-spi
84 rvalbumin cells surrounded by less-condensed perineuronal nets.
85 nes modulate their dynamics independently of perineuronal nets.
86 ith a concomitant reduction in the number of perineuronal nets.
87 n sulphate from the extracellular matrix and perineuronal nets.
88 nsity of both parvalbumin and a component of perineuronal nets.
89 mponents of pericellular aggregates known as perineuronal nets.
90 derstanding the organization and function of perineuronal nets.
91 nity, a distribution pattern consistent with perineuronal nets.
92 cid (GABA)ergic neurons and is secreted into perineuronal nets.
93 scin-R may play a functional role within the perineuronal nets.
94 anglia of transgenic mice; these fibers form perineuronal plexi around a subpopulation of sensory som
95                 We show direct evidence that perineuronal reactive ACs play a major role in maintaini
96 ion of brain parenchyma with more pronounced perineuronal satellitosis.
97 s axonal toxicity directly or indirectly via perineuronal Schwann cells.
98 c), atypical PrPres did not show significant perineuronal, vascular, or perivascular immunoreactivity

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