ライフサイエンスコーパス: cell body

1 n within the three-dimensional volume of the cell body.

2 nd only later spreads to the oligodendrocyte cell body.

3 greater cell force generation and a stiffer cell body.

4 rifugal propagation of Ca(2+) waves into the cell body.

5 nbleached EB1 entering the flagella from the cell body.

6 uma, which, unexpectedly, is confined to the cell body.

7 or the faster polymerization rate within the cell body.

8 lity, similar to cellular cargo, towards the cell body.

9 of axonal processes contacting the neuronal cell body.

10 neck that separates the leader bleb from the cell body.

11 not along the protein transport route in the cell body.

12 re found in keratocyte fragments that lack a cell body.

13 flagellum and from the flagellum back to the cell body.

14 ion of surface area, increases distal to the cell body.

15 the overexpressed mRNA is restricted to the cell body.

16 , are transported discontinuously toward the cell body.

17 membrane protrusions that extend beyond the cell body.

18 the number of dendrites growing out from the cell body.

19 l stimuli can be transmitted deep inside the cell body.

20 the ciliary rootlet links the cilium to the cell body.

21 time and do not involve reorientation of the cell body.

22 ering of polarity transcripts throughout the cell body.

23 microtubule to steer the plus end toward the cell body.

24 d accumulated hypophosphorylated NDK5 in the cell body.

25 an organelle that self-assembles outside the cell body.

26 h are delivered from the growing axon to the cell body.

27 ctivated gametes, aCRY is localized over the cell body.

28 d disc matching the dimensions of a neuron's cell body.

29 fusion barrier between the outer segment and cell body.

30 sulting in the compaction and removal of the cell body.

31 odendrocytes were swollen and had vacuolated cell bodies.

32 n-based contacts with neighboring mesodermal cell bodies.

33 endrites and clusters of their parent nigral cell bodies.

34 s a battery of injury responses in axons and cell bodies.

35 ticular mitochondria restricted to the motor cell bodies.

36 elin forms on axons but avoids dendrites and cell bodies.

37 o changes in Bdnf mRNA in the parent granule cell bodies.

38 r no lipofuscin was detected in motor neuron cell bodies.

39 mum, which covers the size range of typical cell bodies.

40 tors of like-like clustering of motor neuron cell bodies.

41 similar decrease in nerve fiber endings and cell bodies.

42 pairs, despite the regular spacing of their cell bodies.

43 to neuronal synapses, dendrites, axons, and cell bodies.

44 lar channels narrower than the length of the cell body, a fraction of meandering Paramecia buckle the

45 of AVP and OT-immunoreactive (ir) fibers and cell bodies across age and sex within the SBNN has been

46 ells exhibit an anterior/animal pole bias in cell body alignment and movement direction, suggesting t

47 The bucking (self-bending) of the cell body allows the Paramecium to reorient its anterior

48 r for BDNF, deletion of Bdnf from cerebellar cell bodies alone did not perturb the localization of pr

49 f the cochlea, myosin VI is expressed in the cell bodies and along the stereocilia that project from

50 atiotemporal regulation of Nogo-A and NgR in cell bodies and axons of RGCs during ontogeny.

51 o TG neurons and expressed transgenes within cell bodies and axons of sensory neurons in all three br

52 of green fluorescent protein (GFP) label of cell bodies and axons throughout the CN.

53 These include RGC dendrites, cell bodies and axons, the unmyelinated retinal nerve fi

54 is found in recycling endosomes in neuronal cell bodies and axons.

55 eposition of alpha-synuclein within neuronal cell bodies and axons.

56 Because the cell bodies and central projections of these cochlear ne

57 als formed synapses with GFP-negative (host) cell bodies and dendrites and, unexpectedly, with some G

58 terial, opsins were found to be expressed in cell bodies and dendrites of cortical neurons and along

59 tic contacts with auditory efferent neuronal cell bodies and dendrites, as well as unlabeled axon ter

60 rm layers, the sites of the retinal ganglion cell bodies and dendrites, respectively.

61 isoform (2N4R-Tau) was partially retained in cell bodies and dendrites, where it accelerated spine an

62 Col4a3 mutants including distorted podocyte cell bodies and disorganized primary processes.

63 ivated microglia can closely appose neuronal cell bodies and displace axosomatic presynaptic terminal

64 onset most likely exceeds that of the nigral cell bodies and has been estimated to be of the order of

65 lly expressed Channelrhodopsin (ChR2) in CST cell bodies and in axon terminals in cervical spinal cor

66 lular localization is restricted to neuronal cell bodies and is not detected at axon initial segments

67 py, we detected expression of mCherry in VTA cell bodies and local processes.

68 d control for spatial separation of neuronal cell bodies and neural projections, which resembles the

69 lar matrix but could also be observed within cell bodies and neurites as well as within the endotheli

70 expression and translation rates in isolated cell bodies and neurites genome-wide.

71 teome, and translated transcriptome in their cell bodies and neurites, providing a unique resource fo

72 scence intensities of PV immunoreactivity in cell bodies and of WFA labeling and aggrecan immunoreact

73 BM) neurons including the positioning of the cell bodies and peripheral axon pathfinding.

74 n 4 (AQP4) appeared distributed all over the cell bodies and processes of the CD44+ astrocytes, while

75 ntous microprojections arising from podocyte cell bodies and processes, and presence of unique bridgi

76 analysis revealed multiple inclusions in the cell bodies and proximal axons of spinal cord neurons, d

77 rritories with inhibitory inputs enriched on cell bodies and proximal dendrites and excitatory inputs

78 ted that unprocessed pro-NRG2 accumulates on cell bodies and proximal dendrites, and that NMDAR activ

79 ed lattice-like structures that surround the cell bodies and proximal neurites of select classes of i

80 brain, but PDF expression persists in their cell bodies and remaining projections.

81 tina is a highly ordered neuronal network of cell bodies and synaptic neuropils arranged in distinct

82 ation and by slowing degradation of neuronal cell bodies and termini in MPTP-intoxicated mice.

83 by cell contact between the sensory ganglion cell bodies and the hindbrain.

84 mRNA and protein expression in both neuronal cell bodies and the injured axons.

85 ists in sLNvand large ventral lateral neuron cell bodies and their remaining projections.

86 synapses can be different from those in the cell bodies and, consequently, qualitatively different c

87 the accumulation of poly(ADP-ribose) in the cell body and axon and limited axonal growth.

88 sive changes in distribution of mRNAs in the cell body and axon compartments of peripheral sensory ne

89 we studied the underlying mechanisms in the cell body and compared them to the mechanisms in the ner

90 This accumulation involved the entire cell body and distal processes of oligodendrocytes, but

91 abilities of the hook protein connecting the cell body and flagellum play a role in locomotion.

92 and the rotational degrees of freedom of the cell body and flagellum, and we use numerical simulation

93 the NOP-eGFP receptors appear throughout the cell body and in processes.

94 al roles in the transport of AMPARs from the cell body and in the insertion and removal of synaptic A

95 Instead, movement of the cell body and nucleus (nucleokinesis) is disrupted.

96 rhodopsin1-containing vesicles (RLVs) in the cell body and reduced rhodopsin protein.

97 wheel complex that connects the TO with the cell body and the cell membrane.

98 ponents syntaxins 3 and 4, localizing to the cell body and the myelin membrane, respectively.

99 ing due to gas leaks at the interface of the cell body and the rotator.

100 etected by membrane receptors located in the cell body and then transduced to the beating cilia by me

101 d by stimuli at their hair bundles drive the cell body and, in turn, it has been assumed, amplifies t

102 t-derived synapses on GFP-immunoreactive MGE cells bodies and dendrites.

103 es with enlarged cell components (dendrites, cell bodies, and nuclei) or by epithelioid melanocytes w

104 NRG2, accumulate as unprocessed proforms on cell bodies, and their ectodomains are shed by metallopr

105 mbrane, detachment of the flagellum from the cell body, and disruption of mitotic spindles.

106 alization of ATP8A2 to the inner segment and cell body, and increased apoptosis in the retina.

107 tion in the outer segment, metabolism in the cell body, and neurotransmitter release at the synaptic

108 ns have distinct roles in the outer segment, cell body, and synaptic terminal of photoreceptors.

109 llowing retrograde transport to the cortical cell bodies, apoptosis was induced by infrared laser ill

110 Neuronal cell bodies are captured from perfused mouse brain slice

111 which becomes paralyzed by 5-6 mo, where MN cell bodies are fluorescent, enabling the same type of r

112 on of tau in axons at long distance from the cell body are not properly understood.

113 rative program, highlighting the role of the cell body as an arbiter of large-scale axon removal.

114 to accumulate at the plasma membrane of the cell body as expected, but instead accumulates in intrac

115 hich endoplasmic reticulum (ER) enlarges and cell body asymmetrically balloons and finally ruptures.

116 orescent-labelled neurons and counterstained cell bodies at a voxel size of 0.32 x 0.32 x 2.0 mum in

117 nt loss of VGLUT1 terminals on dendrites and cell bodies at both 21 days and 3 months post-crush.

118 into the synaptic neuropil and anchoring of cell bodies at the neuropil border.

119 ErbB4 and NRG2, and pro-NRG2 accumulates on cell bodies atop subsurface cisternae.

120 o the nigrostriatal pathway including nigral cell bodies, axons and striatal terminal fields.

121 the cochlea have a unique motility in their cell body based on mechanoelectric coupling, with which

122 es well with the loss of nigral dopaminergic cell bodies but only correlates with in vitro measures o

123 e of not only measuring the mechanics of the cell body but also the parameters of the pericellular br

124 e mice, MEIG1 is expressed in the whole germ cell bodies, but the protein migrates to the manchette,

125 knockout mice had increased motility of the cell body, but severely impaired retraction of the tail

126 tivity was sufficient to clear RLVs from the cell body by a process dependent on Arf1-GTP levels and

127 ranslation rates between protrusions and the cell body by RNA sequencing (RNA-seq) and quantitative p

128 omes are recruited as single vesicles to the cell body by surfing on filopodia as well as filopodia g

129 Flagellar rotation counter-rotates the cell body, causing MSHA pili to have periodic mechanical

130 , in feeder channels that are wider than the cell body, cells elongate along one side wall of the cha

131 d to grow as they were swept back toward the cell body; coated pits were absent from the correspondin

132 rease in synaptic coverage around motoneuron cell bodies compared with short-term data, which is indi

133 forces with FA monitoring, we show that the cell body contact angle controls the onset of force gene

134 Pelvic ganglia neural cell bodies contained heparanase 1, heparanase 2, and le

135 Cell bodies containing VAChT were not found at any site.

136 his line, increasing the stiffness resisting cell body contraction led to a decrease of the lag time

137 ependent node-and-cable actin network in the cell body cortex.

138 found that photoactivation of PPTg glutamate cell bodies could serve as a direct positive reinforcer

139 A2, PDE11A4 is expressed throughout neuronal cell bodies, dendrites (stratum radiatum), and axons (fi

140 The volume of the neuronal cell body, density of dendritic spines, and glial fibril

141 optotic protein Puma as a key factor in this cell body-derived signal.

142 , the intercalation of post-mitotic neuronal cell bodies during VNC formation.

143 ion of the layer 2/3 pyramidal neuron to the cell body, enhancing the effectiveness of layer 1 input.

144 idirectional manipulation of PPN cholinergic cell bodies exerted opposing effects on locomotor behavi

145 e up to several hundred micrometers from the cell body, extending the leading edge and promoting high

146 o travel from the peripheral terminal to the cell body followed by a return signal to the peripheral

147 The cell bodies form a regular mosaic, suggesting that they

148 t only at the cell poles, but also along the cell bodies, forming a decreasing concentration gradient

149 d to separate the mechanical response of the cell body from deformation of the pericellular layer sur

150 In the cell body, galectin-3 colocalizes with melanosome-destin

151 h model to derive the elastic modulus of the cell body has been demonstrated, the model ability to ch

152 tin protein at the growth cone even when the cell bodies have been removed.

153 Before any myocardial cell bodies have entered the trabecular layer, cardiomyo

154 gy analysis, we document marked variation in cell body helical parameters and flagellum number among

155 the buildup of synaptic proteins in neuronal cell bodies, hence may play an adaptive role to stresses

156 ene are expressed at the surface of neuronal cell bodies; however, they do not associate with the ion

157 erefore quantified AVP- and OT-ir fibers and cell bodies in 22 subregions of the forebrain SBNN in ju

158 fferences in OT-ir fiber fractional areas or cell bodies in any of the 22 subregions of the forebrain

159 ial roles for glial ensheathment of neuronal cell bodies in CNS homeostasis as well as Spz3 as a nove

160 and muscimol to activate or inhibit neuronal cell bodies in distinct locations along the rostro-cauda

161 neurofibrillary tangles observed in neuronal cell bodies in individuals with Alzheimer's disease.

162 ite matter fibres more readily than neuronal cell bodies in STN, which may help explain anatomic vari

163 e exception of the unique presence of RFRP-3 cell bodies in the arcuate nucleus (Arc).

164 m perisomatic clusters around CCKBR-positive cell bodies in the BLA.

165 i-Hebbian LTP induction in interneurons with cell bodies in the CA1 stratum oriens.

166 a(2)delta(3) subunit revealed immunoreactive cell bodies in the ganglion cell layer and inner nuclear

167 The cell bodies in the inner nuclear layer, however, were la

168 ographic maps, where the positions of neuron cell bodies in the projecting field correspond with the

169 e observed in ex vivo vagus nerve and neuron cell bodies in the vagal ganglia.

170 luorescence in the lysosomes of motor neuron cell bodies in the ventral horn of WT mice by 3 mo of ag

171 ting from electrical stimulation of dopamine cell bodies in the ventral tegmental area (VTA).

172 trograde tracing showed that these clustered cell bodies in turn project to the striatum as part of t

173 The feedforward projecting cell bodies in V2 were primarily located in the supragra

174 nerates an abnormal mitochondrial network in cell bodies in vivo and reduces the number of axonal mit

175 endritic arborization and mislocalization of cell bodies in vivo These cellular defects were associat

176 nto a spiral-like form that wraps around the cell body in a spiral-like fashion and enables the cell

177 amino terminus, which is transported to the cell body in an importin-mediated manner.

178 cant change in TlpD localisation towards the cell body in cheAY2-, catalase- or aconitase-deficient b

179 edge was dissociated from the advance of the cell body in dKO cells, which developed extremely elonga

180 ing evidence points to a requirement for the cell body in the degenerative program.

181 retrogradely transported to the motor neuron cell body in the spinal cord, recycled to the plasma mem

182 d embryonic axons might be restricted to the cell body in vivo, in the intact nervous system.

183 rve terminal function compared with neuronal cell bodies, in accordance with the post-mortem literatu

184 In neuronal cell bodies, increased DAcyt was not due to transmitter

185 ncluded loss of glial ensheathment of neuron cell bodies, increased neuronal cell death, and defects

186 served extending from podocyte processes and cell body, indicating significant membrane dynamics acco

187 Optogenetic stimulation of NAc cell bodies induced a positive fMRI signal in the NAc, b

188 axons and its constant supply from neuronal cell bodies into axons is required for axon survival in

189 particularly important for moving DCVs from cell bodies into axons, and then Unc-104 and kinesin-1 f

190 ) moves IFT trains carrying cargoes from the cell body into the flagellum and from the flagellum back

191 t study we found that Islet1(+) motor neuron cell bodies invaded the floor plate of Robo1/2 double mu

192 Dynein synthesized in neuronal cell bodies is conveyed into the axon by slow transport,

193 of organelles from the axon terminals to the cell bodies is essential to the survival and function of

194 Under the subheading 'Spiking of L5 cell bodies is not influenced by spindles', the first se

195 onal contacts, but how glia support neuronal cell bodies is unclear.

196 ptotic machinery being present in axons, the cell body is an active participant in gating axonal casp

197 Orientation of the flagella toward the cell body is critical for determination of wild-type spi

198 the axonal microcompartment relative to the cell body is not well understood.

199 At a molecular level, the cell body is the convergence point of two signaling path

200 These data indicate that the cell body is the focus of Parkin-dependent mitochondrial

201 lls into a protrusive front and a retracting cell body is the hallmark of mesenchymal-like cell migra

202 e detected by spinal afferent neurons, whose cell bodies lie in dorsal root ganglia (DRGs).

203 lly coherent manner, including connectivity, cell body location, and the spatial distribution of syna

204 Ganglion cell body loss, which is normally later in progression,

205 d dentate gyrus, with no frank noradrenergic cell body loss.

206 anied by decreased epidermal innervation and cell-body loss in the dorsal root ganglia.

207 e lateral attachment of the flagellum to the cell body, mediated by the flagellum attachment zone (FA

208 type: young postmitotic neurons have smaller cell bodies, more extensively branched neurites, and red

209 in AVP-ir fiber fractional areas, and AVP-ir cell body numbers, which were mainly observed in the med

210 ord, KChIP1 is coexpressed with Kv4.3 in the cell bodies of a subset of lamina II excitatory interneu

211 Consistent with this, GLR-1 accumulates in cell bodies of apm-2 mutants.

212 -type K(+) channels, particularly within the cell bodies of CA3 pyramidal neurons.

213 eminal ganglia, the location of the neuronal cell bodies of corneal sensory nerve fibers.

214 om glia, DPP10 proteins appear mainly in the cell bodies of DPP10(+) neurons, not only at the plasma

215 n 3 (LC3), were examined in the motor neuron cell bodies of G85R SOD1YFP mice and found to be reduced

216 currents (ISA s) have been recorded from the cell bodies of hippocampal and neocortical interneurons

217 arly in the brain cortex, which contains the cell bodies of neurons and glia.

218 nal population are densely intermingled with cell bodies of others.

219 t spontaneous activity (SA) generated in the cell bodies of primary nociceptors within dorsal root ga

220 reas Kir6.1 was predominant in dendrites and cell bodies of pyramidal neurons.

221 C were inferred to be excitatory because the cell bodies of retrogradely labeled neurons did not cola

222 Dorsal raphe (DR) harbors cell bodies of serotonin-producing neurons that supply s

223 Although the location of the nerve cell bodies of spinal afferents is well known to reside

224 mutated versions of DAT were confined to the cell bodies of the dopaminergic neurons in the fly brain

225 SN that was not present in the corresponding cell bodies of the DRG or the cranial TG.

226 ved in processes, varicosities, and neuronal cell bodies of the olfactory bulb, granular zones of cor

227 kably, the same relationship is not found in cell bodies of the same neurons and throughout the corti

228 ed expression of this opsin primarily to the cell body of mammalian cortical neurons.

229 ominantly asymmetric synapses with orexin-ir cell bodies or dendrites.

230 SPOT can be activated in neuron cell bodies or uncaged in dendrites to enable structural

231 a(2+) when it accumulates either in the cone cell body or outer segment.

232 determined by which neuronal component - the cell body or the neurite connecting the cell body to the

233 is to transport proteins from the OS to the cell body or to prevent entry of non-OS proteins into th

234 ents studied (ie, extracellular [p = 0.001], cell body [p = 0.003], and neuritic/glial-processes [p =

235 n-3, which is predominantly localized to the cell body peripherally along the Golgi zone.

236 of microtubules with plus-ends distal to the cell body (plus-end-out), whereas dendrites contain mixe

237 ular positions of stalks within a rod-shaped cell body: polar in the genus Caulobacter and subpolar o

238 dpf spinal cord demonstrates variable dmrt3 cell body position and dimensions, confirmed by single c

239 The placement of neuronal cell bodies relative to the neuropile differs among spec

240 Here we show that DRG neuron cell bodies release extracellular vesicles, including ex

241 In contrast, while elimination of vCrz(+) cell bodies requires Draper, elimination of vCrz(+) neur

242 Taste buds are innervated by neurons whose cell bodies reside in cranial sensory ganglia.

243 Accumulation of alpha-syn at the cell body resulted in aberrant association with cis-Golg

244 long microtubules from axon tips to neuronal cell bodies (retrograde transport) or from cell bodies t

245 move toward dendritic ends (anterograde) or cell bodies (retrograde), whereas most of them remain st

246 Axonal and cell body RNA samples were separately subjected to high

247 , we measured v and the angular frequency of cell body rotation, Omega, of motile Escherichia coli as

248 ree clusters of TRN neurons that differed in cell body shape and size, dendritic arborization pattern

249 force theory underestimates the influence of cell body shape on speed for helical shaped bacteria.

250 h mitochondria are unable to exit the neuron cell bodies, similar to the kinesin-1/unc-116 mutant.

251 essite can be reduced up to 15 mum away from cell bodies, similar to the reported length of Geobacter

252 p-/m+ mice, reduced primary forebrain neuron cell body size is apparent in embryonic day 15.5 fetuses

253 Snord116p-/m+ mice the reduction in neuronal cell body size was associated with decreased neuronal nu

254 tive neuronal subpopulations, based on their cell body size.

255 g flagella seeing a lower viscosity than the cell body, so that flagella can be seen as nano-rheomete

256 require spatial input; the majority of their cell bodies subsequently move to cover the entire medull

257 This suggests that, when the cell body switches from convex to concave, tension in th

258 Platelets, small anuclear circulating cell bodies that influence a wide variety of physiologic

259 e peripheral terminal of a nociceptor to its cell body that, in turn, induces a signal that travels b

260 the filopodial shaft and surfing toward the cell body, the most common mode of capture; (ii) capturi

261 erve-ending loss occurs before a decrease in cell bodies; this phenotype is indicative of axonal dieb

262 n of a large-scale pattern across the entire cell body; this has been unveiled by studying the distri

263 e Ca(2+) waves increase RhoA activity in the cell body through calcium/calmodulin-dependent protein k

264 The third step is migration of the tumor cell body through the remodeled matrix.

265 transporting mitochondria from the neuronal cell body throughout the bundles of DRG axons.

266 l cell bodies (retrograde transport) or from cell bodies to axon tips (anterograde transport).

267 llows only healthy mitochondria to pass from cell bodies to axons, perhaps to limit the impact of mit

268 rogradely transported from axon terminals to cell bodies to induce cell death.

269 between perisynaptic glia and photoreceptor cell bodies to mediate a novel, long-distance mechanism

270 rial astrocytes and therefore require larger cell bodies to process waste more efficiently.

271 how severed distal axons signal back to the cell body to induce hyperexcitability, loss of inhibitio

272 haracterization of the helical motion of the cell body to lift the 2D data to 3D trajectories.

273 lity, i.e., the ability of their cylindrical cell body to shorten and elongate upon cell depolarizati

274 nsport of Rab5-containing endosomes from the cell body to specific locations of developing axons.

275 itochondria along neuronal microtubules from cell body to synapse is crucial to neuronal function.

276 the cell body or the neurite connecting the cell body to the arbor - has a smaller volume.

277 ll structure and force transmission from the cell body to the leading edge.

278 gesting that the signal transmitted from the cell body to the peripheral terminal is not a newly tran

279 e simply for conducting information from the cell body to the synapses, here we demonstrate that the

280 h associate almost exclusively with neuronal cell bodies) to understand glia-soma interactions.

281 t of the displacement and orientation of the cell body together with a description of the movement of

282 waves, which stochastically migrate from the cell body towards neurite tips, direct microtubule-based

283 eover, localization of aCRY within the algal cell body varies between vegetative cells and the differ

284 uclei, which averages 41.9% and 49.2% of the cell body volume, respectively, but that in turn the com

285 The change in NCX3 in the cell body was associated with a decrease in NCX3 protein

286 gical behaviors within cortical neurons: the cell body was soft and characterized by a solid-like res

287 etter differentiate axons and dendrites from cell bodies, we mapped the tissue in terms of its scatte

288 Among other striking features, outer hair cell bodies were extremely small and were strongly attac

289 e in the inner nuclear layer (INL) and a few cell bodies were in the ganglion cell layer (GCL).

290 ajority of tdTomato and Confetti fluorescent cell bodies were in the inner nuclear layer (INL) and a

291 In contrast, in the cerebellum, the Purkinje cell bodies were the most strongly immunolabeled element

292 h mRNA at the NMJ compared with motor neuron cell bodies where we find higher levels of transcript co

293 in signaling endosomes from distal axons to cell bodies, where they are inserted on soma surfaces an

294 ne major adhesion site at leading end of the cell body, which is linked through actomyosin contractil

295 ated in the synapses but not in the neuronal cells bodies, which was different from the alpha-synucle

296 ith minus-end-out are transported toward the cell body while "correctly" oriented MTs are transported

297 st, hCLRN1(N48K) largely mislocalized to the cell body with a small amount reaching the hair bundle.

298 (PM) contacts were particularly abundant in cell bodies, with large, flat ER cisternae apposed to th

299 peptidoglycan incorporation occurs along the cell body, with the notable exception of a large region

300 mechanism by which the pili surrounding the cell body work together to propel bacteria remains uncle