ライフサイエンスコーパス: multipolar

1 , unipolar, bipolar, inverted pyramidal, and multipolar.

2 monopolar morphology of the P cell becoming multipolar.

3 ng the phenotypic conversion from bipolar to multipolar.

4 halic trigeminal neurons, some of which were multipolar.

5 ied, though the spindles may be short and/or multipolar [3, 4] and the fidelity of chromosome distrib

6 ted the efficacy of a novel linear irrigated multipolar ablation catheter capable of creating linear

7 g CDK2 inhibition, lung cancer cells develop multipolar anaphase and undergo multipolar cell division

8 extra centrosomes generate CIN by promoting multipolar anaphase, a highly abnormal division that pro

9 amplify during papillar endocycles, causing multipolar anaphase.

10 evere HDR disruption additionally results in multipolar anaphases and loss of clonogenic survival.

11 s of immature doublecortin-positive (DCX(+)) multipolar and bipolar neurons in the hippocampal format

12 They displayed multipolar and complex dendritic arbors in ipsilateral L

13 rafish embryos leads to mitotic defects with multipolar and disorganized mitotic spindles.

14 ECs causes increases in centrosome numbers, multipolar and disorganized spindles, and unaligned chro

15 rcollicular nucleus were large and generally multipolar and had extensive, sparsely branching central

16 c conversion of planar epithelial cells into multipolar and invasive mesenchymal cells before differe

17 overall movement is radial, but they become multipolar and move nonradially in the intermediate zone

18 itional dependence of molecular orientation (multipolar) and orbital (quadrupolar) order in the perov

19 they were generally larger, were more often multipolar, and (in cervical enlargement) had stronger N

20 The overall densities of unipolar, bipolar, multipolar, and inverted pyramidal neurons did not diffe

21 ant (e.g., flattened pyramidal, nonpyramidal multipolar, and inverted pyramidal neurons).

22 gets is very diverse and includes pyramidal, multipolar, and neurogliaform cells.

23 cal types of neurons--unipolar, bipolar, and multipolar--are important for information processing and

24 three subtypes of PV-immunoreactive neurons: multipolar, bipolar and spherical-shaped neurons, based

25 have a more heterogeneous representation of multipolar, bipolar, and unipolar interneurons.

26 Neurons typically assume multipolar, bipolar, or unipolar morphologies.

27 in the rat developing neocortex affects the multipolar-bipolar transition of neurons leading to dela

28 somatodendritic morphology into four types: multipolar, bitufted, bipolar, and irregular.

29 AC precursors are initially multipolar but lose neurites as they migrate through the

30 D ablation through sequential mapping with a multipolar catheter effectively achieved an ablation res

31 roanatomical mapping system was used in 70%, multipolar catheter in 51%, and real-time image integrat

32 In 21 patients, a multipolar catheter placed within scar visualized spatia

33 in 45 patients with AF were identified using multipolar catheter recordings.

34 geting the earliest of LPs visualized on the multipolar catheter, and the impact on later LPs was rec

35 With the use of a multipolar catheter, pacing was performed from electrode

36 risk ratio=0.49 [0.33-0.74]), and the use of multipolar catheters (R(2)=0.08; P=0.05; risk ratio=0.75

37 All clinical high-resolution multipolar catheters are of sufficient resolution to acc

38 Contact mapping was performed using biatrial multipolar catheters in 36 AF subjects (29 persistent).

39 and use of scar integration from imaging and multipolar catheters to focus high-density mapping are i

40 by AFM interactions between the dipolar and multipolar Ce moments .

41 Terminals of auditory nerve fibers in the multipolar cell area included both large and small endin

42 selves ensheathed by a layer of processes of multipolar cell body glia.

43 ls with more than two centrosomes to undergo multipolar cell division leading to apoptosis, defined a

44 ells develop multipolar anaphase and undergo multipolar cell division with the resulting progeny apop

45 lls with multiple centrosomes rarely undergo multipolar cell divisions, and the progeny of these divi

46 is required for cells to transit out of the multipolar cell phase and to enter into the cortical pla

47 nregulation of FoxG1 at the beginning of the multipolar cell phase induces Unc5D expression, the timi

48 used anatomical techniques to identify which multipolar cell population receives synaptic innervation

49 The projections of one type of labeled multipolar cell, planar neurons, were traced into the ve

50 Two broadly distinct populations of multipolar cells exist: T-stellate and D-stellate neuron

51 rade tracing data revealed that medium-sized multipolar cells from the magnocellular part of the LRN

52 tly generated by soma-targeting fast-spiking multipolar cells in layer III, which in turn were driven

53 premotor neurons within the OPt, as well as multipolar cells in the nucleus of the posterior commiss

54 Time-lapse imaging of multipolar cells in the subventricular zone revealed tha

55 ells, thick-smooth dendrite cells, and large multipolar cells of the intermediate layer were present

56 We investigated whether multipolar cells of the ventral cochlear nucleus have pr

57 The other type comprised multipolar cells that were located at the origin and int

58 Multipolar cells with onset chopper (O(C)) responses inn

59 We suggest that multipolar cells within the PVCN have the distribution a

60 d terminals, as well as retrogradely labeled multipolar cells, were present in the contralateral OPt,

61 Labeled cells in DCN were either fusiform or multipolar cells, whereas those in Sp5 varied in size an

62 n, and had morphological features of radiate multipolar cells.

63 stem is composed of a considerable number of multipolar centrifugal neurons, resembling the "ectopic"

64 imple point charge models and more elaborate multipolar charge models for the CO-ligand are smaller b

65 er from monkeys in having a preponderance of multipolar ChAT-ir interneurons in the caudate nucleus a

66 f disorganized spindle microtubules owing to multipolar configurations and defects in chromosome segr

67 us identifies the K-fiber meshwork of linked multipolar connectors as a key integrator and determinan

68 The K-fiber mesh is made of linked multipolar connectors.

69 l evaluation of electrograms recorded on the multipolar coronary sinus and ablation catheters was und

70 ring several spectroscopic signatures of the multipolar delocalized exciton, including the S(2) <- S(

71 ently recorded interneuron subtype had short multipolar dendrites and a dense local axonal arborizati

72 e imaging with scDNA-seq, we determined that multipolar divisions at the zygote or two-cell stage wer

73 Thus, multipolar divisions cannot explain observed rates of CI

74 Although most multipolar divisions failed and cell fusion occurred, so

75 oo low to cause mitotic arrest and result in multipolar divisions instead.

76 ase, whereas, severe HDR deficiency leads to multipolar divisions that are prohibitive for cell proli

77 omes in tumor cells create the potential for multipolar divisions that can lead to aneuploidy and cel

78 tosis through a signaling cascade leading to multipolar divisions, and its knockout promotes clusteri

79 nesin-14 HSET, which likely accounts for the multipolar divisions, and overexpression of HSET reduced

80 This aneuploidy resulted from multipolar divisions, chromosome missegregation, and fai

81 cancer cells with extra centrosomes to avoid multipolar divisions.

82 mitosis, avoiding the detrimental effects of multipolar divisions.

83 e injected with neurobiotin were found to be multipolar Dogiel type II neurons.

84 e >250 s) in 10 procedures (group 1), with a multipolar duty-cycled radiofrequency pulmonary group 2)

85 ed radiofrequency, argon plasma coagulation, multipolar electrocoagulation, and photodynamic therapy.

86 ctivation pattern recorded from conventional multipolar electrode catheters was characteristic of clo

87 r otherwise treatment refractory OCD using a multipolar electrode implanted in the ventral anterior c

88 , resulting in e.g. dipolar, quadrupolar, or multipolar emission on demand.

89 In order to facilitate the design of multipolar fluorine-backbone interactions in protein-lig

90 sed at protein interfaces, we postulate that multipolar fluorine-backbone interactions may represent

91 acking the IGF-1 receptor remain arrested as multipolar forming a highly disorganized tissue.

92 na I projection neurons have been described: multipolar, fusiform, and pyramidal.

93 ynapses on somata and dendritic processes of multipolar GABAergic interneurons, recognized sites for

94 The resulting multipolar geometries resemble electrostatic charge conf

95 Individual activated projection neurons were multipolar, globular, or fusiform in shape.

96 These multipolar glycinergic cells were smaller in soma size a

97 well with experimental data for bipolar and multipolar HT-29 colorectal cancer cells.

98 Multipolar interactions involving fluorine and the prote

99 We show that nonlinear multipolar interference allows achieving not only unidir

100 Multipolar interneurones with narrow spikes generated th

101 f the left atrium (LA) was performed using a multipolar Lasso catheter guided by intracardiac echocar

102 y ablation in a linear pattern, an irrigated multipolar linear ablation catheter safely delivers cont

103 te the excitation of 16 distinct high-order, multipolar, localized surface phonon polariton resonance

104 even assuming beamed emission, but a strong multipolar magnetic field can describe its properties.

105 found that most polyploid cells divide in a multipolar manner.

106 e areas of slow conduction with simultaneous multipolar mapping.

107 b(2)Te(5) (GST) can support a diverse set of multipolar Mie resonances with active tunability.

108 with somal translocation induces a switch to multipolar migration.

109 -phase entry, giant nuclei, multinucleation, multipolar mitoses and centrosome hyperamplification.

110 leted cells showed a significant increase of multipolar mitoses and other spindle pole defects.

111 ls with supernumerary centrosomes to undergo multipolar mitoses resulting in apoptotic cell death.

112 acquisition of > or =3 centrosomes-generates multipolar mitoses, aneuploidy, and chromosome instabili

113 to significant increases in multinucleation, multipolar mitoses, failed abscission, asymmetric segreg

114 47 and low-dose paclitaxel induces aberrant, multipolar mitoses, mitotic slippage and multinucleation

115 in abolishes centrosome clustering, yielding multipolar mitoses.

116 ancer cells defined mechanisms that suppress multipolar mitoses.

117 ary nor sufficient to cause the formation of multipolar mitoses.

118 y divide because of mechanisms that suppress multipolar mitoses.

119 Importantly, multipolar mitosis results in global unbalanced chromoso

120 y phosphatase knockdown, multinucleation and multipolar mitosis were markedly reduced, resulting in e

121 undergo centrosome de-clustering, prolonged multipolar mitosis, and cell death.

122 n by shRNA caused focal cytokinesis defects, multipolar mitosis, and multinuclearity as observed in t

123 gression and centrosome number, resulting in multipolar mitosis.

124 The deletion of MdmX induces multipolar mitotic spindle formation and the loss of chr

125 overduplication and has been shown to cause multipolar mitotic spindle formation, a diagnostic hallm

126 Here we show that multipolar mitotic spindles form frequently in mouse pol

127 of microtubule dynamics by MAP2 resulted in multipolar mitotic spindles, defects in cytokinesis and

128 This multipolar mode is less efficient but still leads to suc

129 e unambiguously associated with any specific multipolar mode.

130 may be associated with interference between multipolar modes.

131 ar and bipolar neurons causes them to assume multipolar morphologies.

132 ajority of migratory new neurons exhibited a multipolar morphology and moved in a nonlinear manner fo

133 On the other side, they show rather multipolar morphology lacking thick dendrite contacting

134 ike transcription factor Dar1 determines the multipolar morphology of postmitotic neurons in Drosophi

135 one to the overlaying cortical plate, assume multipolar morphology while passing through the transien

136 in the lower intermediate zone either showed multipolar morphology with short neurites or possessed n

137 yed TH-IR (9 with bipolar morphology, 6 with multipolar morphology) while the remaining 28 neurons di

138 y TH-IR (18 with bipolar morphology, 10 with multipolar morphology).

139 cal phenotypes caused by Merlin loss, namely multipolar morphology, enhanced cell-matrix adhesion, fo

140 ons by transiently adopting a characteristic multipolar morphology.

141 morphology; the remainder had Dogiel type II multipolar morphology.

142 motor activity was necessary to maintain the multipolar morphology.

143 The methods presented here for multipolar needles bring closer the application of needl

144 Using multipolar needles, the new methods presented reduce the

145 and equip the reader with 8 new methods for multipolar needles, where 2 or more electrodes are space

146 By examining the critical behavior of the multipolar nematic order parameter, we show that it driv

147 We uncovered a multipolar nematic phase of matter in the metallic pyroc

148 hat the transcription factor Dar1 determines multipolar neuron morphology in postmitotic neurons by r

149 at these genes are required for Dar1-induced multipolar neuron morphology.

150 We have found that FGFRs regulate multipolar neuron orientation and the morphological chan

151 st common morphological type of CR+ neurons, multipolar neuronal morphology was typical among PV+ neu

152 ad significantly fewer doublecortin-positive multipolar neurons (p < 0.001) and beaded axons (p = 0.0

153 Dar1 is specifically expressed in multipolar neurons and loss of dar1 gradually converts m

154 se data suggest that cochlear nucleus planar multipolar neurons drive the MOC neuron's response to so

155 were also found on globular bushy cells and multipolar neurons in the PVCN and AVCN.

156 ological transformation and migration of the multipolar neurons in the SVZ/IZ.

157 neurons and loss of dar1 gradually converts multipolar neurons into the bipolar or unipolar morpholo

158 ial nucleus of the trapezoid body, and small multipolar neurons of the contralateral ventral nucleus

159 uron types: spherical bushy cells and planar multipolar neurons of the ipsilateral ventral cochlear n

160 Depletion of kinesin-6 results in multipolar neurons that either are stationary or continu

161 Pase and N-cadherin (NCad) are important for multipolar neurons to polarize their migration toward th

162 and vertically oriented bipolar neurons and multipolar neurons were approximately equally frequent a

163 Multipolar neurons were found caudally, dorsal and ventr

164 oneurons, Rohde nucleus cells, small ventral multipolar neurons, and Edinger cells.

165 argest cells, which were pyramidal and spiny multipolar neurons, appeared earliest.

166 orrelated with the number of labeled radiate multipolar neurons, suggesting radiate neurons as the pr

167 rescues the effect of Cx43 knockdown in the multipolar neurons.

168 rom posteroventral cochlear nucleus stellate/multipolar neurons.

169 keletal compartmentalization is conserved in multipolar neurons.

170 ections resulted in labeled cochlear nucleus multipolar neurons.

171 and make synaptic contacts with dendrites of multipolar neurons.

172 possesses a dense core region consisting of multipolar neurons.

173 tecture with a random distribution of simple multipolar neurons.

174 onnected pyramidal neurons (presynaptic) and multipolar or bitufted interneurons (postsynaptic).

175 These cells were multipolar or bitufted, had a widely extending axon, and

176 t a systematic study of the effect of higher-multipolar order plasmon modes on the spectral response

177 is the direct consequence of the underlying multipolar order that is "hidden" in the neutron diffrac

178 attice with an intertwined dipolar and ferro-multipolar order.

179 Recent discoveries of pseudogap, magnetic multipolar ordered and possible d-wave superconducting p

180 ransition to a less directionally persistent multipolar phase of migration.

181 y discovered electronic nematic phases, this multipolar phase spontaneously breaks rotational symmetr

182 in the absence of UNC-6 and SLT-1 induces a multipolar phenotype with undirected outgrowths.

183 nd loss of its function caused a distinctive multipolar phenotype.

184 re-shell nanostars demonstrated a pronounced multipolar plasmon resonance, which has not been observe

185 Multipolar plasmon resonances up to fourth order were me

186 at exhibits optical properties influenced by multipolar plasmonic coupling.

187 ctin cDNAs caused a dramatic accumulation of multipolar progenitor cells within the subventricular zo

188 Rac activation, leading to the formation of multipolar protrusions and increased cell circularity, a

189 romote actin polymerization and formation of multipolar protrusions, thereby retarding cell migration

190 Multipolar Purkinje cells are located in the central reg

191 spond to parallel fiber activation, but only multipolar Purkinje cells showed characteristic all-or-n

192 Patients had a minimum of 10 multipolar recordings of 30 seconds each.

193 ontribution of the higher-order modes in the multipolar region.

194 e an orbital disorder/order transition and a multipolar reorientation transition, each occurring at d

195 Due to their multipolar resonant response and low intrinsic losses th

196 allows for the manipulation of the nonlinear multipolar response of a meta-atom, resulting in e.g. di

197 rates leads to new features appearing in the multipolar response.

198 The great wealth of multipolar responses has not only brought in new physica

199 rates of MT formation and were predominantly multipolar, revealing a function of augmin in stabilizin

200 resent new opportunities for engineering the multipolar scattering response of dielectric optical ant

201 nged metaphase arrest, anaphase bridges, and multipolar segregations.

202 lls (41 out of 131 neurons, i.e., 31%) had a multipolar soma, while the other group (87 out of 131 ne

203 ar, horizontal; and perpendicular bipolar or multipolar somata.

204 , as predicted by quantum theories involving multipolar spin interactions.

205 centrosomes can result in the assembly of a multipolar spindle and lead to chromosome mis-segregatio

206 rosomes from spindle poles, the formation of multipolar spindle arrays and cytokinetic defects.

207 The model results explain why multipolar spindle could inhibit SAC silencing and spind

208 ion of beta-tubulin isotypes and resulted in multipolar spindle formation and apoptosis.

209 Inhibition of centrosome clustering triggers multipolar spindle formation and mitotic catastrophe, of

210 en correlated with an increased incidence of multipolar spindle formation in some cancer cells that c

211 cancer cells, inhibited mitosis and induced multipolar spindle formation in these cells.

212 Loss of control over mitotic progression, multipolar spindle formation, and cytokinesis defects ar

213 ic failure with centrosome amplification and multipolar spindle formation, leading to aneuploidy and

214 ties, including centrosome amplification and multipolar spindle formation, which results in chromosom

215 erary centrosomes, multinucleated cells, and multipolar spindle formation.

216 rosome amplification, chromosome lagging and multipolar spindle formation.

217 ient to produce centrosome amplification and multipolar spindle formation.

218 blastic leukemia cells resulted in increased multipolar spindle frequency that correlated with centro

219 As a result, GRP94 knockdown cells form a multipolar spindle instead of bipolar morphology and con

220 quence of cells passing through a transient 'multipolar spindle intermediate' in which merotelic kine

221 ntrosome and spindle pole numbers, producing multipolar spindles (most ESCRT-III/VPS4 proteins) or mo

222 ntrosomal and mitotic abnormalities, such as multipolar spindles and asymmetric, bipolar spindles wit

223 Multipolar spindles and bipolar spindles with misaligned

224 rturbation of IKK2 promotes the formation of multipolar spindles and chromosome missegregation.

225 Moreover, imaging studies revealed multipolar spindles and chromosome segregation defects i

226 osome replication, resulting in tripolar and multipolar spindles and defective cytokinesis.

227 ell division, resulting in the generation of multipolar spindles and free microtubule-organizing cent

228 ent before anaphase onset, which can lead to multipolar spindles and genomic instability.

229 ed loss of the shRNA screening hits leads to multipolar spindles and heterogeneous chromosome content

230 eated cells, with supernumerary centrosomes, multipolar spindles and lagging chromosomes during anaph

231 cells show an aberrant number of centrosome, multipolar spindles and micronuclei formation.

232 Mitotically arrested cells display multipolar spindles and misalignment of chromosomes, ind

233 tions and accumulation of mitotic cells with multipolar spindles and unaligned chromosomes.

234 reas HBXIP overexpression causes tripolar or multipolar spindles due to excessive centrosome replicat

235 ci of microtubule organization, formation of multipolar spindles from adjacent centrosome pairs, and

236 y in mitosis, amplified centrosomes assemble multipolar spindles in CDK5RAP2 mutant cells.

237 evelopment, as we observe both monopolar and multipolar spindles in Eg5 transgenic mice.

238 Polyploid hepatocytes form multipolar spindles in mitosis, which lead to chromosome

239 l clustering that prevented the formation of multipolar spindles in noncancer cells.

240 Depletion of Kif2a generated multipolar spindles in stage 12 embryos.

241 crosslinks sufficient to stabilize aberrant multipolar spindles may form.

242 pecifically associated with the formation of multipolar spindles only when centrosomes were present.

243 overcome this clustering mechanism to allow multipolar spindles to form at a high frequency.

244 The formation of multipolar spindles via centrosome splitting after LIC d

245 ormation of acentrosomal poles, meaning that multipolar spindles were observable only in cells with a

246 mation of multiple numbers of centrioles and multipolar spindles with abnormal chromosome arrangement

247 Multipolar spindles with poles that contain single centr

248 letion resulted in distorted, elongated, and multipolar spindles, accompanied by aberrant chromosomal

249 RD9-depleted cells have fragmented PCM, form multipolar spindles, activate the spindle assembly check

250 cancer cells increases the frequency of CA, multipolar spindles, anaphase-lagging chromosomes, and m

251 ncluding formation of unstructured spindles, multipolar spindles, and chromosome missegregation, lead

252 l cells, including centrosome amplification, multipolar spindles, and chromosome missegregation.

253 d abnormal cytokinesis with delayed mitosis, multipolar spindles, and increased apoptosis, rescued by

254 ncluding misaligned and lagging chromosomes, multipolar spindles, and increased tetraploidy.

255 not met: 1) collapsed, 2) monopolar, and 3) multipolar spindles, and the computational screen reveal

256 cells with extra centrosomes initially form multipolar spindles, but these spindles ultimately becom

257 ividual depletion enhances the generation of multipolar spindles, increases mitotic transit time, and

258 cancer cells, including multinucleation and multipolar spindles, indicating that these changes are s

259 These AMtOCs assemble multipolar spindles, leading to chromosome missegregatio

260 ng lamin B caused formation of elongated and multipolar spindles, which could be reversed by partiall

261 cts, including chromosome missegregation and multipolar spindles, which eventually lead to the activa

262 increases the number of anaphase bridges and multipolar spindles.

263 soform, induced centrosome amplification and multipolar spindles.

264 g that results in formation of elongated and multipolar spindles.

265 these assembly pathways caused formation of multipolar spindles.

266 romatid separation, lagging chromosomes, and multipolar spindles.

267 ation of the centrosome and the formation of multipolar spindles.

268 a pronounced attenuation at prometaphase and multipolar spindles.

269 myt1 mutant spermatocytes enter meiosis with multipolar spindles.

270 the central region of the lobe, with large, multipolar, spiny dendrites and locally ending axons.

271 mitter interactions ranging from dipolar and multipolar spontaneous emission enhancement, to plasmon-

272 migration was independently disrupted at the multipolar stage and accompanied by premature ectopic ex

273 tion and microtubule organization during the multipolar stage as important determinants of axon forma

274 NAi have revealed that transition out of the multipolar stage depends on the function of filamin A, L

275 The multipolar stage occurs as bipolar progenitor cells beco

276 The multipolar stage therefore seems to be a critical point

277 e passage of migrating neurons through their multipolar stage via p27 signaling and that interference

278 rphological stage of neuronal migration, the multipolar stage, is vulnerable and is disrupted in seve

279 ontinuously from nearly zero at remnant in a multipolar state, to a large value under the maximum ele

280 implications of cooperative quadrupolar and multipolar states for the design of relaxor-like hybrid

281 Rather, at the pyramidal-to-multipolar synapse, raised P(r) increases the transient

282 At the pyramidal-to-multipolar synapse, which shows paired-pulse depression,

283 radial glial cells and are distinct from the multipolar Tbr2((+)) intermediate progenitors, which div

284 up-regulation disrupts the transition from a multipolar to a bipolar neuronal morphology in the inter

285 The change of the morphology from multipolar to bipolar cells was also attenuated.

286 otin1 or Kif20b hindered the transition from multipolar to bipolar cells.

287 e-born neurons fail to correctly switch from multipolar to bipolar morphology, resulting in impaired

288 nsition of newly born migrating neurons from multipolar to bipolar morphology.

289 s, we observe specific roles for LIC1 in the multipolar to bipolar transition and glial-guided neuron

290 rol distinct steps of the migratory process, multipolar to bipolar transition in the intermediate zon

291 r-acceptor molecules varies from delocalized/multipolar to localized/dipolar depending on the environ

292 m a complete failure in progression from the multipolar to the migratory bipolar state, as revealed b

293 suggest that SARA regulates the orientation, multipolar-to-bipolar transition and the positioning of

294 r interactions--such as extremely high-order multipolar transitions, two-plasmon spontaneous emission

295 ten considered "weak", including "orthogonal multipolar" types represented by, for example, F-CO, sul

296 In multipolar vertebrate neurons, action potentials (APs) i

297 The explicit mobile moieties are the ion, multipolar waters, and the carbonyls and amides of the p

298 s with locally branching axons fall into the multipolar (with ventrally protruding dendrites) and fla

299 rons inhibited for Erk1/2 are stalled in the multipolar zone.

300 ed, they cannot be inactivated, resulting in multipolar zygotic spindles.