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1 on channels on the surface of the axons they ensheath.
2 between the oligodendrocyte and the axons it ensheaths.
3 d that only about 20-30% of each synapse was ensheathed.
5 ing oligodendrocytes are generated and axons ensheathed according to a tightly regulated sequence of
6 ine glia (MG) are multifunctional cells that ensheath and provide trophic support to commissural axon
7 from NRG1 type III deficient mice are poorly ensheathed and fail to myelinate; lentiviral-mediated ex
8 y parameters, such as the number of synapses ensheathed and the strength of this ensheathment, we sho
9 al muscle is produced by the muscle cells it ensheathes and by nonmuscle cells located in the surroun
11 tex where neuronal cell bodies reside, while ensheathing and astrocyte-like glia enwrap and infiltrat
12 proteins, erbB2 and erbB3, are expressed on ensheathing and myelinating Schwann cells and rapidly ph
14 specialized, proteolipid-rich membrane that ensheaths and insulates nerve fibers, facilitates the ra
15 disproportionately unmyelinated, aberrantly ensheathed, and hypomyelinated, with reduced conduction
16 precursors, and that most adult perineurial, ensheathing, and astrocyte-like glia are produced after
17 ons, activated microglia closely apposed and ensheathed apical dendrites, neurites, and neuronal peri
18 do not tile: each astrocyte participates in ensheathing approximately one-quarter of all of the axon
22 d Na+ channels and ankyrinG form adjacent to ensheathed axonal segments even in the absence of a myel
28 as 3 months after injury and their processes ensheathed axons near and distal to the lesion, colocali
32 yelin in layer 2/3 and a quarter in layer 4) ensheathes axons of inhibitory neurons, specifically of
35 tebrate midline glia play important roles in ensheathing axons that cross the midline and secreting s
36 o mature oligodendrocytes and are capable of ensheathing axons with myelin without molecular cues fro
38 tion of the oligodendrocyte plasma membrane, ensheaths axons to facilitate electrical conduction.
40 a present on CSF-facing leptomeningeal cells ensheathing blood vessels in the subarachnoid space may
43 t regenerated into grafts, and appropriately ensheathed but did not myelinate sensory axons extending
47 elop the adult neuroblast and are themselves ensheathed by a layer of processes of multipolar cell bo
49 a network of chains of migrating neuroblasts ensheathed by astrocytes and juxtaposed by clusters of i
50 the adult, migrating SVZa-derived cells are ensheathed by astrocytes, although the function of these
52 these neuronal precursors migrate in chains, ensheathed by astrocytic processes, and travel toward th
54 litated by fiber bundles, particularly those ensheathed by fibroblastic reticular cells in the lymph
55 cular network, a meshwork of collagen fibers ensheathed by fibroblastic reticular cells that connects
57 show that individual or a group of axons are ensheathed by inner glial processes, which in turn are e
59 tial proportion of these APP+ spheroids were ensheathed by myelin, a finding that was confirmed in th
60 propagation of action potentials, axons are ensheathed by myelin, a multilayered insulating membrane
61 e primary heart tube is an endocardial tube, ensheathed by myocardial cells, that develops from bilat
62 and ankyrinG are adjacent to axonal segments ensheathed by oligodendrocytes, but at P21, many node-li
65 ive (-IR) neurons have also been shown to be ensheathed by perineuronal nets (PNN), extracellular mat
66 (+) neuronal glutamatergic synapses that are ensheathed by processes from individual developing astro
68 ckout mice develop normally, become properly ensheathed by Schwann cells, and appear to function norm
72 peripheral nerve in the Drosophila larva is ensheathed by three glial layers, which structurally sup
74 xpressed in Schwann cells and the axons they ensheath cause the hereditary motor and sensory neuropat
76 spinal cord transection model and olfactory ensheathing cell (OEC) or fibroblast (FB; control) trans
77 the fact that the neuroprotective olfactory ensheathing cell (OEC) subset is difficult to isolate, m
80 lfactory receptor neuron (ORN) and olfactory ensheathing cell maturation; however, directed outgrowth
81 ork has implicated this pathway in olfactory ensheathing cell support for regeneration of axons from
83 ently discovered type of cell, the olfactory ensheathing cell, which can be obtained from the adult n
85 eeze fracture, P faces of both the axons and ensheathing cells (glia that surround the axon fascicles
86 ne or in combination with cultured olfactory ensheathing cells (OEC) into the lesion cavity 6 weeks a
87 st that correct development of the olfactory ensheathing cells (OEC) is imperative for normal GnRH-1
88 lantation of a mixture of 50% p75+ olfactory ensheathing cells (OECs) and fibroblasts derived from th
101 's gland cells, and GFAP(+)/p75(-) olfactory ensheathing cells (OECs) in the underlying lamina propri
102 allei infection, we infected human olfactory ensheathing cells (OECs) in vitro and measured bacterial
104 ere we describe transplantation of olfactory ensheathing cells (OECs) or Schwann cells derived from t
107 n of the calcium influx pathway in olfactory ensheathing cells (OECs) was performed using Indo-1 calc
108 actory sensory neurons (OSNs), and olfactory ensheathing cells (OECs), but was excluded from mature O
109 t rat Schwann cells (SCs), but not olfactory ensheathing cells (OECs), form a boundary with astrocyte
110 L a population of glial cells, the olfactory ensheathing cells (OECs), surround OSN axon fascicles.
111 for three-dimensional culturing of olfactory ensheathing cells (OECs), which can be used to understan
114 n (GFP)-expressing donor rats [GFP-olfactory ensheathing cells (OECs)] into a region of spinal cord d
116 prove that the NC give rise to the olfactory ensheathing cells and subpopulations of GnRH-1 neurons,
119 ovide evidence that these specialized vessel-ensheathing cells contribute to the S1P that promotes th
122 ared following transplants of pure olfactory ensheathing cells from neonatal animals and mixed olfact
124 cent discovery of the potential of olfactory ensheathing cells has proved a significant advance.
125 ss in a first application of human olfactory ensheathing cells in clinical brachial plexus injury wou
126 l nerve glia play roles similar to olfactory ensheathing cells in supporting axon elongation, yet dif
127 eronasal progenitors, formation of olfactory ensheathing cells in the nasal mucosa, and impairs GnRH-
128 erved in Gli3 mutants from lack of olfactory ensheathing cells in the nasal mucosa, moreover, we disc
129 ounding the olfactory epithelium (OE) and by ensheathing cells in the nerve layer of the ventral olfa
130 models transplantation of cultured olfactory ensheathing cells into an injured spinal cord induces re
131 a of olfactory mucosa and cultured olfactory ensheathing cells into the lesion cavity) 6 weeks after
133 ervations indicate that Sema3A expression by ensheathing cells plays an important role in guiding olf
135 transplantation of cultured adult olfactory ensheathing cells restores the sensory input needed for
136 demonstrate that Schwann cells and olfactory ensheathing cells share a common developmental origin.
138 ultures (containing a mean of ~50% olfactory ensheathing cells) in a population of spinal cord-injure
140 they share features with mammalian olfactory ensheathing cells, the developmental roles of antennal n
142 that migrate inward and to the posterior to ensheath commissural axons, and PMG that migrate inward
147 ydrophobic pocket that adaptively expands to ensheath differing-length lipid chains using a cleft-lik
152 neocortical gray matter is thought to mostly ensheath excitatory axons connecting to subcortical regi
156 ndicate that NG exchanges identities between ensheathing glia (EG) and astrocyte-like glia (ALG).
157 everal studies have suggested that olfactory ensheathing glia (EG) can form Schwann cell (SC)-like my
160 promise are olfactory bulb-derived olfactory ensheathing glia (OEG) transplantation and treadmill ste
162 n anatomical evidence suggest that olfactory ensheathing glia (OEG) transplantation promotes axon reg
163 d adult rat Schwann cells (SCs) or olfactory ensheathing glia (OEG), or both, were transplanted in th
165 ll types in the adult Drosophila brain, with ensheathing glia acting as phagocytes after axotomy, and
169 actions between spinal motor axons and their ensheathing glia are vital for forming and maintaining f
170 lies, gut-induced metabolic reprogramming of ensheathing glia becomes constitutive in old flies owing
171 this, we found that blocking endocytosis in ensheathing glia blocked the induction of plasticity.
173 glial functions, beginning with the role of ensheathing glia in preventing ephaptic coupling, axogli
174 bset of globose basal cells and by olfactory ensheathing glia in the normal mucosa; Hes5 label disapp
176 uction, we discover serotonin signaling from ensheathing glia is required for experience-dependent sy
182 henotype is associated with a failure of the ensheathing glia to correctly wrap peripheral axons.
183 tless FGF receptor acts cell-autonomously in ensheathing glia to regulate process extension so as to
185 uired for this critical period plasticity as ensheathing glia upregulate Draper, invade the VM7 glome
186 e gonadotropin-releasing hormone neurons and ensheathing glia which are also resident in the mesenchy
187 y neurons, non-neuronal cells, and olfactory ensheathing glia, all made from embryonic Pax7+ cells.
188 (outer and inner surface glia, cortex glia, ensheathing glia, and astrocytes), which show within-cla
189 e intestine activates JAK-STAT signalling in ensheathing glia, inducing the expression of glial monoc
193 il is separated from neuronal cell bodies by ensheathing glia, which as we show using dye injection e
194 CDH3 and CDH11 are expressed by olfactory ensheathing glia, which surround OSN axons in the outer
200 that are remarkably similar to those of axon-ensheathing glial cells in unmyelinated invertebrates.
202 ein-blocking antibodies, or olfactory nerves ensheathing glial cells transplanted into the acutely in
203 thelia, including migrating GnRH neurons and ensheathing glial precursors of the migrating mass (MM),
204 coaxial non-lip progenitors; contrastingly, ensheathing granule cells derive principally from LRL.
205 to hypomyelinated mice, iOPCs are capable of ensheathing host axons and generating compact myelin.
207 ons counted, 18% also expressed CB, 31% were ensheathed in PNN, and 7% expressed both CB and PNN.
208 , whereas unmyelinated axons were aberrantly ensheathed in Remak bundles, with increased numbers of a
210 myelinating Schwann cells and the axons they ensheath is mediated by cell adhesion molecules of the C
211 d in the cerebral cortex, pia mater, and pia-ensheathed leptomeningeal vessels in two GBCA-exposed hu
212 The primary non-motile cilium, a membrane-ensheathed, microtubule-bundled organelle, extends from
214 ocytes more efficiently than fetal OPCs, and ensheathed more host axons per donor cell than fetal cel
217 e rise to mature oligodendrocytes that could ensheath multiple host axons when co-cultured with prima
219 on microscopy (EM) images of axons and their ensheathing myelin from both the central and peripheral
222 aggregates of the extracellular matrix which ensheath neuronal cell bodies, primary dendrites and axo
224 e in the cytosolic matrix of astrocytes that ensheath neurons and blood vessels, whereas NR2A/B is co
226 sends paracrine signals to activate TRPA1 of ensheathed nociceptors to sustain mechanical allodynia.
229 y, vascular pattern, or SM cell and pericyte ensheathing of vessels in SM alpha-actin null mice.
231 The signals that determine whether axons are ensheathed or myelinated by Schwann cells have long been
232 omeninges, subpial astrocytes and astrocytes ensheathing penetrating blood vessels at the ventral sur
235 yte-like cells or B-cells, sends projections ensheathing pericytes on SVZ capillaries in young mice.
236 Vertebrate and invertebrate epidermal cells ensheath peripheral arbors of somatosensory neurons, inc
237 We show that Schwann cells, the cells that ensheath peripheral nerve axons, and which traditionally
241 omponent of the perineuronal net matrix that ensheaths principal neurons in the MNTB and the large ca
242 avid C17.2 cell-host axon contacts, and the ensheathing properties of these cells are related to the
243 axonal regrowth, and then remyelinate or re-ensheath regenerated axons, thereby ensuring functional
244 ptors suggests that the extracellular matrix ensheathing RPE microvilli contains ligands for this int
245 se progression that is triggered within axon ensheathing Schwann cells and that can be ameliorated by
246 he potential contribution of peripheral axon ensheathing Schwann cells to ALS by constructing transge
247 remature formation of heminodes around early ensheathing Schwann cells, and altered nerve conduction
250 en localized to protoplasmic astrocytes that ensheath synapses and modulate neuronal activity in the
255 gene that result in a failure of the SGPs to ensheath the GCs, leading to defects in GC development.
257 enesis, SGPs send out cellular extensions to ensheath the individual GCs and promote their developmen
258 is selectively expressed by glial cells that ensheath the migratory neurons (expressing APPL), and th
259 ophila is established by surface glia, which ensheath the nerve cord and insulate it against the pota
260 iated cortex glia that extend processes that ensheath the neuroepithelium, suggesting that glia cells
267 we found that oligodendrocytes repetitively ensheathed the same axons multiple times before any stab
270 ious literature, our data suggest that cells ensheathing the dorsal aorta emerge from a sub-populatio
273 ous to the transporters in the Bergmann glia ensheathing the Purkinje cells), nor did it block the cu
274 olysis of caged Ca(2+) in astrocytic endfeet ensheathing the vessel wall was associated with an 18% i
276 r cellular structure, the perineurium, which ensheaths the motor nerve, forming a flexible, protectiv
279 cells sort individual axons from bundles and ensheath them to generate multiple layers of myelin.
282 7.5), KCNQ4 is also found at calyx terminals ensheathing type I vestibular hair cells where it may be
284 Also, individual photoreceptor terminals are ensheathed within the outer plexiform layer (OPL) by the