ライフサイエンスコーパス: pole

1 end of the cell (old pole) to the other (new pole).

2 that are stabilized in one orientation (self-poling).

3 superior temporal gyrus (STGr) and temporal pole.

4 ated in the same region of the left temporal pole.

5 six were over 10-fold enriched at the animal pole.

6 scale network that converges on the temporal pole.

7 o push the centrosome toward the cell apical pole.

8 hich in Vibrio species are found at the cell pole.

9 ding downregulation of Wnt genes at the oral pole.

10 ithin the perirhinal cortex and the temporal pole.

11 in controlled array positioning at the cell pole.

12 the microtubules fail to reach the posterior pole.

13 n displayed a deficit in active Cdc42 at the pole.

14 rentiating cells that append to its arterial pole.

15 and high toward the caudo-medial (occipital) pole.

16 eft inferior frontal gyrus, and left frontal pole.

17 ffect of damage anchored to the mother's old pole.

18 V patterning aligns along the animal-vegetal pole.

19 daughter, the one receiving the mother's old pole.

20 al gyrus, angular gyrus, and middle temporal pole.

21 ing later stages, it relocates to the distal pole.

22 ad a combination of lesions in the posterior pole.

23 ecific patterns of expression in the frontal pole.

24 ity of the material accumulated at the north pole.

25 e cytoskeletal changes are restricted to one pole.

26 ema pattern is organized around the anterior pole.

27 r clusters are reliably targeted to the cell pole.

28 ral emissions from a vantage point above the poles.

29 (3) sister chromatids segregate to opposite poles.

30 mplex with inverted geometry avoids the cell poles.

31 ors organize into large clusters at the cell poles.

32 d matter along field lines onto the magnetic poles.

33 deformed by axial forces exerted at opposing poles.

34 material from the septum or newly born cell poles.

35 us-ends to cluster spindle microtubules into poles.

36 to allow dynein to cluster microtubules into poles.

37 rtical ring expansion and clearance from the poles.

38 e chromosomes, enabling formation of nascent poles.

39 ning of regulatory proteins to specific cell poles.

40 d not efficiently concentrate at the spindle poles.

41 the chromosomes are embedded in the spindle poles.

42 la: see text] of mRNAs are segregated to the poles.

43 e notable exception of a large region at the poles.

44 f sterols, and their recruitment to the cell poles.

45 thesis in the nucleoid to degradation at the poles.

46 e and ultimately toward the opposite spindle poles.

47 ces that move chromosomes toward the spindle poles.

48 mic microtubules (MTs) from opposite spindle poles.

49 in similar thermal environments at Mercury's poles.

50 , to mainly intraspecific competition at the poles.

51 migration of HmpF-GFPuv to the lagging cell poles.

52 within bacterial cells, particularly to the poles.

53 tached to microtubules from opposite spindle poles.

54 ubules also inhibit RhoA accumulation at the poles.

55 an intrinsic differences between the spindle poles.

56 n an equatorial zone between the two spindle poles.

57 anionic lipid-enriched membrane at the cell poles.

58 poles show a chaotic scene, unlike Saturn's poles.

59 affold and periodically shuttles between its poles.

60 triggers thionine reduction at the cathodic poles.

61 ith specially designed geometry and periodic poling.

62 than 10 DA of nonperfusion in the posterior pole, 11 (84.6%) developed new vessels, OR 74.25 [95% CI

63 on the fovea), and throughout the posterior pole (12 x 9 mm).

64 quent in the periphery than in the posterior pole (46% vs. 76%) and negligible in controls.

65 toplasmic dynein is required for the spindle pole accumulation of Astrin, and dynein-mediated transpo

66 om 13 (31.0%) eyes with a perfused posterior pole (an area encompassing a 5 disc diameter radius cent

67 h chromosomes move toward stationary spindle poles, anaphase B, in which chromosomes move at the same

68 ated by ParP, which tethers arrays to a cell pole anchor, ParC.

69 idging fibre, we show that the forces at the pole and at the kinetochore depend on the bridging fibre

70 network (insula seeds) and between temporal pole and elements of the default mode network in NTSCUs.

71 nctional connectivity between right temporal pole and medial prefrontal cortex, combined with years o

72 omplete PVD with detachment at the posterior pole and periphery.

73 el mRNAs over 4-fold enriched at the vegetal pole and six were over 10-fold enriched at the animal po

74 reductions of cortical thickness in frontal pole and superior frontal gyrus, and similar effects wer

75 nidentified component of the mitotic spindle pole and the centrosome.

76 otif (ester moiety and turn each occupying a pole and the methyl terminal located near the equator).

77 th filamentous (F)-actin and granules at one pole and the nucleus in a specialized uropod, the "nucle

78 s were examined using the standard posterior pole and the peripapillary retinal nerve fiber layer (pR

79 nular lesions were confined to the posterior poles and appeared to have developed at the margins of c

80 ndle, especially concentrated at the spindle poles and inner centromeres in metaphase and translocate

81 anced distribution of Astrin between spindle poles and kinetochores.

82 s to the cell cortex adjacent to the spindle poles and orients the mitotic spindle.

83 ProP concentrates at the poles and septa of Escherichia coli cells in a cardiolip

84 ting sister chromosomes are anchored to cell poles and the chromosome is remodeled into an elongated

85 active pumping of ions and water at the cell poles and the division furrow can also achieve the same

86 al missegregation, misorientation of spindle poles and the generation of extra centrosomes, which is

87 henomena context for Juno's passage over the poles and traverse of Jupiter's hazardous inner radiatio

88 structure with a coiled-coil domain for the 'pole' and four helical 'ribs' spanning the N-terminal TR

89 n right insula, right putamen, left temporal pole, and bilateral thalamus) and function (increased br

90 ate cortex, orbital frontal cortex, temporal pole, and insula, which were correlated with cognitive f

91 be independent of their kinetochore, spindle pole, and nuclear envelope localization.

92 Drosophila Shot localizes to mitotic spindle poles, and its knockdown results in an unfocused spindle

93 ossovers; (2) homologs segregate to opposite poles; and (3) sister chromatids segregate to opposite p

94 e GM-NDI was significantly lower in temporal pole, anterior parahippocampal gyrus, and hippocampus of

95 replicative ("R-class") asymmetry dominating POLE-, APOBEC-, and MSI-associated mutations.

96 The poles are cold because they receive the least energy fro

97 We find spindle poles are largely dispensable, and in fact act as brakes

98 Mother cells inheriting old poles are phenotypically distinct and display increased

99 idate the left medial portion of the frontal pole as particularly altered in major depression.

100 l membrane rather than clustered at the cell poles as in wild type chemosensory arrays.

101 port apparatus is localized to the bacterial poles, as is consistent with many T4SS substrates being

102 er, mitotic exit occurred in the presence of pole-associated chromosomes.

103 Posterior pole asymmetry analysis (PPAA) and central cross-section

104 lary RNFL (cpRNFL) thickness using posterior pole asymmetry analysis (PPAA) and investigated the para

105 ocular pulse amplitude (OPA), the posterior pole asymmetry analysis (PPAA), the peripapillary retina

106 with left dorsal anterior insula and frontal pole atrophy.

107 twork contracted laterally along the pole-to-pole axis without a detectable increase in tension.

108 rally informed subdivisions of human frontal pole between depressed patients and comparison subjects

109 Blazed gratings with single and multi-pole blazing passbands are fabricated and measured showi

110 Cdc5 also localizes to the spindle pole bodies (SPBs) from S phase until the end of mitosis

111 known as centrosomes in animals and spindle pole bodies (SPBs) in fungi, are important for the faith

112 Centrosomes, or spindle pole bodies (SPBs) in yeast, are vital mechanical hubs t

113 such as fungi, centrosomes [known as spindle pole bodies (SPBs)] are essential for cell division.

114 saccharomyces pombe harbors MTOCs at spindle pole bodies, transient MTOCs in the division plane (eMTO

115 st components of the MEN localize to spindle pole bodies.

116 d and acceleration of two separating spindle pole bodies.

117 rchitecture of the core of the yeast spindle pole body (SPB) by Bayesian integrative structure modeli

118 In this state, Cdc14 targets the spindle pole body (SPB) component Spc110 to counterbalance its p

119 romyces cerevisiae) the multilayered spindle pole body (SPB) is embedded in the nuclear envelope (NE)

120 The spindle pole body (SPB) of budding yeast duplicates once per cel

121 the septum initiation network to the spindle pole body (SPB, centrosome equivalent) to control mitoti

122 TOCs; mammalian centrosome and yeast spindle pole body [SPB]) nucleate more astral microtubules on on

123 ing the nuclear envelope in mammals, spindle pole body dynamics in fission yeast, and surveillance of

124 ears that centromeres cluster at the spindle pole body in fission yeast.

125 d three of these genes in centrosome/spindle pole body, centromere, and cohesion function.

126 sion based mechanism, centred on the spindle pole body, for the coordination of DNA replication in S.

127 ars the load of chromosome movement far from poles, but we do not know where and how-physically and m

128 bits a strong partitioning bias for old cell poles by a segregation mechanism that is mediated by ter

129 , followed by separation of chromosome-bound poles by outward sliding.

130 mbe, the mitochondria are pushed to the cell poles by the spindle.

131 Compared with cases with wild-type POLE, cases with POLE mutations were younger at diagnosi

132 omosomes associated with one or both spindle poles, causing a significant mitotic delay.

133 becomes a function of HSET-mediated spindle pole clustering.

134 uatorial and posterior sclera, and posterior pole containing the optic nerve head.

135 ealed chorioretinal atrophy of the posterior pole contiguous with the disc in all but 1 patient that

136 S, pSTS, and the right half of the occipital pole (corresponding to Brodmann's area 17 and serving as

137 It inhibits growth at nascent new poles, creating asymmetry in polar growth.

138 and leads to lagging chromosomes and spindle pole defects.

139 grity and suggest that its removal may cause pole delamination and mitotic failure when spindle force

140 s elongatus PCC 7942 oscillates from pole-to-pole despite the potential spatial constraints imposed b

141 of a Ras-like GTPase, MglA, to leading cell poles determines the moving direction of cells.

142 motactic machinery, resulting in proper cell pole development.

143 poral regulation of gene expression and cell pole differentiation.

144 ler mutants result from a decrease in animal pole-directed migration and are independent of endoderm.

145 gonal optic axes interleaved with orthogonal poling directions, is shown to generate high-quality hyp

146 trol of SrTiO3 film thicknesses and electric poling directions.

147 that bcd RNA is sequestered at the anterior pole during oogenesis, is not translated until fertiliza

148 mosomes, with polar microtubules and spindle poles during metaphase through telophase, and partially

149 poles or cause their relocation between cell poles during reversals akin to a spatial toggle switch.

150 Much attention has been focused on POLE exonuclease domain mutations, which occur frequentl

151 X-ray diffraction pole-figure analysis demonstrates that the texture of Li

152 >, <111>, and <751> orientations using X-ray pole figures.

153 issue at wounds set the location of anterior pole formation: a polarized AP axis, the pre-existing mi

154 stress, caps of polymerized pFn at bacterial poles formed part of mechanically loaded adhesion comple

155 bilateral temporal lobe, including temporal pole, fusiform gyrus, and insula, and extending into occ

156 Mutations in the POLD1 and POLE genes encoding DNA polymerases delta (Poldelta) and

157 The heterogeneous human frontal pole has been identified as a node in the dysfunctional

158 The two poles have much in common, such as light climate, temper

159 sel branching, and tangles) or the posterior pole (hyperfluorescent lesions, absence of foveal avascu

160 perior, and central regions of the posterior pole in 83%, 75%, 67%, 54%, and 25% of eyes, respectivel

161 fate-determining kinase DivJ at the stalked pole in Caulobacter, in cousins such as Asticcacaulis, S

162 ucturally defined medial area of the frontal pole in depressed patients.

163 aging: active Cdc42 was enriched at the cell pole in hypophosphorylated cdc24 mutants, while hyperpho

164 liposomes and ProP concentrated at the cell poles in a CL-independent manner.

165 caused by shortening of the spindle to bring poles in contact with the chromosomes, followed by separ

166 localization of calcium ATPases at one cell pole, in a ring pattern, facing the cross-walls, and by

167 te furrows at both the cell equator and cell poles, in both metaphase and anaphase.

168 lectively localized to the animal or vegetal pole, including determinants of somatic and germline fat

169 is divides around the nucleoid near one cell pole, initially capturing approximately one quarter of o

170 for centrosome number regulation and spindle pole integrity specifically in mES cells.

171 gnment at the metaphase plate and in spindle pole integrity.

172 ore, stabilization of the centrosome-spindle pole interface by the CEP215-HSET complex could promote

173 s concept, suggesting that the left temporal pole is crucial for word comprehension.

174 Due to its vasculature, the temporal pole is not commonly completely lesioned in stroke survi

175 ulting ECL of luminol and H2O2 at the anodic poles is monitored using a photomultiplier tube (PMT) or

176 ind that the fraction of Tsr clusters at the poles is smaller in deletion mutants for Tol-Pal than in

177 he Tibetan Plateau (TP), known as the "Third Pole", is a critical zone for atmospheric mercury (Hg) d

178 ip of planarian head blastemas (the anterior pole) is required for anterior-posterior (AP) and medial

179 g, when the cardiac tube grows between fixed poles, is modulated by the progressive breakdown of the

180 isc and amniotic ectoderm occupying opposite poles-is a vital milestone during human embryo implantat

181 ar photonic crystal, i.e., a 2D periodically-poled LiTaO3 crystal.

182 Spindle pole localization of WDR62 and mitotic progression are d

183 Additionally, FtsZ persisted at the poles longer when ZapA and ZauP were overproduced, and f

184 l microtubules grow out from the two spindle poles, make contact with the cell cortex, and then shrin

185 hydrogen content of deposits near the lunar poles may yield insight into this history, because these

186 ion did not induce formation of acentrosomal poles, meaning that multipolar spindles were observable

187 The involvement of the temporal pole-medial prefrontal cortex circuit in a model highly

188 nt events, while abnormalities in a temporal pole-medial prefrontal cortex circuit might speak to the

189 ts knockdown results in an unfocused spindle pole morphology and a disruption of proper spindle orien

190 hat large cytoplasmic volume affects spindle pole morphology, chromosome alignment, and stringency of

191 pment of mitotic aster asymmetry and spindle pole movement towards the subdomain of cortical ER, wher

192 ead, MAPKBP1 is recruited to mitotic spindle poles (MSPs) during the early phases of mitosis where it

193 h of these tumors harbored the P286R hotspot POLE mutation consistent with the ultramutator phenotype

194 Pathogenic somatic POLE mutations were detected in 66 (1.0%) of 6517 colore

195 d with cases with wild-type POLE, cases with POLE mutations were younger at diagnosis (median 54.5 ye

196 e hotly debated existence of a left temporal-pole network for verbal semantics selectively modulated

197 ed using either birefringent or periodically poled nonlinear crystals, which requires careful dispers

198 iography, we have ascertained that posterior pole nonperfusion of more than 10 DA remains the key ris

199 The HIAPER Pole-to-Pole Observation (HIPPO) program from 2009 to 2011 inter

200 oceans for climate; indeed, the peak equator-pole ocean heat transport on Earth peaks at almost half

201 rms that trap beta1-integrins on the luminal pole of bronchial epithelial cells.

202 inated, unipolar localization at the leading pole of each cell.

203 t APYS1 caused gross malformation of the old pole of M. tuberculosis, with eventual lysis.

204 sufficiently large magnetic fields by writer pole of magnetic hard disks, especially for achieving in

205 reasing incidences toward the multibacillary pole of the clinical spectrum.

206 e process of cellularization in the anterior pole of the early Drosophila embryo to explore how cells

207 ction, decussates at the level of the caudal pole of the facial nerve nucleus in the rostral medulla

208 PA2, OFT progenitors migrate to the arterial pole of the heart and differentiate into OFT lineages.

209 ago due to inoperable mass in the mid-lower pole of the left kidney diagnosed as clear cell RCC with

210 iliated cells that line the posterior dorsal pole of the middle ear cavity which was previously thoug

211 d OFT progenitors co-migrate to the arterial pole of the zebrafish heart tube soon after their specif

212 kinase 1 and Aurora-A, targeted Hsp72 to the poles of cells with amplified centrosomes.

213 rate to HDRs shown to be localized near cell poles of dividing chromosomes, thus mediating equipartit

214 ion septum is necessary for constructing new poles of progeny cells, and cells cannot elongate withou

215 vironments near the locations of the pre-TPW poles of rotation, and a possible link between volcanic

216 d on the phagosomal membrane adjacent to the poles of the bacterium.

217 dispersal capabilities can inhabit opposite poles of the Earth, and dominate extreme environments ov

218 ge microtubule asters that grow out from the poles of the first mitotic spindle.

219 into cardiomyocytes that are accreted to the poles of the heart tube over a well-defined developmenta

220 neuronal activity at the dorsal and ventral poles of the hippocampus have shown that the scale of sp

221 of cell wall material to create the new cell poles of the separated daughter cells.

222 mation of centrosomes, the organelles at the poles of the spindle that can persist as microtubule org

223 ect the flow as an accretion column onto the poles of the white dwarf, a star subclass known as AM He

224 n an oxide electrode through electrochemical poling of a SOC at 2 volts for a few seconds.

225 progenitors migrate directly to the arterial pole, OFT progenitors become temporarily sequestered in

226 lated in the periphery (beyond the posterior pole), only 1 (7.7%) eye developed new vessels, odds rat

227 e visual stimulus, but also at the occipital pole (OP), corresponding to the foveal representation, e

228 Strikingly, the occipital pole (OP), representing foveal locations, showed higher

229 arized motility proteins to the correct cell poles or cause their relocation between cell poles durin

230 termini competing for occupancy of the other pole), or a reverse J-shaped motif (ester moiety and tur

231 he same velocity as outwardly moving spindle poles, or both.

232 ntrated zones undergoing coordinated pole-to-pole oscillation to help ensure that the cytokinetic div

233 go speed, evolving from diffusion to pole-to-pole oscillation, local excursions, and, finally, immobi

234 the geometrical chamber parameters: pole-to-pole oscillations, spiral rotations, and traveling waves

235 sequentially mapped in both atria with a 20-pole PentaRay catheter.

236 the effect of the IYO/RIMA pathway on xylem pole pericycle cells, we provide compelling evidence rei

237 data demonstrate a major role for the phloem-pole pericycle in regulating phloem unloading in roots.

238 es and proteins are diverted into the phloem-pole pericycle, a tissue connected to the protophloem by

239 ese proteins remain restricted to the phloem-pole pericycle.

240 By counteracting MglA near lagging cell poles, PlpA reinforces the polarity axis of MglA and thu

241 the previously implicated genes APC, MUTYH, POLE, POLD1, and NTHL1, although a hereditary etiology i

242 In the posterior pole, positive staining was only observed at the level o

243 ing kinetics are observed through an in situ poling process using a dark-field transmission electron

244 Anterior pole progenitors were specified at the pre-existing midl

245 Anterior pole progenitors were specified broadly on the dorsal-ve

246 We also identified POLE proofreading domain mutations in three endometrioid

247 utations that impair DNA polymerase epsilon (POLE) proofreading.

248 commonly injured orbitofrontal and temporal pole regions CoV was <3.5% for all parameters.

249 e amplification of temperature change at the poles relative to global temperature change) has been st

250 ron numbers across the rostral to the caudal pole resembles primates.

251 ed) enriched mRNAs at the vegetal and animal pole, respectively.

252 mprehensively interrogate animal and vegetal pole RNAs in the fully grown Xenopus laevis oocyte.

253 ent scar (55%) or fovea (16%), and posterior pole scanning for new tumors (11%).

254 merization are sufficient to promote spindle pole separation and the assembly of bipolar spindle in t

255 surements as well as customized detection of poles, septa, fluorescent foci and organelles, determine

256 Images of Jupiter's poles show a chaotic scene, unlike Saturn's poles.

257 ic kilometers of ice have accumulated at the poles since the end of the last ice age ~370,000 years a

258 Furthermore, cells within the anterior pole skewed toward the trunk along their long axis relat

259 ricting fzlA mutant strain develops 'pointy' poles, suggesting that FzlA influences the relative cont

260 reated mice showed better performance in the pole test compared with TAT.beta-Gal-treated controls.

261 ere observed more frequently in the anterior pole than in the embryo trunk.

262 h of the loser) was three times lower at the poles than in the tropics.

263 stral microtubules on one of the two spindle poles than the other.

264 potential pathways operating at the vegetal pole that highlight where future investigations might be

265 This age helps define a key paleomagnetic pole that positions the Kaapvaal Craton at equatorial la

266 phery of the array, forming multiple nascent poles that then coalesce until bipolarity is achieved.

267 tified a mutation in DNA polymerase epsilon (POLE) that associated with an ultramutator phenotype.

268 as increased thickness of the right frontal pole, the right lateral parietal lobules, and the left p

269 forms on the cortex adjacent to one spindle pole, then ingresses down the length of the spindle to p

270 microtubules emanating from the same spindle pole, they activate another mechanosensitive mechanism t

271 zation and then redistributes to the spindle pole to ensure faithful spindle architecture.

272 ABAA receptor subunits from the dorsolateral pole to ventromedial extremities.

273 ally increases from one end of the cell (old pole) to the other (new pole).

274 Once the spindle pole-to-kinetochore contact has been made, the homologue

275 e the network contracted laterally along the pole-to-pole axis without a detectable increase in tensi

276 chococcus elongatus PCC 7942 oscillates from pole-to-pole despite the potential spatial constraints i

277 The HIAPER Pole-to-Pole Observation (HIPPO) program from 2009 to 20

278 in concentrated zones undergoing coordinated pole-to-pole oscillation to help ensure that the cytokin

279 the cargo speed, evolving from diffusion to pole-to-pole oscillation, local excursions, and, finally

280 ndent on the geometrical chamber parameters: pole-to-pole oscillations, spiral rotations, and traveli

281 salt bridges that join the N- and C-terminal poles together.

282 ate can be injected directly into the foetal pole under transvaginal ultrasound guidance in order to

283 he important patterning role of the anterior pole, understanding how it becomes localized during rege

284 s peripheral schisis involving the posterior pole, vascular abnormalities and haemorrhages.

285 egion specificity in the left medial frontal pole volume in depressed patients was demonstrated.

286 In a second approach, frontal pole volume was compared by subdivision-naive multivaria

287 Frontal pole volume was first compared between depressed patient

288 =0.002) between serum VEGF and total frontal pole volume was found in patients with schizophrenia/sch

289 This pole-ward drift is facilitated by anterograde delivery o

290 ecome more sub-tropical, i.e. made dryer via pole-ward expanding subtropical subsidence.

291 old-trapped and processed at Charon's winter pole was proposed as an explanation for the dark colorat

292 a and higher thickness in bilateral temporal pole were found in NTSCUs versus healthy control subject

293 ing of the ANE territory around the anterior pole, whereas high expression levels of sFRP1/5 antagoni

294 ention of anillin and septin in the anterior pole, which are cytokinesis proteins that our genetic da

295 tiating regions, and continues in the venous pole, which gives rise to the SV.

296 ied sequential left-right asymmetries at the poles, which bias the buckling in opposite directions, t

297 dorsolateral prefrontal cortex and temporal pole, while cool executive functions were associated wit

298 tra amplified centrosomes clustered into two poles whose pseudo-bipolar spindles exhibit reduced fide

299 of awake, head-fixed mice as they explored a pole with their whiskers, and simultaneously measured bo

300 ages divided into 3 zones (zone 1 [posterior pole], zone 2 [midperiphery], and zone 3 [far periphery]